Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 19 |
|---|---|
| ensemblid | ENSG00000165029.17 |
| hgncid | 29 |
| symbol | ABCA1 |
| name | ATP binding cassette subfamily A member 1 |
| refseq_nuc | NM_005502.4 |
| refseq_prot | NP_005493.2 |
| ensembl_nuc | ENST00000374736.8 |
| ensembl_prot | ENSP00000363868.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 104781006 |
| end | 104928155 |
| strand | - |
| ver | v1.2 |
| region | chr9:104781006-104928155 |
| region5000 | chr9:104776006-104933155 |
| regionname0 | ABCA1_chr9_104781006_104928155 |
| regionname5000 | ABCA1_chr9_104776006_104933155 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2261 | 59 | 2 | 20 | 21 | 5 | 10 | 16 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002 | 0/0 | 2261 | 39 | 31 | 1 | 7 | 0 | 0 | 4 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003 | 0/0 | 2261 | 31 | 3 | 5 | 19 | 1 | 3 | 13 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004 | 1/0 | 2261 | 28 | 15 | 5 | 2 | 1 | 4 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005 | 0/0 | 2261 | 25 | 12 | 3 | 4 | 0 | 6 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006 | 0/0 | 2261 | 20 | 0 | 4 | 16 | 0 | 0 | 13 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007 | 0/0 | 2261 | 18 | 0 | 2 | 13 | 0 | 3 | 8 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008 | 0/0 | 2261 | 14 | 5 | 2 | 5 | 0 | 2 | 5 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009 | 0/0 | 2261 | 13 | 2 | 3 | 5 | 1 | 2 | 5 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010 | 0/0 | 2261 | 11 | 0 | 8 | 2 | 0 | 1 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0011 | 0/0 | 2261 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012 | 0/0 | 2261 | 8 | 4 | 2 | 2 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0013 | 0/0 | 2261 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014 | 0/0 | 2261 | 5 | 0 | 0 | 3 | 2 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0015 | 0/0 | 2261 | 4 | 3 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0016 | 0/0 | 2261 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0017 | 0/0 | 2261 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0018 | 0/0 | 2261 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0019 | 0/0 | 2261 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0020 | 0/0 | 2261 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0021 | 0/0 | 2261 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0022 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0023 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0024 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0025 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0026 | 0/0 | 2261 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0027 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0028 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0029 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0030 | 0/0 | 2261 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0031 | 0/0 | 2261 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0032 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0033 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0034 | 0/0 | 2261 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0035 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0036 | 0/0 | 2261 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0037 | 0/0 | 2261 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0038 | 0/0 | 2261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 6786 | 42 | 2 | 16 | 10 | 5 | 8 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0002 | 0/0 | 6786 | 18 | 0 | 3 | 14 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0003 | 0/0 | 6786 | 17 | 0 | 2 | 12 | 0 | 3 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0004 | 0/0 | 6786 | 11 | 0 | 1 | 10 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0005 | 0/0 | 6786 | 11 | 0 | 2 | 9 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0006 | 0/0 | 6786 | 10 | 3 | 0 | 5 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0007 | 0/0 | 6786 | 9 | 0 | 8 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0008 | 1/0 | 6786 | 9 | 0 | 2 | 2 | 1 | 3 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0009 | 0/0 | 6786 | 8 | 0 | 1 | 5 | 1 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0010 | 0/0 | 6786 | 7 | 7 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0011 | 0/0 | 6786 | 7 | 1 | 0 | 6 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0012 | 0/0 | 6786 | 7 | 0 | 3 | 4 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0013 | 0/0 | 6786 | 6 | 0 | 0 | 6 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0014 | 0/0 | 6786 | 5 | 1 | 1 | 3 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0015 | 0/0 | 6786 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0016 | 0/0 | 6786 | 4 | 0 | 2 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0017 | 0/0 | 6786 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0018 | 0/0 | 6786 | 4 | 0 | 1 | 3 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0019 | 0/0 | 6786 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0020 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0021 | 0/0 | 6786 | 3 | 2 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0022 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0023 | 0/0 | 6786 | 3 | 0 | 0 | 1 | 2 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0024 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0025 | 0/0 | 6786 | 3 | 2 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0026 | 0/0 | 6786 | 3 | 1 | 0 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0027 | 0/0 | 6786 | 3 | 0 | 0 | 1 | 1 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0028 | 0/0 | 6786 | 3 | 0 | 2 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0029 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0030 | 0/0 | 6786 | 2 | 0 | 0 | 1 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0031 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0032 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0033 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0034 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0035 | 0/0 | 6786 | 2 | 0 | 1 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0036 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0037 | 0/0 | 6786 | 2 | 1 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0038 | 0/0 | 6786 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0039 | 0/0 | 6786 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0040 | 0/0 | 6786 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0041 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0042 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0043 | 0/0 | 6786 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0044 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0045 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0046 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0047 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0048 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0049 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0050 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0051 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0052 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0053 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0054 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0055 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0056 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0057 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0058 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0059 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0060 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0061 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0062 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0063 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0064 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0065 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0066 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0067 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0068 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0069 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0070 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0071 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0072 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0073 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0074 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0075 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0076 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0077 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0078 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0079 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0080 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0081 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0082 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0083 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0084 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0085 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0086 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0087 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0088 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0089 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0090 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0091 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0092 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0093 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0094 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0095 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0096 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0097 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0098 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0099 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0100 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0101 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0102 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0103 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0104 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0105 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0106 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0107 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0108 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0109 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0110 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0111 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0112 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0113 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| c0114 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3623 | 59 | 29 | 16 | 2 | 2 | 9 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0002 | 0/0 | 3619 | 53 | 12 | 10 | 30 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0003 | 0/0 | 3622 | 31 | 3 | 8 | 16 | 1 | 3 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0004 | 1/0 | 3623 | 24 | 4 | 6 | 6 | 2 | 5 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0005 | 0/0 | 3624 | 17 | 15 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0006 | 0/0 | 3623 | 16 | 0 | 2 | 10 | 0 | 4 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0007 | 0/0 | 3623 | 15 | 5 | 4 | 6 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0008 | 0/0 | 3622 | 10 | 10 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0009 | 0/0 | 3624 | 9 | 0 | 3 | 2 | 0 | 4 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0010 | 0/0 | 3620 | 9 | 0 | 5 | 4 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0011 | 0/0 | 3624 | 6 | 0 | 1 | 4 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0012 | 0/0 | 3624 | 5 | 0 | 0 | 5 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0013 | 0/0 | 3619 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0014 | 0/0 | 3622 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0015 | 0/0 | 3623 | 3 | 2 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0016 | 0/0 | 3622 | 3 | 0 | 1 | 1 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0017 | 0/0 | 3622 | 3 | 0 | 0 | 0 | 1 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0018 | 0/0 | 3623 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0019 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0020 | 0/0 | 3623 | 2 | 0 | 0 | 1 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0021 | 0/0 | 3619 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0022 | 0/0 | 3623 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0023 | 0/0 | 3622 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0024 | 0/0 | 3619 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0025 | 0/0 | 3623 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0026 | 0/0 | 3623 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0027 | 0/0 | 3622 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0028 | 0/0 | 3620 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0029 | 0/0 | 3623 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0030 | 0/0 | 3619 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0031 | 0/0 | 3623 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0032 | 0/0 | 3620 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0033 | 0/0 | 3621 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0034 | 0/0 | 3622 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0035 | 0/0 | 3623 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0036 | 0/0 | 3621 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0037 | 0/0 | 3623 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0038 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0039 | 0/0 | 3622 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0040 | 0/0 | 3623 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0041 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0042 | 0/0 | 3622 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0043 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0044 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0045 | 0/0 | 3623 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0046 | 0/0 | 3623 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0047 | 0/0 | 3623 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0048 | 0/0 | 3620 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0049 | 0/0 | 3623 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0050 | 0/0 | 3620 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0051 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| t0052 | 0/0 | 3619 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 6786 | 42 | 2 | 16 | 10 | 5 | 8 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0005 | 0/0 | 6786 | 11 | 0 | 2 | 9 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0035 | 0/0 | 6786 | 2 | 0 | 1 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0092 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0097 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0108 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0109 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0011 | 0/0 | 6786 | 7 | 1 | 0 | 6 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0015 | 0/0 | 6786 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0017 | 0/0 | 6786 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0024 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0025 | 0/0 | 6786 | 3 | 2 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0031 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0032 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0033 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0037 | 0/0 | 6786 | 2 | 1 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0046 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0057 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0058 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0059 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0074 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0075 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0078 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0081 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0085 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002 | 0/0 | 6786 | 18 | 0 | 3 | 14 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0009 | 0/0 | 6786 | 8 | 0 | 1 | 5 | 1 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0038 | 0/0 | 6786 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0056 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0076 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0077 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0008 | 1/0 | 6786 | 9 | 0 | 2 | 2 | 1 | 3 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0029 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0042 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0043 | 0/0 | 6786 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0044 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0064 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0066 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0087 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0096 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0098 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0099 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0107 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0112 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0113 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0114 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0014 | 0/0 | 6786 | 5 | 1 | 1 | 3 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0016 | 0/0 | 6786 | 4 | 0 | 2 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0022 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0026 | 0/0 | 6786 | 3 | 1 | 0 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0036 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0039 | 0/0 | 6786 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0051 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0052 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0070 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0071 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0082 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0084 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004 | 0/0 | 6786 | 11 | 0 | 1 | 10 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0012 | 0/0 | 6786 | 7 | 0 | 3 | 4 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0063 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0089 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003 | 0/0 | 6786 | 17 | 0 | 2 | 12 | 0 | 3 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0090 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006 | 0/0 | 6786 | 10 | 3 | 0 | 5 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0047 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0048 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0049 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0069 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0018 | 0/0 | 6786 | 4 | 0 | 1 | 3 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0021 | 0/0 | 6786 | 3 | 2 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0027 | 0/0 | 6786 | 3 | 0 | 0 | 1 | 1 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0028 | 0/0 | 6786 | 3 | 0 | 2 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010c0007 | 0/0 | 6786 | 9 | 0 | 8 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010c0030 | 0/0 | 6786 | 2 | 0 | 0 | 1 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0011c0010 | 0/0 | 6786 | 7 | 7 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0011c0055 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0040 | 0/0 | 6786 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0041 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0065 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0093 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0102 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0105 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0013c0013 | 0/0 | 6786 | 6 | 0 | 0 | 6 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0023 | 0/0 | 6786 | 3 | 0 | 0 | 1 | 2 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0053 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0054 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0015c0020 | 0/0 | 6786 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0015c0061 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0016c0019 | 0/0 | 6786 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0017c0034 | 0/0 | 6786 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0018c0079 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0018c0080 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0019c0086 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0019c0106 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0020c0045 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0021c0060 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0022c0050 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0023c0072 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0024c0073 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0025c0083 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0026c0111 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0027c0062 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0028c0095 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0029c0110 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0030c0100 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0031c0067 | 0/0 | 6786 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0032c0104 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0033c0101 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0034c0103 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0035c0091 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0036c0094 | 0/0 | 6786 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0037c0088 | 0/0 | 6786 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0038c0068 | 0/0 | 6786 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 10408 | 15 | 1 | 7 | 2 | 2 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0002 | 0/0 | 10404 | 3 | 0 | 2 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0003 | 0/0 | 10407 | 5 | 0 | 2 | 2 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0004 | 0/0 | 10408 | 3 | 0 | 1 | 0 | 1 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0006 | 0/0 | 10408 | 6 | 0 | 2 | 2 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0007 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0011 | 0/0 | 10409 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0012 | 0/0 | 10409 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0023 | 0/0 | 10407 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0039 | 0/0 | 10407 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0043 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0049 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0001t0052 | 0/0 | 10404 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0005t0001 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0005t0002 | 0/0 | 10404 | 8 | 0 | 1 | 7 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0005t0004 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0005t0010 | 0/0 | 10405 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0035t0004 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0035t0009 | 0/0 | 10409 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0092t0012 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0097t0001 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0108t0002 | 0/0 | 10404 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0001c0109t0001 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0011t0004 | 0/0 | 10408 | 3 | 1 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0011t0007 | 0/0 | 10408 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0011t0012 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0011t0020 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0015t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0015t0004 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0015t0013 | 0/0 | 10404 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0015t0031 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0017t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0017t0015 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0017t0026 | 0/0 | 10408 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0024t0008 | 0/0 | 10407 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0025t0007 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0025t0008 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0025t0015 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0031t0001 | 0/0 | 10408 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0032t0001 | 0/0 | 10408 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0033t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0033t0032 | 0/0 | 10405 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0037t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0037t0011 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0046t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0057t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0058t0007 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0059t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0074t0027 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0075t0027 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0078t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0081t0013 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0002c0085t0008 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002t0002 | 0/0 | 10404 | 12 | 0 | 3 | 9 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002t0003 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002t0007 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002t0010 | 0/0 | 10405 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002t0014 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002t0028 | 0/0 | 10405 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0002t0050 | 0/0 | 10405 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0009t0001 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0009t0003 | 0/0 | 10407 | 4 | 0 | 0 | 2 | 1 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0009t0006 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0009t0046 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0009t0051 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0038t0003 | 0/0 | 10407 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0038t0005 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0056t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0076t0002 | 0/0 | 10404 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0003c0077t0005 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0008t0001 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0008t0003 | 0/0 | 10407 | 3 | 0 | 2 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0008t0004 | 1/0 | 10408 | 2 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0008t0006 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0008t0016 | 0/0 | 10407 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0008t0028 | 0/0 | 10405 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0029t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0029t0005 | 0/0 | 10409 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0042t0008 | 0/0 | 10407 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0043t0003 | 0/0 | 10407 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0044t0007 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0044t0013 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0064t0007 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0066t0008 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0087t0009 | 0/0 | 10409 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0096t0007 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0098t0005 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0099t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0107t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0112t0005 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0113t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0004c0114t0005 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0014t0003 | 0/0 | 10407 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0014t0005 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0014t0006 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0014t0011 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0016t0001 | 0/0 | 10408 | 3 | 0 | 2 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0016t0011 | 0/0 | 10409 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0022t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0022t0021 | 0/0 | 10404 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0026t0004 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0026t0009 | 0/0 | 10409 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0026t0024 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0036t0001 | 0/0 | 10408 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0039t0017 | 0/0 | 10407 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0051t0019 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0052t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0070t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0071t0041 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0082t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0005c0084t0014 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0002 | 0/0 | 10404 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0003 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0004 | 0/0 | 10408 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0005 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0006 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0010 | 0/0 | 10405 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0011 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0042 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0004t0045 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0012t0001 | 0/0 | 10408 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0012t0002 | 0/0 | 10404 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0012t0010 | 0/0 | 10405 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0063t0003 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0006c0089t0003 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0002 | 0/0 | 10404 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0003 | 0/0 | 10407 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0004 | 0/0 | 10408 | 3 | 0 | 0 | 2 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0006 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0009 | 0/0 | 10409 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0011 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0014 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0016 | 0/0 | 10407 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0020 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0033 | 0/0 | 10406 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0003t0035 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0007c0090t0007 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0001 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0003 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0005 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0006 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0007 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0012 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0014 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0015 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0022 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0006t0047 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0047t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0048t0030 | 0/0 | 10404 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0049t0004 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0008c0069t0008 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0018t0003 | 0/0 | 10407 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0018t0004 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0018t0038 | 0/0 | 10409 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0021t0001 | 0/0 | 10408 | 2 | 1 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0021t0004 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0027t0004 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0027t0006 | 0/0 | 10408 | 2 | 0 | 0 | 1 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0028t0009 | 0/0 | 10409 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0009c0028t0048 | 0/0 | 10405 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010c0007t0002 | 0/0 | 10404 | 4 | 0 | 4 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010c0007t0003 | 0/0 | 10407 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010c0007t0010 | 0/0 | 10405 | 4 | 0 | 4 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010c0030t0001 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0010c0030t0022 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0011c0010t0005 | 0/0 | 10409 | 6 | 6 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0011c0010t0037 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0011c0055t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0040t0029 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0040t0040 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0041t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0041t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0065t0007 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0093t0001 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0102t0007 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0012c0105t0024 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0013c0013t0002 | 0/0 | 10404 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0013c0013t0003 | 0/0 | 10407 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0013c0013t0025 | 0/0 | 10408 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0023t0007 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0023t0017 | 0/0 | 10407 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0023t0036 | 0/0 | 10406 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0053t0002 | 0/0 | 10404 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0014c0054t0010 | 0/0 | 10405 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0015c0020t0001 | 0/0 | 10408 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0015c0020t0004 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0015c0061t0001 | 0/0 | 10408 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0016c0019t0006 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0016c0019t0018 | 0/0 | 10408 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0017c0034t0001 | 0/0 | 10408 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0018c0079t0004 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0018c0080t0004 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0019c0086t0003 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0019c0106t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0020c0045t0002 | 0/0 | 10404 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0021c0060t0001 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0022c0050t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0023c0072t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0024c0073t0019 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0025c0083t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0026c0111t0002 | 0/0 | 10404 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0027c0062t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0028c0095t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0029c0110t0002 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0030c0100t0009 | 0/0 | 10409 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0031c0067t0006 | 0/0 | 10408 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0032c0104t0005 | 0/0 | 10409 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0033c0101t0001 | 0/0 | 10408 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0034c0103t0007 | 0/0 | 10408 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0035c0091t0008 | 0/0 | 10407 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0036c0094t0009 | 0/0 | 10409 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0037c0088t0034 | 0/0 | 10407 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| a0038c0068t0044 | 0/0 | 10404 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | copy fasta | chr9 | 104776006 | 104933155 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0012g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0023g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0023g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0039g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0043g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0049g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0001t0052g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0005t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0035t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0035t0009g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0092t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0097t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0108t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0001c0109t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0011t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0011t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0011t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0011t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0011t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0011t0012g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0011t0020g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0015t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0015t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0015t0013g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0015t0013g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0015t0031g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0017t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0017t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0017t0026g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0017t0026g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0024t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0024t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0024t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0025t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0025t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0025t0015g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0031t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0031t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0032t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0032t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0033t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0033t0032g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0037t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0037t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0046t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0057t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0058t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0059t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0074t0027g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0075t0027g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0078t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0081t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0002c0085t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0010g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0014g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0028g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0002t0050g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0046g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0009t0051g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0038t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0038t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0056t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0076t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0003c0077t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0004g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0016g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0008t0028g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0029t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0029t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0029t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0042t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0042t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0043t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0043t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0044t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0044t0013g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0064t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0066t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0087t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0096t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0098t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0099t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0107t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0112t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0113t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0004c0114t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0014t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0014t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0014t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0014t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0014t0011g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0016t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0016t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0016t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0016t0011g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0022t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0022t0021g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0022t0021g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0026t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0026t0009g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0026t0024g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0036t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0036t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0039t0017g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0039t0017g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0051t0019g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0052t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0070t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0071t0041g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0082t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0005c0084t0014g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0011g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0042g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0004t0045g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0012t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0012t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0012t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0012t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0012t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0012t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0012t0010g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0063t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0006c0089t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0011g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0014g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0016g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0016g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0020g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0033g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0003t0035g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0007c0090t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0014g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0022g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0006t0047g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0047t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0048t0030g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0049t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0008c0069t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0018t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0018t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0018t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0018t0038g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0021t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0021t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0021t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0027t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0027t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0027t0006g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0028t0009g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0028t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0009c0028t0048g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0010g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0010g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0010g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0007t0010g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0030t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0010c0030t0022g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0010t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0010t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0010t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0010t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0010t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0010t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0010t0037g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0011c0055t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0040t0029g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0040t0040g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0041t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0041t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0065t0007g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0093t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0102t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0012c0105t0024g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0013c0013t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0013c0013t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0013c0013t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0013c0013t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0013c0013t0025g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0013c0013t0025g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0014c0023t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0014c0023t0017g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0014c0023t0036g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0014c0053t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0014c0054t0010g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0015c0020t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0015c0020t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0015c0020t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0015c0061t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0016c0019t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0016c0019t0018g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0016c0019t0018g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0016c0019t0018g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0017c0034t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0017c0034t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0018c0079t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0018c0080t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0019c0086t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0019c0106t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0020c0045t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0021c0060t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0022c0050t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0023c0072t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0024c0073t0019g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0025c0083t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0026c0111t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0027c0062t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0028c0095t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0029c0110t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0030c0100t0009g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0031c0067t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0032c0104t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0033c0101t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0034c0103t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0035c0091t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0036c0094t0009g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0037c0088t0034g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| a0038c0068t0044g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0052 | g0318 | EUR | GBR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00099 | hp2 | a0003 | c0009 | t0003 | g0209 | EUR | GBR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00408 | hp1 | a0026 | c0111 | t0002 | g0065 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00408 | hp2 | a0007 | c0003 | t0035 | g0061 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00423 | hp1 | a0005 | c0014 | t0006 | g0052 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00423 | hp2 | a0003 | c0002 | t0014 | g0066 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00544 | hp2 | a0001 | c0108 | t0002 | g0113 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00558 | hp1 | a0003 | c0009 | t0051 | g0145 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00558 | hp2 | a0006 | c0012 | t0002 | g0060 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00609 | hp1 | a0012 | c0040 | t0040 | g0055 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00609 | hp2 | a0006 | c0004 | t0004 | g0227 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00621 | hp1 | a0003 | c0002 | t0002 | g0041 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00621 | hp2 | a0007 | c0003 | t0011 | g0072 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00642 | hp1 | a0005 | c0016 | t0001 | g0009 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00673 | hp1 | a0003 | c0002 | t0028 | g0261 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00673 | hp2 | a0002 | c0037 | t0011 | g0116 | EAS | CHS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00738 | hp1 | a0003 | c0009 | t0001 | g0279 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00741 | hp1 | a0009 | c0018 | t0004 | g0292 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG00741 | hp2 | a0010 | c0007 | t0010 | g0200 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01070 | hp1 | a0009 | c0028 | t0009 | g0092 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01070 | hp2 | a0001 | c0001 | t0011 | g0085 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01071 | hp1 | a0009 | c0028 | t0009 | g0093 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01071 | hp2 | a0001 | c0097 | t0001 | g0106 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01081 | hp1 | a0004 | c0008 | t0003 | g0294 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01081 | hp2 | a0008 | c0048 | t0030 | g0022 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01099 | hp1 | a0004 | c0096 | t0007 | g0020 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01099 | hp2 | a0010 | c0007 | t0010 | g0201 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01106 | hp1 | a0012 | c0065 | t0007 | g0182 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01109 | hp1 | a0018 | c0079 | t0004 | g0314 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01168 | hp2 | a0001 | c0001 | t0039 | g0246 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01169 | hp1 | a0007 | c0003 | t0016 | g0242 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01175 | hp2 | a0005 | c0016 | t0001 | g0010 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01192 | hp2 | a0004 | c0064 | t0007 | g0175 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01243 | hp1 | a0006 | c0012 | t0001 | g0212 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01243 | hp2 | a0018 | c0080 | t0004 | g0107 | AMR | PUR | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01255 | hp1 | a0006 | c0004 | t0004 | g0067 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01255 | hp2 | a0002 | c0025 | t0015 | g0283 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01257 | hp1 | a0037 | c0088 | t0034 | g0298 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01257 | hp2 | a0008 | c0049 | t0004 | g0103 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01261 | hp2 | a0010 | c0007 | t0010 | g0185 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01346 | hp1 | a0010 | c0007 | t0010 | g0139 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01346 | hp2 | a0003 | c0038 | t0003 | g0293 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01361 | hp1 | a0001 | c0005 | t0001 | g0050 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01361 | hp2 | a0006 | c0012 | t0001 | g0090 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01433 | hp1 | a0010 | c0007 | t0002 | g0012 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0058 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01496 | hp1 | a0005 | c0014 | t0003 | g0173 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0047 | AMR | CLM | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01515 | hp1 | a0001 | c0001 | t0049 | g0034 | EUR | IBS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01515 | hp2 | a0014 | c0023 | t0036 | g0104 | EUR | IBS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01517 | hp1 | a0014 | c0023 | t0017 | g0105 | EUR | IBS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01884 | hp1 | a0002 | c0078 | t0001 | g0216 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01884 | hp2 | a0002 | c0017 | t0026 | g0163 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01891 | hp1 | a0005 | c0071 | t0041 | g0311 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01891 | hp2 | a0004 | c0042 | t0008 | g0158 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01934 | hp2 | a0010 | c0007 | t0002 | g0013 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01952 | hp1 | a0004 | c0043 | t0003 | g0136 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01952 | hp2 | a0012 | c0093 | t0001 | g0108 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01975 | hp1 | a0010 | c0007 | t0002 | g0015 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01975 | hp2 | a0001 | c0035 | t0009 | g0071 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01978 | hp2 | a0006 | c0012 | t0010 | g0198 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01993 | hp1 | a0021 | c0060 | t0001 | g0078 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG01993 | hp2 | a0010 | c0007 | t0002 | g0125 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02004 | hp1 | a0007 | c0003 | t0003 | g0014 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02004 | hp2 | a0003 | c0002 | t0002 | g0069 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02027 | hp1 | a0002 | c0011 | t0007 | g0247 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02027 | hp2 | a0006 | c0004 | t0003 | g0190 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02055 | hp1 | a0009 | c0021 | t0001 | g0174 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02055 | hp2 | a0005 | c0036 | t0001 | g0091 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02056 | hp1 | a0007 | c0003 | t0009 | g0156 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02056 | hp2 | a0014 | c0053 | t0002 | g0146 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02080 | hp1 | a0003 | c0002 | t0002 | g0126 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02083 | hp1 | a0013 | c0013 | t0025 | g0032 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02083 | hp2 | a0005 | c0084 | t0014 | g0215 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02129 | hp1 | a0007 | c0003 | t0004 | g0027 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02129 | hp2 | a0013 | c0013 | t0025 | g0033 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02132 | hp1 | a0001 | c0001 | t0012 | g0144 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02132 | hp2 | a0003 | c0009 | t0003 | g0138 | EAS | KHV | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02145 | hp1 | a0011 | c0010 | t0005 | g0255 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02145 | hp2 | a0009 | c0021 | t0004 | g0204 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02148 | hp1 | a0003 | c0002 | t0002 | g0040 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02155 | hp1 | a0010 | c0007 | t0003 | g0149 | EAS | CDX | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02155 | hp2 | a0002 | c0011 | t0004 | g0263 | EAS | CDX | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02257 | hp1 | a0004 | c0042 | t0008 | g0083 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02257 | hp2 | a0002 | c0017 | t0026 | g0276 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02258 | hp1 | a0005 | c0022 | t0021 | g0141 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02258 | hp2 | a0002 | c0031 | t0001 | g0152 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02280 | hp1 | a0032 | c0104 | t0005 | g0168 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02280 | hp2 | a0002 | c0058 | t0007 | g0143 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02293 | hp1 | a0004 | c0008 | t0003 | g0197 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02293 | hp2 | a0001 | c0005 | t0002 | g0017 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02300 | hp1 | a0034 | c0103 | t0007 | g0240 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02300 | hp2 | a0003 | c0002 | t0002 | g0070 | AMR | PEL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02451 | hp1 | a0038 | c0068 | t0044 | g0272 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02451 | hp2 | a0005 | c0014 | t0005 | g0245 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02572 | hp1 | a0022 | c0050 | t0001 | g0166 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02572 | hp2 | a0012 | c0102 | t0007 | g0188 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02602 | hp1 | a0003 | c0002 | t0050 | g0068 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0297 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02615 | hp1 | a0004 | c0098 | t0005 | g0303 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02615 | hp2 | a0017 | c0034 | t0001 | g0153 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02622 | hp1 | a0015 | c0020 | t0004 | g0005 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02622 | hp2 | a0004 | c0114 | t0005 | g0304 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02630 | hp1 | a0004 | c0029 | t0005 | g0162 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02630 | hp2 | a0008 | c0006 | t0015 | g0095 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02647 | hp1 | a0003 | c0056 | t0001 | g0288 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02647 | hp2 | a0024 | c0073 | t0019 | g0231 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02698 | hp1 | a0001 | c0109 | t0001 | g0232 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0193 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02717 | hp1 | a0028 | c0095 | t0002 | g0114 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02717 | hp2 | a0015 | c0020 | t0001 | g0006 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02723 | hp1 | a0033 | c0101 | t0001 | g0308 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02723 | hp2 | a0002 | c0032 | t0001 | g0317 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02735 | hp1 | a0005 | c0016 | t0011 | g0075 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02735 | hp2 | a0009 | c0021 | t0001 | g0189 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0054 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02738 | hp2 | a0004 | c0008 | t0003 | g0289 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02809 | hp1 | a0004 | c0113 | t0002 | g0159 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02809 | hp2 | a0003 | c0038 | t0005 | g0307 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02818 | hp1 | a0002 | c0081 | t0013 | g0277 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02818 | hp2 | a0002 | c0011 | t0004 | g0112 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02886 | hp1 | a0011 | c0010 | t0005 | g0287 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02886 | hp2 | a0002 | c0025 | t0007 | g0237 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02895 | hp1 | a0002 | c0085 | t0008 | g0142 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02895 | hp2 | a0002 | c0015 | t0013 | g0305 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02896 | hp1 | a0002 | c0024 | t0008 | g0008 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02896 | hp2 | a0004 | c0029 | t0005 | g0023 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02897 | hp1 | a0002 | c0024 | t0008 | g0003 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02897 | hp2 | a0002 | c0015 | t0013 | g0306 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02922 | hp1 | a0005 | c0082 | t0002 | g0282 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02922 | hp2 | a0011 | c0010 | t0005 | g0258 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02965 | hp1 | a0008 | c0047 | t0002 | g0244 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02965 | hp2 | a0002 | c0032 | t0001 | g0025 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02970 | hp1 | a0004 | c0107 | t0002 | g0236 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02970 | hp2 | a0008 | c0069 | t0008 | g0096 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02976 | hp1 | a0002 | c0075 | t0027 | g0150 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02976 | hp2 | a0005 | c0026 | t0024 | g0157 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03041 | hp1 | a0015 | c0020 | t0001 | g0160 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03041 | hp2 | a0011 | c0010 | t0005 | g0169 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03098 | hp1 | a0002 | c0025 | t0008 | g0285 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03098 | hp2 | a0002 | c0046 | t0002 | g0154 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03130 | hp1 | a0005 | c0036 | t0001 | g0273 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03130 | hp2 | a0005 | c0022 | t0002 | g0284 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03139 | hp1 | a0019 | c0086 | t0003 | g0100 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03139 | hp2 | a0029 | c0110 | t0002 | g0165 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03195 | hp1 | a0004 | c0029 | t0001 | g0099 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03195 | hp2 | a0005 | c0052 | t0001 | g0281 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03209 | hp1 | a0012 | c0041 | t0002 | g0230 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03209 | hp2 | a0002 | c0057 | t0001 | g0148 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03225 | hp1 | a0012 | c0105 | t0024 | g0217 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03225 | hp2 | a0002 | c0015 | t0002 | g0315 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03239 | hp1 | a0009 | c0027 | t0006 | g0267 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03239 | hp2 | a0008 | c0006 | t0047 | g0056 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03453 | hp1 | a0025 | c0083 | t0001 | g0313 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03453 | hp2 | a0008 | c0006 | t0007 | g0111 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03486 | hp1 | a0005 | c0070 | t0001 | g0316 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03486 | hp2 | a0005 | c0051 | t0019 | g0164 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03490 | hp1 | a0001 | c0001 | t0023 | g0295 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03490 | hp2 | a0007 | c0003 | t0004 | g0048 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03491 | hp1 | a0005 | c0039 | t0017 | g0018 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03491 | hp2 | a0005 | c0016 | t0001 | g0049 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03492 | hp1 | a0005 | c0039 | t0017 | g0019 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03492 | hp2 | a0001 | c0001 | t0023 | g0296 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03516 | hp1 | a0004 | c0099 | t0001 | g0110 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03516 | hp2 | a0002 | c0017 | t0015 | g0101 | AFR | ESN | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03540 | hp1 | a0002 | c0037 | t0001 | g0275 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03540 | hp2 | a0011 | c0010 | t0005 | g0097 | AFR | GWD | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03579 | hp1 | a0011 | c0055 | t0001 | g0259 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03579 | hp2 | a0004 | c0112 | t0005 | g0098 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03688 | hp1 | a0007 | c0003 | t0006 | g0051 | SAS | STU | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03688 | hp2 | a0001 | c0035 | t0004 | g0011 | SAS | STU | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03704 | hp1 | a0003 | c0009 | t0003 | g0073 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03704 | hp2 | a0008 | c0006 | t0001 | g0087 | SAS | PJL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03831 | hp1 | a0004 | c0087 | t0009 | g0118 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03831 | hp2 | a0015 | c0061 | t0001 | g0080 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03834 | hp1 | a0007 | c0003 | t0020 | g0179 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0239 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03927 | hp1 | a0003 | c0076 | t0002 | g0130 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03927 | hp2 | a0004 | c0008 | t0004 | g0264 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03942 | hp1 | a0004 | c0008 | t0001 | g0036 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG04199 | hp2 | a0036 | c0094 | t0009 | g0079 | SAS | STU | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG04204 | hp1 | a0005 | c0026 | t0004 | g0042 | SAS | STU | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG04204 | hp2 | a0030 | c0100 | t0009 | g0268 | SAS | STU | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18522 | hp1 | a0002 | c0059 | t0001 | g0235 | AFR | YRI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18522 | hp2 | a0002 | c0015 | t0031 | g0084 | AFR | YRI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18747 | hp1 | a0001 | c0005 | t0004 | g0167 | EAS | CHB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18747 | hp2 | a0007 | c0003 | t0003 | g0229 | EAS | CHB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18906 | hp1 | a0008 | c0006 | t0003 | g0187 | AFR | YRI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18906 | hp2 | a0012 | c0041 | t0001 | g0274 | AFR | YRI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18941 | hp1 | a0003 | c0009 | t0006 | g0186 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18941 | hp2 | a0012 | c0040 | t0029 | g0001 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18942 | hp1 | a0001 | c0005 | t0010 | g0043 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18942 | hp2 | a0002 | c0011 | t0020 | g0171 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18944 | hp2 | a0006 | c0012 | t0002 | g0028 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18949 | hp1 | a0007 | c0003 | t0009 | g0260 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18949 | hp2 | a0008 | c0006 | t0014 | g0221 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18953 | hp1 | a0001 | c0005 | t0002 | g0031 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18953 | hp2 | a0008 | c0006 | t0012 | g0081 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18960 | hp1 | a0008 | c0006 | t0005 | g0063 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18960 | hp2 | a0001 | c0005 | t0002 | g0062 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18962 | hp1 | a0003 | c0009 | t0046 | g0219 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18962 | hp2 | a0007 | c0003 | t0033 | g0035 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18964 | hp1 | a0014 | c0054 | t0010 | g0251 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18964 | hp2 | a0016 | c0019 | t0018 | g0177 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18967 | hp1 | a0006 | c0004 | t0006 | g0249 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18967 | hp2 | a0013 | c0013 | t0002 | g0262 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18969 | hp1 | a0001 | c0005 | t0002 | g0192 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18969 | hp2 | a0016 | c0019 | t0018 | g0117 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18970 | hp1 | a0003 | c0002 | t0010 | g0270 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18970 | hp2 | a0007 | c0003 | t0014 | g0030 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18978 | hp1 | a0006 | c0063 | t0003 | g0151 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18978 | hp2 | a0016 | c0019 | t0018 | g0131 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18979 | hp1 | a0006 | c0004 | t0042 | g0265 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18979 | hp2 | a0008 | c0006 | t0006 | g0057 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18982 | hp1 | a0013 | c0013 | t0003 | g0256 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18982 | hp2 | a0016 | c0019 | t0006 | g0250 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18983 | hp1 | a0003 | c0002 | t0002 | g0044 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18983 | hp2 | a0006 | c0012 | t0002 | g0226 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18984 | hp1 | a0006 | c0012 | t0002 | g0140 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18985 | hp1 | a0007 | c0003 | t0002 | g0037 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18985 | hp2 | a0014 | c0023 | t0007 | g0115 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18990 | hp1 | a0003 | c0002 | t0002 | g0205 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18990 | hp2 | a0007 | c0003 | t0002 | g0038 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18991 | hp1 | a0006 | c0089 | t0003 | g0180 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18991 | hp2 | a0002 | c0011 | t0012 | g0134 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18992 | hp1 | a0003 | c0009 | t0003 | g0178 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18992 | hp2 | a0008 | c0006 | t0022 | g0135 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18998 | hp1 | a0009 | c0027 | t0006 | g0224 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18999 | hp1 | a0003 | c0002 | t0002 | g0045 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18999 | hp2 | a0009 | c0018 | t0003 | g0253 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19001 | hp1 | a0003 | c0002 | t0003 | g0127 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19001 | hp2 | a0002 | c0011 | t0004 | g0213 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19002 | hp1 | a0007 | c0003 | t0016 | g0029 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19002 | hp2 | a0003 | c0002 | t0002 | g0184 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19007 | hp1 | a0005 | c0014 | t0003 | g0243 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19007 | hp2 | a0001 | c0092 | t0012 | g0220 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19009 | hp1 | a0013 | c0013 | t0003 | g0207 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19009 | hp2 | a0006 | c0004 | t0010 | g0252 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19010 | hp2 | a0006 | c0004 | t0002 | g0132 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19011 | hp2 | a0006 | c0004 | t0002 | g0133 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19030 | hp1 | a0004 | c0066 | t0008 | g0007 | AFR | LWK | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19030 | hp2 | a0035 | c0091 | t0008 | g0161 | AFR | LWK | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19043 | hp1 | a0003 | c0077 | t0005 | g0312 | AFR | LWK | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19043 | hp2 | a0004 | c0044 | t0013 | g0280 | AFR | LWK | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19060 | hp1 | a0002 | c0011 | t0007 | g0119 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19060 | hp2 | a0001 | c0005 | t0002 | g0123 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19066 | hp1 | a0013 | c0013 | t0003 | g0120 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19066 | hp2 | a0006 | c0004 | t0005 | g0206 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19068 | hp1 | a0004 | c0008 | t0006 | g0202 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19068 | hp2 | a0001 | c0005 | t0002 | g0129 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19078 | hp1 | a0003 | c0002 | t0002 | g0172 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19080 | hp1 | a0001 | c0005 | t0002 | g0254 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19080 | hp2 | a0031 | c0067 | t0006 | g0223 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19081 | hp1 | a0003 | c0002 | t0007 | g0059 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19081 | hp2 | a0007 | c0003 | t0004 | g0170 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19082 | hp1 | a0003 | c0002 | t0002 | g0122 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19082 | hp2 | a0007 | c0090 | t0007 | g0046 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19083 | hp1 | a0009 | c0028 | t0048 | g0241 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19083 | hp2 | a0010 | c0030 | t0022 | g0191 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19084 | hp1 | a0009 | c0018 | t0003 | g0248 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19084 | hp2 | a0006 | c0004 | t0045 | g0155 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19088 | hp1 | a0009 | c0018 | t0038 | g0228 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19088 | hp2 | a0001 | c0001 | t0012 | g0039 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19090 | hp1 | a0001 | c0005 | t0002 | g0064 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19090 | hp2 | a0005 | c0014 | t0011 | g0222 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19091 | hp1 | a0003 | c0002 | t0002 | g0257 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19091 | hp2 | a0004 | c0008 | t0028 | g0199 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19240 | hp1 | a0002 | c0074 | t0027 | g0290 | AFR | YRI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA19240 | hp2 | a0011 | c0010 | t0005 | g0286 | AFR | YRI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20129 | hp1 | a0002 | c0033 | t0032 | g0024 | AFR | ASW | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20129 | hp2 | a0004 | c0044 | t0007 | g0302 | AFR | ASW | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20752 | hp2 | a0009 | c0027 | t0004 | g0124 | EUR | TSI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0194 | EUR | TSI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20805 | hp2 | a0004 | c0008 | t0016 | g0266 | EUR | TSI | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20905 | hp1 | a0005 | c0026 | t0009 | g0076 | SAS | GIH | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20905 | hp2 | a0010 | c0030 | t0001 | g0053 | SAS | GIH | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02109 | hp1 | a0011 | c0010 | t0037 | g0181 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02109 | hp2 | a0005 | c0022 | t0021 | g0147 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02486 | hp1 | a0023 | c0072 | t0001 | g0309 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02486 | hp2 | a0002 | c0031 | t0001 | g0278 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02559 | hp1 | a0004 | c0043 | t0003 | g0128 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG02559 | hp2 | a0002 | c0017 | t0002 | g0271 | AFR | ACB | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03471 | hp1 | a0019 | c0106 | t0001 | g0094 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG03471 | hp2 | a0002 | c0015 | t0004 | g0004 | AFR | MSL | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG06807 | hp1 | a0017 | c0034 | t0001 | g0300 | AFR | USA | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| HG06807 | hp2 | a0002 | c0024 | t0008 | g0109 | AFR | USA | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18955 | hp1 | a0020 | c0045 | t0002 | g0299 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA18955 | hp2 | a0006 | c0004 | t0011 | g0269 | EAS | JPT | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA20300 | hp2 | a0002 | c0033 | t0002 | g0301 | AFR | USA | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA21309 | hp1 | a0001 | c0001 | t0043 | g0002 | AFR | LWK | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| NA21309 | hp2 | a0027 | c0062 | t0001 | g0310 | AFR | LWK | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0195 | REF | REF | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| homoSapiens_grch38 | hp1 | a0004 | c0008 | t0004 | g0234 | REF | REF | ABCA1_chr9_104776006_104933155 | ABCA1 | chr9 | 104776006 | 104933155 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104784372
|
G | T | 3 | a0022a0023a0033 | 3 | HG02486.hp1 HG02572.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.6729C>A | p.Asp2243Glu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 7042/10408 | 6729/6786 | 2243/2261 | chr9 | 104784372 | ||
| chr9:104792796
|
T | G | 1 | a0029 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.5747A>C | p.Glu1916Ala | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/50 | 6060/10408 | 5747/6786 | 1916/2261 | chr9 | 104792796 | ||
| chr9:104798522
|
C | T | 1 | a0031 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.5020G>A | p.Val1674Ile | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/50 | 5333/10408 | 5020/6786 | 1674/2261 | chr9 | 104798522 | ||
| chr9:104800523
|
T | C | 15 | a0001a0003a0006others(12): Show | 151 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(148): Show |
missense_variant | MODERATE | c.4760A>G | p.Lys1587Arg | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/50 | 5073/10408 | 4760/6786 | 1587/2261 | chr9 | 104800523 | ||
| chr9:104814451
|
T | G | 1 | a0018 | 2 | HG01109.hp1 HG01243.hp2 |
missense_variant | MODERATE | c.3763A>C | p.Ser1255Arg | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 26/50 | 4076/10408 | 3763/6786 | 1255/2261 | chr9 | 104814451 | ||
| chr9:104817351
|
C | G | 11 | a0011a0015a0017others(8): Show | 22 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(19): Show |
missense_variant | MODERATE | c.3516G>C | p.Glu1172Asp | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/50 | 3829/10408 | 3516/6786 | 1172/2261 | chr9 | 104817351 | ||
| chr9:104817352
|
T | C | 1 | a0030 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.3515A>G | p.Glu1172Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/50 | 3828/10408 | 3515/6786 | 1172/2261 | chr9 | 104817352 | ||
| chr9:104819706
|
G | C | 1 | a0016 | 4 | NA18964.hp2 NA18969.hp2 NA18978.hp2 others(1): Show |
missense_variant | MODERATE | c.3121C>G | p.Leu1041Val | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/50 | 3434/10408 | 3121/6786 | 1041/2261 | chr9 | 104819706 | ||
| chr9:104819977
|
T | C | 1 | a0034 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.3053A>G | p.Asp1018Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 21/50 | 3366/10408 | 3053/6786 | 1018/2261 | chr9 | 104819977 | ||
| chr9:104822664
|
C | A | 1 | a0031 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.2660G>T | p.Cys887Phe | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/50 | 2973/10408 | 2660/6786 | 887/2261 | chr9 | 104822664 | ||
| chr9:104824472
|
T | C | 17 | a0002a0003a0006others(14): Show | 145 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(142): Show |
missense_variant | MODERATE | c.2649A>G | p.Ile883Met | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/50 | 2962/10408 | 2649/6786 | 883/2261 | chr9 | 104824472 | ||
| chr9:104824519
|
C | T | 1 | a0035 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2602G>A | p.Glu868Lys | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/50 | 2915/10408 | 2602/6786 | 868/2261 | chr9 | 104824519 | ||
| chr9:104825752
|
C | T | 4 | a0006a0007a0013others(1): Show | 49 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(46): Show |
missense_variant | MODERATE | c.2473G>A | p.Val825Ile | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/50 | 2786/10408 | 2473/6786 | 825/2261 | chr9 | 104825752 | ||
| chr9:104826957
|
C | G | 1 | a0036 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.2328G>C | p.Lys776Asn | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/50 | 2641/10408 | 2328/6786 | 776/2261 | chr9 | 104826957 | ||
| chr9:104826965
|
T | G | 1 | a0021 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.2320A>C | p.Thr774Pro | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/50 | 2633/10408 | 2320/6786 | 774/2261 | chr9 | 104826965 | ||
| chr9:104826974
|
C | T | 6 | a0008a0010a0017others(3): Show | 31 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(28): Show |
missense_variant | MODERATE | c.2311G>A | p.Val771Met | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/50 | 2624/10408 | 2311/6786 | 771/2261 | chr9 | 104826974 | ||
| chr9:104830980
|
T | C | 1 | a0026 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.1837A>G | p.Lys613Glu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/50 | 2150/10408 | 1837/6786 | 613/2261 | chr9 | 104830980 | ||
| chr9:104837015
|
A | G | 1 | a0037 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1276T>C | p.Phe426Leu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/50 | 1589/10408 | 1276/6786 | 426/2261 | chr9 | 104837015 | ||
| chr9:104837555
|
T | C | 1 | a0025 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1067A>G | p.Asn356Ser | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/50 | 1380/10408 | 1067/6786 | 356/2261 | chr9 | 104837555 | ||
| chr9:104858586
|
C | T | 20 | a0002a0003a0005others(17): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
missense_variant | MODERATE | c.656G>A | p.Arg219Lys | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/50 | 969/10408 | 656/6786 | 219/2261 | chr9 | 104858586 | ||
| chr9:104858608
|
A | T | 1 | a0038 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.634T>A | p.Ser212Thr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/50 | 947/10408 | 634/6786 | 212/2261 | chr9 | 104858608 | ||
| chr9:104858680
|
G | T | 1 | a0020 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.562C>A | p.Gln188Lys | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/50 | 875/10408 | 562/6786 | 188/2261 | chr9 | 104858680 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104785486
|
A | C | 1 | a0019c0106 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.6555T>G | p.Ser2185Ser | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/50 | 6868/10408 | 6555/6786 | 2185/2261 | chr9 | 104785486 | ||
| chr9:104785591
|
C | T | 7 | a0002c0024a0002c0032a0002c0085others(4): Show | 10 | HG01081.hp2 HG01109.hp1 HG02647.hp1 others(7): Show |
synonymous_variant | LOW | c.6450G>A | p.Pro2150Pro | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/50 | 6763/10408 | 6450/6786 | 2150/2261 | chr9 | 104785591 | ||
| chr9:104787941
|
G | A | 24 | a0002c0025a0002c0058a0002c0075others(21): Show | 35 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(32): Show |
synonymous_variant | LOW | c.6183C>T | p.Gly2061Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/50 | 6496/10408 | 6183/6786 | 2061/2261 | chr9 | 104787941 | ||
| chr9:104788486
|
C | T | 1 | a0002c0074 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.6009G>A | p.Gly2003Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/50 | 6322/10408 | 6009/6786 | 2003/2261 | chr9 | 104788486 | ||
| chr9:104791957
|
G | A | 1 | a0002c0075 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.5799C>T | p.Cys1933Cys | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/50 | 6112/10408 | 5799/6786 | 1933/2261 | chr9 | 104791957 | ||
| chr9:104791993
|
A | G | 16 | a0002c0033a0002c0057a0002c0078others(13): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
synonymous_variant | LOW | c.5763T>C | p.Tyr1921Tyr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/50 | 6076/10408 | 5763/6786 | 1921/2261 | chr9 | 104791993 | ||
| chr9:104796122
|
G | A | 1 | a0014c0054 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.5313C>T | p.Thr1771Thr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/50 | 5626/10408 | 5313/6786 | 1771/2261 | chr9 | 104796122 | ||
| chr9:104798448
|
G | A | 1 | a0004c0099 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.5094C>T | p.Tyr1698Tyr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/50 | 5407/10408 | 5094/6786 | 1698/2261 | chr9 | 104798448 | ||
| chr9:104804649
|
C | A | 1 | a0001c0097 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.4536G>T | p.Thr1512Thr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/50 | 4849/10408 | 4536/6786 | 1512/2261 | chr9 | 104804649 | ||
| chr9:104806265
|
C | A | 14 | a0002c0046a0002c0057a0002c0058others(11): Show | 16 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
synonymous_variant | LOW | c.4440G>T | p.Gly1480Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/50 | 4753/10408 | 4440/6786 | 1480/2261 | chr9 | 104806265 | ||
| chr9:104806265
|
C | T | 1 | a0002c0059 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.4440G>A | p.Gly1480Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/50 | 4753/10408 | 4440/6786 | 1480/2261 | chr9 | 104806265 | ||
| chr9:104806424
|
C | T | 13 | a0001c0005a0001c0108a0003c0002others(10): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
synonymous_variant | LOW | c.4281G>A | p.Thr1427Thr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/50 | 4594/10408 | 4281/6786 | 1427/2261 | chr9 | 104806424 | ||
| chr9:104812679
|
C | T | 5 | a0002c0015a0002c0059a0004c0044others(2): Show | 12 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(9): Show |
synonymous_variant | LOW | c.3945G>A | p.Gly1315Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/50 | 4258/10408 | 3945/6786 | 1315/2261 | chr9 | 104812679 | ||
| chr9:104816197
|
C | T | 14 | a0002c0017a0002c0024a0002c0032others(11): Show | 21 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(18): Show |
synonymous_variant | LOW | c.3684G>A | p.Arg1228Arg | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/50 | 3997/10408 | 3684/6786 | 1228/2261 | chr9 | 104816197 | ||
| chr9:104816248
|
T | C | 10 | a0011c0010a0015c0020a0017c0034others(7): Show | 19 | HG02109.hp1 HG02145.hp1 HG02300.hp1 others(16): Show |
synonymous_variant | LOW | c.3633A>G | p.Glu1211Glu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/50 | 3946/10408 | 3633/6786 | 1211/2261 | chr9 | 104816248 | ||
| chr9:104818761
|
G | A | 9 | a0002c0015a0002c0031a0002c0033others(6): Show | 18 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(15): Show |
synonymous_variant | LOW | c.3364C>T | p.Leu1122Leu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/50 | 3677/10408 | 3364/6786 | 1122/2261 | chr9 | 104818761 | ||
| chr9:104821467
|
G | A | 2 | a0002c0031a0012c0093 | 3 | HG01952.hp2 HG02258.hp2 HG02486.hp2 |
synonymous_variant | LOW | c.2868C>T | p.Thr956Thr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/50 | 3181/10408 | 2868/6786 | 956/2261 | chr9 | 104821467 | ||
| chr9:104822510
|
C | T | 3 | a0004c0112a0004c0113a0004c0114 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2814G>A | p.Gly938Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/50 | 3127/10408 | 2814/6786 | 938/2261 | chr9 | 104822510 | ||
| chr9:104827089
|
C | T | 2 | a0006c0063a0006c0089 | 2 | NA18978.hp1 NA18991.hp1 |
synonymous_variant | LOW | c.2196G>A | p.Gln732Gln | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/50 | 2509/10408 | 2196/6786 | 732/2261 | chr9 | 104827089 | ||
| chr9:104828991
|
G | T | 47 | a0001c0092a0002c0011a0002c0015others(44): Show | 139 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
synonymous_variant | LOW | c.2040C>A | p.Ile680Ile | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/50 | 2353/10408 | 2040/6786 | 680/2261 | chr9 | 104828991 | ||
| chr9:104831702
|
G | A | 2 | a0012c0105a0032c0104 | 2 | HG02280.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.1635C>T | p.Ser545Ser | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/50 | 1948/10408 | 1635/6786 | 545/2261 | chr9 | 104831702 | ||
| chr9:104831807
|
T | C | 1 | a0002c0032 | 2 | HG02723.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.1530A>G | p.Leu510Leu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/50 | 1843/10408 | 1530/6786 | 510/2261 | chr9 | 104831807 | ||
| chr9:104832706
|
T | G | 1 | a0031c0067 | 1 | NA19080.hp2 | synonymous_variant | LOW | c.1377A>C | p.Thr459Thr | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/50 | 1690/10408 | 1377/6786 | 459/2261 | chr9 | 104832706 | ||
| chr9:104840385
|
C | T | 25 | a0002c0046a0004c0087a0004c0112others(22): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
synonymous_variant | LOW | c.948G>A | p.Gly316Gly | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/50 | 1261/10408 | 948/6786 | 316/2261 | chr9 | 104840385 | ||
| chr9:104840397
|
G | A | 20 | a0001c0108a0001c0109a0002c0033others(17): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
synonymous_variant | LOW | c.936C>T | p.Pro312Pro | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/50 | 1249/10408 | 936/6786 | 312/2261 | chr9 | 104840397 | ||
| chr9:104858591
|
T | C | 3 | a0004c0112a0004c0113a0004c0114 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.651A>G | p.Leu217Leu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/50 | 964/10408 | 651/6786 | 217/2261 | chr9 | 104858591 | ||
| chr9:104861748
|
C | T | 50 | a0001c0035a0002c0011a0002c0017others(47): Show | 148 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
synonymous_variant | LOW | c.474G>A | p.Leu158Leu | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/50 | 787/10408 | 474/6786 | 158/2261 | chr9 | 104861748 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104781061
|
A | G | 1 | a0013c0013t0025 | 2 | HG02083.hp1 HG02129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3254T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 3254 | chr9 | 104781061 | |||||
| chr9:104781064
|
A | G | 2 | a0005c0026t0024a0012c0105t0024 | 2 | HG02976.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3251T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 3251 | chr9 | 104781064 | |||||
| chr9:104781069
|
G | A | 1 | a0009c0028t0048 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3246C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 3246 | chr9 | 104781069 | |||||
| chr9:104781095
|
T | C | 4 | a0001c0001t0049a0005c0039t0017a0014c0023t0017others(1): Show | 5 | HG01515.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3220A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 3220 | chr9 | 104781095 | |||||
| chr9:104781415
|
TAAC | T | 46 | a0001c0001t0002a0001c0001t0043a0001c0001t0052others(43): Show | 79 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2897_*2899delGTT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 2897 | chr9 | 104781415 | |||||
| chr9:104781610
|
C | T | 1 | a0002c0017t0026 | 2 | HG01884.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2705G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 2705 | chr9 | 104781610 | |||||
| chr9:104781677
|
G | A | 2 | a0003c0002t0028a0004c0008t0028 | 2 | HG00673.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2638C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 2638 | chr9 | 104781677 | |||||
| chr9:104782004
|
T | C | 36 | a0001c0001t0003a0001c0001t0006a0001c0001t0023others(33): Show | 61 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2311A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 2311 | chr9 | 104782004 | |||||
| chr9:104782025
|
C | T | 1 | a0012c0040t0040 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2290G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 2290 | chr9 | 104782025 | |||||
| chr9:104782102
|
A | G | 2 | a0005c0051t0019a0024c0073t0019 | 2 | HG02647.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2213T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 2213 | chr9 | 104782102 | |||||
| chr9:104782226
|
C | T | 1 | a0001c0001t0043 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2089G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 2089 | chr9 | 104782226 | |||||
| chr9:104782404
|
G | A | 22 | a0001c0001t0007a0001c0001t0012a0001c0092t0012others(19): Show | 25 | HG00558.hp1 HG01099.hp1 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1911C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1911 | chr9 | 104782404 | |||||
| chr9:104782419
|
C | T | 177 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(174): Show | 273 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*1896G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1896 | chr9 | 104782419 | |||||
| chr9:104782525
|
G | A | 1 | a0009c0018t0038 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1790C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1790 | chr9 | 104782525 | |||||
| chr9:104782662
|
A | T | 15 | a0003c0038t0005a0003c0077t0005a0004c0029t0005others(12): Show | 21 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1653T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1653 | chr9 | 104782662 | |||||
| chr9:104782733
|
A | G | 1 | a0006c0004t0042 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1582T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1582 | chr9 | 104782733 | |||||
| chr9:104782848
|
T | TA | 16 | a0003c0038t0005a0003c0077t0005a0004c0029t0005others(13): Show | 22 | HG00408.hp2 HG01891.hp1 HG02145.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1466dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1466 | chr9 | 104782848 | |||||
| chr9:104782848
|
TA | T | 91 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(88): Show | 151 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*1466delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1466 | chr9 | 104782848 | |||||
| chr9:104782875
|
G | A | 112 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(109): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1440C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1440 | chr9 | 104782875 | |||||
| chr9:104782893
|
C | T | 1 | a0001c0001t0023 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1422G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1422 | chr9 | 104782893 | |||||
| chr9:104782973
|
C | A | 1 | a0003c0002t0050 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1342G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1342 | chr9 | 104782973 | |||||
| chr9:104783055
|
G | C | 2 | a0008c0006t0022a0010c0030t0022 | 2 | NA18992.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1260C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1260 | chr9 | 104783055 | |||||
| chr9:104783135
|
C | T | 1 | a0008c0006t0047 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1180G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 1180 | chr9 | 104783135 | |||||
| chr9:104783441
|
C | T | 3 | a0002c0017t0015a0002c0025t0015a0008c0006t0015 | 3 | HG01255.hp2 HG02630.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*874G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 874 | chr9 | 104783441 | |||||
| chr9:104783622
|
G | A | 111 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(108): Show | 175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*693C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 693 | chr9 | 104783622 | |||||
| chr9:104783826
|
T | G | 1 | a0038c0068t0044 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*489A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 489 | chr9 | 104783826 | |||||
| chr9:104783899
|
G | A | 2 | a0002c0074t0027a0002c0075t0027 | 2 | HG02976.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*416C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 416 | chr9 | 104783899 | |||||
| chr9:104783920
|
A | T | 15 | a0003c0038t0005a0003c0077t0005a0004c0029t0005others(12): Show | 21 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*395T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 395 | chr9 | 104783920 | |||||
| chr9:104783947
|
T | C | 2 | a0003c0009t0051a0006c0004t0045 | 2 | HG00558.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 368 | chr9 | 104783947 | |||||
| chr9:104783993
|
CA | C | 9 | a0003c0002t0014a0003c0009t0046a0005c0084t0014others(6): Show | 9 | HG00408.hp2 HG00423.hp2 HG01257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*321delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 321 | chr9 | 104783993 | |||||
| chr9:104784219
|
A | G | 6 | a0002c0015t0013a0002c0015t0031a0002c0033t0032others(3): Show | 7 | HG01081.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*96T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 96 | chr9 | 104784219 | |||||
| chr9:104784240
|
C | T | 1 | a0008c0048t0030 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 50/50 | 75 | chr9 | 104784240 | |||||
| chr9:104903697
|
C | G | 41 | a0001c0001t0006a0001c0001t0011a0001c0001t0012others(38): Show | 53 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-18G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/50 | 18 | chr9 | 104903697 | |||||
| chr9:104903754
|
G | GC | 41 | a0001c0001t0006a0001c0001t0011a0001c0001t0012others(38): Show | 53 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-76dupG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/50 | 76 | chr9 | 104903754 | |||||
| chr9:104928104
|
G | T | 1 | a0012c0040t0029 | 1 | NA18941.hp2 | 5_prime_UTR_variant | MODIFIER | c.-262C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/50 | 24425 | chr9 | 104928104 | |||||
| chr9:104928121
|
G | C | 1 | a0001c0001t0052 | 1 | HG00099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-279C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/50 | 24442 | chr9 | 104928121 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:104784620
|
A | G | 20 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(17): Show | 20 | HG00642.hp2 HG00738.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.6646-165T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784620 | ||||||
| chr9:104784671
|
G | A | 1 | a0002c0085t0008g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6646-216C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784671 | ||||||
| chr9:104784725
|
C | T | 1 | a0005c0036t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6646-270G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784725 | ||||||
| chr9:104784743
|
G | A | 247 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.6646-288C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784743 | ||||||
| chr9:104784766
|
C | T | 3 | a0015c0020t0001g0006a0015c0020t0004g0005a0027c0062t0001g0310 | 3 | HG02622.hp1 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6646-311G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784766 | ||||||
| chr9:104784779
|
G | A | 5 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(2): Show | 5 | HG01081.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.6646-324C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784779 | ||||||
| chr9:104784790
|
C | A | 3 | a0002c0017t0015g0101a0002c0025t0015g0283a0008c0006t0015g0095 | 3 | HG01255.hp2 HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6646-335G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784790 | ||||||
| chr9:104784791
|
G | A | 1 | a0004c0098t0005g0303 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6646-336C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784791 | ||||||
| chr9:104784800
|
T | C | 8 | a0002c0037t0001g0275a0011c0010t0005g0097a0011c0010t0005g0169others(5): Show | 8 | HG02145.hp1 HG02615.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.6646-345A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784800 | ||||||
| chr9:104784821
|
T | C | 1 | a0002c0059t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6646-366A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784821 | ||||||
| chr9:104784832
|
C | T | 2 | a0002c0017t0026g0163a0002c0017t0026g0276 | 2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.6646-377G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784832 | ||||||
| chr9:104784934
|
A | G | 77 | a0001c0001t0001g0077a0001c0001t0001g0176a0001c0001t0001g0196others(74): Show | 77 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.6645+462T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784934 | ||||||
| chr9:104784936
|
G | A | 66 | a0001c0001t0001g0196a0001c0001t0003g0210a0001c0001t0004g0193others(63): Show | 66 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.6645+460C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784936 | ||||||
| chr9:104784949
|
C | T | 108 | a0001c0001t0001g0195a0001c0001t0001g0238a0001c0001t0002g0074others(105): Show | 108 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.6645+447G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784949 | ||||||
| chr9:104784963
|
C | T | 1 | a0007c0003t0016g0029 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.6645+433G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784963 | ||||||
| chr9:104784992
|
C | T | 3 | a0001c0001t0003g0089a0001c0001t0006g0047a0001c0001t0006g0058 | 3 | HG01168.hp1 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.6645+404G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104784992 | ||||||
| chr9:104785341
|
C | G | 98 | a0001c0001t0002g0074a0001c0001t0002g0233a0001c0001t0052g0318others(95): Show | 98 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.6645+55G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 49/49 | chr9 | 104785341 | ||||||
| chr9:104785877
|
G | T | 7 | a0011c0010t0005g0097a0011c0010t0005g0169a0011c0010t0005g0255others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6402-238C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104785877 | ||||||
| chr9:104785890
|
G | C | 4 | a0004c0008t0003g0289a0005c0014t0011g0222a0013c0013t0025g0032others(1): Show | 4 | HG02083.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.6402-251C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104785890 | ||||||
| chr9:104785969
|
T | A | 56 | a0001c0001t0001g0195a0001c0001t0002g0233a0001c0005t0001g0050others(53): Show | 56 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.6401+329A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104785969 | ||||||
| chr9:104785971
|
G | A | 1 | a0007c0003t0004g0027 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6401+327C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104785971 | ||||||
| chr9:104785981
|
C | T | 2 | a0004c0029t0005g0162a0004c0112t0005g0098 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.6401+317G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104785981 | ||||||
| chr9:104786094
|
C | A | 306 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.6401+204G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104786094 | ||||||
| chr9:104786113
|
G | A | 1 | a0006c0004t0011g0269 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.6401+185C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104786113 | ||||||
| chr9:104786147
|
A | G | 1 | a0001c0005t0001g0050 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6401+151T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104786147 | ||||||
| chr9:104786181
|
T | C | 77 | a0001c0001t0012g0144a0001c0005t0004g0167a0002c0011t0004g0213others(74): Show | 77 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.6401+117A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104786181 | ||||||
| chr9:104786212
|
G | T | 306 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.6401+86C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104786212 | ||||||
| chr9:104786285
|
T | C | 51 | a0001c0001t0012g0144a0001c0005t0004g0167a0002c0011t0004g0213others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.6401+13A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 48/49 | chr9 | 104786285 | ||||||
| chr9:104786537
|
A | G | 51 | a0001c0001t0012g0144a0001c0005t0004g0167a0002c0011t0004g0213others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.6309-147T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 47/49 | chr9 | 104786537 | ||||||
| chr9:104786605
|
A | C | 3 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0066t0008g0007 | 3 | HG01891.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6309-215T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 47/49 | chr9 | 104786605 | ||||||
| chr9:104786784
|
G | A | 3 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0033t0032g0024 | 3 | HG01884.hp2 HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6308+89C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 47/49 | chr9 | 104786784 | ||||||
| chr9:104786812
|
C | T | 1 | a0012c0065t0007g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.6308+61G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 47/49 | chr9 | 104786812 | ||||||
| chr9:104787010
|
G | A | 18 | a0002c0025t0007g0237a0002c0058t0007g0143a0002c0078t0001g0216others(15): Show | 18 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.6205-34C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/49 | chr9 | 104787010 | ||||||
| chr9:104787024
|
C | A | 1 | a0013c0013t0003g0120 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6205-48G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/49 | chr9 | 104787024 | ||||||
| chr9:104787139
|
T | A | 1 | a0025c0083t0001g0313 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6205-163A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/49 | chr9 | 104787139 | ||||||
| chr9:104787175
|
G | T | 4 | a0002c0017t0015g0101a0004c0029t0005g0023a0008c0006t0015g0095others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.6205-199C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/49 | chr9 | 104787175 | ||||||
| chr9:104787279
|
A | G | 7 | a0011c0010t0005g0097a0011c0010t0005g0169a0011c0010t0005g0255others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6205-303T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/49 | chr9 | 104787279 | ||||||
| chr9:104787312
|
C | G | 40 | a0001c0001t0012g0144a0001c0005t0004g0167a0002c0011t0004g0213others(37): Show | 40 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.6205-336G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/49 | chr9 | 104787312 | ||||||
| chr9:104787546
|
G | A | 54 | a0001c0001t0001g0195a0001c0001t0002g0233a0001c0005t0001g0050others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.6204+374C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 46/49 | chr9 | 104787546 | ||||||
| chr9:104788123
|
A | G | 10 | a0003c0077t0005g0312a0004c0098t0005g0303a0011c0010t0005g0097others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.6070-69T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788123 | ||||||
| chr9:104788146
|
G | C | 1 | a0002c0032t0001g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6070-92C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788146 | ||||||
| chr9:104788230
|
T | C | 4 | a0004c0008t0003g0289a0005c0014t0011g0222a0013c0013t0025g0032others(1): Show | 4 | HG02083.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.6070-176A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788230 | ||||||
| chr9:104788343
|
A | C | 1 | a0004c0008t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6069+83T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788343 | ||||||
| chr9:104788351
|
C | T | 3 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0066t0008g0007 | 3 | HG01891.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6069+75G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788351 | ||||||
| chr9:104788358
|
A | G | 124 | a0001c0001t0002g0233a0001c0005t0001g0050a0001c0005t0002g0017others(121): Show | 124 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.6069+68T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788358 | ||||||
| chr9:104788364
|
CA | C | 16 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.6069+61delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788364 | ||||||
| chr9:104788402
|
C | G | 12 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(9): Show | 12 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.6069+24G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788402 | ||||||
| chr9:104788407
|
T | C | 1 | a0033c0101t0001g0308 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.6069+19A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 45/49 | chr9 | 104788407 | ||||||
| chr9:104788740
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5928-173C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104788740 | ||||||
| chr9:104788899
|
C | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(38): Show | 41 | HG00738.hp2 HG01071.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.5928-332G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104788899 | ||||||
| chr9:104788939
|
C | T | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5928-372G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104788939 | ||||||
| chr9:104788966
|
A | C | 41 | a0001c0005t0004g0167a0002c0011t0004g0213a0002c0011t0004g0263others(38): Show | 41 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.5928-399T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104788966 | ||||||
| chr9:104789119
|
G | A | 3 | a0001c0001t0006g0225a0001c0001t0007g0183a0001c0001t0012g0039 | 3 | NA18984.hp2 NA19078.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.5928-552C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789119 | ||||||
| chr9:104789248
|
C | T | 38 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(35): Show | 38 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.5928-681G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789248 | ||||||
| chr9:104789257
|
C | T | 55 | a0001c0001t0001g0088a0001c0001t0001g0203a0001c0001t0002g0074others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.5928-690G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789257 | ||||||
| chr9:104789378
|
C | T | 17 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(14): Show | 17 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.5928-811G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789378 | ||||||
| chr9:104789379
|
G | T | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5928-812C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789379 | ||||||
| chr9:104789445
|
T | A | 81 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(78): Show | 81 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.5928-878A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789445 | ||||||
| chr9:104789465
|
C | T | 16 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0057t0001g0148others(13): Show | 16 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.5928-898G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789465 | ||||||
| chr9:104789771
|
C | CCACT | 81 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(78): Show | 81 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.5927+1147_5927+115 others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789771 | ||||||
| chr9:104789780
|
T | C | 19 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(16): Show | 19 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.5927+1142A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789780 | ||||||
| chr9:104789816
|
G | A | 2 | a0022c0050t0001g0166a0023c0072t0001g0309 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.5927+1106C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789816 | ||||||
| chr9:104789889
|
C | G | 17 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(14): Show | 17 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.5927+1033G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789889 | ||||||
| chr9:104789914
|
T | C | 2 | a0004c0064t0007g0175a0004c0096t0007g0020 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.5927+1008A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789914 | ||||||
| chr9:104789930
|
C | T | 1 | a0015c0061t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5927+992G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104789930 | ||||||
| chr9:104790085
|
A | C | 1 | a0004c0008t0028g0199 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.5927+837T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790085 | ||||||
| chr9:104790096
|
C | CA | 95 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.5927+825dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790096 | ||||||
| chr9:104790096
|
C | CAA | 23 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(20): Show | 23 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.5927+824_5927+825d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790096 | ||||||
| chr9:104790220
|
A | G | 6 | a0005c0026t0024g0157a0005c0036t0001g0273a0005c0070t0001g0316others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.5927+702T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790220 | ||||||
| chr9:104790255
|
T | C | 2 | a0002c0024t0008g0003a0002c0024t0008g0008 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5927+667A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790255 | ||||||
| chr9:104790339
|
T | C | 25 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(22): Show | 25 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.5927+583A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790339 | ||||||
| chr9:104790414
|
G | A | 118 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.5927+508C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790414 | ||||||
| chr9:104790494
|
T | A | 1 | a0002c0032t0001g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5927+428A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790494 | ||||||
| chr9:104790596
|
T | C | 1 | a0034c0103t0007g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5927+326A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790596 | ||||||
| chr9:104790643
|
A | G | 118 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.5927+279T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790643 | ||||||
| chr9:104790658
|
A | G | 118 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.5927+264T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790658 | ||||||
| chr9:104790760
|
T | C | 19 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0057t0001g0148others(16): Show | 19 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.5927+162A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790760 | ||||||
| chr9:104790904
|
A | G | 122 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(119): Show | 122 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.5927+18T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 44/49 | chr9 | 104790904 | ||||||
| chr9:104791190
|
T | C | 2 | a0002c0032t0001g0025a0002c0032t0001g0317 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.5821-162A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791190 | ||||||
| chr9:104791197
|
A | T | 120 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(117): Show | 120 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.5821-169T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791197 | ||||||
| chr9:104791207
|
G | A | 1 | a0003c0009t0051g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.5821-179C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791207 | ||||||
| chr9:104791243
|
A | G | 116 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(113): Show | 116 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.5821-215T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791243 | ||||||
| chr9:104791284
|
C | A | 5 | a0009c0018t0003g0248a0016c0019t0006g0250a0016c0019t0018g0117others(2): Show | 5 | NA18964.hp2 NA18969.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.5821-256G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791284 | ||||||
| chr9:104791340
|
G | A | 8 | a0002c0025t0007g0237a0002c0058t0007g0143a0004c0029t0005g0023others(5): Show | 8 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.5821-312C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791340 | ||||||
| chr9:104791458
|
T | C | 2 | a0002c0015t0002g0315a0007c0003t0006g0051 | 2 | HG03225.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.5821-430A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791458 | ||||||
| chr9:104791503
|
G | GGCTCACT | 117 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(114): Show | 117 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.5820+432_5820+433i others(9): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791503 | ||||||
| chr9:104791788
|
C | T | 118 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.5820+148G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791788 | ||||||
| chr9:104791912
|
G | A | 1 | a0008c0049t0004g0103 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.5820+24C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 43/49 | chr9 | 104791912 | ||||||
| chr9:104792135
|
G | A | 17 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0057t0001g0148others(14): Show | 17 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.5758-137C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792135 | ||||||
| chr9:104792158
|
C | T | 2 | a0022c0050t0001g0166a0023c0072t0001g0309 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.5758-160G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792158 | ||||||
| chr9:104792167
|
C | T | 3 | a0004c0008t0003g0289a0006c0004t0005g0206a0006c0004t0010g0252 | 3 | HG02738.hp2 NA19009.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.5758-169G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792167 | ||||||
| chr9:104792214
|
C | T | 1 | a0003c0056t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5758-216G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792214 | ||||||
| chr9:104792240
|
T | C | 118 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.5758-242A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792240 | ||||||
| chr9:104792253
|
T | C | 170 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.5758-255A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792253 | ||||||
| chr9:104792376
|
A | G | 2 | a0013c0013t0025g0032a0013c0013t0025g0033 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.5758-378T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792376 | ||||||
| chr9:104792463
|
A | G | 43 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(40): Show | 43 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.5757+323T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792463 | ||||||
| chr9:104792464
|
A | T | 118 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.5757+322T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792464 | ||||||
| chr9:104792538
|
A | T | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5757+248T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792538 | ||||||
| chr9:104792547
|
T | G | 43 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0007g0119others(40): Show | 43 | HG00423.hp1 HG01255.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.5757+239A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 42/49 | chr9 | 104792547 | ||||||
| chr9:104792953
|
G | T | 2 | a0003c0002t0002g0172a0006c0012t0002g0060 | 2 | HG00558.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.5637-47C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 41/49 | chr9 | 104792953 | ||||||
| chr9:104792975
|
G | A | 1 | a0027c0062t0001g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5637-69C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 41/49 | chr9 | 104792975 | ||||||
| chr9:104793025
|
G | A | 43 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0007g0119others(40): Show | 43 | HG00423.hp1 HG01255.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.5637-119C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 41/49 | chr9 | 104793025 | ||||||
| chr9:104793325
|
G | A | 15 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(12): Show | 15 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.5507-25C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104793325 | ||||||
| chr9:104793430
|
C | G | 93 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0004g0213others(90): Show | 93 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.5507-130G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104793430 | ||||||
| chr9:104793566
|
C | A | 1 | a0004c0044t0007g0302 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5507-266G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104793566 | ||||||
| chr9:104793673
|
T | C | 2 | a0002c0085t0008g0142a0008c0006t0015g0095 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.5507-373A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104793673 | ||||||
| chr9:104793720
|
G | C | 1 | a0016c0019t0018g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.5507-420C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104793720 | ||||||
| chr9:104793877
|
A | C | 1 | a0001c0001t0011g0085 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5506+510T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104793877 | ||||||
| chr9:104794068
|
T | C | 68 | a0001c0005t0004g0167a0002c0011t0004g0112a0002c0011t0007g0119others(65): Show | 68 | HG00423.hp1 HG00642.hp1 HG01175.hp2 others(65): Show |
intron_variant | MODIFIER | c.5506+319A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104794068 | ||||||
| chr9:104794071
|
T | C | 1 | a0005c0036t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5506+316A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104794071 | ||||||
| chr9:104794135
|
G | A | 189 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.5506+252C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104794135 | ||||||
| chr9:104794136
|
C | A | 189 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.5506+251G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 40/49 | chr9 | 104794136 | ||||||
| chr9:104794512
|
T | TA | 80 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0024t0008g0003others(77): Show | 80 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(77): Show |
splice_region_variant&intron_variant | LOW | c.5383-3dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794512 | ||||||
| chr9:104794512
|
T | TAA | 24 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(21): Show | 24 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.5383-4_5383-3dupTT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794512 | ||||||
| chr9:104794512
|
T | TAAA | 143 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
splice_region_variant&intron_variant | LOW | c.5383-5_5383-3dupTT others(1): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794512 | ||||||
| chr9:104794512
|
T | TAAAA | 8 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0001g0196others(5): Show | 8 | HG01346.hp2 HG01978.hp1 HG02148.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.5383-6_5383-3dupTT others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794512 | ||||||
| chr9:104794512
|
TA | T | 40 | a0002c0011t0004g0112a0002c0011t0007g0119a0002c0011t0007g0247others(37): Show | 40 | HG00423.hp1 HG00642.hp1 HG01175.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.5383-3delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794512 | ||||||
| chr9:104794677
|
T | G | 11 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(8): Show | 11 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5383-167A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794677 | ||||||
| chr9:104794699
|
T | C | 2 | a0002c0032t0001g0025a0002c0032t0001g0317 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.5383-189A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794699 | ||||||
| chr9:104794749
|
G | GTATGGAG others(17): Show |
1 | a0002c0011t0004g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5383-263_5383-240d others(26): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794749 | ||||||
| chr9:104794851
|
G | A | 1 | a0008c0006t0007g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5383-341C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794851 | ||||||
| chr9:104794896
|
T | C | 39 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.5383-386A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104794896 | ||||||
| chr9:104795034
|
G | A | 1 | a0004c0008t0003g0294 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5383-524C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795034 | ||||||
| chr9:104795065
|
C | T | 1 | a0011c0010t0005g0287 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5383-555G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795065 | ||||||
| chr9:104795185
|
G | A | 1 | a0004c0112t0005g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5383-675C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795185 | ||||||
| chr9:104795293
|
G | A | 6 | a0002c0025t0007g0237a0002c0058t0007g0143a0004c0064t0007g0175others(3): Show | 6 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.5382+760C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795293 | ||||||
| chr9:104795312
|
G | A | 5 | a0001c0001t0006g0225a0001c0001t0007g0183a0001c0001t0012g0039others(2): Show | 5 | NA18962.hp1 NA18984.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.5382+741C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795312 | ||||||
| chr9:104795397
|
T | C | 1 | a0009c0021t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5382+656A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795397 | ||||||
| chr9:104795484
|
A | G | 2 | a0008c0006t0001g0087a0008c0006t0047g0056 | 2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.5382+569T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795484 | ||||||
| chr9:104795512
|
G | A | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5382+541C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795512 | ||||||
| chr9:104795528
|
G | A | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5382+525C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795528 | ||||||
| chr9:104795535
|
G | A | 8 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0074t0027g0290others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.5382+518C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795535 | ||||||
| chr9:104795584
|
A | G | 302 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.5382+469T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795584 | ||||||
| chr9:104795590
|
G | T | 1 | a0001c0001t0052g0318 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5382+463C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795590 | ||||||
| chr9:104795595
|
G | A | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5382+458C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795595 | ||||||
| chr9:104795688
|
T | C | 1 | a0001c0035t0009g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.5382+365A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795688 | ||||||
| chr9:104795750
|
G | A | 1 | a0003c0077t0005g0312 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5382+303C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795750 | ||||||
| chr9:104795968
|
A | G | 8 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0074t0027g0290others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.5382+85T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 39/49 | chr9 | 104795968 | ||||||
| chr9:104796231
|
G | A | 1 | a0003c0009t0003g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5238-34C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 38/49 | chr9 | 104796231 | ||||||
| chr9:104796471
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5122-47T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796471 | ||||||
| chr9:104796485
|
A | G | 32 | a0002c0057t0001g0148a0002c0078t0001g0216a0002c0085t0008g0142others(29): Show | 32 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.5122-61T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796485 | ||||||
| chr9:104796640
|
C | G | 1 | a0003c0002t0050g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5122-216G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796640 | ||||||
| chr9:104796656
|
C | A | 29 | a0002c0057t0001g0148a0002c0078t0001g0216a0004c0029t0001g0099others(26): Show | 29 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.5122-232G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796656 | ||||||
| chr9:104796691
|
C | T | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5122-267G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796691 | ||||||
| chr9:104796698
|
T | C | 1 | a0008c0006t0015g0095 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5122-274A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796698 | ||||||
| chr9:104796702
|
C | A | 35 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(32): Show | 35 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.5122-278G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796702 | ||||||
| chr9:104796778
|
G | A | 277 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.5122-354C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104796778 | ||||||
| chr9:104797025
|
A | G | 12 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(9): Show | 12 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.5122-601T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797025 | ||||||
| chr9:104797187
|
T | C | 7 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0074t0027g0290others(4): Show | 7 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.5122-763A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797187 | ||||||
| chr9:104797198
|
T | C | 35 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(32): Show | 35 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.5122-774A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797198 | ||||||
| chr9:104797243
|
A | C | 1 | a0008c0006t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5122-819T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797243 | ||||||
| chr9:104797574
|
C | CG | 89 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.5121+846dupC | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797574 | ||||||
| chr9:104797614
|
C | T | 29 | a0002c0057t0001g0148a0002c0078t0001g0216a0004c0029t0001g0099others(26): Show | 29 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.5121+807G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797614 | ||||||
| chr9:104797694
|
C | T | 1 | a0009c0018t0003g0248 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.5121+727G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797694 | ||||||
| chr9:104797838
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.5121+583C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797838 | ||||||
| chr9:104797849
|
T | A | 3 | a0002c0017t0026g0163a0002c0017t0026g0276a0004c0107t0002g0236 | 3 | HG01884.hp2 HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5121+572A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797849 | ||||||
| chr9:104797908
|
T | C | 1 | a0002c0017t0015g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5121+513A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797908 | ||||||
| chr9:104797938
|
C | T | 1 | a0011c0010t0005g0287 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5121+483G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104797938 | ||||||
| chr9:104798010
|
G | A | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(35): Show | 38 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.5121+411C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104798010 | ||||||
| chr9:104798115
|
G | C | 3 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0066t0008g0007 | 3 | HG01891.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5121+306C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104798115 | ||||||
| chr9:104798143
|
G | C | 6 | a0002c0017t0026g0163a0002c0017t0026g0276a0004c0107t0002g0236others(3): Show | 6 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5121+278C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104798143 | ||||||
| chr9:104798173
|
T | C | 32 | a0002c0057t0001g0148a0002c0078t0001g0216a0002c0085t0008g0142others(29): Show | 32 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.5121+248A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104798173 | ||||||
| chr9:104798232
|
T | C | 4 | a0015c0020t0001g0006a0015c0020t0001g0160a0015c0020t0004g0005others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5121+189A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104798232 | ||||||
| chr9:104798366
|
A | G | 39 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0057t0001g0148others(36): Show | 39 | HG01884.hp1 HG01884.hp2 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.5121+55T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104798366 | ||||||
| chr9:104798375
|
T | C | 1 | a0002c0025t0008g0285 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5121+46A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 37/49 | chr9 | 104798375 | ||||||
| chr9:104799171
|
T | C | 7 | a0002c0025t0007g0237a0002c0058t0007g0143a0004c0064t0007g0175others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.4944-573A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799171 | ||||||
| chr9:104799394
|
T | TCA | 85 | a0001c0001t0007g0183a0001c0001t0052g0318a0001c0005t0001g0050others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.4943+423_4943+424d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
T | TCACA | 27 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0011g0085others(24): Show | 27 | HG00408.hp1 HG00544.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.4943+421_4943+424d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
T | TCACACA | 23 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0195others(20): Show | 23 | HG00642.hp2 HG01169.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.4943+419_4943+424d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
T | TCACACAC others(1): Show |
52 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(49): Show | 52 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.4943+417_4943+424d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
T | TCACACAC others(3): Show |
26 | a0001c0001t0001g0208a0001c0001t0001g0238a0001c0001t0002g0233others(23): Show | 26 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.4943+415_4943+424d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
T | TCACACAC others(5): Show |
7 | a0001c0109t0001g0232a0002c0011t0007g0119a0002c0011t0007g0247others(4): Show | 7 | HG01255.hp2 HG01891.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.4943+413_4943+424d others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
T | TCACACAC others(7): Show |
18 | a0001c0001t0001g0077a0001c0001t0001g0176a0002c0011t0004g0112others(15): Show | 18 | HG00609.hp2 HG01261.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.4943+411_4943+424d others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
T | TCACACAC others(9): Show |
3 | a0004c0066t0008g0007a0005c0014t0006g0052a0016c0019t0006g0250 | 3 | HG00423.hp1 NA18982.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4943+409_4943+424d others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
TCA | T | 5 | a0002c0025t0008g0285a0003c0002t0002g0045a0004c0008t0001g0036others(2): Show | 5 | HG03098.hp1 HG03927.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.4943+423_4943+424d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
TCACACAC others(1): Show |
T | 15 | a0004c0008t0003g0289a0004c0113t0002g0159a0005c0070t0001g0316others(12): Show | 15 | HG00408.hp2 HG00609.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.4943+417_4943+424d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
TCACACAC others(3): Show |
T | 25 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(22): Show | 25 | HG00621.hp2 HG00673.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.4943+415_4943+424d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
TCACACAC others(5): Show |
T | 2 | a0004c0112t0005g0098a0008c0047t0002g0244 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4943+413_4943+424d others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
TCACACAC others(7): Show |
T | 2 | a0004c0064t0007g0175a0004c0096t0007g0020 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.4943+411_4943+424d others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
TCACACAC others(13): Show |
T | 13 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4943+405_4943+424d others(22): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104799394
|
TCACACAC others(15): Show |
T | 1 | a0006c0004t0005g0206 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4943+403_4943+424d others(24): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 36/49 | chr9 | 104799394 | ||||||
| chr9:104800002
|
T | C | 1 | a0007c0003t0020g0179 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4774-14A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/49 | chr9 | 104800002 | ||||||
| chr9:104800005
|
C | T | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4774-17G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/49 | chr9 | 104800005 | ||||||
| chr9:104800042
|
G | A | 3 | a0005c0051t0019g0164a0005c0082t0002g0282a0012c0093t0001g0108 | 3 | HG01952.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4774-54C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/49 | chr9 | 104800042 | ||||||
| chr9:104800144
|
C | G | 2 | a0005c0036t0001g0273a0005c0070t0001g0316 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4774-156G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/49 | chr9 | 104800144 | ||||||
| chr9:104800226
|
A | G | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4774-238T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/49 | chr9 | 104800226 | ||||||
| chr9:104800255
|
G | A | 1 | a0008c0006t0012g0081 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4773+255C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/49 | chr9 | 104800255 | ||||||
| chr9:104800276
|
G | A | 147 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.4773+234C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 35/49 | chr9 | 104800276 | ||||||
| chr9:104800658
|
T | A | 2 | a0004c0112t0005g0098a0008c0047t0002g0244 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4699-74A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104800658 | ||||||
| chr9:104800919
|
G | A | 2 | a0002c0015t0013g0305a0002c0015t0013g0306 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4699-335C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104800919 | ||||||
| chr9:104800946
|
T | C | 39 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.4699-362A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104800946 | ||||||
| chr9:104800988
|
T | C | 220 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.4699-404A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104800988 | ||||||
| chr9:104801049
|
T | C | 3 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109 | 3 | HG02896.hp1 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4699-465A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801049 | ||||||
| chr9:104801116
|
T | TAAAA | 68 | a0001c0001t0011g0085a0001c0005t0002g0254a0002c0011t0004g0213others(65): Show | 68 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.4699-536_4699-533d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801116 | ||||||
| chr9:104801116
|
T | TAAAAA | 239 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.4699-537_4699-533d others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801116 | ||||||
| chr9:104801116
|
T | TAAAAAA | 8 | a0002c0017t0002g0271a0002c0017t0026g0163a0002c0017t0026g0276others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.4699-538_4699-533d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801116 | ||||||
| chr9:104801156
|
G | A | 93 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.4699-572C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801156 | ||||||
| chr9:104801283
|
A | C | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4699-699T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801283 | ||||||
| chr9:104801312
|
C | T | 41 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(38): Show | 41 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.4699-728G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801312 | ||||||
| chr9:104801322
|
T | C | 300 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.4698+732A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801322 | ||||||
| chr9:104801344
|
C | T | 1 | a0001c0001t0011g0085 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4698+710G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801344 | ||||||
| chr9:104801381
|
G | A | 1 | a0014c0053t0002g0146 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4698+673C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801381 | ||||||
| chr9:104801392
|
CTA | C | 39 | a0002c0011t0004g0112a0002c0011t0007g0119a0002c0011t0007g0247others(36): Show | 39 | HG00423.hp1 HG00642.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.4698+660_4698+661d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801392 | ||||||
| chr9:104801406
|
G | A | 28 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(25): Show | 28 | HG00738.hp2 HG01071.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.4698+648C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801406 | ||||||
| chr9:104801426
|
T | A | 3 | a0005c0051t0019g0164a0005c0082t0002g0282a0012c0093t0001g0108 | 3 | HG01952.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4698+628A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801426 | ||||||
| chr9:104801471
|
C | T | 29 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(26): Show | 29 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.4698+583G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801471 | ||||||
| chr9:104801498
|
G | A | 2 | a0010c0007t0010g0200a0010c0007t0010g0201 | 2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.4698+556C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801498 | ||||||
| chr9:104801552
|
G | GT | 8 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4698+501dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801552 | ||||||
| chr9:104801599
|
C | T | 39 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.4698+455G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801599 | ||||||
| chr9:104801733
|
G | A | 39 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.4698+321C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801733 | ||||||
| chr9:104801788
|
C | T | 3 | a0002c0033t0002g0301a0002c0033t0032g0024a0005c0071t0041g0311 | 3 | HG01891.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4698+266G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801788 | ||||||
| chr9:104801791
|
G | A | 1 | a0007c0003t0003g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4698+263C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801791 | ||||||
| chr9:104801796
|
G | A | 166 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.4698+258C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801796 | ||||||
| chr9:104801942
|
A | C | 1 | a0010c0007t0002g0015 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4698+112T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104801942 | ||||||
| chr9:104802047
|
A | G | 1 | a0004c0008t0028g0199 | 1 | NA19091.hp2 | splice_region_variant&intron_variant | LOW | c.4698+7T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 34/49 | chr9 | 104802047 | ||||||
| chr9:104802185
|
C | G | 39 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.4593-26G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802185 | ||||||
| chr9:104802289
|
CAG | C | 145 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.4593-132_4593-131d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802289 | ||||||
| chr9:104802395
|
T | C | 44 | a0002c0011t0004g0112a0002c0011t0007g0119a0002c0011t0007g0247others(41): Show | 44 | HG00423.hp1 HG00642.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.4593-236A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802395 | ||||||
| chr9:104802430
|
T | A | 1 | a0001c0005t0002g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4593-271A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802430 | ||||||
| chr9:104802460
|
T | G | 307 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.4593-301A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802460 | ||||||
| chr9:104802558
|
C | T | 38 | a0002c0011t0004g0112a0002c0011t0007g0119a0002c0011t0007g0247others(35): Show | 38 | HG00423.hp1 HG00642.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.4593-399G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802558 | ||||||
| chr9:104802565
|
T | C | 145 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.4593-406A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802565 | ||||||
| chr9:104802586
|
T | C | 8 | a0002c0017t0002g0271a0002c0017t0026g0163a0002c0017t0026g0276others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.4593-427A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802586 | ||||||
| chr9:104802637
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4593-478C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802637 | ||||||
| chr9:104802658
|
G | A | 40 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(37): Show | 40 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.4593-499C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802658 | ||||||
| chr9:104802830
|
G | A | 6 | a0005c0026t0024g0157a0005c0036t0001g0273a0005c0070t0001g0316others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4592+454C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802830 | ||||||
| chr9:104802862
|
C | T | 1 | a0012c0102t0007g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4592+422G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802862 | ||||||
| chr9:104802907
|
G | A | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4592+377C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104802907 | ||||||
| chr9:104803032
|
A | G | 1 | a0008c0006t0015g0095 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4592+252T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104803032 | ||||||
| chr9:104803215
|
C | G | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4592+69G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104803215 | ||||||
| chr9:104803234
|
C | T | 2 | a0004c0112t0005g0098a0008c0047t0002g0244 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4592+50G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104803234 | ||||||
| chr9:104803250
|
C | A | 1 | a0019c0106t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4592+34G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 33/49 | chr9 | 104803250 | ||||||
| chr9:104803343
|
A | T | 1 | a0007c0003t0009g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4560-27T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803343 | ||||||
| chr9:104803609
|
C | CT | 34 | a0002c0057t0001g0148a0002c0078t0001g0216a0002c0085t0008g0142others(31): Show | 34 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.4560-294dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803609 | ||||||
| chr9:104803629
|
G | C | 1 | a0002c0031t0001g0278 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4560-313C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803629 | ||||||
| chr9:104803638
|
G | A | 39 | a0002c0011t0004g0263a0002c0011t0020g0171a0002c0037t0011g0116others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.4560-322C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803638 | ||||||
| chr9:104803712
|
A | G | 39 | a0002c0011t0004g0263a0002c0011t0020g0171a0002c0037t0011g0116others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.4560-396T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803712 | ||||||
| chr9:104803768
|
C | T | 7 | a0002c0025t0007g0237a0002c0058t0007g0143a0004c0064t0007g0175others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.4560-452G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803768 | ||||||
| chr9:104803817
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4560-501C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803817 | ||||||
| chr9:104803830
|
C | G | 8 | a0002c0017t0002g0271a0002c0017t0026g0163a0002c0017t0026g0276others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.4560-514G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803830 | ||||||
| chr9:104803852
|
C | T | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4560-536G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104803852 | ||||||
| chr9:104804019
|
T | C | 2 | a0022c0050t0001g0166a0023c0072t0001g0309 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.4559+607A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104804019 | ||||||
| chr9:104804081
|
G | A | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4559+545C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104804081 | ||||||
| chr9:104804099
|
A | G | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4559+527T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104804099 | ||||||
| chr9:104804234
|
C | CA | 40 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(37): Show | 40 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.4559+391dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104804234 | ||||||
| chr9:104804596
|
C | A | 271 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.4559+30G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104804596 | ||||||
| chr9:104804603
|
G | A | 2 | a0013c0013t0025g0032a0013c0013t0025g0033 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.4559+23C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 32/49 | chr9 | 104804603 | ||||||
| chr9:104804818
|
C | T | 1 | a0002c0017t0015g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4465-98G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104804818 | ||||||
| chr9:104804978
|
T | C | 1 | a0002c0025t0008g0285 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4465-258A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104804978 | ||||||
| chr9:104805135
|
C | T | 10 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(7): Show | 10 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4465-415G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805135 | ||||||
| chr9:104805191
|
C | T | 2 | a0008c0069t0008g0096a0035c0091t0008g0161 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4465-471G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805191 | ||||||
| chr9:104805193
|
G | A | 10 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(7): Show | 10 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4465-473C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805193 | ||||||
| chr9:104805201
|
A | G | 6 | a0002c0025t0007g0237a0004c0064t0007g0175a0004c0096t0007g0020others(3): Show | 6 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.4465-481T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805201 | ||||||
| chr9:104805236
|
G | T | 9 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4465-516C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805236 | ||||||
| chr9:104805367
|
G | A | 1 | a0009c0028t0048g0241 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4465-647C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805367 | ||||||
| chr9:104805637
|
C | CCCAGGCC others(45): Show |
1 | a0004c0029t0005g0162 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4464+552_4464+603d others(54): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805637 | ||||||
| chr9:104805683
|
T | C | 4 | a0002c0017t0002g0271a0002c0017t0026g0163a0002c0017t0026g0276others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.4464+558A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805683 | ||||||
| chr9:104805830
|
C | T | 15 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(12): Show | 15 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.4464+411G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805830 | ||||||
| chr9:104805843
|
G | A | 1 | a0023c0072t0001g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4464+398C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805843 | ||||||
| chr9:104805922
|
C | T | 1 | a0001c0001t0049g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4464+319G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805922 | ||||||
| chr9:104805926
|
G | A | 29 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(26): Show | 29 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.4464+315C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805926 | ||||||
| chr9:104805931
|
C | A | 1 | a0001c0001t0006g0239 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4464+310G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805931 | ||||||
| chr9:104805976
|
G | A | 3 | a0005c0051t0019g0164a0005c0082t0002g0282a0012c0093t0001g0108 | 3 | HG01952.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4464+265C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104805976 | ||||||
| chr9:104806109
|
A | AAAAAAAC | 8 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4464+125_4464+131d others(9): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104806109 | ||||||
| chr9:104806229
|
A | G | 1 | a0009c0027t0006g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4464+12T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 31/49 | chr9 | 104806229 | ||||||
| chr9:104806521
|
C | T | 6 | a0005c0026t0024g0157a0005c0036t0001g0273a0005c0070t0001g0316others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4275-91G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104806521 | ||||||
| chr9:104806528
|
G | C | 1 | a0003c0077t0005g0312 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4275-98C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104806528 | ||||||
| chr9:104806655
|
T | G | 3 | a0022c0050t0001g0166a0023c0072t0001g0309a0024c0073t0019g0231 | 3 | HG02486.hp1 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.4275-225A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104806655 | ||||||
| chr9:104806739
|
C | T | 1 | a0009c0018t0003g0248 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4275-309G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104806739 | ||||||
| chr9:104806740
|
G | A | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4275-310C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104806740 | ||||||
| chr9:104807028
|
A | T | 6 | a0005c0026t0024g0157a0005c0036t0001g0273a0005c0070t0001g0316others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4275-598T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807028 | ||||||
| chr9:104807056
|
T | C | 164 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.4275-626A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807056 | ||||||
| chr9:104807086
|
C | T | 10 | a0002c0058t0007g0143a0002c0078t0001g0216a0004c0029t0001g0099others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.4275-656G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807086 | ||||||
| chr9:104807105
|
G | A | 2 | a0004c0112t0005g0098a0008c0047t0002g0244 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4275-675C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807105 | ||||||
| chr9:104807312
|
G | A | 3 | a0003c0009t0003g0178a0006c0063t0003g0151a0006c0089t0003g0180 | 3 | NA18978.hp1 NA18991.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.4275-882C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807312 | ||||||
| chr9:104807493
|
T | C | 10 | a0002c0058t0007g0143a0002c0078t0001g0216a0004c0029t0001g0099others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.4275-1063A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807493 | ||||||
| chr9:104807581
|
G | A | 1 | a0001c0001t0012g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4275-1151C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807581 | ||||||
| chr9:104807761
|
C | T | 1 | a0002c0075t0027g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4275-1331G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807761 | ||||||
| chr9:104807818
|
A | T | 3 | a0002c0033t0002g0301a0002c0033t0032g0024a0005c0071t0041g0311 | 3 | HG01891.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4275-1388T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807818 | ||||||
| chr9:104807822
|
T | A | 22 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(19): Show | 22 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.4275-1392A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807822 | ||||||
| chr9:104807835
|
T | A | 1 | a0006c0004t0011g0269 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4275-1405A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807835 | ||||||
| chr9:104807843
|
T | TACACAC | 7 | a0004c0113t0002g0159a0005c0036t0001g0091a0005c0052t0001g0281others(4): Show | 7 | HG01081.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4275-1414_4275-141 others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807843 | ||||||
| chr9:104807843
|
T | TACACACA others(1): Show |
3 | a0002c0046t0002g0154a0002c0057t0001g0148a0025c0083t0001g0313 | 3 | HG03098.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4275-1414_4275-141 others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807843 | ||||||
| chr9:104807845
|
T | C | 13 | a0002c0046t0002g0154a0002c0057t0001g0148a0004c0113t0002g0159others(10): Show | 13 | HG01081.hp2 HG02055.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.4275-1415A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807845 | ||||||
| chr9:104807845
|
T | TACAC | 6 | a0001c0001t0001g0088a0001c0001t0039g0246a0015c0020t0001g0006others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.4275-1419_4275-141 others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807845 | ||||||
| chr9:104807845
|
T | TATAC | 27 | a0002c0011t0004g0263a0002c0011t0020g0171a0002c0037t0011g0116others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.4275-1416_4275-141 others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807845 | ||||||
| chr9:104807845
|
TAC | T | 5 | a0002c0033t0002g0301a0002c0033t0032g0024a0003c0002t0002g0172others(2): Show | 5 | HG00558.hp2 HG01891.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.4275-1417_4275-141 others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807845 | ||||||
| chr9:104807845
|
TACAC | T | 153 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.4275-1419_4275-141 others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807845 | ||||||
| chr9:104807845
|
TACACAC | T | 26 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(23): Show | 26 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.4275-1421_4275-141 others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807845 | ||||||
| chr9:104807845
|
TACACACA others(1): Show |
T | 11 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.4275-1423_4275-141 others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807845 | ||||||
| chr9:104807847
|
C | T | 6 | a0001c0001t0003g0086a0002c0017t0002g0271a0002c0017t0026g0163others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4275-1417G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807847 | ||||||
| chr9:104807849
|
C | T | 6 | a0001c0001t0003g0086a0002c0033t0002g0301a0002c0033t0032g0024others(3): Show | 6 | HG00558.hp2 HG01109.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.4275-1419G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807849 | ||||||
| chr9:104807851
|
C | T | 148 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.4275-1421G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807851 | ||||||
| chr9:104807853
|
C | T | 158 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.4275-1423G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807853 | ||||||
| chr9:104807855
|
C | T | 9 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.4275-1425G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807855 | ||||||
| chr9:104807871
|
CACACAT | C | 4 | a0002c0017t0002g0271a0002c0017t0026g0163a0002c0017t0026g0276others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.4275-1447_4275-144 others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807871 | ||||||
| chr9:104807877
|
T | C | 34 | a0002c0011t0004g0263a0002c0031t0001g0152a0002c0031t0001g0278others(31): Show | 34 | HG00423.hp1 HG01081.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.4275-1447A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807877 | ||||||
| chr9:104807879
|
T | C | 8 | a0011c0010t0005g0255a0011c0010t0005g0258a0011c0010t0005g0287others(5): Show | 8 | HG02145.hp1 HG02300.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.4275-1449A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807879 | ||||||
| chr9:104807884
|
A | T | 287 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.4275-1454T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807884 | ||||||
| chr9:104807885
|
T | A | 287 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.4275-1455A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807885 | ||||||
| chr9:104807885
|
T | TTA | 17 | a0002c0031t0001g0152a0002c0031t0001g0278a0005c0014t0006g0052others(14): Show | 17 | HG00423.hp1 HG01243.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.4275-1457_4275-145 others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807885 | ||||||
| chr9:104807914
|
ATTG | A | 82 | a0002c0011t0004g0112a0002c0011t0004g0263a0002c0011t0007g0119others(79): Show | 82 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.4275-1487_4275-148 others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807914 | ||||||
| chr9:104807960
|
A | C | 26 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(23): Show | 26 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.4274+1506T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104807960 | ||||||
| chr9:104808013
|
A | G | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4274+1453T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808013 | ||||||
| chr9:104808016
|
C | T | 1 | a0002c0011t0004g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4274+1450G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808016 | ||||||
| chr9:104808122
|
A | AT | 9 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4274+1343dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808122 | ||||||
| chr9:104808164
|
G | A | 1 | a0001c0005t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4274+1302C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808164 | ||||||
| chr9:104808198
|
G | A | 3 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0066t0008g0007 | 3 | HG01891.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4274+1268C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808198 | ||||||
| chr9:104808246
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4274+1220G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808246 | ||||||
| chr9:104808433
|
C | G | 129 | a0001c0001t0001g0088a0001c0001t0039g0246a0002c0011t0004g0112others(126): Show | 129 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.4274+1033G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808433 | ||||||
| chr9:104808522
|
G | A | 13 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.4274+944C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808522 | ||||||
| chr9:104808927
|
G | A | 307 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.4274+539C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808927 | ||||||
| chr9:104808960
|
C | T | 86 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.4274+506G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104808960 | ||||||
| chr9:104809094
|
G | A | 178 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.4274+372C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104809094 | ||||||
| chr9:104809248
|
GACGTGCT others(4): Show |
G | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4274+207_4274+217d others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 30/49 | chr9 | 104809248 | ||||||
| chr9:104809743
|
G | A | 6 | a0002c0025t0007g0237a0004c0064t0007g0175a0004c0096t0007g0020others(3): Show | 6 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.4176-179C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104809743 | ||||||
| chr9:104809838
|
T | G | 9 | a0001c0001t0001g0088a0001c0001t0039g0246a0002c0025t0008g0285others(6): Show | 9 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.4176-274A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104809838 | ||||||
| chr9:104809853
|
T | A | 16 | a0002c0085t0008g0142a0011c0010t0005g0097a0011c0010t0005g0169others(13): Show | 16 | HG02109.hp1 HG02145.hp1 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.4176-289A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104809853 | ||||||
| chr9:104809937
|
T | C | 1 | a0002c0085t0008g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4176-373A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104809937 | ||||||
| chr9:104810141
|
C | CAT | 37 | a0001c0001t0002g0074a0001c0001t0003g0086a0001c0001t0004g0193others(34): Show | 37 | HG00609.hp1 HG00673.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.4176-579_4176-578d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
C | CATAT | 14 | a0001c0108t0002g0113a0002c0031t0001g0152a0002c0031t0001g0278others(11): Show | 14 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.4176-581_4176-578d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
C | CATATAT | 5 | a0002c0015t0031g0084a0003c0076t0002g0130a0014c0053t0002g0146others(2): Show | 5 | HG02056.hp2 HG02300.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4176-583_4176-578d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
C | CATATATA others(1): Show |
3 | a0001c0001t0012g0144a0003c0009t0001g0279a0003c0009t0003g0209 | 3 | HG00099.hp2 HG00738.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.4176-585_4176-578d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
CAT | C | 24 | a0002c0046t0002g0154a0002c0057t0001g0148a0004c0008t0003g0197others(21): Show | 24 | HG00642.hp1 HG01099.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.4176-579_4176-578d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
CATAT | C | 26 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(23): Show | 26 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.4176-581_4176-578d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
CATATAT | C | 16 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0058t0007g0143others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4176-583_4176-578d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
CATATATA others(1): Show |
C | 12 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0032t0001g0025others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.4176-585_4176-578d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810141
|
CATATATA others(3): Show |
C | 10 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0024t0008g0003others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.4176-587_4176-578d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810141 | ||||||
| chr9:104810145
|
T | C | 1 | a0012c0105t0024g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4176-581A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810145 | ||||||
| chr9:104810150
|
A | G | 1 | a0007c0003t0011g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4176-586T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810150 | ||||||
| chr9:104810158
|
ATATATAT others(4): Show |
A | 2 | a0004c0112t0005g0098a0008c0047t0002g0244 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4176-605_4176-595d others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810158 | ||||||
| chr9:104810164
|
ATATAC | A | 9 | a0001c0001t0001g0088a0001c0001t0039g0246a0002c0025t0008g0285others(6): Show | 9 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.4176-605_4176-601d others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810164 | ||||||
| chr9:104810169
|
C | A | 1 | a0003c0009t0003g0073 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4176-605G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810169 | ||||||
| chr9:104810170
|
T | C | 12 | a0001c0001t0001g0088a0001c0001t0039g0246a0002c0025t0008g0285others(9): Show | 12 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.4176-606A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810170 | ||||||
| chr9:104810182
|
A | T | 13 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.4175+618T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810182 | ||||||
| chr9:104810672
|
A | G | 2 | a0018c0079t0004g0314a0018c0080t0004g0107 | 2 | HG01109.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.4175+128T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810672 | ||||||
| chr9:104810769
|
C | T | 6 | a0005c0026t0024g0157a0005c0036t0001g0273a0005c0070t0001g0316others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4175+31G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 29/49 | chr9 | 104810769 | ||||||
| chr9:104811055
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0196 | 2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.4051-131C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811055 | ||||||
| chr9:104811065
|
T | G | 1 | a0012c0040t0029g0001 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4051-141A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811065 | ||||||
| chr9:104811201
|
T | G | 1 | a0009c0018t0003g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4051-277A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811201 | ||||||
| chr9:104811217
|
G | A | 7 | a0001c0001t0006g0214a0006c0004t0003g0190a0006c0004t0004g0227others(4): Show | 7 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.4051-293C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811217 | ||||||
| chr9:104811248
|
T | C | 15 | a0002c0058t0007g0143a0002c0078t0001g0216a0004c0029t0001g0099others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.4051-324A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811248 | ||||||
| chr9:104811476
|
G | A | 35 | a0002c0011t0004g0112a0002c0011t0007g0119a0002c0011t0007g0247others(32): Show | 35 | HG00423.hp1 HG00642.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.4051-552C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811476 | ||||||
| chr9:104811828
|
T | C | 3 | a0008c0006t0005g0063a0008c0006t0006g0057a0008c0006t0022g0135 | 3 | NA18960.hp1 NA18979.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.4050+746A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811828 | ||||||
| chr9:104811907
|
C | T | 1 | a0012c0040t0040g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4050+667G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104811907 | ||||||
| chr9:104812093
|
T | C | 1 | a0006c0012t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4050+481A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812093 | ||||||
| chr9:104812229
|
C | T | 5 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(2): Show | 5 | HG02723.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4050+345G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812229 | ||||||
| chr9:104812237
|
G | A | 1 | a0002c0075t0027g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4050+337C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812237 | ||||||
| chr9:104812304
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4050+270A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812304 | ||||||
| chr9:104812469
|
TCC | T | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277 | 3 | HG02258.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4050+103_4050+104d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812469 | ||||||
| chr9:104812472
|
G | T | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277 | 3 | HG02258.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4050+102C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812472 | ||||||
| chr9:104812473
|
G | T | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277 | 3 | HG02258.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4050+101C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812473 | ||||||
| chr9:104812476
|
T | G | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277 | 3 | HG02258.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4050+98A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812476 | ||||||
| chr9:104812477
|
C | A | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277 | 3 | HG02258.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4050+97G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812477 | ||||||
| chr9:104812478
|
C | T | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277 | 3 | HG02258.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4050+96G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812478 | ||||||
| chr9:104812479
|
A | T | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277 | 3 | HG02258.hp2 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4050+95T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 28/49 | chr9 | 104812479 | ||||||
| chr9:104812939
|
G | T | 1 | a0006c0004t0003g0190 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3902-217C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 27/49 | chr9 | 104812939 | ||||||
| chr9:104813000
|
G | T | 22 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(19): Show | 22 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.3902-278C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 27/49 | chr9 | 104813000 | ||||||
| chr9:104813052
|
A | G | 2 | a0003c0009t0006g0186a0006c0004t0006g0249 | 2 | NA18941.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.3902-330T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 27/49 | chr9 | 104813052 | ||||||
| chr9:104813296
|
A | C | 1 | a0001c0001t0003g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3902-574T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 27/49 | chr9 | 104813296 | ||||||
| chr9:104813494
|
A | T | 1 | a0002c0075t0027g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3901+624T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 27/49 | chr9 | 104813494 | ||||||
| chr9:104813965
|
G | A | 104 | a0001c0001t0001g0088a0001c0001t0039g0246a0002c0011t0004g0112others(101): Show | 104 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.3901+153C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 27/49 | chr9 | 104813965 | ||||||
| chr9:104814367
|
A | G | 5 | a0002c0017t0002g0271a0002c0017t0026g0163a0002c0017t0026g0276others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.3787+60T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 26/49 | chr9 | 104814367 | ||||||
| chr9:104814375
|
A | G | 9 | a0002c0058t0007g0143a0002c0078t0001g0216a0004c0029t0001g0099others(6): Show | 9 | HG01884.hp1 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3787+52T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 26/49 | chr9 | 104814375 | ||||||
| chr9:104814384
|
A | G | 4 | a0002c0075t0027g0150a0022c0050t0001g0166a0023c0072t0001g0309others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3787+43T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 26/49 | chr9 | 104814384 | ||||||
| chr9:104814541
|
G | A | 23 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.3739-66C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104814541 | ||||||
| chr9:104814762
|
G | A | 1 | a0003c0002t0007g0059 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3739-287C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104814762 | ||||||
| chr9:104814885
|
C | G | 2 | a0003c0002t0002g0040a0006c0012t0010g0198 | 2 | HG01978.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3739-410G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104814885 | ||||||
| chr9:104814919
|
T | C | 3 | a0022c0050t0001g0166a0023c0072t0001g0309a0024c0073t0019g0231 | 3 | HG02486.hp1 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3739-444A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104814919 | ||||||
| chr9:104814937
|
G | A | 11 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.3739-462C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104814937 | ||||||
| chr9:104814940
|
A | G | 11 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.3739-465T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104814940 | ||||||
| chr9:104815015
|
T | A | 1 | a0001c0001t0043g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3739-540A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815015 | ||||||
| chr9:104815018
|
A | T | 18 | a0002c0085t0008g0142a0004c0008t0003g0289a0011c0010t0005g0097others(15): Show | 18 | HG02109.hp1 HG02145.hp1 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.3739-543T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815018 | ||||||
| chr9:104815042
|
G | A | 1 | a0003c0002t0003g0127 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3739-567C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815042 | ||||||
| chr9:104815051
|
A | T | 1 | a0004c0114t0005g0304 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3739-576T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815051 | ||||||
| chr9:104815253
|
G | T | 21 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(18): Show | 21 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.3739-778C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815253 | ||||||
| chr9:104815583
|
G | A | 1 | a0019c0086t0003g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3738+560C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815583 | ||||||
| chr9:104815767
|
C | G | 35 | a0002c0011t0004g0112a0002c0011t0007g0119a0002c0011t0007g0247others(32): Show | 35 | HG00423.hp1 HG00642.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.3738+376G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815767 | ||||||
| chr9:104815778
|
A | T | 10 | a0001c0001t0001g0088a0001c0001t0003g0297a0001c0001t0039g0246others(7): Show | 10 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.3738+365T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815778 | ||||||
| chr9:104815822
|
A | C | 33 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0020g0171others(30): Show | 33 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.3738+321T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104815822 | ||||||
| chr9:104816005
|
C | T | 1 | a0029c0110t0002g0165 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3738+138G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104816005 | ||||||
| chr9:104816020
|
T | C | 12 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.3738+123A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104816020 | ||||||
| chr9:104816053
|
A | G | 3 | a0015c0020t0001g0006a0015c0020t0001g0160a0015c0020t0004g0005 | 3 | HG02622.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3738+90T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104816053 | ||||||
| chr9:104816120
|
C | T | 18 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0013g0305others(15): Show | 18 | HG00673.hp2 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3738+23G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 25/49 | chr9 | 104816120 | ||||||
| chr9:104816395
|
G | A | 3 | a0004c0112t0005g0098a0008c0047t0002g0244a0032c0104t0005g0168 | 3 | HG02280.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3536-50C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104816395 | ||||||
| chr9:104816468
|
T | G | 7 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(4): Show | 7 | HG01884.hp1 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3536-123A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104816468 | ||||||
| chr9:104816483
|
T | A | 1 | a0007c0090t0007g0046 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3536-138A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104816483 | ||||||
| chr9:104816607
|
A | G | 6 | a0005c0026t0024g0157a0005c0036t0001g0273a0005c0070t0001g0316others(3): Show | 6 | HG01109.hp1 HG01243.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3536-262T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104816607 | ||||||
| chr9:104816971
|
C | G | 27 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(24): Show | 27 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.3535+361G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104816971 | ||||||
| chr9:104817092
|
A | G | 2 | a0002c0085t0008g0142a0004c0008t0003g0289 | 2 | HG02738.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3535+240T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104817092 | ||||||
| chr9:104817183
|
G | A | 29 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(26): Show | 29 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.3535+149C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104817183 | ||||||
| chr9:104817191
|
A | C | 25 | a0001c0001t0001g0176a0002c0011t0004g0263a0002c0037t0011g0116others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.3535+141T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104817191 | ||||||
| chr9:104817266
|
G | C | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3535+66C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104817266 | ||||||
| chr9:104817267
|
C | G | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3535+65G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 24/49 | chr9 | 104817267 | ||||||
| chr9:104817469
|
C | T | 1 | a0004c0008t0003g0294 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3463-65G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817469 | ||||||
| chr9:104817470
|
G | A | 2 | a0004c0008t0003g0289a0004c0008t0006g0202 | 2 | HG02738.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3463-66C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817470 | ||||||
| chr9:104817473
|
G | A | 2 | a0004c0008t0003g0289a0004c0008t0006g0202 | 2 | HG02738.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3463-69C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817473 | ||||||
| chr9:104817537
|
T | C | 6 | a0002c0025t0007g0237a0004c0064t0007g0175a0004c0096t0007g0020others(3): Show | 6 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.3463-133A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817537 | ||||||
| chr9:104817599
|
C | T | 15 | a0002c0011t0004g0112a0002c0011t0007g0119a0002c0011t0007g0247others(12): Show | 15 | HG00423.hp1 HG01255.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3463-195G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817599 | ||||||
| chr9:104817818
|
T | A | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-414A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817818 | ||||||
| chr9:104817819
|
T | C | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-415A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817819 | ||||||
| chr9:104817820
|
G | A | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-416C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817820 | ||||||
| chr9:104817823
|
G | A | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-419C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817823 | ||||||
| chr9:104817824
|
A | G | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-420T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817824 | ||||||
| chr9:104817827
|
T | C | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-423A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817827 | ||||||
| chr9:104817828
|
T | G | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-424A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817828 | ||||||
| chr9:104817830
|
T | G | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-426A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817830 | ||||||
| chr9:104817831
|
A | T | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-427T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817831 | ||||||
| chr9:104817832
|
A | G | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-428T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817832 | ||||||
| chr9:104817833
|
C | T | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-429G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817833 | ||||||
| chr9:104817834
|
A | T | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3463-430T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817834 | ||||||
| chr9:104817922
|
T | C | 7 | a0005c0026t0024g0157a0005c0036t0001g0091a0005c0036t0001g0273others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.3463-518A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817922 | ||||||
| chr9:104817929
|
G | C | 8 | a0002c0025t0007g0237a0003c0077t0005g0312a0004c0064t0007g0175others(5): Show | 8 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.3463-525C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817929 | ||||||
| chr9:104817986
|
T | G | 1 | a0007c0003t0020g0179 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3463-582A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817986 | ||||||
| chr9:104817992
|
G | A | 1 | a0018c0079t0004g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3463-588C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104817992 | ||||||
| chr9:104818008
|
T | C | 1 | a0005c0070t0001g0316 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3463-604A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818008 | ||||||
| chr9:104818136
|
G | A | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3462+527C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818136 | ||||||
| chr9:104818146
|
A | G | 7 | a0002c0025t0007g0237a0003c0077t0005g0312a0004c0064t0007g0175others(4): Show | 7 | HG01099.hp1 HG01106.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.3462+517T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818146 | ||||||
| chr9:104818169
|
TA | T | 98 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.3462+493delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818169 | ||||||
| chr9:104818199
|
C | T | 25 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(22): Show | 25 | HG00642.hp1 HG01081.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.3462+464G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818199 | ||||||
| chr9:104818367
|
T | C | 2 | a0005c0036t0001g0273a0005c0070t0001g0316 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3462+296A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818367 | ||||||
| chr9:104818376
|
G | A | 43 | a0001c0001t0001g0088a0001c0001t0001g0176a0001c0001t0003g0297others(40): Show | 43 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.3462+287C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818376 | ||||||
| chr9:104818378
|
C | T | 3 | a0001c0001t0006g0239a0001c0001t0023g0295a0001c0001t0023g0296 | 3 | HG03490.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3462+285G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818378 | ||||||
| chr9:104818561
|
T | C | 44 | a0001c0001t0001g0088a0001c0001t0001g0176a0001c0001t0003g0297others(41): Show | 44 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.3462+102A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 23/49 | chr9 | 104818561 | ||||||
| chr9:104818948
|
A | G | 1 | a0003c0056t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3242-65T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104818948 | ||||||
| chr9:104818958
|
G | T | 1 | a0003c0056t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3242-75C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104818958 | ||||||
| chr9:104819026
|
C | T | 48 | a0001c0001t0001g0088a0001c0001t0001g0176a0001c0001t0006g0214others(45): Show | 48 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.3242-143G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819026 | ||||||
| chr9:104819090
|
A | G | 3 | a0002c0011t0020g0171a0004c0008t0003g0289a0004c0008t0006g0202 | 3 | HG02738.hp2 NA18942.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3242-207T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819090 | ||||||
| chr9:104819142
|
G | A | 16 | a0002c0011t0020g0171a0002c0024t0008g0003a0002c0024t0008g0008others(13): Show | 16 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.3242-259C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819142 | ||||||
| chr9:104819160
|
A | G | 1 | a0002c0075t0027g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3242-277T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819160 | ||||||
| chr9:104819255
|
C | T | 14 | a0002c0015t0031g0084a0002c0025t0015g0283a0002c0059t0001g0235others(11): Show | 14 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3241+331G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819255 | ||||||
| chr9:104819316
|
T | C | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3241+270A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819316 | ||||||
| chr9:104819390
|
T | C | 4 | a0001c0001t0001g0102a0002c0011t0020g0171a0004c0008t0003g0289others(1): Show | 4 | HG02738.hp2 NA18942.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.3241+196A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819390 | ||||||
| chr9:104819468
|
A | C | 95 | a0001c0001t0001g0203a0001c0001t0001g0218a0001c0001t0002g0233others(92): Show | 95 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.3241+118T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 22/49 | chr9 | 104819468 | ||||||
| chr9:104820079
|
G | A | 2 | a0002c0031t0001g0152a0002c0031t0001g0278 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2961-10C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820079 | ||||||
| chr9:104820180
|
T | C | 1 | a0016c0019t0018g0131 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2961-111A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820180 | ||||||
| chr9:104820342
|
T | C | 2 | a0002c0032t0001g0025a0002c0032t0001g0317 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2961-273A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820342 | ||||||
| chr9:104820499
|
G | A | 43 | a0002c0011t0007g0119a0002c0011t0007g0247a0002c0011t0012g0134others(40): Show | 43 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.2961-430C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820499 | ||||||
| chr9:104820506
|
T | G | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2961-437A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820506 | ||||||
| chr9:104820532
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2961-463G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820532 | ||||||
| chr9:104820619
|
C | T | 1 | a0007c0003t0016g0029 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2961-550G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820619 | ||||||
| chr9:104820620
|
G | A | 2 | a0015c0020t0001g0006a0015c0020t0004g0005 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2961-551C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820620 | ||||||
| chr9:104820717
|
C | G | 26 | a0001c0097t0001g0106a0001c0108t0002g0113a0001c0109t0001g0232others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.2961-648G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820717 | ||||||
| chr9:104820763
|
C | CG | 81 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0015t0013g0305others(78): Show | 81 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.2960+611dupC | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820763 | ||||||
| chr9:104820935
|
C | T | 1 | a0002c0057t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2960+440G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104820935 | ||||||
| chr9:104821019
|
C | T | 1 | a0036c0094t0009g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2960+356G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821019 | ||||||
| chr9:104821020
|
G | A | 2 | a0005c0022t0021g0141a0005c0022t0021g0147 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2960+355C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821020 | ||||||
| chr9:104821085
|
A | C | 1 | a0003c0002t0003g0127 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2960+290T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821085 | ||||||
| chr9:104821086
|
C | A | 1 | a0003c0002t0003g0127 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2960+289G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821086 | ||||||
| chr9:104821136
|
G | A | 3 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0058t0007g0143 | 3 | HG01884.hp2 HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2960+239C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821136 | ||||||
| chr9:104821233
|
C | G | 1 | a0034c0103t0007g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2960+142G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821233 | ||||||
| chr9:104821249
|
T | G | 22 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(19): Show | 22 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2960+126A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821249 | ||||||
| chr9:104821357
|
C | T | 7 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0037t0001g0275others(4): Show | 7 | HG01884.hp2 HG01952.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2960+18G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 20/49 | chr9 | 104821357 | ||||||
| chr9:104821596
|
C | T | 1 | a0006c0004t0045g0155 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2829-90G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104821596 | ||||||
| chr9:104821634
|
C | T | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2829-128G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104821634 | ||||||
| chr9:104821673
|
G | A | 8 | a0002c0025t0008g0285a0002c0057t0001g0148a0011c0010t0005g0097others(5): Show | 8 | HG02145.hp1 HG02922.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2829-167C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104821673 | ||||||
| chr9:104821750
|
C | T | 317 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.2829-244G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104821750 | ||||||
| chr9:104821931
|
A | G | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2829-425T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104821931 | ||||||
| chr9:104822028
|
T | C | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2828+468A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822028 | ||||||
| chr9:104822038
|
G | A | 5 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2828+458C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822038 | ||||||
| chr9:104822060
|
C | T | 5 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2828+436G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822060 | ||||||
| chr9:104822070
|
T | C | 27 | a0001c0097t0001g0106a0001c0108t0002g0113a0001c0109t0001g0232others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.2828+426A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822070 | ||||||
| chr9:104822152
|
C | A | 1 | a0002c0032t0001g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2828+344G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822152 | ||||||
| chr9:104822161
|
G | A | 8 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0046t0002g0154others(5): Show | 8 | HG02280.hp1 HG02300.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2828+335C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822161 | ||||||
| chr9:104822168
|
G | C | 1 | a0002c0032t0001g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2828+328C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822168 | ||||||
| chr9:104822206
|
T | C | 1 | a0002c0059t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2828+290A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822206 | ||||||
| chr9:104822216
|
C | A | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2828+280G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822216 | ||||||
| chr9:104822276
|
C | G | 1 | a0002c0011t0012g0134 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2828+220G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822276 | ||||||
| chr9:104822410
|
A | G | 1 | a0009c0021t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2828+86T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822410 | ||||||
| chr9:104822461
|
T | C | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2828+35A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 19/49 | chr9 | 104822461 | ||||||
| chr9:104822719
|
G | C | 9 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2657-52C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104822719 | ||||||
| chr9:104822735
|
G | C | 57 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0017t0015g0101others(54): Show | 57 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.2657-68C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104822735 | ||||||
| chr9:104822742
|
C | T | 3 | a0001c0001t0002g0233a0001c0001t0023g0295a0001c0001t0023g0296 | 3 | HG01175.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2657-75G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104822742 | ||||||
| chr9:104822932
|
C | T | 30 | a0008c0006t0001g0087a0008c0006t0003g0187a0008c0006t0005g0063others(27): Show | 30 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.2657-265G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104822932 | ||||||
| chr9:104823035
|
T | G | 76 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(73): Show | 76 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2657-368A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823035 | ||||||
| chr9:104823064
|
G | GA | 80 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0017t0015g0101others(77): Show | 80 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.2657-398dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823064 | ||||||
| chr9:104823321
|
C | T | 3 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2657-654G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823321 | ||||||
| chr9:104823347
|
C | T | 1 | a0002c0085t0008g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2657-680G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823347 | ||||||
| chr9:104823446
|
G | A | 6 | a0008c0006t0003g0187a0008c0048t0030g0022a0017c0034t0001g0153others(3): Show | 6 | HG01081.hp2 HG02615.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2657-779C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823446 | ||||||
| chr9:104823520
|
A | C | 1 | a0002c0085t0008g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2657-853T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823520 | ||||||
| chr9:104823560
|
G | A | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2657-893C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823560 | ||||||
| chr9:104823957
|
C | A | 57 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0017t0015g0101others(54): Show | 57 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.2656+508G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104823957 | ||||||
| chr9:104824239
|
CAAAG | C | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2656+222_2656+225d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104824239 | ||||||
| chr9:104824390
|
C | T | 2 | a0003c0009t0001g0279a0003c0009t0003g0209 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2656+75G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104824390 | ||||||
| chr9:104824405
|
A | G | 4 | a0012c0105t0024g0217a0024c0073t0019g0231a0032c0104t0005g0168others(1): Show | 4 | HG02280.hp1 HG02300.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2656+60T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 18/49 | chr9 | 104824405 | ||||||
| chr9:104824615
|
T | A | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2543-37A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104824615 | ||||||
| chr9:104824756
|
C | T | 1 | a0002c0059t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2543-178G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104824756 | ||||||
| chr9:104824890
|
C | T | 6 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2543-312G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104824890 | ||||||
| chr9:104825044
|
G | A | 4 | a0001c0001t0002g0074a0001c0001t0011g0085a0001c0001t0052g0318others(1): Show | 4 | HG00099.hp1 HG01070.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2543-466C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825044 | ||||||
| chr9:104825295
|
C | T | 1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2542+388G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825295 | ||||||
| chr9:104825392
|
G | C | 3 | a0003c0002t0002g0122a0003c0002t0002g0257a0003c0076t0002g0130 | 3 | HG03927.hp1 NA19082.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2542+291C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825392 | ||||||
| chr9:104825485
|
T | A | 4 | a0003c0056t0001g0288a0018c0079t0004g0314a0018c0080t0004g0107others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2542+198A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825485 | ||||||
| chr9:104825499
|
T | A | 4 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277others(1): Show | 4 | HG01952.hp2 HG02258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2542+184A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825499 | ||||||
| chr9:104825554
|
A | C | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2542+129T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825554 | ||||||
| chr9:104825565
|
A | C | 1 | a0007c0003t0003g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2542+118T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825565 | ||||||
| chr9:104825565
|
A | G | 1 | a0037c0088t0034g0298 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2542+118T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 17/49 | chr9 | 104825565 | ||||||
| chr9:104825904
|
A | G | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2338-17T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104825904 | ||||||
| chr9:104825981
|
T | C | 4 | a0003c0056t0001g0288a0018c0079t0004g0314a0018c0080t0004g0107others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338-94A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104825981 | ||||||
| chr9:104826047
|
G | A | 31 | a0008c0006t0001g0087a0008c0006t0003g0187a0008c0006t0005g0063others(28): Show | 31 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2338-160C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826047 | ||||||
| chr9:104826090
|
C | T | 1 | a0003c0002t0002g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2338-203G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826090 | ||||||
| chr9:104826091
|
T | C | 1 | a0003c0002t0002g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2338-204A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826091 | ||||||
| chr9:104826196
|
C | T | 5 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338-309G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826196 | ||||||
| chr9:104826214
|
C | T | 5 | a0008c0006t0005g0063a0008c0006t0006g0057a0008c0006t0012g0081others(2): Show | 5 | NA18953.hp2 NA18960.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338-327G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826214 | ||||||
| chr9:104826216
|
G | T | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2338-329C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826216 | ||||||
| chr9:104826291
|
A | G | 139 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(136): Show | 139 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.2338-404T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826291 | ||||||
| chr9:104826332
|
T | G | 4 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277others(1): Show | 4 | HG01952.hp2 HG02258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2338-445A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826332 | ||||||
| chr9:104826496
|
C | T | 139 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(136): Show | 139 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.2337+452G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826496 | ||||||
| chr9:104826712
|
C | T | 5 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2337+236G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826712 | ||||||
| chr9:104826713
|
G | A | 1 | a0003c0077t0005g0312 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2337+235C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826713 | ||||||
| chr9:104826793
|
G | T | 22 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(19): Show | 22 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2337+155C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826793 | ||||||
| chr9:104826830
|
G | T | 5 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+118C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826830 | ||||||
| chr9:104826853
|
A | T | 191 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(188): Show | 191 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.2337+95T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 16/49 | chr9 | 104826853 | ||||||
| chr9:104827192
|
A | T | 2 | a0005c0016t0001g0009a0005c0016t0001g0010 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2116-23T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827192 | ||||||
| chr9:104827286
|
C | T | 31 | a0008c0006t0001g0087a0008c0006t0003g0187a0008c0006t0005g0063others(28): Show | 31 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2116-117G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827286 | ||||||
| chr9:104827299
|
A | T | 138 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(135): Show | 138 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.2116-130T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827299 | ||||||
| chr9:104827349
|
C | T | 138 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(135): Show | 138 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.2116-180G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827349 | ||||||
| chr9:104827429
|
C | T | 17 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(14): Show | 17 | HG01952.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2116-260G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827429 | ||||||
| chr9:104827463
|
C | T | 190 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(187): Show | 190 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.2116-294G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827463 | ||||||
| chr9:104827514
|
C | G | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2116-345G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827514 | ||||||
| chr9:104827534
|
C | T | 8 | a0006c0004t0005g0206a0006c0004t0006g0249a0006c0004t0010g0252others(5): Show | 8 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2116-365G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827534 | ||||||
| chr9:104827666
|
G | C | 37 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.2116-497C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104827666 | ||||||
| chr9:104828141
|
C | A | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2115+775G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828141 | ||||||
| chr9:104828165
|
C | T | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2115+751G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828165 | ||||||
| chr9:104828346
|
C | T | 22 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(19): Show | 22 | HG01952.hp2 HG02109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2115+570G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828346 | ||||||
| chr9:104828377
|
G | C | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2115+539C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828377 | ||||||
| chr9:104828440
|
A | G | 1 | a0001c0005t0002g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2115+476T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828440 | ||||||
| chr9:104828488
|
C | T | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2115+428G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828488 | ||||||
| chr9:104828676
|
G | A | 6 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0037t0001g0275others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2115+240C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828676 | ||||||
| chr9:104828743
|
C | T | 58 | a0001c0092t0012g0220a0002c0015t0013g0305a0002c0015t0013g0306others(55): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.2115+173G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828743 | ||||||
| chr9:104828801
|
G | T | 40 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2115+115C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828801 | ||||||
| chr9:104828831
|
AT | A | 5 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2115+84delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828831 | ||||||
| chr9:104828835
|
T | C | 40 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.2115+81A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 15/49 | chr9 | 104828835 | ||||||
| chr9:104829197
|
G | A | 58 | a0001c0092t0012g0220a0002c0015t0013g0305a0002c0015t0013g0306others(55): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1893-59C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829197 | ||||||
| chr9:104829282
|
G | A | 5 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1893-144C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829282 | ||||||
| chr9:104829292
|
A | G | 2 | a0002c0032t0001g0025a0002c0032t0001g0317 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1893-154T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829292 | ||||||
| chr9:104829342
|
T | C | 3 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0058t0007g0143 | 3 | HG01884.hp2 HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1893-204A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829342 | ||||||
| chr9:104829480
|
C | G | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1893-342G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829480 | ||||||
| chr9:104829498
|
A | G | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-360T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829498 | ||||||
| chr9:104829526
|
C | T | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1893-388G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829526 | ||||||
| chr9:104829583
|
T | C | 1 | a0002c0025t0007g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1893-445A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829583 | ||||||
| chr9:104829627
|
A | C | 16 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1893-489T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829627 | ||||||
| chr9:104829856
|
T | C | 4 | a0006c0004t0005g0206a0006c0004t0006g0249a0006c0004t0010g0252others(1): Show | 4 | HG02056.hp2 NA18967.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-718A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829856 | ||||||
| chr9:104829908
|
C | A | 140 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0011t0004g0213others(137): Show | 140 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1893-770G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829908 | ||||||
| chr9:104829943
|
T | TAC | 14 | a0001c0001t0001g0082a0001c0001t0001g0291a0001c0001t0003g0297others(11): Show | 14 | HG01070.hp2 HG01081.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1893-807_1893-806d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
T | TACAC | 4 | a0001c0001t0001g0102a0001c0001t0002g0137a0001c0005t0004g0167others(1): Show | 4 | HG02717.hp1 NA18747.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-809_1893-806d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
T | TACACAC | 4 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-811_1893-806d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
T | TACACACA others(1): Show |
3 | a0005c0052t0001g0281a0017c0034t0001g0153a0017c0034t0001g0300 | 3 | HG02615.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1893-813_1893-806d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
TAC | T | 28 | a0001c0001t0001g0176a0002c0025t0008g0285a0002c0057t0001g0148others(25): Show | 28 | HG01099.hp1 HG01192.hp2 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.1893-807_1893-806d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
TACAC | T | 33 | a0001c0001t0001g0088a0001c0001t0039g0246a0001c0108t0002g0113others(30): Show | 33 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1893-809_1893-806d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
TACACAC | T | 61 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1893-811_1893-806d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
TACACACA others(1): Show |
T | 13 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(10): Show | 13 | HG01169.hp1 HG01515.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1893-813_1893-806d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
TACACACA others(3): Show |
T | 60 | a0001c0092t0012g0220a0002c0015t0013g0305a0002c0015t0013g0306others(57): Show | 60 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1893-815_1893-806d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829943
|
TACACACA others(5): Show |
T | 2 | a0012c0105t0024g0217a0032c0104t0005g0168 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1893-817_1893-806d others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829943 | ||||||
| chr9:104829945
|
C | T | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1893-807G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104829945 | ||||||
| chr9:104830075
|
C | T | 3 | a0001c0001t0001g0176a0004c0064t0007g0175a0004c0096t0007g0020 | 3 | HG01099.hp1 HG01192.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1892+850G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830075 | ||||||
| chr9:104830077
|
G | A | 11 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1892+848C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830077 | ||||||
| chr9:104830084
|
G | A | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+841C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830084 | ||||||
| chr9:104830272
|
G | A | 1 | a0008c0049t0004g0103 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1892+653C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830272 | ||||||
| chr9:104830360
|
T | G | 24 | a0001c0108t0002g0113a0001c0109t0001g0232a0004c0043t0003g0128others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1892+565A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830360 | ||||||
| chr9:104830427
|
C | T | 2 | a0005c0016t0001g0009a0005c0016t0001g0010 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1892+498G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830427 | ||||||
| chr9:104830468
|
T | C | 1 | a0030c0100t0009g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1892+457A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830468 | ||||||
| chr9:104830551
|
G | A | 2 | a0010c0007t0010g0200a0010c0007t0010g0201 | 2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1892+374C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830551 | ||||||
| chr9:104830615
|
G | A | 1 | a0019c0106t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1892+310C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830615 | ||||||
| chr9:104830689
|
CA | C | 40 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1892+235delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830689 | ||||||
| chr9:104830696
|
A | T | 7 | a0001c0001t0001g0195a0001c0001t0001g0208a0001c0001t0001g0218others(4): Show | 7 | HG00738.hp2 HG01071.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1892+229T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830696 | ||||||
| chr9:104830701
|
T | A | 1 | a0007c0003t0016g0029 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1892+224A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830701 | ||||||
| chr9:104830721
|
T | C | 6 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1892+204A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830721 | ||||||
| chr9:104830802
|
C | G | 1 | a0002c0081t0013g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1892+123G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830802 | ||||||
| chr9:104830840
|
C | T | 1 | a0002c0059t0001g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1892+85G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830840 | ||||||
| chr9:104830901
|
A | T | 223 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(220): Show | 223 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1892+24T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 14/49 | chr9 | 104830901 | ||||||
| chr9:104831130
|
T | C | 3 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1716-29A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831130 | ||||||
| chr9:104831149
|
T | TA | 35 | a0001c0001t0003g0089a0001c0001t0006g0054a0001c0005t0002g0123others(32): Show | 35 | HG00558.hp1 HG01109.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.1716-49dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831149 | ||||||
| chr9:104831149
|
T | TAA | 83 | a0001c0092t0012g0220a0002c0011t0007g0119a0002c0011t0007g0247others(80): Show | 83 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1716-50_1716-49dup others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831149 | ||||||
| chr9:104831149
|
T | TAAA | 16 | a0003c0009t0003g0073a0006c0004t0002g0132a0006c0004t0003g0190others(13): Show | 16 | HG00408.hp2 HG00558.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1716-51_1716-49dup others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831149 | ||||||
| chr9:104831149
|
TA | T | 58 | a0001c0001t0006g0225a0001c0001t0011g0085a0001c0001t0049g0034others(55): Show | 58 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1716-49delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831149 | ||||||
| chr9:104831149
|
TAA | T | 27 | a0008c0006t0003g0187a0008c0006t0005g0063a0008c0006t0006g0057others(24): Show | 27 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1716-50_1716-49del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831149 | ||||||
| chr9:104831221
|
C | CT | 10 | a0005c0016t0011g0075a0009c0021t0001g0189a0012c0041t0001g0274others(7): Show | 10 | HG01106.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716-121dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831221 | ||||||
| chr9:104831339
|
T | C | 25 | a0001c0108t0002g0113a0001c0109t0001g0232a0002c0085t0008g0142others(22): Show | 25 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1716-238A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831339 | ||||||
| chr9:104831343
|
G | A | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716-242C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831343 | ||||||
| chr9:104831406
|
T | C | 19 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304others(16): Show | 19 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1715+216A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831406 | ||||||
| chr9:104831569
|
T | C | 1 | a0007c0003t0009g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1715+53A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 13/49 | chr9 | 104831569 | ||||||
| chr9:104832005
|
T | C | 9 | a0002c0015t0031g0084a0002c0033t0002g0301a0002c0033t0032g0024others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510-178A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832005 | ||||||
| chr9:104832083
|
A | G | 46 | a0001c0108t0002g0113a0001c0109t0001g0232a0004c0029t0001g0099others(43): Show | 46 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1510-256T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832083 | ||||||
| chr9:104832107
|
T | G | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1510-280A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832107 | ||||||
| chr9:104832175
|
C | T | 1 | a0008c0049t0004g0103 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1510-348G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832175 | ||||||
| chr9:104832193
|
T | C | 37 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(34): Show | 37 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1510-366A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832193 | ||||||
| chr9:104832226
|
G | C | 1 | a0014c0054t0010g0251 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1509+348C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832226 | ||||||
| chr9:104832228
|
T | A | 1 | a0014c0054t0010g0251 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1509+346A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832228 | ||||||
| chr9:104832234
|
A | G | 124 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0011t0004g0213others(121): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1509+340T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832234 | ||||||
| chr9:104832382
|
T | A | 1 | a0002c0037t0011g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1509+192A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832382 | ||||||
| chr9:104832417
|
G | A | 28 | a0008c0006t0001g0087a0008c0006t0003g0187a0008c0006t0005g0063others(25): Show | 28 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1509+157C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832417 | ||||||
| chr9:104832453
|
A | G | 2 | a0002c0032t0001g0025a0002c0032t0001g0317 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1509+121T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832453 | ||||||
| chr9:104832489
|
CT | C | 24 | a0001c0108t0002g0113a0001c0109t0001g0232a0004c0043t0003g0128others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1509+84delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 12/49 | chr9 | 104832489 | ||||||
| chr9:104832920
|
G | A | 1 | a0001c0005t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1312-149C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104832920 | ||||||
| chr9:104832929
|
G | A | 28 | a0008c0006t0001g0087a0008c0006t0003g0187a0008c0006t0005g0063others(25): Show | 28 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1312-158C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104832929 | ||||||
| chr9:104833195
|
G | A | 16 | a0006c0004t0002g0132a0006c0004t0002g0133a0006c0004t0003g0190others(13): Show | 16 | HG00408.hp2 HG00558.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1312-424C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833195 | ||||||
| chr9:104833321
|
A | C | 121 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0011t0004g0213others(118): Show | 121 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1312-550T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833321 | ||||||
| chr9:104833403
|
A | G | 38 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(35): Show | 38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1312-632T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833403 | ||||||
| chr9:104833444
|
A | G | 4 | a0003c0056t0001g0288a0018c0079t0004g0314a0018c0080t0004g0107others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-673T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833444 | ||||||
| chr9:104833466
|
G | A | 1 | a0007c0003t0011g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1312-695C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833466 | ||||||
| chr9:104833690
|
C | T | 5 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-919G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833690 | ||||||
| chr9:104833697
|
C | A | 126 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0011t0004g0213others(123): Show | 126 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1312-926G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833697 | ||||||
| chr9:104833741
|
G | A | 3 | a0003c0002t0002g0040a0003c0002t0002g0069a0003c0002t0002g0070 | 3 | HG02004.hp2 HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1312-970C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833741 | ||||||
| chr9:104833756
|
A | C | 1 | a0011c0010t0005g0287 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1312-985T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833756 | ||||||
| chr9:104833806
|
G | A | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312-1035C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833806 | ||||||
| chr9:104833820
|
T | C | 86 | a0001c0092t0012g0220a0002c0015t0013g0305a0002c0015t0013g0306others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1312-1049A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833820 | ||||||
| chr9:104833843
|
G | A | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1312-1072C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833843 | ||||||
| chr9:104833906
|
CTGCACAG others(909): Show |
C | 43 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(40): Show | 43 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1312-2051_1312-113 others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833906 | ||||||
| chr9:104833924
|
G | A | 83 | a0001c0092t0012g0220a0002c0015t0013g0305a0002c0015t0013g0306others(80): Show | 83 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1312-1153C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833924 | ||||||
| chr9:104833927
|
A | C | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1312-1156T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104833927 | ||||||
| chr9:104834004
|
T | C | 92 | a0001c0092t0012g0220a0002c0015t0013g0305a0002c0015t0013g0306others(89): Show | 92 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1312-1233A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834004 | ||||||
| chr9:104834105
|
G | A | 1 | a0019c0106t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1312-1334C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834105 | ||||||
| chr9:104834130
|
C | G | 78 | a0001c0108t0002g0113a0001c0109t0001g0232a0004c0042t0008g0083others(75): Show | 78 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1312-1359G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834130 | ||||||
| chr9:104834293
|
G | A | 1 | a0008c0006t0006g0057 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1312-1522C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834293 | ||||||
| chr9:104834309
|
C | T | 6 | a0005c0036t0001g0091a0005c0036t0001g0273a0005c0052t0001g0281others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-1538G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834309 | ||||||
| chr9:104834321
|
T | C | 56 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277others(53): Show | 56 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1312-1550A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834321 | ||||||
| chr9:104834447
|
C | T | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-1676G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834447 | ||||||
| chr9:104834462
|
T | C | 52 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304others(49): Show | 52 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1312-1691A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834462 | ||||||
| chr9:104834550
|
C | G | 1 | a0037c0088t0034g0298 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1312-1779G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834550 | ||||||
| chr9:104834565
|
AC | A | 6 | a0002c0017t0015g0101a0012c0041t0001g0274a0012c0041t0002g0230others(3): Show | 6 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-1795delG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834565 | ||||||
| chr9:104834573
|
G | A | 85 | a0001c0092t0012g0220a0002c0015t0013g0305a0002c0015t0013g0306others(82): Show | 85 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1312-1802C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834573 | ||||||
| chr9:104834650
|
G | C | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-1879C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834650 | ||||||
| chr9:104834714
|
G | A | 12 | a0002c0025t0008g0285a0002c0057t0001g0148a0003c0056t0001g0288others(9): Show | 12 | HG01109.hp1 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1312-1943C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834714 | ||||||
| chr9:104834864
|
C | G | 1 | a0006c0004t0002g0133 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1312-2093G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834864 | ||||||
| chr9:104834959
|
G | A | 1 | a0002c0025t0008g0285 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1311+2021C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834959 | ||||||
| chr9:104834971
|
G | A | 6 | a0002c0081t0013g0277a0012c0105t0024g0217a0024c0073t0019g0231others(3): Show | 6 | HG02280.hp1 HG02300.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+2009C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834971 | ||||||
| chr9:104834975
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1311+2005C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834975 | ||||||
| chr9:104834976
|
C | T | 1 | a0006c0012t0002g0226 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1311+2004G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104834976 | ||||||
| chr9:104835028
|
C | T | 1 | a0011c0010t0005g0287 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1311+1952G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835028 | ||||||
| chr9:104835056
|
C | T | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1311+1924G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835056 | ||||||
| chr9:104835105
|
G | A | 1 | a0012c0040t0040g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1311+1875C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835105 | ||||||
| chr9:104835221
|
C | T | 1 | a0007c0003t0009g0260 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1311+1759G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835221 | ||||||
| chr9:104835223
|
G | A | 52 | a0004c0087t0009g0118a0004c0112t0005g0098a0004c0113t0002g0159others(49): Show | 52 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1311+1757C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835223 | ||||||
| chr9:104835246
|
CA | C | 117 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0011t0004g0213others(114): Show | 117 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1311+1733delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835246 | ||||||
| chr9:104835292
|
G | A | 1 | a0002c0081t0013g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1311+1688C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835292 | ||||||
| chr9:104835311
|
T | C | 5 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(2): Show | 5 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+1669A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835311 | ||||||
| chr9:104835441
|
A | G | 232 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(229): Show | 232 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.1311+1539T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835441 | ||||||
| chr9:104835564
|
T | C | 1 | a0006c0012t0002g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1311+1416A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104835564 | ||||||
| chr9:104836118
|
A | T | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+862T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104836118 | ||||||
| chr9:104836158
|
C | T | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1311+822G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104836158 | ||||||
| chr9:104836201
|
T | C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1311+779A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104836201 | ||||||
| chr9:104836338
|
G | A | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+642C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104836338 | ||||||
| chr9:104836459
|
C | T | 280 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0203others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1311+521G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104836459 | ||||||
| chr9:104836562
|
G | C | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(1): Show | 4 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+418C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104836562 | ||||||
| chr9:104836603
|
T | G | 42 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1311+377A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 11/49 | chr9 | 104836603 | ||||||
| chr9:104837109
|
G | A | 55 | a0001c0092t0012g0220a0002c0017t0015g0101a0002c0025t0007g0237others(52): Show | 55 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1195-13C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/49 | chr9 | 104837109 | ||||||
| chr9:104837124
|
G | A | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-28C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/49 | chr9 | 104837124 | ||||||
| chr9:104837131
|
AAGG | A | 53 | a0002c0046t0002g0154a0004c0087t0009g0118a0004c0112t0005g0098others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.1195-38_1195-36del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/49 | chr9 | 104837131 | ||||||
| chr9:104837157
|
G | GC | 222 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(219): Show | 222 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1195-62_1195-61ins others(1): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/49 | chr9 | 104837157 | ||||||
| chr9:104837200
|
T | C | 131 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0011t0004g0213others(128): Show | 131 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1195-104A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/49 | chr9 | 104837200 | ||||||
| chr9:104837288
|
T | A | 2 | a0002c0081t0013g0277a0038c0068t0044g0272 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1194+140A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/49 | chr9 | 104837288 | ||||||
| chr9:104837347
|
A | G | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1194+81T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 10/49 | chr9 | 104837347 | ||||||
| chr9:104837574
|
A | G | 1 | a0001c0001t0006g0239 | 1 | HG03834.hp2 | splice_region_variant&intron_variant | LOW | c.1055-7T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104837574 | ||||||
| chr9:104837656
|
T | C | 17 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304others(14): Show | 17 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1055-89A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104837656 | ||||||
| chr9:104837847
|
C | T | 4 | a0003c0056t0001g0288a0018c0079t0004g0314a0018c0080t0004g0107others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-280G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104837847 | ||||||
| chr9:104837883
|
T | C | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1055-316A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104837883 | ||||||
| chr9:104837887
|
A | G | 227 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(224): Show | 227 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1055-320T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104837887 | ||||||
| chr9:104837912
|
A | G | 53 | a0002c0046t0002g0154a0004c0087t0009g0118a0004c0112t0005g0098others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.1055-345T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104837912 | ||||||
| chr9:104837970
|
T | C | 38 | a0001c0108t0002g0113a0001c0109t0001g0232a0002c0033t0002g0301others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1055-403A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104837970 | ||||||
| chr9:104838123
|
C | G | 55 | a0001c0092t0012g0220a0002c0017t0015g0101a0002c0025t0007g0237others(52): Show | 55 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1055-556G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838123 | ||||||
| chr9:104838298
|
T | C | 222 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(219): Show | 222 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1055-731A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838298 | ||||||
| chr9:104838305
|
C | CA | 63 | a0001c0001t0002g0137a0001c0001t0006g0054a0001c0092t0012g0220others(60): Show | 63 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1055-739dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838305 | ||||||
| chr9:104838305
|
C | CAA | 6 | a0006c0004t0006g0249a0006c0004t0011g0269a0006c0012t0010g0198others(3): Show | 6 | HG00621.hp2 HG01978.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-740_1055-739d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838305 | ||||||
| chr9:104838453
|
C | CA | 163 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0011t0004g0213others(160): Show | 163 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1055-887dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838453 | ||||||
| chr9:104838453
|
C | CAA | 21 | a0003c0002t0002g0040a0004c0112t0005g0098a0004c0113t0002g0159others(18): Show | 21 | HG00621.hp2 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1055-888_1055-887d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838453 | ||||||
| chr9:104838534
|
G | A | 53 | a0002c0046t0002g0154a0004c0087t0009g0118a0004c0112t0005g0098others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.1055-967C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838534 | ||||||
| chr9:104838600
|
G | A | 4 | a0012c0105t0024g0217a0024c0073t0019g0231a0032c0104t0005g0168others(1): Show | 4 | HG02280.hp1 HG02300.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055-1033C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838600 | ||||||
| chr9:104838616
|
C | CA | 64 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0247others(61): Show | 64 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1055-1050dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838616 | ||||||
| chr9:104838616
|
CA | C | 11 | a0001c0001t0006g0047a0002c0017t0026g0163a0002c0017t0026g0276others(8): Show | 11 | HG01081.hp1 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1055-1050delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838616 | ||||||
| chr9:104838875
|
T | C | 1 | a0005c0084t0014g0215 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1055-1308A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838875 | ||||||
| chr9:104838941
|
C | A | 4 | a0003c0056t0001g0288a0018c0079t0004g0314a0018c0080t0004g0107others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+1338G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838941 | ||||||
| chr9:104838995
|
A | G | 84 | a0001c0092t0012g0220a0002c0011t0004g0112a0002c0015t0002g0315others(81): Show | 84 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1054+1284T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104838995 | ||||||
| chr9:104839137
|
T | C | 8 | a0002c0025t0008g0285a0002c0057t0001g0148a0011c0010t0005g0097others(5): Show | 8 | HG02145.hp1 HG02922.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054+1142A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839137 | ||||||
| chr9:104839155
|
G | T | 8 | a0002c0025t0008g0285a0002c0057t0001g0148a0011c0010t0005g0097others(5): Show | 8 | HG02145.hp1 HG02922.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054+1124C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839155 | ||||||
| chr9:104839231
|
T | C | 170 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(167): Show | 170 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1054+1048A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839231 | ||||||
| chr9:104839260
|
G | A | 226 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(223): Show | 226 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.1054+1019C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839260 | ||||||
| chr9:104839264
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0039g0246 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1054+1015C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839264 | ||||||
| chr9:104839288
|
A | G | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1054+991T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839288 | ||||||
| chr9:104839344
|
T | C | 42 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1054+935A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839344 | ||||||
| chr9:104839422
|
G | A | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+857C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839422 | ||||||
| chr9:104839517
|
G | GTTT | 38 | a0001c0108t0002g0113a0001c0109t0001g0232a0002c0033t0002g0301others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1054+761_1054+762i others(5): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839517 | ||||||
| chr9:104839520
|
C | T | 127 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(124): Show | 127 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1054+759G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839520 | ||||||
| chr9:104839521
|
T | TTTG | 103 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(100): Show | 103 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1054+755_1054+757d others(5): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839521 | ||||||
| chr9:104839581
|
C | T | 2 | a0005c0026t0009g0076a0036c0094t0009g0079 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1054+698G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839581 | ||||||
| chr9:104839652
|
AC | A | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+626delG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839652 | ||||||
| chr9:104839653
|
C | A | 6 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0037t0001g0275others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054+626G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839653 | ||||||
| chr9:104839660
|
CAAAT | C | 162 | a0001c0092t0012g0220a0001c0108t0002g0113a0001c0109t0001g0232others(159): Show | 162 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1054+615_1054+618d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839660 | ||||||
| chr9:104839875
|
C | T | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1054+404G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104839875 | ||||||
| chr9:104840061
|
T | G | 30 | a0001c0108t0002g0113a0001c0109t0001g0232a0002c0033t0002g0301others(27): Show | 30 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1054+218A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 9/49 | chr9 | 104840061 | ||||||
| chr9:104840532
|
A | AT | 73 | a0001c0092t0012g0220a0002c0017t0015g0101a0002c0017t0026g0163others(70): Show | 73 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.814-14dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840532 | ||||||
| chr9:104840548
|
G | T | 1 | a0015c0061t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.814-29C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840548 | ||||||
| chr9:104840762
|
G | A | 38 | a0001c0108t0002g0113a0001c0109t0001g0232a0002c0033t0002g0301others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.814-243C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840762 | ||||||
| chr9:104840876
|
C | G | 2 | a0002c0085t0008g0142a0019c0106t0001g0094 | 2 | HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.814-357G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840876 | ||||||
| chr9:104840893
|
C | T | 53 | a0002c0046t0002g0154a0004c0087t0009g0118a0004c0112t0005g0098others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.814-374G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840893 | ||||||
| chr9:104840902
|
G | C | 1 | a0002c0025t0007g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.814-383C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840902 | ||||||
| chr9:104840925
|
TAA | T | 53 | a0002c0046t0002g0154a0004c0087t0009g0118a0004c0112t0005g0098others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.814-408_814-407del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840925 | ||||||
| chr9:104840929
|
A | G | 1 | a0001c0001t0007g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.814-410T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840929 | ||||||
| chr9:104840997
|
T | C | 36 | a0002c0046t0002g0154a0004c0087t0009g0118a0005c0016t0001g0009others(33): Show | 36 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.814-478A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104840997 | ||||||
| chr9:104841003
|
A | G | 53 | a0002c0046t0002g0154a0004c0087t0009g0118a0004c0112t0005g0098others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.814-484T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841003 | ||||||
| chr9:104841023
|
G | A | 5 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(2): Show | 5 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-504C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841023 | ||||||
| chr9:104841158
|
G | C | 53 | a0002c0046t0002g0154a0004c0087t0009g0118a0004c0112t0005g0098others(50): Show | 53 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.814-639C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841158 | ||||||
| chr9:104841173
|
C | T | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0065t0007g0182others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-654G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841173 | ||||||
| chr9:104841288
|
A | G | 4 | a0003c0056t0001g0288a0018c0079t0004g0314a0018c0080t0004g0107others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-769T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841288 | ||||||
| chr9:104841441
|
AAAAAAG | A | 125 | a0001c0092t0012g0220a0002c0017t0015g0101a0002c0017t0026g0163others(122): Show | 125 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.814-928_814-923del others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841441 | ||||||
| chr9:104841586
|
G | A | 3 | a0001c0001t0006g0225a0001c0001t0007g0183a0001c0001t0012g0039 | 3 | NA18984.hp2 NA19078.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.814-1067C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841586 | ||||||
| chr9:104841643
|
GC | G | 72 | a0001c0092t0012g0220a0002c0017t0015g0101a0002c0017t0026g0163others(69): Show | 72 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.814-1125delG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841643 | ||||||
| chr9:104841682
|
G | C | 39 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(36): Show | 39 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.814-1163C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841682 | ||||||
| chr9:104841761
|
T | C | 57 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(54): Show | 57 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.814-1242A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841761 | ||||||
| chr9:104841823
|
A | G | 37 | a0001c0108t0002g0113a0002c0033t0002g0301a0002c0033t0032g0024others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.814-1304T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841823 | ||||||
| chr9:104841916
|
G | T | 227 | a0001c0092t0012g0220a0001c0108t0002g0113a0002c0011t0004g0112others(224): Show | 227 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.814-1397C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841916 | ||||||
| chr9:104841941
|
C | T | 1 | a0012c0102t0007g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.814-1422G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104841941 | ||||||
| chr9:104842104
|
C | T | 39 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(36): Show | 39 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.814-1585G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842104 | ||||||
| chr9:104842113
|
T | A | 53 | a0001c0092t0012g0220a0002c0017t0015g0101a0002c0025t0007g0237others(50): Show | 53 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.814-1594A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842113 | ||||||
| chr9:104842204
|
C | A | 5 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1685G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842204 | ||||||
| chr9:104842226
|
C | T | 36 | a0002c0046t0002g0154a0004c0087t0009g0118a0005c0016t0001g0009others(33): Show | 36 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.814-1707G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842226 | ||||||
| chr9:104842301
|
G | T | 45 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(42): Show | 45 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.814-1782C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842301 | ||||||
| chr9:104842441
|
A | C | 240 | a0001c0001t0004g0194a0001c0001t0011g0085a0001c0005t0002g0062others(237): Show | 240 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.814-1922T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842441 | ||||||
| chr9:104842541
|
G | A | 2 | a0007c0003t0004g0048a0007c0003t0006g0051 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.814-2022C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842541 | ||||||
| chr9:104842637
|
T | C | 51 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(48): Show | 51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.814-2118A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842637 | ||||||
| chr9:104842676
|
T | C | 56 | a0002c0015t0031g0084a0002c0017t0002g0271a0002c0017t0026g0163others(53): Show | 56 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.814-2157A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842676 | ||||||
| chr9:104842751
|
C | A | 1 | a0001c0108t0002g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.814-2232G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842751 | ||||||
| chr9:104842763
|
C | A | 1 | a0006c0063t0003g0151 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.814-2244G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842763 | ||||||
| chr9:104842831
|
C | T | 5 | a0003c0056t0001g0288a0005c0082t0002g0282a0018c0079t0004g0314others(2): Show | 5 | HG01109.hp1 HG01243.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-2312G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842831 | ||||||
| chr9:104842893
|
C | T | 2 | a0003c0002t0028g0261a0003c0009t0006g0186 | 2 | HG00673.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.814-2374G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842893 | ||||||
| chr9:104842923
|
C | T | 1 | a0009c0027t0004g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.814-2404G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842923 | ||||||
| chr9:104842924
|
C | T | 1 | a0001c0001t0002g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.814-2405G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842924 | ||||||
| chr9:104842958
|
A | G | 1 | a0003c0002t0002g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.814-2439T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104842958 | ||||||
| chr9:104843063
|
C | T | 77 | a0002c0011t0004g0263a0002c0011t0007g0119a0002c0011t0007g0247others(74): Show | 77 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.813+2414G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843063 | ||||||
| chr9:104843136
|
C | G | 3 | a0013c0013t0003g0256a0013c0013t0025g0032a0013c0013t0025g0033 | 3 | HG02083.hp1 HG02129.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.813+2341G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843136 | ||||||
| chr9:104843240
|
C | G | 15 | a0002c0017t0002g0271a0002c0025t0008g0285a0002c0057t0001g0148others(12): Show | 15 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.813+2237G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843240 | ||||||
| chr9:104843240
|
C | T | 6 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+2237G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843240 | ||||||
| chr9:104843242
|
T | G | 1 | a0028c0095t0002g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.813+2235A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843242 | ||||||
| chr9:104843288
|
C | T | 1 | a0019c0106t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.813+2189G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843288 | ||||||
| chr9:104843357
|
G | T | 4 | a0002c0046t0002g0154a0003c0077t0005g0312a0012c0105t0024g0217others(1): Show | 4 | HG02280.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+2120C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843357 | ||||||
| chr9:104843601
|
C | T | 1 | a0010c0007t0010g0139 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.813+1876G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843601 | ||||||
| chr9:104843669
|
T | G | 2 | a0017c0034t0001g0153a0017c0034t0001g0300 | 2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.813+1808A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843669 | ||||||
| chr9:104843728
|
G | C | 8 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(5): Show | 8 | HG01106.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+1749C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843728 | ||||||
| chr9:104843763
|
C | T | 31 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0037t0011g0116others(28): Show | 31 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.813+1714G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843763 | ||||||
| chr9:104843764
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.813+1713C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843764 | ||||||
| chr9:104843793
|
ATCT | A | 8 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(5): Show | 8 | HG01106.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+1681_813+1683d others(5): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843793 | ||||||
| chr9:104843819
|
T | C | 1 | a0013c0013t0003g0207 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.813+1658A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843819 | ||||||
| chr9:104843835
|
G | T | 2 | a0006c0004t0042g0265a0007c0003t0033g0035 | 2 | NA18962.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.813+1642C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843835 | ||||||
| chr9:104843848
|
T | A | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.813+1629A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843848 | ||||||
| chr9:104843888
|
G | A | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.813+1589C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104843888 | ||||||
| chr9:104844008
|
A | AT | 8 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(5): Show | 8 | HG01106.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+1468dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844008 | ||||||
| chr9:104844027
|
G | GA | 6 | a0003c0002t0002g0172a0004c0112t0005g0098a0004c0113t0002g0159others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+1449dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844027 | ||||||
| chr9:104844027
|
GA | G | 57 | a0002c0017t0002g0271a0002c0017t0015g0101a0002c0017t0026g0163others(54): Show | 57 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.813+1449delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844027 | ||||||
| chr9:104844027
|
GAA | G | 35 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0031t0001g0152others(32): Show | 35 | HG01106.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.813+1448_813+1449d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844027 | ||||||
| chr9:104844038
|
A | C | 8 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(5): Show | 8 | HG01106.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+1439T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844038 | ||||||
| chr9:104844102
|
C | T | 8 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(5): Show | 8 | HG01106.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+1375G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844102 | ||||||
| chr9:104844165
|
C | T | 5 | a0001c0001t0006g0225a0001c0001t0007g0183a0001c0001t0012g0039others(2): Show | 5 | NA18970.hp2 NA18984.hp2 NA19078.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+1312G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844165 | ||||||
| chr9:104844166
|
G | C | 8 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(5): Show | 8 | HG01106.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+1311C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844166 | ||||||
| chr9:104844233
|
G | A | 8 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(5): Show | 8 | HG01106.hp1 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+1244C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844233 | ||||||
| chr9:104844301
|
C | A | 2 | a0012c0105t0024g0217a0032c0104t0005g0168 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.813+1176G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844301 | ||||||
| chr9:104844302
|
C | G | 2 | a0012c0105t0024g0217a0032c0104t0005g0168 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.813+1175G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844302 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3251): Show |
1 | a0002c0011t0012g0134 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3260): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3261): Show |
1 | a0014c0053t0002g0146 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3270): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3251): Show |
1 | a0003c0002t0014g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3260): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3252): Show |
1 | a0002c0011t0004g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3261): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3251): Show |
1 | a0013c0013t0003g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3260): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3261): Show |
1 | a0009c0027t0006g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3270): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3258): Show |
1 | a0003c0038t0003g0293 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3267): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3262): Show |
1 | a0003c0076t0002g0130 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3271): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3262): Show |
1 | a0010c0007t0003g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3271): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3259): Show |
1 | a0008c0006t0012g0081 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3268): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3210): Show |
1 | a0003c0002t0002g0041 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3219): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3262): Show |
1 | a0003c0002t0002g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3271): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3259): Show |
1 | a0002c0011t0004g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3268): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3252): Show |
1 | a0013c0013t0025g0032 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3261): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3264): Show |
1 | a0003c0002t0002g0172 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3273): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3260): Show |
1 | a0003c0009t0001g0279 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3269): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3260): Show |
1 | a0020c0045t0002g0299 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3269): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3254): Show |
1 | a0014c0023t0007g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3263): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3261): Show |
1 | a0003c0009t0003g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3270): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3260): Show |
1 | a0008c0006t0006g0057 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3269): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3259): Show |
1 | a0003c0002t0002g0257 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3268): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3260): Show |
1 | a0002c0011t0007g0247 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3269): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3245): Show |
1 | a0003c0009t0003g0178 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3254): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3253): Show |
1 | a0013c0013t0003g0120 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3262): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3253): Show |
1 | a0013c0013t0025g0033 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3262): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3252): Show |
1 | a0003c0002t0002g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3261): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3261): Show |
1 | a0003c0002t0003g0127 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3270): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3251): Show |
1 | a0003c0009t0046g0219 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3260): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3257): Show |
1 | a0003c0009t0003g0073 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3266): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3258): Show |
3 | a0003c0002t0002g0184a0003c0002t0002g0205a0003c0009t0003g0209 | 3 | HG00099.hp2 NA18990.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.813+1170_813+1171i others(3267): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3259): Show |
1 | a0003c0009t0051g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3268): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3258): Show |
1 | a0008c0006t0005g0063 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3267): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3242): Show |
1 | a0016c0019t0018g0177 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3251): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3207): Show |
1 | a0003c0002t0002g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3216): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3251): Show |
1 | a0013c0013t0003g0207 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3260): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3253): Show |
1 | a0013c0013t0002g0262 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3262): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3566): Show |
1 | a0003c0002t0002g0045 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3575): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3386): Show |
1 | a0003c0002t0002g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3395): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3387): Show |
1 | a0003c0002t0002g0069 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3396): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3385): Show |
1 | a0003c0002t0010g0270 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3394): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(2798): Show |
1 | a0003c0002t0002g0070 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(2807): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(2841): Show |
1 | a0002c0011t0020g0171 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.813+1170_813+1171i others(2850): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(2841): Show |
1 | a0003c0002t0007g0059 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(2850): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3252): Show |
1 | a0003c0009t0006g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3261): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3251): Show |
1 | a0003c0002t0028g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3260): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844306
|
T | TAAAAAAG others(3210): Show |
1 | a0002c0011t0007g0119 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.813+1170_813+1171i others(3219): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844306 | ||||||
| chr9:104844339
|
A | C | 1 | a0005c0036t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.813+1138T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844339 | ||||||
| chr9:104844638
|
G | A | 1 | a0005c0036t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.813+839C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844638 | ||||||
| chr9:104844728
|
G | A | 1 | a0017c0034t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.813+749C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844728 | ||||||
| chr9:104844780
|
T | A | 101 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(98): Show | 101 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(98): Show |
intron_variant | MODIFIER | c.813+697A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844780 | ||||||
| chr9:104844824
|
CAA | C | 14 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0075t0027g0150others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.813+651_813+652del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844824 | ||||||
| chr9:104844931
|
T | C | 53 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(50): Show | 53 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.813+546A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844931 | ||||||
| chr9:104844945
|
T | C | 10 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.813+532A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104844945 | ||||||
| chr9:104845084
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0196 | 2 | HG02148.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.813+393C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104845084 | ||||||
| chr9:104845090
|
G | C | 3 | a0001c0092t0012g0220a0007c0003t0011g0072a0012c0040t0040g0055 | 3 | HG00609.hp1 HG00621.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.813+387C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104845090 | ||||||
| chr9:104845139
|
G | C | 54 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(51): Show | 54 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.813+338C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104845139 | ||||||
| chr9:104845235
|
CT | C | 3 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.813+241delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104845235 | ||||||
| chr9:104845446
|
C | T | 1 | a0005c0036t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.813+31G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104845446 | ||||||
| chr9:104845460
|
G | A | 6 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(3): Show | 6 | HG01106.hp1 HG03098.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+17C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 8/49 | chr9 | 104845460 | ||||||
| chr9:104845588
|
C | T | 1 | a0004c0099t0001g0110 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.721-19G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104845588 | ||||||
| chr9:104845863
|
A | G | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(1): Show | 4 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-294T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104845863 | ||||||
| chr9:104846038
|
T | C | 6 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(3): Show | 6 | HG01106.hp1 HG03098.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-469A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846038 | ||||||
| chr9:104846081
|
C | T | 1 | a0010c0007t0003g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.721-512G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846081 | ||||||
| chr9:104846341
|
C | T | 59 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(56): Show | 59 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.721-772G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846341 | ||||||
| chr9:104846373
|
G | A | 6 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(3): Show | 6 | HG01106.hp1 HG03098.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-804C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846373 | ||||||
| chr9:104846506
|
T | C | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.721-937A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846506 | ||||||
| chr9:104846527
|
T | C | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.721-958A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846527 | ||||||
| chr9:104846564
|
T | C | 6 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(3): Show | 6 | HG01106.hp1 HG03098.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-995A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846564 | ||||||
| chr9:104846673
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.721-1104G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846673 | ||||||
| chr9:104846784
|
G | A | 31 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0037t0011g0116others(28): Show | 31 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.721-1215C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846784 | ||||||
| chr9:104846808
|
CAGAT | C | 10 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0059t0001g0235others(7): Show | 10 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.721-1243_721-1240d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846808 | ||||||
| chr9:104846840
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.721-1271T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104846840 | ||||||
| chr9:104847163
|
G | A | 2 | a0008c0047t0002g0244a0008c0069t0008g0096 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.721-1594C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847163 | ||||||
| chr9:104847195
|
C | G | 104 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(101): Show | 104 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.721-1626G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847195 | ||||||
| chr9:104847664
|
C | T | 7 | a0004c0029t0001g0099a0004c0029t0005g0162a0004c0098t0005g0303others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-2095G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847664 | ||||||
| chr9:104847677
|
A | G | 42 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(39): Show | 42 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.721-2108T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847677 | ||||||
| chr9:104847728
|
C | T | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0105t0024g0217others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-2159G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847728 | ||||||
| chr9:104847794
|
G | A | 12 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(9): Show | 12 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.721-2225C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847794 | ||||||
| chr9:104847871
|
T | C | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0105t0024g0217others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-2302A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847871 | ||||||
| chr9:104847884
|
T | C | 1 | a0026c0111t0002g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.721-2315A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847884 | ||||||
| chr9:104847935
|
A | T | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-2366T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104847935 | ||||||
| chr9:104848057
|
T | C | 1 | a0005c0052t0001g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.721-2488A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848057 | ||||||
| chr9:104848188
|
T | C | 8 | a0010c0007t0002g0012a0010c0007t0002g0013a0010c0007t0002g0015others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-2619A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848188 | ||||||
| chr9:104848359
|
A | C | 1 | a0008c0006t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.721-2790T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848359 | ||||||
| chr9:104848366
|
A | C | 5 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0105t0024g0217others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-2797T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848366 | ||||||
| chr9:104848524
|
A | G | 1 | a0002c0085t0008g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.721-2955T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848524 | ||||||
| chr9:104848609
|
G | A | 6 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(3): Show | 6 | HG01106.hp1 HG03098.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-3040C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848609 | ||||||
| chr9:104848616
|
G | GA | 16 | a0001c0005t0002g0017a0002c0025t0008g0285a0002c0031t0001g0152others(13): Show | 16 | HG02258.hp2 HG02280.hp1 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.721-3048dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848616 | ||||||
| chr9:104848616
|
GA | G | 84 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(81): Show | 84 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.721-3048delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848616 | ||||||
| chr9:104848713
|
C | G | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-3144G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848713 | ||||||
| chr9:104848788
|
G | A | 1 | a0001c0005t0002g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.721-3219C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848788 | ||||||
| chr9:104848851
|
A | G | 23 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0057t0001g0148others(20): Show | 23 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.721-3282T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848851 | ||||||
| chr9:104848961
|
A | C | 5 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-3392T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848961 | ||||||
| chr9:104848998
|
C | T | 6 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312others(3): Show | 6 | HG01106.hp1 HG03098.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-3429G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848998 | ||||||
| chr9:104848999
|
G | A | 54 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(51): Show | 54 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.721-3430C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104848999 | ||||||
| chr9:104849056
|
G | T | 17 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(14): Show | 17 | HG01106.hp1 HG01884.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.721-3487C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849056 | ||||||
| chr9:104849096
|
T | C | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-3527A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849096 | ||||||
| chr9:104849284
|
G | T | 1 | a0007c0090t0007g0046 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.721-3715C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849284 | ||||||
| chr9:104849285
|
T | G | 1 | a0007c0090t0007g0046 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.721-3716A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849285 | ||||||
| chr9:104849286
|
G | T | 1 | a0007c0090t0007g0046 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.721-3717C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849286 | ||||||
| chr9:104849303
|
A | G | 5 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-3734T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849303 | ||||||
| chr9:104849328
|
T | C | 1 | a0008c0006t0015g0095 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.721-3759A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849328 | ||||||
| chr9:104849382
|
G | A | 1 | a0022c0050t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.721-3813C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849382 | ||||||
| chr9:104849382
|
GTTTAA | G | 10 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.721-3818_721-3814d others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849382 | ||||||
| chr9:104849502
|
T | C | 1 | a0008c0006t0007g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.721-3933A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849502 | ||||||
| chr9:104849546
|
T | C | 31 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0037t0011g0116others(28): Show | 31 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.721-3977A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849546 | ||||||
| chr9:104849549
|
T | A | 38 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(35): Show | 38 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.721-3980A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104849549 | ||||||
| chr9:104850119
|
T | TTTTG | 16 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(13): Show | 16 | HG01257.hp1 HG01257.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.721-4554_721-4551d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850119 | ||||||
| chr9:104850119
|
T | TTTTGTTT others(1): Show |
167 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(164): Show | 167 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.721-4558_721-4551d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850119 | ||||||
| chr9:104850119
|
T | TTTTGTTT others(5): Show |
1 | a0003c0002t0002g0069 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.721-4562_721-4551d others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850119 | ||||||
| chr9:104850178
|
G | C | 4 | a0002c0031t0001g0152a0002c0031t0001g0278a0002c0081t0013g0277others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-4609C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850178 | ||||||
| chr9:104850183
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.721-4614C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850183 | ||||||
| chr9:104850292
|
T | A | 2 | a0002c0011t0012g0134a0008c0006t0012g0081 | 2 | NA18953.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.721-4723A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850292 | ||||||
| chr9:104850352
|
C | T | 1 | a0008c0006t0014g0221 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.721-4783G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850352 | ||||||
| chr9:104850504
|
TAAAAG | T | 31 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0037t0011g0116others(28): Show | 31 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.721-4940_721-4936d others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850504 | ||||||
| chr9:104850607
|
A | C | 12 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(9): Show | 12 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.721-5038T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850607 | ||||||
| chr9:104850608
|
T | A | 12 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(9): Show | 12 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.721-5039A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850608 | ||||||
| chr9:104850641
|
A | G | 6 | a0012c0041t0001g0274a0012c0041t0002g0230a0012c0105t0024g0217others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-5072T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850641 | ||||||
| chr9:104850730
|
A | C | 1 | a0009c0021t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.721-5161T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850730 | ||||||
| chr9:104850769
|
A | G | 12 | a0002c0011t0004g0213a0002c0011t0020g0171a0003c0002t0002g0044others(9): Show | 12 | HG00423.hp2 HG02083.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.721-5200T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850769 | ||||||
| chr9:104850798
|
T | C | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-5229A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850798 | ||||||
| chr9:104850801
|
C | G | 10 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.721-5232G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850801 | ||||||
| chr9:104850808
|
A | G | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.721-5239T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850808 | ||||||
| chr9:104850834
|
C | T | 13 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(10): Show | 13 | HG01106.hp1 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-5265G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850834 | ||||||
| chr9:104850846
|
T | C | 1 | a0003c0002t0003g0127 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.721-5277A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850846 | ||||||
| chr9:104850878
|
G | A | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-5309C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104850878 | ||||||
| chr9:104851083
|
C | A | 13 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(10): Show | 13 | HG01106.hp1 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-5514G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851083 | ||||||
| chr9:104851321
|
A | G | 12 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(9): Show | 12 | HG01081.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.721-5752T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851321 | ||||||
| chr9:104851389
|
G | A | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-5820C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851389 | ||||||
| chr9:104851397
|
G | A | 5 | a0012c0041t0002g0230a0012c0105t0024g0217a0019c0106t0001g0094others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-5828C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851397 | ||||||
| chr9:104851413
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.721-5844T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851413 | ||||||
| chr9:104851568
|
T | A | 19 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(16): Show | 19 | HG01081.hp2 HG02145.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.721-5999A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851568 | ||||||
| chr9:104851602
|
C | T | 313 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.721-6033G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851602 | ||||||
| chr9:104851768
|
C | T | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.721-6199G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851768 | ||||||
| chr9:104851833
|
T | A | 6 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-6264A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851833 | ||||||
| chr9:104851851
|
C | T | 9 | a0002c0017t0015g0101a0002c0024t0008g0003a0002c0024t0008g0008others(6): Show | 9 | HG02109.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-6282G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851851 | ||||||
| chr9:104851852
|
G | A | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721-6283C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851852 | ||||||
| chr9:104851936
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.721-6367C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104851936 | ||||||
| chr9:104852012
|
C | T | 5 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-6443G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104852012 | ||||||
| chr9:104852183
|
C | T | 2 | a0002c0017t0015g0101a0005c0026t0009g0076 | 2 | HG03516.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.720+6339G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104852183 | ||||||
| chr9:104852575
|
T | C | 1 | a0023c0072t0001g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.720+5947A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104852575 | ||||||
| chr9:104852895
|
A | C | 2 | a0004c0029t0001g0099a0028c0095t0002g0114 | 2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.720+5627T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104852895 | ||||||
| chr9:104853066
|
A | G | 1 | a0008c0006t0006g0057 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.720+5456T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853066 | ||||||
| chr9:104853168
|
T | G | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.720+5354A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853168 | ||||||
| chr9:104853235
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.720+5287A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853235 | ||||||
| chr9:104853271
|
C | A | 6 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+5251G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853271 | ||||||
| chr9:104853372
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.720+5150G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853372 | ||||||
| chr9:104853372
|
CCA | C | 3 | a0002c0037t0001g0275a0002c0046t0002g0154a0003c0077t0005g0312 | 3 | HG03098.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.720+5148_720+5149d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853372 | ||||||
| chr9:104853558
|
C | T | 2 | a0019c0106t0001g0094a0035c0091t0008g0161 | 2 | HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.720+4964G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853558 | ||||||
| chr9:104853571
|
G | A | 6 | a0012c0041t0002g0230a0012c0105t0024g0217a0019c0106t0001g0094others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4951C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853571 | ||||||
| chr9:104853634
|
A | AT | 15 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(12): Show | 15 | HG01081.hp2 HG01106.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+4887dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853634 | ||||||
| chr9:104853649
|
T | C | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.720+4873A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853649 | ||||||
| chr9:104853677
|
C | G | 15 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(12): Show | 15 | HG01081.hp2 HG01106.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+4845G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853677 | ||||||
| chr9:104853753
|
T | C | 2 | a0005c0014t0003g0243a0009c0018t0003g0253 | 2 | NA18999.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.720+4769A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853753 | ||||||
| chr9:104853803
|
G | A | 11 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+4719C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853803 | ||||||
| chr9:104853892
|
G | A | 1 | a0005c0014t0003g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.720+4630C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853892 | ||||||
| chr9:104853950
|
G | C | 1 | a0006c0004t0004g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.720+4572C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853950 | ||||||
| chr9:104853986
|
G | C | 15 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(12): Show | 15 | HG01081.hp2 HG01106.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+4536C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104853986 | ||||||
| chr9:104854053
|
T | C | 2 | a0002c0037t0001g0275a0003c0077t0005g0312 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.720+4469A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854053 | ||||||
| chr9:104854229
|
A | G | 1 | a0002c0011t0004g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.720+4293T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854229 | ||||||
| chr9:104854235
|
C | A | 6 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4287G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854235 | ||||||
| chr9:104854235
|
C | T | 7 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(4): Show | 7 | HG02109.hp1 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+4287G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854235 | ||||||
| chr9:104854458
|
TA | T | 27 | a0002c0025t0007g0237a0005c0016t0001g0009a0005c0016t0001g0010others(24): Show | 27 | HG00642.hp1 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.720+4063delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854458 | ||||||
| chr9:104854478
|
G | A | 6 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4044C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854478 | ||||||
| chr9:104854497
|
G | A | 6 | a0004c0066t0008g0007a0004c0112t0005g0098a0004c0113t0002g0159others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4025C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854497 | ||||||
| chr9:104854711
|
T | C | 8 | a0004c0029t0001g0099a0004c0029t0005g0023a0004c0029t0005g0162others(5): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+3811A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104854711 | ||||||
| chr9:104855000
|
G | C | 6 | a0012c0041t0002g0230a0012c0105t0024g0217a0019c0106t0001g0094others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+3522C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855000 | ||||||
| chr9:104855056
|
C | T | 81 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(78): Show | 81 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.720+3466G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855056 | ||||||
| chr9:104855152
|
C | T | 81 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(78): Show | 81 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.720+3370G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855152 | ||||||
| chr9:104855153
|
G | A | 34 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0031g0084others(31): Show | 34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.720+3369C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855153 | ||||||
| chr9:104855181
|
C | A | 1 | a0004c0008t0006g0202 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.720+3341G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855181 | ||||||
| chr9:104855194
|
C | A | 1 | a0003c0009t0003g0209 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.720+3328G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855194 | ||||||
| chr9:104855238
|
G | A | 5 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+3284C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855238 | ||||||
| chr9:104855271
|
A | C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.720+3251T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855271 | ||||||
| chr9:104855279
|
T | C | 316 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.720+3243A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855279 | ||||||
| chr9:104855354
|
G | A | 6 | a0002c0057t0001g0148a0005c0022t0002g0284a0005c0022t0021g0141others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+3168C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855354 | ||||||
| chr9:104855402
|
C | T | 2 | a0015c0020t0001g0006a0015c0020t0004g0005 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.720+3120G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855402 | ||||||
| chr9:104855447
|
C | T | 6 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+3075G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855447 | ||||||
| chr9:104855725
|
C | T | 2 | a0012c0105t0024g0217a0032c0104t0005g0168 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.720+2797G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855725 | ||||||
| chr9:104855752
|
C | T | 1 | a0006c0012t0010g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.720+2770G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104855752 | ||||||
| chr9:104856017
|
G | A | 1 | a0003c0002t0050g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.720+2505C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856017 | ||||||
| chr9:104856175
|
A | G | 3 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.720+2347T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856175 | ||||||
| chr9:104856254
|
A | T | 25 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0031g0084others(22): Show | 25 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.720+2268T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856254 | ||||||
| chr9:104856400
|
T | C | 177 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(174): Show | 177 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.720+2122A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856400 | ||||||
| chr9:104856453
|
C | T | 44 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(41): Show | 44 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.720+2069G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856453 | ||||||
| chr9:104856672
|
A | T | 1 | a0014c0053t0002g0146 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.720+1850T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856672 | ||||||
| chr9:104856677
|
T | C | 1 | a0009c0018t0003g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.720+1845A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856677 | ||||||
| chr9:104856782
|
G | A | 186 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(183): Show | 186 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.720+1740C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856782 | ||||||
| chr9:104856853
|
G | A | 1 | a0002c0025t0008g0285 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.720+1669C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856853 | ||||||
| chr9:104856913
|
C | T | 31 | a0002c0033t0002g0301a0002c0033t0032g0024a0002c0037t0011g0116others(28): Show | 31 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.720+1609G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856913 | ||||||
| chr9:104856970
|
G | C | 1 | a0004c0008t0004g0264 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.720+1552C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856970 | ||||||
| chr9:104856985
|
T | C | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.720+1537A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856985 | ||||||
| chr9:104856986
|
G | A | 2 | a0002c0037t0001g0275a0003c0077t0005g0312 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.720+1536C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104856986 | ||||||
| chr9:104857065
|
G | A | 1 | a0007c0003t0016g0242 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.720+1457C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857065 | ||||||
| chr9:104857069
|
C | A | 81 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(78): Show | 81 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.720+1453G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857069 | ||||||
| chr9:104857087
|
T | C | 1 | a0001c0035t0004g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.720+1435A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857087 | ||||||
| chr9:104857229
|
A | G | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.720+1293T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857229 | ||||||
| chr9:104857235
|
G | A | 44 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(41): Show | 44 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.720+1287C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857235 | ||||||
| chr9:104857258
|
G | A | 25 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0031g0084others(22): Show | 25 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.720+1264C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857258 | ||||||
| chr9:104857335
|
C | T | 1 | a0002c0081t0013g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+1187G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857335 | ||||||
| chr9:104857339
|
C | T | 177 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(174): Show | 177 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.720+1183G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857339 | ||||||
| chr9:104857389
|
C | T | 2 | a0002c0037t0001g0275a0003c0077t0005g0312 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.720+1133G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857389 | ||||||
| chr9:104857403
|
T | G | 81 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(78): Show | 81 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.720+1119A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857403 | ||||||
| chr9:104857465
|
C | T | 25 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0015t0031g0084others(22): Show | 25 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.720+1057G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857465 | ||||||
| chr9:104857482
|
G | A | 6 | a0012c0041t0002g0230a0012c0105t0024g0217a0019c0106t0001g0094others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+1040C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857482 | ||||||
| chr9:104857527
|
T | A | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.720+995A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857527 | ||||||
| chr9:104857531
|
C | T | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.720+991G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857531 | ||||||
| chr9:104857704
|
C | CAAAA | 13 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0075t0027g0150others(10): Show | 13 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+817_720+818ins others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857704 | ||||||
| chr9:104857813
|
C | G | 1 | a0008c0006t0022g0135 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.720+709G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857813 | ||||||
| chr9:104857843
|
C | G | 181 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(178): Show | 181 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.720+679G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857843 | ||||||
| chr9:104857966
|
T | C | 1 | a0003c0077t0005g0312 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.720+556A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104857966 | ||||||
| chr9:104858018
|
C | T | 184 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(181): Show | 184 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.720+504G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104858018 | ||||||
| chr9:104858051
|
G | A | 177 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(174): Show | 177 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.720+471C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104858051 | ||||||
| chr9:104858094
|
A | G | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.720+428T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104858094 | ||||||
| chr9:104858106
|
C | T | 127 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(124): Show | 127 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.720+416G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104858106 | ||||||
| chr9:104858335
|
C | G | 1 | a0002c0017t0015g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.720+187G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104858335 | ||||||
| chr9:104858347
|
G | T | 1 | a0008c0006t0047g0056 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.720+175C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 7/49 | chr9 | 104858347 | ||||||
| chr9:104858791
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.544-93T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104858791 | ||||||
| chr9:104858817
|
G | T | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.544-119C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104858817 | ||||||
| chr9:104858859
|
A | C | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.544-161T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104858859 | ||||||
| chr9:104858906
|
C | A | 1 | a0004c0064t0007g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.544-208G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104858906 | ||||||
| chr9:104858907
|
C | A | 1 | a0004c0064t0007g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.544-209G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104858907 | ||||||
| chr9:104859018
|
A | G | 1 | a0023c0072t0001g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.544-320T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859018 | ||||||
| chr9:104859176
|
C | T | 18 | a0002c0011t0004g0112a0002c0017t0002g0271a0002c0025t0008g0285others(15): Show | 18 | HG01081.hp2 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.544-478G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859176 | ||||||
| chr9:104859357
|
A | G | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.544-659T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859357 | ||||||
| chr9:104859391
|
G | A | 46 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(43): Show | 46 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.544-693C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859391 | ||||||
| chr9:104859392
|
ACCACAAG others(61): Show |
A | 6 | a0012c0041t0002g0230a0012c0105t0024g0217a0019c0106t0001g0094others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-762_544-695del others(68): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859392 | ||||||
| chr9:104859640
|
T | C | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.544-942A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859640 | ||||||
| chr9:104859696
|
A | G | 172 | a0001c0001t0001g0208a0002c0011t0004g0112a0002c0011t0004g0213others(169): Show | 172 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.544-998T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859696 | ||||||
| chr9:104859772
|
C | T | 1 | a0003c0056t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.544-1074G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859772 | ||||||
| chr9:104859817
|
A | G | 172 | a0001c0001t0001g0208a0002c0011t0004g0112a0002c0011t0004g0213others(169): Show | 172 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.544-1119T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859817 | ||||||
| chr9:104859981
|
G | A | 6 | a0002c0011t0012g0134a0003c0009t0003g0178a0008c0006t0005g0063others(3): Show | 6 | NA18953.hp2 NA18960.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-1283C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104859981 | ||||||
| chr9:104860053
|
C | CA | 28 | a0001c0001t0002g0233a0001c0001t0003g0297a0001c0001t0006g0054others(25): Show | 28 | HG01081.hp2 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.544-1356dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860053 | ||||||
| chr9:104860053
|
C | CAA | 27 | a0002c0015t0004g0004a0002c0015t0031g0084a0002c0037t0001g0275others(24): Show | 27 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.544-1357_544-1356d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860053 | ||||||
| chr9:104860085
|
C | T | 1 | a0008c0006t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-1387G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860085 | ||||||
| chr9:104860202
|
A | G | 172 | a0001c0001t0001g0208a0002c0011t0004g0112a0002c0011t0004g0213others(169): Show | 172 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.543+1477T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860202 | ||||||
| chr9:104860217
|
A | C | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.543+1462T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860217 | ||||||
| chr9:104860433
|
A | C | 8 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+1246T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860433 | ||||||
| chr9:104860551
|
C | T | 171 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(168): Show | 171 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.543+1128G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860551 | ||||||
| chr9:104860595
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.543+1084G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860595 | ||||||
| chr9:104860602
|
A | C | 3 | a0002c0031t0001g0152a0002c0031t0001g0278a0024c0073t0019g0231 | 3 | HG02258.hp2 HG02486.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.543+1077T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860602 | ||||||
| chr9:104860615
|
A | T | 1 | a0005c0082t0002g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.543+1064T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860615 | ||||||
| chr9:104860620
|
A | G | 8 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+1059T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860620 | ||||||
| chr9:104860743
|
T | G | 1 | a0035c0091t0008g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+936A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860743 | ||||||
| chr9:104860755
|
C | CT | 21 | a0001c0001t0001g0195a0002c0074t0027g0290a0003c0009t0006g0186others(18): Show | 21 | HG01106.hp1 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.543+923dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860755 | ||||||
| chr9:104860755
|
C | CTT | 148 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(145): Show | 148 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.543+922_543+923dup others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860755 | ||||||
| chr9:104860755
|
C | CTTT | 14 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0025t0008g0285others(11): Show | 14 | HG00741.hp2 HG01255.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.543+921_543+923dup others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860755 | ||||||
| chr9:104860813
|
A | G | 169 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(166): Show | 169 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.543+866T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860813 | ||||||
| chr9:104860819
|
T | C | 170 | a0001c0005t0010g0043a0002c0011t0004g0112a0002c0011t0004g0213others(167): Show | 170 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.543+860A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860819 | ||||||
| chr9:104860828
|
C | T | 169 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(166): Show | 169 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.543+851G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860828 | ||||||
| chr9:104860843
|
G | A | 2 | a0012c0041t0002g0230a0033c0101t0001g0308 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.543+836C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860843 | ||||||
| chr9:104860888
|
C | T | 3 | a0004c0066t0008g0007a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.543+791G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860888 | ||||||
| chr9:104860962
|
G | C | 1 | a0002c0085t0008g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.543+717C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860962 | ||||||
| chr9:104860968
|
A | C | 169 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(166): Show | 169 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.543+711T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104860968 | ||||||
| chr9:104861014
|
C | T | 6 | a0012c0041t0002g0230a0012c0105t0024g0217a0019c0106t0001g0094others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+665G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861014 | ||||||
| chr9:104861045
|
C | T | 169 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(166): Show | 169 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.543+634G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861045 | ||||||
| chr9:104861056
|
A | C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.543+623T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861056 | ||||||
| chr9:104861097
|
C | T | 6 | a0012c0041t0002g0230a0012c0105t0024g0217a0019c0106t0001g0094others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+582G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861097 | ||||||
| chr9:104861233
|
G | A | 6 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+446C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861233 | ||||||
| chr9:104861289
|
G | T | 167 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(164): Show | 167 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.543+390C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861289 | ||||||
| chr9:104861345
|
C | T | 167 | a0002c0011t0004g0112a0002c0011t0004g0213a0002c0011t0004g0263others(164): Show | 167 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.543+334G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861345 | ||||||
| chr9:104861372
|
T | A | 53 | a0002c0011t0004g0112a0002c0015t0002g0315a0002c0015t0004g0004others(50): Show | 53 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.543+307A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861372 | ||||||
| chr9:104861469
|
T | G | 120 | a0001c0035t0004g0011a0001c0035t0009g0071a0002c0011t0004g0112others(117): Show | 120 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.543+210A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861469 | ||||||
| chr9:104861526
|
G | C | 23 | a0002c0017t0002g0271a0002c0017t0026g0163a0002c0017t0026g0276others(20): Show | 23 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.543+153C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 6/49 | chr9 | 104861526 | ||||||
| chr9:104861842
|
CA | C | 148 | a0001c0035t0004g0011a0001c0035t0009g0071a0002c0011t0004g0112others(145): Show | 148 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.422-43delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104861842 | ||||||
| chr9:104861928
|
C | T | 1 | a0003c0038t0003g0293 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.422-128G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104861928 | ||||||
| chr9:104861961
|
A | G | 133 | a0001c0001t0001g0082a0002c0011t0004g0112a0002c0011t0007g0119others(130): Show | 133 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.422-161T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104861961 | ||||||
| chr9:104862049
|
T | TAC | 116 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0088others(113): Show | 116 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.422-251_422-250dup others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862049 | ||||||
| chr9:104862049
|
T | TACAC | 19 | a0002c0015t0004g0004a0002c0032t0001g0317a0002c0074t0027g0290others(16): Show | 19 | HG00558.hp2 HG01109.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.422-253_422-250dup others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862049 | ||||||
| chr9:104862049
|
T | TACACAC | 4 | a0002c0015t0002g0315a0002c0037t0001g0275a0003c0077t0005g0312others(1): Show | 4 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-255_422-250dup others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862049 | ||||||
| chr9:104862049
|
TACAC | T | 5 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0025t0015g0283others(2): Show | 5 | HG01255.hp2 HG01884.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-253_422-250del others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862049 | ||||||
| chr9:104862051
|
C | A | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-251G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862051 | ||||||
| chr9:104862065
|
CACACACA others(5): Show |
C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-277_422-266del others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862065 | ||||||
| chr9:104862071
|
CACACAT | C | 42 | a0002c0011t0004g0263a0002c0011t0007g0119a0002c0011t0007g0247others(39): Show | 42 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.422-277_422-272del others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862071 | ||||||
| chr9:104862073
|
CACAT | C | 3 | a0002c0011t0004g0213a0009c0018t0038g0228a0013c0013t0003g0207 | 3 | NA19001.hp2 NA19009.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.422-277_422-274del others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862073 | ||||||
| chr9:104862102
|
T | C | 52 | a0002c0011t0004g0112a0002c0025t0007g0237a0002c0025t0008g0285others(49): Show | 52 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.422-302A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862102 | ||||||
| chr9:104862103
|
C | CT | 16 | a0002c0017t0002g0271a0002c0024t0008g0003a0002c0024t0008g0008others(13): Show | 16 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.422-304dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862103 | ||||||
| chr9:104862103
|
CT | C | 6 | a0001c0001t0006g0047a0002c0017t0026g0163a0002c0017t0026g0276others(3): Show | 6 | HG01255.hp2 HG01496.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-304delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862103 | ||||||
| chr9:104862108
|
T | C | 52 | a0002c0011t0004g0112a0002c0025t0007g0237a0002c0025t0008g0285others(49): Show | 52 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.422-308A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862108 | ||||||
| chr9:104862126
|
C | T | 5 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0025t0015g0283others(2): Show | 5 | HG01255.hp2 HG01884.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-326G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862126 | ||||||
| chr9:104862157
|
G | A | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.422-357C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862157 | ||||||
| chr9:104862196
|
C | T | 4 | a0002c0011t0004g0213a0002c0011t0004g0263a0003c0002t0002g0172others(1): Show | 4 | HG02155.hp2 NA19001.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-396G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862196 | ||||||
| chr9:104862270
|
A | ATT | 50 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(47): Show | 50 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.422-472_422-471dup others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862270 | ||||||
| chr9:104862413
|
T | TTTGCTTT others(18): Show |
118 | a0001c0001t0001g0016a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.422-614_422-613ins others(25): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862413 | ||||||
| chr9:104862417
|
C | T | 118 | a0001c0001t0001g0016a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.422-617G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862417 | ||||||
| chr9:104862418
|
T | G | 118 | a0001c0001t0001g0016a0002c0011t0004g0112a0002c0011t0004g0213others(115): Show | 118 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.422-618A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862418 | ||||||
| chr9:104862462
|
G | A | 3 | a0004c0112t0005g0098a0004c0113t0002g0159a0004c0114t0005g0304 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.422-662C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862462 | ||||||
| chr9:104862597
|
C | G | 56 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(53): Show | 56 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.422-797G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862597 | ||||||
| chr9:104862631
|
T | G | 1 | a0002c0017t0015g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.422-831A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862631 | ||||||
| chr9:104862631
|
T | TGCTGGGC others(23): Show |
1 | a0005c0014t0011g0222 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.422-832_422-831ins others(30): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862631 | ||||||
| chr9:104862631
|
T | TGCTGGGC others(63): Show |
1 | a0002c0033t0032g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.422-832_422-831ins others(70): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862631 | ||||||
| chr9:104862631
|
TGCCGGGC others(53): Show |
T | 1 | a0010c0007t0002g0125 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.422-891_422-832del others(60): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862631 | ||||||
| chr9:104862634
|
C | T | 242 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0088others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.422-834G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862634 | ||||||
| chr9:104862635
|
G | C | 4 | a0001c0001t0012g0144a0001c0005t0010g0043a0004c0008t0028g0199others(1): Show | 4 | HG02132.hp1 NA18942.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-835C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862635 | ||||||
| chr9:104862635
|
GGGCCGGG others(57): Show |
G | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.422-899_422-836del others(64): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862635 | ||||||
| chr9:104862637
|
G | C | 2 | a0004c0008t0006g0202a0004c0066t0008g0007 | 2 | NA19030.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.422-837C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862637 | ||||||
| chr9:104862638
|
CCGGGCCG others(98): Show |
C | 56 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(53): Show | 56 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.422-943_422-839del | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862638 | ||||||
| chr9:104862639
|
C | A | 1 | a0005c0014t0011g0222 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.422-839G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862639 | ||||||
| chr9:104862639
|
C | CGGGCCGG others(33): Show |
1 | a0015c0020t0001g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.422-840_422-839ins others(40): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862639 | ||||||
| chr9:104862639
|
CGGGCCGG others(16): Show |
C | 1 | a0004c0066t0008g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.422-862_422-840del others(23): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862639 | ||||||
| chr9:104862639
|
CGGGCCGG others(36): Show |
C | 3 | a0001c0001t0012g0144a0006c0004t0010g0252a0035c0091t0008g0161 | 3 | HG02132.hp1 NA19009.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.422-882_422-840del others(43): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862639 | ||||||
| chr9:104862640
|
G | C | 2 | a0001c0005t0010g0043a0002c0017t0015g0101 | 2 | HG03516.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.422-840C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862640 | ||||||
| chr9:104862640
|
GGGCCGGG others(52): Show |
G | 1 | a0004c0029t0005g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.422-899_422-841del others(59): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862640 | ||||||
| chr9:104862641
|
G | C | 1 | a0001c0005t0010g0043 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.422-841C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862641 | ||||||
| chr9:104862641
|
GGCCGGGC others(58): Show |
G | 2 | a0004c0029t0001g0099a0012c0105t0024g0217 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.422-906_422-842del others(65): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862641 | ||||||
| chr9:104862642
|
G | C | 52 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0238others(49): Show | 52 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.422-842C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862642 | ||||||
| chr9:104862643
|
CCGGGCCG others(47): Show |
C | 2 | a0001c0001t0001g0016a0005c0016t0011g0075 | 2 | HG02735.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.422-897_422-844del others(54): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862643 | ||||||
| chr9:104862644
|
C | A | 1 | a0001c0005t0010g0043 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.422-844G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
C | CGGGCAGC others(8): Show |
1 | a0004c0064t0007g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.422-845_422-844ins others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
C | CGGGCAGC others(28): Show |
1 | a0005c0014t0003g0243 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.422-845_422-844ins others(35): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGG | C | 7 | a0001c0001t0001g0291a0002c0025t0007g0237a0002c0046t0002g0154others(4): Show | 7 | HG01255.hp1 HG01433.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-847_422-845del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(6): Show |
C | 1 | a0010c0007t0002g0015 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.422-857_422-845del others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(11): Show |
C | 3 | a0001c0001t0004g0193a0003c0076t0002g0130a0005c0026t0004g0042 | 3 | HG02698.hp2 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.422-862_422-845del others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(20): Show |
C | 2 | a0001c0001t0001g0238a0001c0109t0001g0232 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.422-871_422-845del others(27): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(21): Show |
C | 2 | a0003c0009t0003g0209a0010c0007t0010g0185 | 2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.422-872_422-845del others(28): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(26): Show |
C | 4 | a0005c0016t0001g0049a0010c0007t0002g0013a0010c0007t0010g0200others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-877_422-845del others(33): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(31): Show |
C | 2 | a0004c0029t0005g0162a0004c0099t0001g0110 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.422-882_422-845del others(38): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(40): Show |
C | 2 | a0012c0102t0007g0188a0019c0086t0003g0100 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.422-891_422-845del others(47): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(41): Show |
C | 4 | a0008c0006t0001g0087a0008c0006t0007g0111a0009c0021t0001g0174others(1): Show | 4 | HG01346.hp1 HG02055.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-892_422-845del others(48): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862644
|
CGGGCCGG others(46): Show |
C | 2 | a0004c0098t0005g0303a0028c0095t0002g0114 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.422-897_422-845del others(53): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862644 | ||||||
| chr9:104862645
|
G | C | 16 | a0001c0005t0010g0043a0002c0011t0004g0112a0002c0025t0008g0285others(13): Show | 16 | HG00738.hp1 HG01081.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.422-845C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862645 | ||||||
| chr9:104862645
|
GGGCCGGG others(47): Show |
G | 5 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0013g0280others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-899_422-846del others(54): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862645 | ||||||
| chr9:104862646
|
G | C | 7 | a0001c0005t0010g0043a0002c0011t0004g0112a0003c0002t0050g0068others(4): Show | 7 | HG00738.hp1 HG01257.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.422-846C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862646 | ||||||
| chr9:104862646
|
GGCCGGGC others(59): Show |
G | 1 | a0029c0110t0002g0165 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.422-912_422-847del others(66): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862646 | ||||||
| chr9:104862646
|
GGCCGGGC others(71): Show |
G | 3 | a0001c0001t0006g0054a0012c0065t0007g0182a0027c0062t0001g0310 | 3 | HG01106.hp1 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.422-924_422-847del others(78): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862646 | ||||||
| chr9:104862647
|
G | A | 6 | a0002c0011t0004g0112a0003c0002t0050g0068a0003c0009t0001g0279others(3): Show | 6 | HG00738.hp1 HG01257.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-847C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862647 | ||||||
| chr9:104862647
|
G | C | 37 | a0001c0001t0001g0102a0001c0001t0002g0137a0001c0001t0004g0194others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.422-847C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862647 | ||||||
| chr9:104862648
|
C | A | 9 | a0002c0025t0008g0285a0002c0059t0001g0235a0008c0048t0030g0022others(6): Show | 9 | HG01081.hp2 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-848G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862648 | ||||||
| chr9:104862649
|
C | A | 39 | a0001c0035t0009g0071a0002c0017t0002g0271a0002c0024t0008g0003others(36): Show | 39 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.422-849G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGG | C | 4 | a0002c0011t0004g0112a0007c0003t0016g0029a0008c0006t0047g0056others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-851_422-850del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGG | C | 8 | a0002c0025t0008g0285a0003c0002t0002g0041a0006c0004t0003g0190others(5): Show | 8 | HG00621.hp1 HG01081.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-852_422-850del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGGCCGG others(6): Show |
C | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.422-862_422-850del others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGGCCGG others(11): Show |
C | 4 | a0001c0092t0012g0220a0006c0004t0002g0132a0007c0003t0011g0072others(1): Show | 4 | HG00621.hp2 HG03579.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-867_422-850del others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGGCCGG others(21): Show |
C | 2 | a0001c0005t0002g0064a0001c0005t0004g0167 | 2 | NA18747.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.422-877_422-850del others(28): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGGCCGG others(26): Show |
C | 3 | a0006c0012t0001g0090a0007c0003t0009g0156a0007c0003t0014g0030 | 3 | HG01361.hp2 HG02056.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.422-882_422-850del others(33): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGGCCGG others(31): Show |
C | 1 | a0004c0044t0007g0302 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.422-887_422-850del others(38): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGGCCGG others(35): Show |
C | 9 | a0001c0001t0002g0137a0001c0001t0004g0194a0001c0005t0002g0062others(6): Show | 9 | HG00408.hp2 HG00558.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-891_422-850del others(42): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862649
|
CGGGCCGG others(41): Show |
C | 3 | a0002c0085t0008g0142a0004c0107t0002g0236a0008c0006t0015g0095 | 3 | HG02630.hp2 HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.422-897_422-850del others(48): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862649 | ||||||
| chr9:104862650
|
G | A | 4 | a0001c0005t0010g0043a0002c0025t0007g0237a0004c0008t0028g0199others(1): Show | 4 | HG01433.hp1 HG02886.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-850C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862650 | ||||||
| chr9:104862650
|
G | C | 6 | a0001c0001t0001g0291a0004c0008t0006g0202a0005c0052t0001g0281others(3): Show | 6 | HG01255.hp1 HG03195.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-850C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862650 | ||||||
| chr9:104862651
|
G | A | 3 | a0001c0001t0001g0291a0004c0008t0006g0202a0006c0004t0004g0067 | 3 | HG01255.hp1 NA19068.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.422-851C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862651 | ||||||
| chr9:104862651
|
G | C | 28 | a0001c0005t0010g0043a0001c0035t0009g0071a0002c0025t0007g0237others(25): Show | 28 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.422-851C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862651 | ||||||
| chr9:104862651
|
GGCCGGGC others(48): Show |
G | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.422-906_422-852del others(55): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862651 | ||||||
| chr9:104862652
|
G | C | 36 | a0001c0001t0001g0077a0001c0001t0001g0195a0001c0001t0001g0218others(33): Show | 36 | HG00609.hp1 HG00738.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.422-852C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862652 | ||||||
| chr9:104862653
|
C | A | 2 | a0005c0052t0001g0281a0008c0006t0003g0187 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.422-853G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862653 | ||||||
| chr9:104862654
|
C | A | 3 | a0001c0035t0004g0011a0004c0064t0007g0175a0005c0014t0003g0243 | 3 | HG01192.hp2 HG03688.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.422-854G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862654 | ||||||
| chr9:104862654
|
CGG | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0218a0004c0008t0004g0264 | 3 | HG00738.hp2 HG01261.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.422-856_422-855del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862654 | ||||||
| chr9:104862654
|
CGGG | C | 7 | a0001c0001t0001g0195a0001c0001t0001g0291a0002c0046t0002g0154others(4): Show | 7 | HG03098.hp2 HG03195.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.422-857_422-855del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862654 | ||||||
| chr9:104862654
|
CGGGCCGG others(6): Show |
C | 3 | a0001c0005t0001g0050a0002c0015t0013g0305a0002c0015t0013g0306 | 3 | HG01361.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.422-867_422-855del others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862654 | ||||||
| chr9:104862654
|
CGGGCCGG others(26): Show |
C | 1 | a0038c0068t0044g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.422-887_422-855del others(33): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862654 | ||||||
| chr9:104862654
|
CGGGCCGG others(30): Show |
C | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.422-891_422-855del others(37): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862654 | ||||||
| chr9:104862654
|
CGGGCCGG others(36): Show |
C | 1 | a0007c0003t0033g0035 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.422-897_422-855del others(43): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862654 | ||||||
| chr9:104862655
|
G | A | 6 | a0002c0011t0004g0112a0007c0003t0009g0260a0007c0003t0016g0029others(3): Show | 6 | HG02145.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-855C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862655 | ||||||
| chr9:104862655
|
G | C | 9 | a0001c0005t0010g0043a0002c0025t0007g0237a0002c0037t0001g0275others(6): Show | 9 | HG00621.hp1 HG01255.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-855C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862655 | ||||||
| chr9:104862656
|
G | A | 6 | a0001c0005t0010g0043a0002c0025t0007g0237a0003c0002t0002g0041others(3): Show | 6 | HG00621.hp1 HG01433.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-856C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862656 | ||||||
| chr9:104862656
|
G | C | 15 | a0002c0011t0004g0112a0002c0025t0008g0285a0002c0037t0001g0275others(12): Show | 15 | HG01081.hp2 HG01255.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.422-856C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862656 | ||||||
| chr9:104862656
|
GGCCGGGC others(43): Show |
G | 1 | a0030c0100t0009g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.422-906_422-857del others(50): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862656 | ||||||
| chr9:104862656
|
GGCCGGGC others(55): Show |
G | 3 | a0001c0001t0012g0039a0018c0079t0004g0314a0018c0080t0004g0107 | 3 | HG01109.hp1 HG01243.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.422-918_422-857del others(62): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862656 | ||||||
| chr9:104862657
|
G | A | 7 | a0002c0025t0008g0285a0006c0004t0004g0067a0008c0048t0030g0022others(4): Show | 7 | HG01081.hp2 HG01255.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-857C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862657 | ||||||
| chr9:104862657
|
G | C | 35 | a0001c0001t0001g0077a0001c0001t0001g0218a0001c0001t0002g0074others(32): Show | 35 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.422-857C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862657 | ||||||
| chr9:104862659
|
C | A | 37 | a0001c0035t0009g0071a0002c0017t0002g0271a0002c0024t0008g0003others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.422-859G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862659
|
C | CCCCACCC others(3): Show |
1 | a0002c0015t0031g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.422-860_422-859ins others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862659
|
C | CCCCCACC others(28): Show |
1 | a0001c0005t0002g0254 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.422-860_422-859ins others(35): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862659
|
CGG | C | 3 | a0002c0017t0026g0163a0006c0004t0004g0067a0006c0012t0010g0198 | 3 | HG01255.hp1 HG01884.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.422-861_422-860del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862659
|
CGGG | C | 9 | a0001c0001t0002g0074a0002c0025t0007g0237a0003c0002t0002g0041others(6): Show | 9 | HG00621.hp1 HG01106.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-862_422-860del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862659
|
CGGGCCGG others(11): Show |
C | 1 | a0004c0096t0007g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.422-877_422-860del others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862659
|
CGGGCCGG others(16): Show |
C | 1 | a0006c0012t0002g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.422-882_422-860del others(23): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862659
|
CGGGCCGG others(25): Show |
C | 2 | a0012c0040t0040g0055a0034c0103t0007g0240 | 2 | HG00609.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.422-891_422-860del others(32): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862659 | ||||||
| chr9:104862660
|
G | A | 8 | a0001c0001t0001g0077a0001c0001t0001g0218a0001c0001t0001g0291others(5): Show | 8 | HG00738.hp2 HG01261.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-860C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862660 | ||||||
| chr9:104862660
|
G | C | 18 | a0001c0001t0001g0195a0001c0005t0002g0254a0001c0005t0010g0043others(15): Show | 18 | HG00673.hp2 HG01081.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.422-860C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862660 | ||||||
| chr9:104862660
|
GGGCCGGG others(32): Show |
G | 1 | a0036c0094t0009g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.422-899_422-861del others(39): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862660 | ||||||
| chr9:104862661
|
G | A | 9 | a0001c0001t0001g0195a0002c0011t0004g0112a0002c0037t0011g0116others(6): Show | 9 | HG00673.hp2 HG02145.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-861C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862661 | ||||||
| chr9:104862661
|
G | C | 17 | a0001c0001t0001g0077a0001c0001t0001g0218a0001c0001t0001g0291others(14): Show | 17 | HG00738.hp2 HG01261.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.422-861C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862661 | ||||||
| chr9:104862661
|
G | GCCCCCCA others(8): Show |
1 | a0004c0043t0003g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422-862_422-861ins others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862661 | ||||||
| chr9:104862661
|
GGCCGGGC others(38): Show |
G | 1 | a0007c0090t0007g0046 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.422-906_422-862del others(45): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862661 | ||||||
| chr9:104862661
|
GGCCGGGC others(50): Show |
G | 1 | a0025c0083t0001g0313 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.422-918_422-862del others(57): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862661 | ||||||
| chr9:104862661
|
GGCCGGGC others(63): Show |
G | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-931_422-862del others(70): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862661 | ||||||
| chr9:104862662
|
G | A | 5 | a0001c0005t0010g0043a0002c0059t0001g0235a0005c0052t0001g0281others(2): Show | 5 | HG02145.hp1 HG03195.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-862C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862662 | ||||||
| chr9:104862662
|
G | C | 42 | a0001c0001t0001g0077a0001c0001t0001g0195a0001c0001t0001g0218others(39): Show | 42 | HG00673.hp2 HG00738.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.422-862C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862662 | ||||||
| chr9:104862663
|
C | A | 5 | a0002c0025t0008g0285a0008c0048t0030g0022a0011c0010t0005g0097others(2): Show | 5 | HG01081.hp2 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-863G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862663 | ||||||
| chr9:104862664
|
C | A | 12 | a0001c0035t0004g0011a0002c0017t0002g0271a0002c0033t0002g0301others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-864G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862664 | ||||||
| chr9:104862664
|
CGGG | C | 9 | a0001c0001t0006g0047a0002c0017t0015g0101a0002c0025t0008g0285others(6): Show | 9 | HG01081.hp2 HG01496.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-867_422-865del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862664 | ||||||
| chr9:104862664
|
CGGGCCGG others(11): Show |
C | 1 | a0032c0104t0005g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.422-882_422-865del others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862664 | ||||||
| chr9:104862664
|
CGGGCCGG others(20): Show |
C | 4 | a0001c0001t0006g0225a0001c0005t0002g0123a0001c0005t0002g0129others(1): Show | 4 | NA18942.hp1 NA18984.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-891_422-865del others(27): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862664 | ||||||
| chr9:104862664
|
CGGGCCGG others(21): Show |
C | 1 | a0007c0003t0009g0260 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.422-892_422-865del others(28): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862664 | ||||||
| chr9:104862664
|
CGGGCCGG others(26): Show |
C | 1 | a0001c0001t0007g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.422-897_422-865del others(33): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862664 | ||||||
| chr9:104862665
|
G | A | 14 | a0001c0005t0002g0254a0002c0015t0031g0084a0002c0017t0026g0163others(11): Show | 14 | HG00621.hp1 HG01255.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.422-865C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862665 | ||||||
| chr9:104862665
|
G | C | 28 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0102others(25): Show | 28 | HG00673.hp2 HG00738.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.422-865C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862665 | ||||||
| chr9:104862666
|
G | A | 16 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0218others(13): Show | 16 | HG00738.hp2 HG01106.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.422-866C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862666 | ||||||
| chr9:104862666
|
G | C | 23 | a0001c0001t0001g0026a0001c0001t0001g0195a0001c0005t0002g0254others(20): Show | 23 | HG00621.hp1 HG00673.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.422-866C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862666 | ||||||
| chr9:104862666
|
GGCCGGGC others(39): Show |
G | 1 | a0005c0036t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.422-912_422-867del others(46): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862666 | ||||||
| chr9:104862666
|
GGCCGGGC others(51): Show |
G | 1 | a0005c0082t0002g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.422-924_422-867del others(58): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862666 | ||||||
| chr9:104862667
|
G | A | 7 | a0001c0001t0001g0195a0002c0011t0004g0112a0007c0003t0016g0029others(4): Show | 7 | HG02818.hp2 HG02922.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-867C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862667 | ||||||
| chr9:104862667
|
G | C | 44 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(41): Show | 44 | HG00621.hp1 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.422-867C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862667 | ||||||
| chr9:104862668
|
C | A | 5 | a0002c0037t0011g0116a0002c0059t0001g0235a0005c0052t0001g0281others(2): Show | 5 | HG00673.hp2 HG02145.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-868G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862668 | ||||||
| chr9:104862669
|
C | A | 30 | a0001c0001t0001g0026a0001c0035t0004g0011a0001c0035t0009g0071others(27): Show | 30 | HG01070.hp1 HG01071.hp1 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.422-869G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862669 | ||||||
| chr9:104862669
|
CGG | C | 8 | a0001c0001t0001g0082a0001c0001t0001g0195a0001c0001t0011g0085others(5): Show | 8 | HG01070.hp2 HG01169.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-871_422-870del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862669 | ||||||
| chr9:104862669
|
CGGG | C | 15 | a0001c0001t0001g0102a0001c0001t0001g0291a0001c0001t0002g0074others(12): Show | 15 | HG01106.hp2 HG01975.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.422-872_422-870del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862669 | ||||||
| chr9:104862669
|
CGGGCCGG others(15): Show |
C | 1 | a0002c0015t0004g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.422-891_422-870del others(22): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862669 | ||||||
| chr9:104862670
|
G | A | 1 | a0009c0021t0004g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.422-870C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862670 | ||||||
| chr9:104862670
|
G | C | 35 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0218others(32): Show | 35 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.422-870C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862670 | ||||||
| chr9:104862670
|
GGGCCGGG others(22): Show |
G | 3 | a0005c0016t0001g0009a0005c0016t0001g0010a0005c0071t0041g0311 | 3 | HG00642.hp1 HG01175.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.422-899_422-871del others(29): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862670 | ||||||
| chr9:104862671
|
G | A | 24 | a0001c0001t0004g0021a0001c0001t0006g0047a0001c0005t0001g0050others(21): Show | 24 | HG00621.hp1 HG00621.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.422-871C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862671 | ||||||
| chr9:104862671
|
G | C | 17 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0218others(14): Show | 17 | HG00673.hp2 HG00738.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.422-871C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862671 | ||||||
| chr9:104862671
|
GGCCGGGC others(34): Show |
G | 1 | a0002c0015t0002g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.422-912_422-872del others(41): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862671 | ||||||
| chr9:104862671
|
GGCCGGGC others(40): Show |
G | 1 | a0009c0018t0004g0292 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.422-918_422-872del others(47): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862671 | ||||||
| chr9:104862672
|
G | A | 11 | a0001c0001t0001g0077a0001c0001t0001g0218a0002c0025t0008g0285others(8): Show | 11 | HG00738.hp2 HG01081.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-872C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862672 | ||||||
| chr9:104862672
|
G | C | 46 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0195others(43): Show | 46 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.422-872C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862672 | ||||||
| chr9:104862673
|
CCGGGCCG others(33): Show |
C | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.422-913_422-874del others(40): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862673 | ||||||
| chr9:104862674
|
C | A | 8 | a0001c0035t0009g0071a0002c0025t0015g0283a0002c0033t0002g0301others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-874G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862674 | ||||||
| chr9:104862674
|
C | CCCCA | 5 | a0001c0001t0001g0077a0001c0001t0001g0218a0002c0037t0001g0275others(2): Show | 5 | HG00738.hp2 HG01261.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-875_422-874ins others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862674 | ||||||
| chr9:104862674
|
C | CGGGCAGG others(13): Show |
2 | a0002c0024t0008g0003a0002c0024t0008g0008 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.422-875_422-874ins others(20): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862674 | ||||||
| chr9:104862674
|
CGGG | C | 19 | a0001c0001t0004g0021a0001c0001t0006g0047a0001c0005t0001g0050others(16): Show | 19 | HG00621.hp1 HG00621.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.422-877_422-875del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862674 | ||||||
| chr9:104862674
|
CGGGCCGG others(4): Show |
C | 1 | a0002c0031t0001g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.422-885_422-875del others(11): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862674 | ||||||
| chr9:104862675
|
G | A | 27 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0102others(24): Show | 27 | HG00099.hp2 HG00673.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.422-875C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862675 | ||||||
| chr9:104862675
|
G | C | 19 | a0001c0001t0001g0077a0001c0001t0001g0218a0002c0015t0031g0084others(16): Show | 19 | HG00738.hp2 HG01081.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.422-875C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862675 | ||||||
| chr9:104862675
|
GGGCCGGG others(17): Show |
G | 2 | a0005c0014t0005g0245a0006c0004t0006g0249 | 2 | HG02451.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.422-899_422-876del others(24): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862675 | ||||||
| chr9:104862676
|
G | A | 1 | a0009c0021t0004g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.422-876C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862676 | ||||||
| chr9:104862676
|
G | C | 44 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(41): Show | 44 | HG00099.hp2 HG00673.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.422-876C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862676 | ||||||
| chr9:104862676
|
GGCCGGGC others(29): Show |
G | 1 | a0002c0032t0001g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.422-912_422-877del others(36): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862676 | ||||||
| chr9:104862677
|
G | A | 12 | a0002c0015t0031g0084a0002c0017t0015g0101a0002c0017t0026g0163others(9): Show | 12 | HG01255.hp1 HG01884.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-877C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862677 | ||||||
| chr9:104862677
|
G | C | 56 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.422-877C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862677 | ||||||
| chr9:104862678
|
C | A | 6 | a0002c0025t0008g0285a0008c0048t0030g0022a0011c0010t0005g0097others(3): Show | 6 | HG01081.hp2 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-878G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862678 | ||||||
| chr9:104862679
|
C | A | 16 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(13): Show | 16 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.422-879G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862679 | ||||||
| chr9:104862679
|
C | CCCCACCC others(3): Show |
1 | a0001c0001t0052g0318 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.422-880_422-879ins others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862679 | ||||||
| chr9:104862679
|
CGGG | C | 22 | a0001c0001t0001g0088a0001c0001t0001g0203a0001c0001t0003g0089others(19): Show | 22 | HG00642.hp2 HG01071.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-882_422-880del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862679 | ||||||
| chr9:104862680
|
G | A | 26 | a0001c0001t0001g0077a0001c0001t0001g0218a0001c0001t0004g0021others(23): Show | 26 | HG00621.hp1 HG00621.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.422-880C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862680 | ||||||
| chr9:104862680
|
G | C | 45 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0102others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.422-880C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862680 | ||||||
| chr9:104862680
|
GGGCCGGG others(12): Show |
G | 2 | a0002c0075t0027g0150a0003c0009t0046g0219 | 2 | HG02976.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.422-899_422-881del others(19): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862680 | ||||||
| chr9:104862681
|
G | A | 31 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0102others(28): Show | 31 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.422-881C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862681 | ||||||
| chr9:104862681
|
G | C | 36 | a0001c0001t0001g0077a0001c0001t0001g0218a0001c0001t0004g0021others(33): Show | 36 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.422-881C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862681 | ||||||
| chr9:104862681
|
G | GCA | 3 | a0005c0052t0001g0281a0008c0006t0003g0187a0011c0010t0005g0258 | 3 | HG02922.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.422-882_422-881ins others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862681 | ||||||
| chr9:104862682
|
G | A | 1 | a0002c0037t0011g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.422-882C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862682 | ||||||
| chr9:104862682
|
G | C | 74 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.422-882C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862682 | ||||||
| chr9:104862683
|
C | A | 9 | a0002c0015t0031g0084a0002c0017t0015g0101a0002c0017t0026g0163others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-883G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862683 | ||||||
| chr9:104862684
|
C | A | 8 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0033t0002g0301others(5): Show | 8 | HG02647.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-884G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862684 | ||||||
| chr9:104862684
|
C | CGGGCAGG others(8): Show |
1 | a0002c0024t0008g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.422-885_422-884ins others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862684 | ||||||
| chr9:104862684
|
CGGG | C | 6 | a0001c0001t0039g0246a0001c0001t0043g0002a0001c0005t0002g0192others(3): Show | 6 | HG00423.hp1 HG01168.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-887_422-885del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862684 | ||||||
| chr9:104862685
|
G | A | 2 | a0001c0001t0052g0318a0009c0021t0004g0204 | 2 | HG00099.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.422-885C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862685 | ||||||
| chr9:104862685
|
G | C | 89 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(86): Show | 89 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.422-885C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862685 | ||||||
| chr9:104862686
|
G | A | 47 | a0001c0001t0001g0077a0001c0001t0001g0088a0001c0001t0001g0203others(44): Show | 47 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.422-886C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862686 | ||||||
| chr9:104862686
|
G | C | 53 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0102others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.422-886C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862686 | ||||||
| chr9:104862686
|
GGCCGGGC others(13): Show |
G | 2 | a0007c0003t0020g0179a0009c0027t0006g0267 | 2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.422-906_422-887del others(20): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862686 | ||||||
| chr9:104862687
|
G | A | 43 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0102others(40): Show | 43 | HG00099.hp2 HG01070.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.422-887C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862687 | ||||||
| chr9:104862687
|
G | C | 67 | a0001c0001t0001g0077a0001c0001t0001g0088a0001c0001t0001g0203others(64): Show | 67 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.422-887C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862687 | ||||||
| chr9:104862689
|
C | A | 20 | a0002c0015t0031g0084a0002c0017t0015g0101a0002c0017t0026g0163others(17): Show | 20 | HG00673.hp2 HG01255.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.422-889G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCACCCCC others(19): Show |
1 | a0001c0001t0039g0246 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(26): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCACCCCC others(55): Show |
1 | a0005c0014t0006g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.422-890_422-889ins others(62): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCACCCCC others(67): Show |
1 | a0001c0001t0043g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.422-890_422-889ins others(74): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCA | 5 | a0001c0001t0001g0077a0001c0001t0001g0218a0002c0037t0001g0275others(2): Show | 5 | HG00738.hp2 HG01261.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-890_422-889ins others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(14): Show |
2 | a0001c0001t0001g0088a0001c0001t0003g0089 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.422-890_422-889ins others(21): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(26): Show |
1 | a0002c0017t0026g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(33): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(44): Show |
2 | a0006c0004t0011g0269a0017c0034t0001g0300 | 2 | HG06807.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.422-890_422-889ins others(51): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(50): Show |
2 | a0001c0001t0003g0210a0007c0003t0004g0048 | 2 | HG03490.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.422-890_422-889ins others(57): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(56): Show |
1 | a0001c0001t0049g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.422-890_422-889ins others(63): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(62): Show |
1 | a0001c0001t0001g0203 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(69): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(68): Show |
1 | a0001c0005t0002g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.422-890_422-889ins others(75): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(80): Show |
2 | a0001c0097t0001g0106a0012c0093t0001g0108 | 2 | HG01071.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.422-890_422-889ins others(87): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCACCCC others(122): Show |
1 | a0005c0084t0014g0215 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(129): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(15): Show |
1 | a0001c0001t0001g0195 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.422-890_422-889ins others(22): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(27): Show |
3 | a0003c0077t0005g0312a0004c0008t0001g0036a0023c0072t0001g0309 | 3 | HG02486.hp1 HG03942.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.422-890_422-889ins others(34): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(33): Show |
2 | a0004c0008t0003g0289a0007c0003t0016g0242 | 2 | HG01169.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.422-890_422-889ins others(40): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(39): Show |
1 | a0006c0012t0002g0226 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(46): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(45): Show |
2 | a0001c0001t0002g0074a0007c0003t0002g0038 | 2 | HG01106.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.422-890_422-889ins others(52): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(57): Show |
1 | a0009c0021t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(64): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(63): Show |
1 | a0001c0001t0001g0026 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(70): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(69): Show |
1 | a0004c0008t0003g0294 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.422-890_422-889ins others(76): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(81): Show |
2 | a0001c0001t0001g0082a0001c0005t0002g0031 | 2 | HG01934.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.422-890_422-889ins others(88): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(87): Show |
1 | a0005c0014t0003g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.422-890_422-889ins others(94): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(93): Show |
1 | a0010c0030t0022g0191 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(100): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
C | CCCCACCC others(36): Show |
1 | a0001c0108t0002g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.422-890_422-889ins others(43): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
CGG | C | 22 | a0001c0001t0001g0102a0001c0001t0001g0238a0001c0001t0001g0291others(19): Show | 22 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.422-891_422-890del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862689
|
CGGG | C | 29 | a0001c0001t0004g0021a0001c0005t0001g0050a0001c0005t0002g0254others(26): Show | 29 | HG00621.hp1 HG00621.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.422-892_422-890del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862689 | ||||||
| chr9:104862690
|
G | C | 64 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(61): Show | 64 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.422-890C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862690 | ||||||
| chr9:104862691
|
G | A | 2 | a0009c0021t0004g0204a0038c0068t0044g0272 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-891C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862691
|
G | C | 56 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(53): Show | 56 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.422-891C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862691
|
G | GCA | 3 | a0002c0025t0008g0285a0011c0010t0005g0097a0011c0010t0005g0169 | 3 | HG03041.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.422-892_422-891ins others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862691
|
G | GCCCCCCA others(8): Show |
1 | a0002c0058t0007g0143 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422-892_422-891ins others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862691
|
G | GCCCCCCA others(32): Show |
1 | a0002c0017t0002g0271 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.422-892_422-891ins others(39): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862691
|
G | GCCCCCCA others(50): Show |
2 | a0006c0004t0002g0133a0015c0020t0004g0005 | 2 | HG02622.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.422-892_422-891ins others(57): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862691
|
G | GCCCCCCA others(80): Show |
1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.422-892_422-891ins others(87): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862691
|
GGCCGGGC others(8): Show |
G | 1 | a0015c0061t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.422-906_422-892del others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862691 | ||||||
| chr9:104862692
|
G | A | 4 | a0001c0001t0006g0047a0002c0059t0001g0235a0011c0010t0005g0255others(1): Show | 4 | HG01496.hp2 HG02145.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-892C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862692 | ||||||
| chr9:104862692
|
G | C | 113 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.422-892C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862692 | ||||||
| chr9:104862693
|
C | A | 6 | a0005c0052t0001g0281a0008c0006t0003g0187a0008c0048t0030g0022others(3): Show | 6 | HG01081.hp2 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-893G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862693 | ||||||
| chr9:104862694
|
C | A | 8 | a0002c0057t0001g0148a0004c0044t0007g0302a0005c0022t0002g0284others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-894G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862694 | ||||||
| chr9:104862694
|
C | CCCCACCC others(57): Show |
1 | a0001c0001t0006g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.422-895_422-894ins others(64): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862694 | ||||||
| chr9:104862694
|
C | CCCCACCC others(69): Show |
1 | a0014c0054t0010g0251 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.422-895_422-894ins others(76): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862694 | ||||||
| chr9:104862694
|
C | T | 1 | a0010c0007t0002g0125 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.422-894G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862694 | ||||||
| chr9:104862694
|
CGGG | C | 5 | a0001c0001t0003g0297a0002c0031t0001g0152a0002c0059t0001g0235others(2): Show | 5 | HG02129.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-897_422-895del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862694 | ||||||
| chr9:104862695
|
G | A | 131 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.422-895C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862695 | ||||||
| chr9:104862695
|
G | C | 11 | a0001c0001t0006g0047a0004c0044t0007g0302a0005c0052t0001g0281others(8): Show | 11 | HG01081.hp2 HG01496.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.422-895C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862695 | ||||||
| chr9:104862696
|
G | C | 144 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.422-896C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862696 | ||||||
| chr9:104862696
|
G | GCCCCCAA others(19): Show |
2 | a0001c0001t0023g0295a0001c0001t0023g0296 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.422-897_422-896ins others(26): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862696 | ||||||
| chr9:104862696
|
G | GCCCCCCA others(73): Show |
1 | a0007c0003t0003g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.422-897_422-896ins others(80): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862696 | ||||||
| chr9:104862696
|
G | GCCCCCCA others(97): Show |
2 | a0001c0001t0001g0196a0016c0019t0006g0250 | 2 | HG02148.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.422-897_422-896ins others(104): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862696 | ||||||
| chr9:104862696
|
GGCCGGCC others(15): Show |
G | 1 | a0026c0111t0002g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.422-918_422-897del others(22): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862696 | ||||||
| chr9:104862697
|
G | A | 5 | a0002c0025t0008g0285a0009c0021t0004g0204a0011c0010t0005g0097others(2): Show | 5 | HG02145.hp2 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-897C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862697 | ||||||
| chr9:104862697
|
G | C | 139 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.422-897C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862697 | ||||||
| chr9:104862698
|
CCG | C | 6 | a0005c0052t0001g0281a0008c0006t0003g0187a0008c0048t0030g0022others(3): Show | 6 | HG01081.hp2 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-900_422-899del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862698 | ||||||
| chr9:104862699
|
C | A | 11 | a0002c0025t0015g0283a0002c0057t0001g0148a0005c0022t0002g0284others(8): Show | 11 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-899G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862699 | ||||||
| chr9:104862699
|
C | G | 2 | a0002c0059t0001g0235a0011c0010t0005g0255 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.422-899G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862699 | ||||||
| chr9:104862700
|
G | A | 2 | a0001c0001t0006g0047a0014c0054t0010g0251 | 2 | HG01496.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.422-900C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862700 | ||||||
| chr9:104862700
|
G | C | 153 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.422-900C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862700 | ||||||
| chr9:104862701
|
G | A | 156 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.422-901C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | C | 19 | a0001c0001t0006g0047a0002c0075t0027g0150a0003c0009t0046g0219others(16): Show | 19 | HG00642.hp1 HG01175.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.422-901C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GC | 6 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0024t0008g0109others(3): Show | 6 | HG02896.hp1 HG02897.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-902dupG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(30): Show |
1 | a0002c0081t0013g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(37): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(36): Show |
1 | a0001c0001t0001g0176 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(43): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(54): Show |
1 | a0001c0001t0006g0214 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(61): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(60): Show |
1 | a0007c0003t0004g0170 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(67): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(66): Show |
1 | a0001c0001t0006g0058 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(73): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(72): Show |
1 | a0002c0078t0001g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(79): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(84): Show |
4 | a0001c0005t0002g0017a0004c0008t0003g0197a0005c0014t0003g0243others(1): Show | 4 | HG02293.hp1 HG02293.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-902_422-901ins others(91): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GCCCCCCA others(84): Show |
1 | a0015c0020t0001g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(91): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(102): Show |
1 | a0005c0022t0002g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(109): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(156): Show |
1 | a0011c0010t0005g0287 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(163): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(94): Show |
1 | a0005c0051t0019g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(101): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(19): Show |
1 | a0011c0010t0037g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(26): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(85): Show |
1 | a0009c0018t0003g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(92): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(92): Show |
1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(99): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(57): Show |
1 | a0002c0057t0001g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(64): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(127): Show |
1 | a0005c0022t0021g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(134): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(139): Show |
1 | a0005c0022t0021g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(146): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCAGGGC others(68): Show |
1 | a0015c0020t0001g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(75): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCCCCC others(49): Show |
1 | a0002c0033t0002g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(56): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCCCCC others(61): Show |
1 | a0002c0033t0032g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(68): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGCC others(77): Show |
1 | a0037c0088t0034g0298 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(84): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGCC others(83): Show |
1 | a0008c0006t0022g0135 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(90): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGCC others(107): Show |
2 | a0006c0004t0004g0227a0007c0003t0002g0037 | 2 | HG00609.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.422-902_422-901ins others(114): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGCC others(98): Show |
1 | a0020c0045t0002g0299 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(105): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGCC others(88): Show |
1 | a0001c0001t0003g0211 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(95): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGCC others(99): Show |
1 | a0005c0039t0017g0018 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(106): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(39): Show |
1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(46): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(88): Show |
1 | a0003c0056t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(95): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(94): Show |
1 | a0006c0012t0001g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(101): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(110): Show |
1 | a0005c0039t0017g0019 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(117): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(63): Show |
1 | a0016c0019t0018g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(70): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(87): Show |
2 | a0001c0001t0001g0121a0008c0006t0006g0057 | 2 | HG01978.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.422-902_422-901ins others(94): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(62): Show |
1 | a0001c0001t0003g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(69): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(75): Show |
1 | a0021c0060t0001g0078 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(82): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(72): Show |
1 | a0001c0001t0002g0233 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(79): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(97): Show |
1 | a0017c0034t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.422-902_422-901ins others(104): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(119): Show |
1 | a0007c0003t0003g0014 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(126): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(143): Show |
1 | a0006c0063t0003g0151 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(150): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862701
|
G | GGCCGGGC others(147): Show |
1 | a0006c0089t0003g0180 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.422-902_422-901ins others(154): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862701 | ||||||
| chr9:104862702
|
C | G | 5 | a0001c0035t0004g0011a0004c0064t0007g0175a0009c0027t0004g0124others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-902G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862702 | ||||||
| chr9:104862702
|
CCCCCACC others(4): Show |
C | 1 | a0001c0035t0009g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.422-913_422-903del others(11): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862702 | ||||||
| chr9:104862704
|
C | A | 1 | a0009c0021t0004g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.422-904G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862704 | ||||||
| chr9:104862705
|
C | G | 15 | a0002c0025t0008g0285a0002c0059t0001g0235a0004c0064t0007g0175others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.422-905G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862705 | ||||||
| chr9:104862706
|
C | G | 5 | a0001c0035t0004g0011a0004c0064t0007g0175a0009c0027t0004g0124others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-906G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862706 | ||||||
| chr9:104862707
|
A | C | 11 | a0001c0001t0006g0239a0002c0074t0027g0290a0004c0029t0001g0099others(8): Show | 11 | HG01192.hp2 HG02145.hp2 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-907T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862707 | ||||||
| chr9:104862707
|
A | G | 5 | a0001c0001t0011g0085a0001c0035t0004g0011a0009c0027t0004g0124others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-907T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862707 | ||||||
| chr9:104862708
|
C | G | 1 | a0001c0035t0004g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.422-908G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862708 | ||||||
| chr9:104862710
|
C | G | 3 | a0009c0027t0004g0124a0009c0028t0009g0092a0009c0028t0009g0093 | 3 | HG01070.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.422-910G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862710 | ||||||
| chr9:104862711
|
C | G | 15 | a0001c0035t0004g0011a0002c0025t0008g0285a0002c0059t0001g0235others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.422-911G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862711 | ||||||
| chr9:104862712
|
C | G | 1 | a0001c0035t0004g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.422-912G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862712 | ||||||
| chr9:104862712
|
CA | C | 3 | a0009c0027t0004g0124a0009c0028t0009g0092a0009c0028t0009g0093 | 3 | HG01070.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.422-913delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862712 | ||||||
| chr9:104862713
|
A | ACCCCCAC others(67): Show |
1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-914_422-913ins others(74): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862713 | ||||||
| chr9:104862713
|
A | C | 5 | a0001c0035t0004g0011a0002c0015t0002g0315a0002c0032t0001g0317others(2): Show | 5 | HG02055.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-913T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862713 | ||||||
| chr9:104862717
|
C | G | 7 | a0002c0025t0008g0285a0002c0059t0001g0235a0005c0052t0001g0281others(4): Show | 7 | HG01081.hp2 HG03041.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.422-917G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862717 | ||||||
| chr9:104862719
|
A | C | 6 | a0001c0001t0012g0039a0009c0018t0004g0292a0018c0079t0004g0314others(3): Show | 6 | HG00408.hp1 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-919T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862719 | ||||||
| chr9:104862723
|
C | G | 1 | a0008c0006t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-923G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862723 | ||||||
| chr9:104862725
|
A | C | 4 | a0001c0001t0006g0054a0005c0082t0002g0282a0012c0065t0007g0182others(1): Show | 4 | HG01106.hp1 HG02738.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-925T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862725 | ||||||
| chr9:104862731
|
A | C | 1 | a0007c0003t0009g0260 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.422-931T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862731 | ||||||
| chr9:104862737
|
A | G | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-937T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862737 | ||||||
| chr9:104862743
|
A | C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-943T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862743 | ||||||
| chr9:104862749
|
A | G | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-949T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862749 | ||||||
| chr9:104862750
|
C | A | 1 | a0007c0003t0004g0170 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.422-950G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862750 | ||||||
| chr9:104862750
|
C | CCCCCACC others(17): Show |
1 | a0007c0003t0004g0027 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.422-951_422-950ins others(24): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862750 | ||||||
| chr9:104862750
|
C | CCCCCACC others(47): Show |
1 | a0006c0012t0002g0028 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.422-951_422-950ins others(54): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862750 | ||||||
| chr9:104862794
|
A | T | 1 | a0022c0050t0001g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.422-994T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862794 | ||||||
| chr9:104862865
|
C | T | 56 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(53): Show | 56 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.422-1065G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104862865 | ||||||
| chr9:104863031
|
G | A | 56 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(53): Show | 56 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.422-1231C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863031 | ||||||
| chr9:104863166
|
T | C | 1 | a0005c0036t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.422-1366A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863166 | ||||||
| chr9:104863253
|
G | A | 4 | a0002c0017t0026g0163a0002c0017t0026g0276a0002c0032t0001g0025others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-1453C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863253 | ||||||
| chr9:104863521
|
G | T | 1 | a0009c0021t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.422-1721C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863521 | ||||||
| chr9:104863522
|
C | T | 56 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(53): Show | 56 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.422-1722G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863522 | ||||||
| chr9:104863651
|
A | G | 66 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(63): Show | 66 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.422-1851T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863651 | ||||||
| chr9:104863827
|
G | A | 54 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(51): Show | 54 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.422-2027C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863827 | ||||||
| chr9:104863903
|
C | T | 3 | a0001c0001t0001g0026a0001c0005t0002g0192a0001c0005t0002g0254 | 3 | HG02080.hp2 NA18969.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.422-2103G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863903 | ||||||
| chr9:104863908
|
G | T | 56 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(53): Show | 56 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.422-2108C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863908 | ||||||
| chr9:104863955
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.422-2155C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863955 | ||||||
| chr9:104863990
|
A | T | 2 | a0012c0041t0002g0230a0033c0101t0001g0308 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.422-2190T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104863990 | ||||||
| chr9:104864003
|
A | G | 61 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(58): Show | 61 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.422-2203T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864003 | ||||||
| chr9:104864108
|
C | T | 122 | a0001c0001t0001g0016a0001c0001t0011g0085a0001c0001t0043g0002others(119): Show | 122 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.422-2308G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864108 | ||||||
| chr9:104864208
|
A | G | 11 | a0001c0001t0043g0002a0002c0015t0031g0084a0002c0057t0001g0148others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-2408T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864208 | ||||||
| chr9:104864261
|
C | T | 62 | a0002c0011t0004g0213a0002c0011t0004g0263a0002c0011t0007g0119others(59): Show | 62 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.422-2461G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864261 | ||||||
| chr9:104864307
|
C | T | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.422-2507G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864307 | ||||||
| chr9:104864380
|
C | T | 3 | a0001c0005t0002g0254a0008c0006t0014g0221a0016c0019t0018g0131 | 3 | NA18949.hp2 NA18978.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.422-2580G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864380 | ||||||
| chr9:104864393
|
G | A | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-2593C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864393 | ||||||
| chr9:104864452
|
T | C | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.422-2652A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864452 | ||||||
| chr9:104864583
|
G | A | 1 | a0036c0094t0009g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.422-2783C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864583 | ||||||
| chr9:104864606
|
C | A | 1 | a0010c0007t0002g0015 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.422-2806G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864606 | ||||||
| chr9:104864619
|
G | A | 7 | a0002c0031t0001g0152a0002c0074t0027g0290a0002c0078t0001g0216others(4): Show | 7 | HG01884.hp1 HG01952.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-2819C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864619 | ||||||
| chr9:104864639
|
C | T | 1 | a0004c0066t0008g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.422-2839G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864639 | ||||||
| chr9:104864762
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.422-2962G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864762 | ||||||
| chr9:104864831
|
G | C | 1 | a0002c0025t0015g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.422-3031C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864831 | ||||||
| chr9:104864902
|
G | A | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.422-3102C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864902 | ||||||
| chr9:104864947
|
A | G | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.422-3147T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864947 | ||||||
| chr9:104864952
|
T | C | 1 | a0006c0012t0010g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.422-3152A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864952 | ||||||
| chr9:104864978
|
G | A | 150 | a0001c0001t0001g0016a0001c0001t0001g0102a0001c0001t0001g0121others(147): Show | 150 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.422-3178C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104864978 | ||||||
| chr9:104865041
|
A | G | 12 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0017t0015g0101others(9): Show | 12 | HG02615.hp1 HG02886.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-3241T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865041 | ||||||
| chr9:104865361
|
T | C | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.422-3561A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865361 | ||||||
| chr9:104865367
|
T | C | 9 | a0002c0032t0001g0025a0002c0033t0002g0301a0002c0033t0032g0024others(6): Show | 9 | HG02622.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-3567A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865367 | ||||||
| chr9:104865515
|
C | CA | 9 | a0001c0001t0001g0208a0001c0001t0006g0058a0001c0001t0007g0183others(6): Show | 9 | HG01255.hp2 HG01433.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-3716dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865515 | ||||||
| chr9:104865515
|
C | CAAAAAAA others(3): Show |
9 | a0001c0035t0004g0011a0002c0017t0026g0163a0002c0032t0001g0317others(6): Show | 9 | HG01192.hp2 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-3725_422-3716d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865515 | ||||||
| chr9:104865515
|
C | CAAAAAAA others(4): Show |
8 | a0002c0017t0026g0276a0002c0037t0001g0275a0002c0058t0007g0143others(5): Show | 8 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-3726_422-3716d others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865515 | ||||||
| chr9:104865515
|
C | CAAAAAAA others(5): Show |
2 | a0018c0080t0004g0107a0023c0072t0001g0309 | 2 | HG01243.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.422-3727_422-3716d others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865515 | ||||||
| chr9:104865515
|
C | CAAAAAAA others(6): Show |
1 | a0018c0079t0004g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.422-3728_422-3716d others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865515 | ||||||
| chr9:104865693
|
A | C | 7 | a0002c0017t0026g0276a0002c0037t0001g0275a0003c0077t0005g0312others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-3893T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865693 | ||||||
| chr9:104865706
|
A | C | 7 | a0002c0017t0026g0276a0002c0037t0001g0275a0003c0077t0005g0312others(4): Show | 7 | HG01109.hp1 HG01243.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-3906T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865706 | ||||||
| chr9:104865907
|
G | A | 200 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0082others(197): Show | 200 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.422-4107C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104865907 | ||||||
| chr9:104866094
|
G | C | 5 | a0002c0032t0001g0317a0005c0036t0001g0091a0008c0047t0002g0244others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-4294C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866094 | ||||||
| chr9:104866109
|
A | G | 4 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0011g0085others(1): Show | 4 | HG01070.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-4309T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866109 | ||||||
| chr9:104866119
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.422-4319G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866119 | ||||||
| chr9:104866122
|
C | T | 8 | a0002c0032t0001g0025a0002c0033t0002g0301a0002c0033t0032g0024others(5): Show | 8 | HG02622.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-4322G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866122 | ||||||
| chr9:104866155
|
T | C | 5 | a0002c0032t0001g0317a0005c0036t0001g0091a0008c0047t0002g0244others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-4355A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866155 | ||||||
| chr9:104866158
|
T | C | 1 | a0001c0001t0007g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.422-4358A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866158 | ||||||
| chr9:104866225
|
G | A | 1 | a0006c0004t0003g0190 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.422-4425C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866225 | ||||||
| chr9:104866431
|
T | C | 15 | a0002c0017t0026g0163a0002c0032t0001g0317a0002c0058t0007g0143others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.422-4631A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866431 | ||||||
| chr9:104866434
|
C | T | 2 | a0018c0079t0004g0314a0018c0080t0004g0107 | 2 | HG01109.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.422-4634G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866434 | ||||||
| chr9:104866452
|
A | C | 18 | a0001c0035t0004g0011a0002c0017t0026g0163a0002c0032t0001g0317others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.422-4652T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866452 | ||||||
| chr9:104866498
|
T | A | 18 | a0001c0035t0004g0011a0002c0017t0026g0163a0002c0032t0001g0317others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.422-4698A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866498 | ||||||
| chr9:104866568
|
A | C | 1 | a0032c0104t0005g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.422-4768T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866568 | ||||||
| chr9:104866611
|
T | A | 16 | a0001c0035t0004g0011a0002c0025t0015g0283a0002c0032t0001g0317others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.422-4811A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866611 | ||||||
| chr9:104866751
|
G | A | 1 | a0027c0062t0001g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422-4951C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866751 | ||||||
| chr9:104866753
|
G | T | 3 | a0002c0017t0026g0276a0002c0025t0015g0283a0008c0069t0008g0096 | 3 | HG01255.hp2 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.422-4953C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866753 | ||||||
| chr9:104866777
|
C | T | 32 | a0001c0001t0001g0082a0001c0001t0001g0102a0001c0001t0001g0208others(29): Show | 32 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.422-4977G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866777 | ||||||
| chr9:104866780
|
G | A | 1 | a0002c0033t0032g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.422-4980C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866780 | ||||||
| chr9:104866823
|
T | C | 185 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0102others(182): Show | 185 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(182): Show |
intron_variant | MODIFIER | c.422-5023A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866823 | ||||||
| chr9:104866997
|
G | T | 2 | a0001c0005t0002g0031a0007c0003t0003g0229 | 2 | NA18747.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.422-5197C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104866997 | ||||||
| chr9:104867055
|
C | T | 33 | a0001c0001t0001g0208a0001c0001t0004g0021a0001c0001t0006g0054others(30): Show | 33 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.422-5255G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104867055 | ||||||
| chr9:104867281
|
G | A | 2 | a0002c0025t0015g0283a0038c0068t0044g0272 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-5481C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104867281 | ||||||
| chr9:104867320
|
C | A | 11 | a0001c0001t0003g0297a0001c0035t0004g0011a0002c0025t0015g0283others(8): Show | 11 | HG01192.hp2 HG01255.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.422-5520G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104867320 | ||||||
| chr9:104867387
|
A | G | 3 | a0002c0017t0026g0163a0017c0034t0001g0300a0025c0083t0001g0313 | 3 | HG01884.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.422-5587T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104867387 | ||||||
| chr9:104867464
|
A | G | 2 | a0007c0003t0009g0156a0007c0003t0009g0260 | 2 | HG02056.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.422-5664T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104867464 | ||||||
| chr9:104867747
|
C | A | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-5947G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104867747 | ||||||
| chr9:104868149
|
C | T | 2 | a0001c0001t0003g0297a0008c0047t0002g0244 | 2 | HG02602.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.422-6349G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868149 | ||||||
| chr9:104868152
|
A | G | 180 | a0001c0001t0001g0082a0001c0001t0001g0208a0001c0001t0001g0218others(177): Show | 180 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(177): Show |
intron_variant | MODIFIER | c.422-6352T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868152 | ||||||
| chr9:104868171
|
C | T | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.422-6371G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868171 | ||||||
| chr9:104868189
|
G | A | 2 | a0002c0025t0015g0283a0038c0068t0044g0272 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-6389C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868189 | ||||||
| chr9:104868231
|
T | C | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.422-6431A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868231 | ||||||
| chr9:104868276
|
T | C | 1 | a0004c0029t0005g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.422-6476A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868276 | ||||||
| chr9:104868289
|
T | C | 12 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0017t0015g0101others(9): Show | 12 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-6489A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868289 | ||||||
| chr9:104868301
|
G | A | 2 | a0001c0001t0003g0297a0008c0047t0002g0244 | 2 | HG02602.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.422-6501C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868301 | ||||||
| chr9:104868339
|
C | T | 37 | a0001c0001t0001g0208a0001c0001t0004g0021a0001c0001t0006g0054others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.422-6539G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868339 | ||||||
| chr9:104868416
|
A | T | 2 | a0001c0001t0003g0210a0007c0003t0033g0035 | 2 | NA18962.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.422-6616T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868416 | ||||||
| chr9:104868424
|
C | T | 2 | a0002c0025t0015g0283a0038c0068t0044g0272 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-6624G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868424 | ||||||
| chr9:104868465
|
A | G | 2 | a0002c0025t0015g0283a0038c0068t0044g0272 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-6665T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868465 | ||||||
| chr9:104868472
|
G | A | 1 | a0001c0001t0003g0211 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.422-6672C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868472 | ||||||
| chr9:104868578
|
C | T | 1 | a0001c0001t0001g0195 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.422-6778G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868578 | ||||||
| chr9:104868615
|
C | T | 2 | a0002c0025t0015g0283a0038c0068t0044g0272 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-6815G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868615 | ||||||
| chr9:104868758
|
G | A | 2 | a0002c0025t0015g0283a0038c0068t0044g0272 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-6958C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868758 | ||||||
| chr9:104868787
|
ATCCAGGC others(46): Show |
A | 1 | a0001c0001t0006g0239 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.422-7040_422-6988d others(55): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868787 | ||||||
| chr9:104868790
|
C | T | 78 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(75): Show | 78 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.422-6990G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868790 | ||||||
| chr9:104868843
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.422-7043G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868843 | ||||||
| chr9:104868853
|
G | A | 58 | a0001c0001t0001g0208a0001c0001t0004g0021a0001c0001t0006g0054others(55): Show | 58 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.422-7053C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868853 | ||||||
| chr9:104868914
|
G | A | 2 | a0002c0025t0015g0283a0038c0068t0044g0272 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422-7114C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104868914 | ||||||
| chr9:104869026
|
G | A | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-7226C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869026 | ||||||
| chr9:104869031
|
G | GA | 37 | a0001c0001t0001g0208a0001c0001t0004g0021a0001c0001t0006g0054others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.422-7232dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869031 | ||||||
| chr9:104869054
|
G | C | 1 | a0008c0006t0007g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.422-7254C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869054 | ||||||
| chr9:104869068
|
G | C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-7268C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869068 | ||||||
| chr9:104869114
|
C | T | 1 | a0001c0108t0002g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.422-7314G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869114 | ||||||
| chr9:104869240
|
GA | G | 4 | a0001c0001t0001g0102a0002c0011t0020g0171a0003c0002t0002g0045others(1): Show | 4 | NA18942.hp2 NA18970.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-7441delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869240 | ||||||
| chr9:104869310
|
T | A | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.422-7510A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869310 | ||||||
| chr9:104869369
|
T | C | 1 | a0002c0058t0007g0143 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422-7569A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869369 | ||||||
| chr9:104869491
|
C | T | 1 | a0003c0002t0003g0127 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.422-7691G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869491 | ||||||
| chr9:104869626
|
G | A | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.422-7826C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869626 | ||||||
| chr9:104869817
|
G | T | 1 | a0007c0003t0004g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.422-8017C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869817 | ||||||
| chr9:104869876
|
A | G | 21 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0017t0026g0163others(18): Show | 21 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.422-8076T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869876 | ||||||
| chr9:104869915
|
GGTTAA | G | 68 | a0001c0001t0004g0021a0001c0001t0006g0054a0001c0001t0039g0246others(65): Show | 68 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.422-8120_422-8116d others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104869915 | ||||||
| chr9:104870040
|
T | C | 21 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0017t0026g0163others(18): Show | 21 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.422-8240A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870040 | ||||||
| chr9:104870080
|
T | G | 1 | a0005c0016t0001g0049 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.422-8280A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870080 | ||||||
| chr9:104870120
|
CAG | C | 35 | a0001c0001t0004g0021a0001c0001t0006g0054a0001c0001t0039g0246others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.422-8322_422-8321d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870120 | ||||||
| chr9:104870152
|
A | G | 2 | a0018c0079t0004g0314a0018c0080t0004g0107 | 2 | HG01109.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.422-8352T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870152 | ||||||
| chr9:104870209
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.422-8409A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870209 | ||||||
| chr9:104870334
|
A | G | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-8534T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870334 | ||||||
| chr9:104870342
|
C | T | 17 | a0002c0017t0026g0276a0002c0037t0001g0275a0002c0046t0002g0154others(14): Show | 17 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.422-8542G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870342 | ||||||
| chr9:104870363
|
G | A | 35 | a0001c0001t0004g0021a0001c0001t0006g0054a0001c0001t0039g0246others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.422-8563C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870363 | ||||||
| chr9:104870379
|
C | G | 78 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(75): Show | 78 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.422-8579G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870379 | ||||||
| chr9:104870380
|
G | A | 15 | a0002c0037t0001g0275a0002c0057t0001g0148a0003c0077t0005g0312others(12): Show | 15 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.422-8580C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870380 | ||||||
| chr9:104870514
|
T | C | 1 | a0012c0041t0001g0274 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.422-8714A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870514 | ||||||
| chr9:104870524
|
G | A | 1 | a0004c0044t0007g0302 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.422-8724C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870524 | ||||||
| chr9:104870653
|
A | G | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.422-8853T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870653 | ||||||
| chr9:104870654
|
T | C | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.422-8854A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870654 | ||||||
| chr9:104870655
|
A | C | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.422-8855T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870655 | ||||||
| chr9:104870672
|
C | T | 12 | a0002c0032t0001g0025a0002c0033t0002g0301a0002c0033t0032g0024others(9): Show | 12 | HG02145.hp1 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-8872G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870672 | ||||||
| chr9:104870743
|
T | C | 1 | a0001c0001t0002g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.422-8943A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870743 | ||||||
| chr9:104870770
|
A | G | 147 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(144): Show | 147 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.422-8970T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870770 | ||||||
| chr9:104870835
|
G | A | 9 | a0001c0001t0001g0088a0001c0001t0003g0089a0004c0008t0003g0289others(6): Show | 9 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-9035C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870835 | ||||||
| chr9:104870889
|
G | C | 1 | a0007c0003t0004g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.422-9089C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870889 | ||||||
| chr9:104870961
|
G | A | 1 | a0010c0007t0010g0185 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.422-9161C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870961 | ||||||
| chr9:104870968
|
C | T | 113 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(110): Show | 113 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.422-9168G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104870968 | ||||||
| chr9:104871342
|
G | C | 132 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(129): Show | 132 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.422-9542C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871342 | ||||||
| chr9:104871444
|
A | C | 82 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(79): Show | 82 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.422-9644T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871444 | ||||||
| chr9:104871496
|
C | A | 6 | a0001c0001t0043g0002a0002c0074t0027g0290a0002c0085t0008g0142others(3): Show | 6 | HG02723.hp1 HG02895.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-9696G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871496 | ||||||
| chr9:104871506
|
C | T | 1 | a0001c0005t0004g0167 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.422-9706G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871506 | ||||||
| chr9:104871534
|
G | C | 4 | a0001c0035t0004g0011a0004c0064t0007g0175a0005c0036t0001g0091others(1): Show | 4 | HG01192.hp2 HG02055.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-9734C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871534 | ||||||
| chr9:104871564
|
A | G | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.422-9764T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871564 | ||||||
| chr9:104871709
|
C | G | 1 | a0003c0002t0002g0205 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.422-9909G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871709 | ||||||
| chr9:104871821
|
G | C | 13 | a0001c0001t0003g0297a0002c0024t0008g0003a0002c0024t0008g0008others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-10021C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871821 | ||||||
| chr9:104871953
|
C | T | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-10153G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871953 | ||||||
| chr9:104871985
|
G | C | 7 | a0001c0001t0003g0210a0002c0011t0012g0134a0003c0009t0003g0178others(4): Show | 7 | NA18953.hp2 NA18962.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-10185C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104871985 | ||||||
| chr9:104872043
|
AT | A | 8 | a0002c0033t0002g0301a0002c0033t0032g0024a0004c0066t0008g0007others(5): Show | 8 | HG02145.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-10244delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872043 | ||||||
| chr9:104872090
|
T | A | 8 | a0002c0033t0002g0301a0002c0033t0032g0024a0004c0066t0008g0007others(5): Show | 8 | HG02145.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-10290A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872090 | ||||||
| chr9:104872103
|
G | A | 1 | a0002c0025t0008g0285 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.422-10303C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872103 | ||||||
| chr9:104872120
|
A | G | 17 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0017t0026g0163others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.422-10320T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872120 | ||||||
| chr9:104872359
|
G | A | 135 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(132): Show | 135 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.422-10559C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872359 | ||||||
| chr9:104872410
|
A | G | 8 | a0002c0033t0002g0301a0002c0033t0032g0024a0004c0066t0008g0007others(5): Show | 8 | HG02145.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-10610T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872410 | ||||||
| chr9:104872502
|
A | G | 36 | a0001c0001t0003g0297a0002c0015t0013g0305a0002c0015t0013g0306others(33): Show | 36 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.421+10537T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872502 | ||||||
| chr9:104872529
|
G | A | 1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421+10510C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872529 | ||||||
| chr9:104872550
|
G | C | 13 | a0002c0017t0026g0163a0004c0042t0008g0083a0004c0042t0008g0158others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+10489C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872550 | ||||||
| chr9:104872629
|
A | G | 5 | a0006c0004t0005g0206a0013c0013t0002g0262a0013c0013t0003g0120others(2): Show | 5 | NA18967.hp2 NA18985.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+10410T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872629 | ||||||
| chr9:104872670
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0203 | 2 | HG00642.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.421+10369G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872670 | ||||||
| chr9:104872903
|
C | T | 1 | a0006c0004t0004g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.421+10136G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104872903 | ||||||
| chr9:104873226
|
T | C | 14 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0017t0015g0101others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+9813A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104873226 | ||||||
| chr9:104873427
|
C | T | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+9612G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104873427 | ||||||
| chr9:104873428
|
G | A | 2 | a0018c0079t0004g0314a0018c0080t0004g0107 | 2 | HG01109.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.421+9611C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104873428 | ||||||
| chr9:104873443
|
G | A | 6 | a0002c0017t0026g0276a0002c0025t0015g0283a0002c0032t0001g0025others(3): Show | 6 | HG01255.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+9596C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104873443 | ||||||
| chr9:104873588
|
C | T | 183 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(180): Show | 183 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(180): Show |
intron_variant | MODIFIER | c.421+9451G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104873588 | ||||||
| chr9:104873612
|
T | C | 3 | a0002c0032t0001g0025a0003c0056t0001g0288a0011c0010t0005g0097 | 3 | HG02647.hp1 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.421+9427A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104873612 | ||||||
| chr9:104874074
|
C | T | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.421+8965G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874074 | ||||||
| chr9:104874278
|
G | A | 74 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(71): Show | 74 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.421+8761C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874278 | ||||||
| chr9:104874395
|
C | T | 1 | a0033c0101t0001g0308 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.421+8644G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874395 | ||||||
| chr9:104874426
|
C | A | 183 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(180): Show | 183 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(180): Show |
intron_variant | MODIFIER | c.421+8613G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874426 | ||||||
| chr9:104874455
|
T | C | 6 | a0002c0017t0026g0276a0002c0025t0015g0283a0002c0032t0001g0025others(3): Show | 6 | HG01255.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+8584A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874455 | ||||||
| chr9:104874490
|
C | T | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.421+8549G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874490 | ||||||
| chr9:104874526
|
G | A | 10 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0017t0015g0101others(7): Show | 10 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.421+8513C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874526 | ||||||
| chr9:104874564
|
C | T | 6 | a0002c0017t0026g0276a0002c0025t0015g0283a0002c0032t0001g0025others(3): Show | 6 | HG01255.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+8475G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874564 | ||||||
| chr9:104874687
|
G | A | 6 | a0002c0017t0026g0276a0002c0025t0015g0283a0002c0032t0001g0025others(3): Show | 6 | HG01255.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+8352C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874687 | ||||||
| chr9:104874750
|
AGCCAGCC others(39): Show |
A | 2 | a0001c0001t0001g0238a0001c0001t0004g0193 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.421+8243_421+8288d others(48): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874750 | ||||||
| chr9:104874758
|
GCCCCGTC others(85): Show |
G | 18 | a0001c0001t0043g0002a0002c0024t0008g0003a0002c0024t0008g0008others(15): Show | 18 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.421+8189_421+8280d others(94): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874758 | ||||||
| chr9:104874782
|
G | A | 2 | a0009c0028t0009g0092a0009c0028t0009g0093 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.421+8257C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874782 | ||||||
| chr9:104874788
|
C | T | 12 | a0002c0015t0002g0315a0002c0015t0004g0004a0002c0017t0015g0101others(9): Show | 12 | HG01109.hp1 HG01243.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+8251G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874788 | ||||||
| chr9:104874804
|
G | A | 1 | a0007c0003t0006g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.421+8235C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874804 | ||||||
| chr9:104874804
|
GCCCCGTC others(39): Show |
G | 2 | a0003c0002t0002g0257a0022c0050t0001g0166 | 2 | HG02572.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.421+8189_421+8234d others(48): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874804 | ||||||
| chr9:104874850
|
A | G | 18 | a0001c0001t0003g0297a0002c0015t0013g0305a0002c0015t0013g0306others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.421+8189T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874850 | ||||||
| chr9:104874850
|
ACCCCGTC others(39): Show |
A | 6 | a0002c0017t0026g0276a0002c0025t0015g0283a0002c0032t0001g0025others(3): Show | 6 | HG01255.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+8143_421+8188d others(48): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874850 | ||||||
| chr9:104874854
|
C | T | 7 | a0001c0001t0006g0225a0001c0001t0012g0039a0001c0092t0012g0220others(4): Show | 7 | HG00673.hp1 NA18962.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+8185G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874854 | ||||||
| chr9:104874864
|
G | A | 1 | a0010c0007t0002g0015 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.421+8175C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874864 | ||||||
| chr9:104874888
|
G | A | 30 | a0001c0001t0003g0297a0002c0015t0013g0305a0002c0015t0013g0306others(27): Show | 30 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.421+8151C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874888 | ||||||
| chr9:104874932
|
C | T | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+8107G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874932 | ||||||
| chr9:104874966
|
G | A | 4 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0011g0085others(1): Show | 4 | HG01070.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+8073C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874966 | ||||||
| chr9:104874970
|
G | A | 3 | a0001c0001t0001g0102a0003c0002t0002g0045a0003c0002t0010g0270 | 3 | NA18970.hp1 NA18998.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.421+8069C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104874970 | ||||||
| chr9:104875025
|
A | G | 183 | a0001c0001t0001g0082a0001c0001t0001g0218a0001c0001t0001g0291others(180): Show | 183 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(180): Show |
intron_variant | MODIFIER | c.421+8014T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875025 | ||||||
| chr9:104875054
|
G | A | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.421+7985C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875054 | ||||||
| chr9:104875055
|
A | T | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.421+7984T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875055 | ||||||
| chr9:104875089
|
G | T | 5 | a0002c0017t0026g0276a0002c0032t0001g0025a0003c0056t0001g0288others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+7950C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875089 | ||||||
| chr9:104875144
|
A | T | 7 | a0006c0004t0005g0206a0013c0013t0002g0262a0013c0013t0003g0120others(4): Show | 7 | NA18967.hp2 NA18982.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+7895T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875144 | ||||||
| chr9:104875211
|
C | T | 4 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+7828G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875211 | ||||||
| chr9:104875274
|
C | T | 3 | a0011c0010t0005g0169a0011c0010t0005g0287a0032c0104t0005g0168 | 3 | HG02280.hp1 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.421+7765G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875274 | ||||||
| chr9:104875327
|
G | A | 6 | a0002c0057t0001g0148a0005c0022t0021g0141a0005c0022t0021g0147others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+7712C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875327 | ||||||
| chr9:104875344
|
T | A | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+7695A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875344 | ||||||
| chr9:104875351
|
C | CA | 50 | a0001c0001t0001g0208a0001c0001t0004g0021a0001c0001t0006g0054others(47): Show | 50 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.421+7687dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875351 | ||||||
| chr9:104875407
|
A | G | 6 | a0001c0001t0006g0225a0001c0001t0012g0039a0001c0092t0012g0220others(3): Show | 6 | NA18962.hp1 NA18984.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+7632T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875407 | ||||||
| chr9:104875480
|
C | T | 1 | a0004c0008t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.421+7559G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875480 | ||||||
| chr9:104875582
|
A | C | 23 | a0001c0001t0003g0297a0002c0015t0013g0305a0002c0015t0013g0306others(20): Show | 23 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.421+7457T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875582 | ||||||
| chr9:104875656
|
A | T | 14 | a0001c0001t0003g0297a0002c0024t0008g0003a0002c0024t0008g0008others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.421+7383T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875656 | ||||||
| chr9:104875660
|
T | TA | 37 | a0001c0001t0001g0208a0001c0001t0004g0021a0001c0001t0006g0054others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.421+7378dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875660 | ||||||
| chr9:104875781
|
G | C | 10 | a0001c0001t0003g0297a0002c0015t0013g0305a0002c0015t0013g0306others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.421+7258C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875781 | ||||||
| chr9:104875842
|
G | A | 1 | a0001c0035t0009g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.421+7197C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875842 | ||||||
| chr9:104875860
|
C | T | 1 | a0003c0009t0003g0073 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.421+7179G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875860 | ||||||
| chr9:104875992
|
G | A | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.421+7047C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104875992 | ||||||
| chr9:104876116
|
A | G | 1 | a0024c0073t0019g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.421+6923T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104876116 | ||||||
| chr9:104876226
|
A | G | 82 | a0001c0001t0001g0082a0001c0001t0003g0210a0001c0001t0003g0211others(79): Show | 82 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.421+6813T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104876226 | ||||||
| chr9:104876688
|
AG | A | 40 | a0001c0001t0004g0021a0001c0001t0006g0054a0001c0001t0043g0002others(37): Show | 40 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.421+6350delC | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104876688 | ||||||
| chr9:104876807
|
G | C | 1 | a0012c0041t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.421+6232C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104876807 | ||||||
| chr9:104876899
|
G | A | 21 | a0001c0001t0004g0021a0001c0001t0006g0054a0001c0001t0043g0002others(18): Show | 21 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+6140C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104876899 | ||||||
| chr9:104877016
|
A | C | 8 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+6023T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104877016 | ||||||
| chr9:104877133
|
G | A | 110 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(107): Show | 110 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.421+5906C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104877133 | ||||||
| chr9:104877420
|
A | T | 1 | a0003c0009t0006g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.421+5619T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104877420 | ||||||
| chr9:104877743
|
C | A | 1 | a0005c0014t0005g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.421+5296G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104877743 | ||||||
| chr9:104877775
|
A | G | 3 | a0003c0056t0001g0288a0011c0010t0005g0097a0012c0093t0001g0108 | 3 | HG01952.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.421+5264T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104877775 | ||||||
| chr9:104878026
|
G | A | 3 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278 | 3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.421+5013C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878026 | ||||||
| chr9:104878056
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.421+4983G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878056 | ||||||
| chr9:104878344
|
T | G | 12 | a0002c0057t0001g0148a0002c0081t0013g0277a0004c0044t0013g0280others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+4695A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878344 | ||||||
| chr9:104878407
|
G | A | 24 | a0001c0001t0003g0297a0002c0015t0004g0004a0002c0017t0015g0101others(21): Show | 24 | HG01109.hp1 HG01884.hp2 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.421+4632C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878407 | ||||||
| chr9:104878438
|
G | C | 1 | a0004c0008t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.421+4601C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878438 | ||||||
| chr9:104878505
|
G | T | 29 | a0001c0001t0003g0297a0002c0015t0004g0004a0002c0017t0015g0101others(26): Show | 29 | HG01109.hp1 HG01255.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.421+4534C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878505 | ||||||
| chr9:104878529
|
A | G | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+4510T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878529 | ||||||
| chr9:104878632
|
T | C | 1 | a0008c0047t0002g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.421+4407A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878632 | ||||||
| chr9:104878924
|
G | A | 2 | a0002c0037t0001g0275a0003c0077t0005g0312 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.421+4115C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104878924 | ||||||
| chr9:104879011
|
G | T | 1 | a0008c0006t0007g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421+4028C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879011 | ||||||
| chr9:104879039
|
C | T | 1 | a0006c0004t0002g0132 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.421+4000G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879039 | ||||||
| chr9:104879073
|
T | TA | 28 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(25): Show | 28 | HG01109.hp1 HG01255.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.421+3965dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879073 | ||||||
| chr9:104879086
|
G | A | 29 | a0001c0001t0003g0297a0002c0015t0004g0004a0002c0017t0015g0101others(26): Show | 29 | HG01109.hp1 HG01255.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.421+3953C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879086 | ||||||
| chr9:104879200
|
C | A | 1 | a0033c0101t0001g0308 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.421+3839G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879200 | ||||||
| chr9:104879460
|
G | T | 19 | a0002c0057t0001g0148a0004c0042t0008g0083a0004c0042t0008g0158others(16): Show | 19 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.421+3579C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879460 | ||||||
| chr9:104879738
|
A | G | 29 | a0001c0001t0003g0297a0002c0015t0004g0004a0002c0017t0015g0101others(26): Show | 29 | HG01109.hp1 HG01255.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.421+3301T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879738 | ||||||
| chr9:104879758
|
C | T | 4 | a0004c0008t0028g0199a0006c0004t0011g0269a0006c0012t0010g0198others(1): Show | 4 | HG01978.hp2 NA18955.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+3281G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879758 | ||||||
| chr9:104879930
|
T | C | 162 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0003g0297others(159): Show | 162 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.421+3109A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104879930 | ||||||
| chr9:104880006
|
C | T | 175 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0003g0297others(172): Show | 175 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(172): Show |
intron_variant | MODIFIER | c.421+3033G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104880006 | ||||||
| chr9:104880111
|
C | T | 1 | a0007c0003t0004g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.421+2928G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104880111 | ||||||
| chr9:104880799
|
T | A | 164 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0003g0297others(161): Show | 164 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(161): Show |
intron_variant | MODIFIER | c.421+2240A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104880799 | ||||||
| chr9:104880839
|
C | A | 28 | a0001c0001t0003g0297a0002c0015t0004g0004a0002c0017t0015g0101others(25): Show | 28 | HG01109.hp1 HG01255.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.421+2200G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104880839 | ||||||
| chr9:104881018
|
G | C | 28 | a0001c0001t0003g0297a0002c0015t0004g0004a0002c0017t0015g0101others(25): Show | 28 | HG01109.hp1 HG01255.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.421+2021C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881018 | ||||||
| chr9:104881080
|
C | A | 9 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.421+1959G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881080 | ||||||
| chr9:104881152
|
G | A | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.421+1887C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881152 | ||||||
| chr9:104881249
|
A | C | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.421+1790T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881249 | ||||||
| chr9:104881309
|
T | C | 8 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(5): Show | 8 | HG01243.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1730A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881309 | ||||||
| chr9:104881313
|
T | C | 5 | a0002c0015t0002g0315a0002c0015t0013g0305a0002c0015t0013g0306others(2): Show | 5 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+1726A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881313 | ||||||
| chr9:104881474
|
CA | C | 8 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(5): Show | 8 | HG01243.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1564delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881474 | ||||||
| chr9:104881505
|
G | A | 43 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(40): Show | 43 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.421+1534C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881505 | ||||||
| chr9:104881529
|
T | C | 86 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(83): Show | 86 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.421+1510A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881529 | ||||||
| chr9:104881655
|
G | A | 1 | a0001c0001t0039g0246 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.421+1384C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881655 | ||||||
| chr9:104881840
|
C | T | 1 | a0012c0040t0040g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.421+1199G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881840 | ||||||
| chr9:104881843
|
G | C | 21 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(18): Show | 21 | HG01884.hp2 HG02257.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+1196C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881843 | ||||||
| chr9:104881857
|
A | T | 9 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.421+1182T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104881857 | ||||||
| chr9:104882006
|
G | A | 83 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(80): Show | 83 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.421+1033C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882006 | ||||||
| chr9:104882028
|
T | TA | 13 | a0001c0001t0002g0233a0001c0001t0003g0086a0001c0109t0001g0232others(10): Show | 13 | HG01109.hp1 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.421+1010dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAA | 11 | a0001c0001t0039g0246a0002c0037t0001g0275a0002c0074t0027g0290others(8): Show | 11 | HG01168.hp2 HG01952.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.421+1009_421+1010d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAA | 6 | a0002c0025t0015g0283a0007c0003t0003g0014a0010c0007t0002g0012others(3): Show | 6 | HG01255.hp2 HG01433.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+1007_421+1010d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAA | 6 | a0001c0001t0001g0016a0001c0005t0002g0017a0001c0005t0002g0254others(3): Show | 6 | HG00621.hp1 HG01975.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+1006_421+1010d others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(2): Show |
6 | a0001c0001t0001g0195a0002c0015t0013g0305a0003c0038t0005g0307others(3): Show | 6 | HG02809.hp2 HG02895.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+1002_421+1010d others(11): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(3): Show |
1 | a0023c0072t0001g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.421+1001_421+1010d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0088 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.421+1000_421+1010d others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(5): Show |
2 | a0005c0039t0017g0018a0005c0039t0017g0019 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.421+999_421+1010du others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0003g0089 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.421+998_421+1010du others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(7): Show |
1 | a0004c0008t0003g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421+997_421+1010du others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(9): Show |
1 | a0011c0055t0001g0259 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.421+995_421+1010du others(17): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(10): Show |
5 | a0001c0001t0001g0077a0001c0108t0002g0113a0003c0002t0002g0257others(2): Show | 5 | HG00544.hp2 HG00738.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+994_421+1010du others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(11): Show |
14 | a0001c0001t0001g0102a0001c0001t0004g0193a0001c0005t0004g0167others(11): Show | 14 | HG02083.hp1 HG02698.hp2 HG03704.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+993_421+1010du others(19): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(12): Show |
9 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0003g0210others(6): Show | 9 | HG00609.hp2 HG00642.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+992_421+1010du others(20): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(13): Show |
17 | a0001c0001t0001g0026a0001c0001t0001g0176a0002c0031t0001g0152others(14): Show | 17 | HG00408.hp1 HG01517.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.421+991_421+1010du others(21): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(14): Show |
9 | a0001c0001t0002g0137a0001c0005t0002g0062a0003c0002t0002g0122others(6): Show | 9 | HG01515.hp2 HG02027.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+990_421+1010du others(22): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(15): Show |
3 | a0001c0001t0001g0121a0007c0003t0002g0038a0007c0003t0035g0061 | 3 | HG00408.hp2 HG01978.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.421+989_421+1010du others(23): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(16): Show |
6 | a0001c0005t0002g0064a0002c0011t0020g0171a0003c0002t0007g0059others(3): Show | 6 | NA18942.hp2 NA18982.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+988_421+1010du others(24): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(18): Show |
2 | a0001c0001t0001g0238a0001c0001t0007g0183 | 2 | HG04199.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.421+986_421+1010du others(26): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(19): Show |
2 | a0004c0008t0004g0264a0005c0014t0003g0243 | 2 | HG03927.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.421+985_421+1010du others(27): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
T | TAAAAAAA others(25): Show |
1 | a0005c0014t0003g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.421+1010_421+1011i others(34): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
TA | T | 35 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0006g0054others(32): Show | 35 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.421+1010delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
TAA | T | 22 | a0002c0024t0008g0008a0002c0057t0001g0148a0004c0042t0008g0083others(19): Show | 22 | HG00558.hp2 HG01891.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+1009_421+1010d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
TAAAAA | T | 6 | a0001c0001t0001g0218a0001c0097t0001g0106a0002c0058t0007g0143others(3): Show | 6 | HG00738.hp2 HG00741.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+1006_421+1010d others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
TAAAAAA | T | 9 | a0001c0001t0006g0214a0003c0002t0002g0205a0004c0099t0001g0110others(6): Show | 9 | HG00544.hp1 HG02056.hp2 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.421+1005_421+1010d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
TAAAAAAA | T | 75 | a0001c0001t0004g0194a0001c0001t0006g0058a0001c0001t0006g0225others(72): Show | 75 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.421+1004_421+1010d others(9): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
TAAAAAAA others(4): Show |
T | 1 | a0010c0030t0022g0191 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.421+1000_421+1010d others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882028
|
TAAAAAAA others(6): Show |
T | 3 | a0003c0009t0003g0209a0007c0003t0016g0242a0007c0003t0020g0179 | 3 | HG00099.hp2 HG01169.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.421+998_421+1010de others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882028 | ||||||
| chr9:104882038
|
A | C | 20 | a0002c0057t0001g0148a0004c0042t0008g0083a0004c0042t0008g0158others(17): Show | 20 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.421+1001T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882038 | ||||||
| chr9:104882042
|
A | C | 20 | a0002c0057t0001g0148a0004c0042t0008g0083a0004c0042t0008g0158others(17): Show | 20 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.421+997T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882042 | ||||||
| chr9:104882046
|
A | C | 20 | a0002c0057t0001g0148a0004c0042t0008g0083a0004c0042t0008g0158others(17): Show | 20 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.421+993T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882046 | ||||||
| chr9:104882049
|
A | AAAAAAAA others(11): Show |
1 | a0020c0045t0002g0299 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.421+989_421+990ins others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882049 | ||||||
| chr9:104882235
|
A | C | 1 | a0023c0072t0001g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.421+804T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882235 | ||||||
| chr9:104882270
|
C | T | 6 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(3): Show | 6 | HG00621.hp1 HG01109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+769G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882270 | ||||||
| chr9:104882424
|
T | C | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+615A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882424 | ||||||
| chr9:104882456
|
A | C | 83 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(80): Show | 83 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.421+583T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882456 | ||||||
| chr9:104882549
|
C | T | 84 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(81): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.421+490G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882549 | ||||||
| chr9:104882563
|
G | T | 1 | a0004c0066t0008g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421+476C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882563 | ||||||
| chr9:104882778
|
G | T | 3 | a0002c0017t0026g0163a0017c0034t0001g0300a0025c0083t0001g0313 | 3 | HG01884.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.421+261C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882778 | ||||||
| chr9:104882799
|
C | T | 106 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(103): Show | 106 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.421+240G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882799 | ||||||
| chr9:104882902
|
C | T | 1 | a0004c0066t0008g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421+137G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882902 | ||||||
| chr9:104882920
|
G | A | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.421+119C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882920 | ||||||
| chr9:104882929
|
C | T | 13 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(10): Show | 13 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.421+110G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882929 | ||||||
| chr9:104882963
|
A | C | 9 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.421+76T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882963 | ||||||
| chr9:104882980
|
T | C | 2 | a0001c0005t0004g0167a0003c0002t0002g0172 | 2 | NA18747.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.421+59A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104882980 | ||||||
| chr9:104883014
|
G | A | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+25C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 5/49 | chr9 | 104883014 | ||||||
| chr9:104883196
|
G | T | 21 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(18): Show | 21 | HG01884.hp2 HG02257.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.303-39C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883196 | ||||||
| chr9:104883293
|
A | G | 1 | a0019c0106t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.303-136T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883293 | ||||||
| chr9:104883393
|
T | C | 22 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(19): Show | 22 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.303-236A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883393 | ||||||
| chr9:104883410
|
C | G | 1 | a0003c0002t0002g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.303-253G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883410 | ||||||
| chr9:104883625
|
C | G | 19 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(16): Show | 19 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.303-468G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883625 | ||||||
| chr9:104883641
|
T | C | 22 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(19): Show | 22 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.303-484A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883641 | ||||||
| chr9:104883691
|
C | CT | 84 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(81): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.303-535_303-534ins others(1): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883691 | ||||||
| chr9:104883728
|
G | A | 80 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(77): Show | 80 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.303-571C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883728 | ||||||
| chr9:104883798
|
C | T | 1 | a0001c0109t0001g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.302+629G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883798 | ||||||
| chr9:104883943
|
C | A | 2 | a0002c0059t0001g0235a0019c0106t0001g0094 | 2 | HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.302+484G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883943 | ||||||
| chr9:104883979
|
T | C | 84 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(81): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.302+448A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104883979 | ||||||
| chr9:104884008
|
C | T | 84 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(81): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.302+419G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104884008 | ||||||
| chr9:104884352
|
A | G | 1 | a0002c0025t0007g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.302+75T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104884352 | ||||||
| chr9:104884363
|
G | A | 1 | a0001c0001t0006g0239 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.302+64C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 4/49 | chr9 | 104884363 | ||||||
| chr9:104884738
|
C | T | 37 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(34): Show | 37 | HG00609.hp1 HG00642.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.161-170G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104884738 | ||||||
| chr9:104884796
|
G | A | 111 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(108): Show | 111 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.161-228C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104884796 | ||||||
| chr9:104884825
|
C | T | 8 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-257G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104884825 | ||||||
| chr9:104884840
|
A | G | 157 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(154): Show | 157 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.161-272T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104884840 | ||||||
| chr9:104884939
|
C | T | 167 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(164): Show | 167 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.161-371G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104884939 | ||||||
| chr9:104884965
|
G | A | 4 | a0001c0001t0001g0121a0003c0002t0002g0040a0003c0002t0002g0069others(1): Show | 4 | HG01978.hp1 HG02004.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-397C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104884965 | ||||||
| chr9:104884971
|
C | T | 3 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278 | 3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.161-403G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104884971 | ||||||
| chr9:104885010
|
C | T | 1 | a0003c0009t0003g0209 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.161-442G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885010 | ||||||
| chr9:104885191
|
G | A | 1 | a0004c0066t0008g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.161-623C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885191 | ||||||
| chr9:104885223
|
C | T | 21 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(18): Show | 21 | HG01884.hp2 HG01952.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-655G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885223 | ||||||
| chr9:104885374
|
G | A | 30 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(27): Show | 30 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-806C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885374 | ||||||
| chr9:104885479
|
AAC | A | 30 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(27): Show | 30 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-913_161-912del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885479 | ||||||
| chr9:104885491
|
T | G | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.161-923A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885491 | ||||||
| chr9:104885574
|
A | G | 2 | a0001c0001t0001g0102a0003c0002t0002g0045 | 2 | NA18998.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.161-1006T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885574 | ||||||
| chr9:104885655
|
C | T | 1 | a0002c0033t0032g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.161-1087G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885655 | ||||||
| chr9:104885692
|
C | T | 11 | a0002c0057t0001g0148a0004c0044t0013g0280a0005c0022t0002g0284others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-1124G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885692 | ||||||
| chr9:104885697
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0203 | 2 | HG00642.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.161-1129C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885697 | ||||||
| chr9:104885699
|
A | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0203 | 2 | HG00642.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.161-1131T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885699 | ||||||
| chr9:104885705
|
T | C | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1137A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885705 | ||||||
| chr9:104885711
|
C | T | 1 | a0001c0001t0039g0246 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.161-1143G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885711 | ||||||
| chr9:104885899
|
G | A | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.161-1331C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885899 | ||||||
| chr9:104885927
|
C | T | 2 | a0008c0006t0003g0187a0012c0102t0007g0188 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.161-1359G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104885927 | ||||||
| chr9:104886047
|
G | C | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-1479C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886047 | ||||||
| chr9:104886123
|
A | G | 1 | a0018c0080t0004g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.161-1555T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886123 | ||||||
| chr9:104886128
|
G | A | 89 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(86): Show | 89 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.161-1560C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886128 | ||||||
| chr9:104886149
|
G | A | 30 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(27): Show | 30 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-1581C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886149 | ||||||
| chr9:104886177
|
G | A | 45 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(42): Show | 45 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.161-1609C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886177 | ||||||
| chr9:104886195
|
TC | T | 89 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(86): Show | 89 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.161-1628delG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886195 | ||||||
| chr9:104886198
|
T | G | 89 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(86): Show | 89 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.161-1630A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886198 | ||||||
| chr9:104886238
|
T | C | 45 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(42): Show | 45 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.161-1670A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886238 | ||||||
| chr9:104886273
|
G | A | 1 | a0002c0011t0004g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.161-1705C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886273 | ||||||
| chr9:104886274
|
C | A | 7 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0024t0008g0109others(4): Show | 7 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-1706G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886274 | ||||||
| chr9:104886314
|
A | G | 30 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(27): Show | 30 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-1746T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886314 | ||||||
| chr9:104886371
|
C | T | 45 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(42): Show | 45 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.161-1803G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886371 | ||||||
| chr9:104886403
|
T | C | 1 | a0002c0017t0026g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.161-1835A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886403 | ||||||
| chr9:104886510
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-1942C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886510 | ||||||
| chr9:104886684
|
T | C | 48 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(45): Show | 48 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.161-2116A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886684 | ||||||
| chr9:104886814
|
T | C | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-2246A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886814 | ||||||
| chr9:104886871
|
G | A | 1 | a0012c0105t0024g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.160+2231C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886871 | ||||||
| chr9:104886871
|
G | C | 1 | a0006c0004t0002g0132 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.160+2231C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104886871 | ||||||
| chr9:104887099
|
A | G | 48 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(45): Show | 48 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.160+2003T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887099 | ||||||
| chr9:104887135
|
G | A | 2 | a0007c0003t0009g0156a0007c0003t0009g0260 | 2 | HG02056.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.160+1967C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887135 | ||||||
| chr9:104887138
|
C | T | 48 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(45): Show | 48 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.160+1964G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887138 | ||||||
| chr9:104887222
|
G | A | 1 | a0006c0004t0010g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.160+1880C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887222 | ||||||
| chr9:104887276
|
A | AAAAC | 48 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(45): Show | 48 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.160+1822_160+1825d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887276 | ||||||
| chr9:104887325
|
C | T | 48 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(45): Show | 48 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.160+1777G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887325 | ||||||
| chr9:104887330
|
A | T | 48 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(45): Show | 48 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.160+1772T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887330 | ||||||
| chr9:104887369
|
G | C | 1 | a0004c0008t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.160+1733C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887369 | ||||||
| chr9:104887388
|
C | G | 2 | a0009c0018t0004g0292a0021c0060t0001g0078 | 2 | HG00741.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.160+1714G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887388 | ||||||
| chr9:104887406
|
A | G | 1 | a0033c0101t0001g0308 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.160+1696T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887406 | ||||||
| chr9:104887450
|
C | CA | 49 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(46): Show | 49 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+1651dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887450 | ||||||
| chr9:104887476
|
C | A | 2 | a0002c0074t0027g0290a0005c0052t0001g0281 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.160+1626G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887476 | ||||||
| chr9:104887477
|
G | A | 2 | a0002c0017t0026g0276a0002c0085t0008g0142 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.160+1625C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887477 | ||||||
| chr9:104887617
|
C | T | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+1485G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887617 | ||||||
| chr9:104887703
|
A | G | 50 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(47): Show | 50 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.160+1399T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887703 | ||||||
| chr9:104887705
|
A | G | 1 | a0010c0030t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.160+1397T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887705 | ||||||
| chr9:104887722
|
C | CT | 33 | a0001c0001t0002g0074a0001c0001t0002g0233a0001c0109t0001g0232others(30): Show | 33 | HG00738.hp1 HG01106.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.160+1379dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887722 | ||||||
| chr9:104887722
|
C | CTTT | 17 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(14): Show | 17 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.160+1377_160+1379d others(5): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887722 | ||||||
| chr9:104887722
|
CT | C | 79 | a0001c0001t0004g0194a0001c0001t0006g0047a0001c0001t0006g0058others(76): Show | 79 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.160+1379delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887722 | ||||||
| chr9:104887752
|
A | G | 21 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(18): Show | 21 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+1350T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104887752 | ||||||
| chr9:104888001
|
G | A | 2 | a0002c0017t0026g0276a0002c0085t0008g0142 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.160+1101C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888001 | ||||||
| chr9:104888036
|
T | C | 49 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(46): Show | 49 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+1066A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888036 | ||||||
| chr9:104888052
|
T | C | 1 | a0003c0002t0028g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.160+1050A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888052 | ||||||
| chr9:104888058
|
G | GGT | 11 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0049g0034others(8): Show | 11 | HG01433.hp2 HG01496.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+1042_160+1043d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
G | GGTGGGTG others(5): Show |
4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+1043_160+1044i others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
G | GGTGGGTG others(7): Show |
15 | a0002c0017t0026g0276a0002c0057t0001g0148a0002c0081t0013g0277others(12): Show | 15 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.160+1043_160+1044i others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
G | GGTGT | 27 | a0001c0001t0003g0297a0001c0005t0002g0031a0001c0035t0004g0011others(24): Show | 27 | HG00609.hp1 HG01192.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.160+1040_160+1043d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
G | GGTGTGT | 60 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(57): Show | 60 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.160+1038_160+1043d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
G | GGTGTGTG others(1): Show |
4 | a0004c0043t0003g0128a0004c0043t0003g0136a0007c0003t0009g0260others(1): Show | 4 | HG01952.hp1 HG02559.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+1036_160+1043d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
G | GGTGTGTG others(3): Show |
1 | a0003c0002t0050g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.160+1034_160+1043d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
GGTGT | G | 8 | a0001c0001t0001g0176a0001c0001t0002g0074a0001c0001t0004g0193others(5): Show | 8 | HG00099.hp1 HG01106.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+1040_160+1043d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888058
|
GGTGTGTG others(3): Show |
G | 2 | a0002c0025t0015g0283a0012c0093t0001g0108 | 2 | HG01255.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.160+1034_160+1043d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888058 | ||||||
| chr9:104888062
|
T | G | 27 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(24): Show | 27 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+1040A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888062 | ||||||
| chr9:104888064
|
T | G | 30 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(27): Show | 30 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.160+1038A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888064 | ||||||
| chr9:104888066
|
T | G | 3 | a0001c0005t0002g0123a0001c0005t0002g0129a0002c0011t0004g0263 | 3 | HG02155.hp2 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.160+1036A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888066 | ||||||
| chr9:104888073
|
G | A | 19 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(16): Show | 19 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+1029C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888073 | ||||||
| chr9:104888074
|
T | G | 27 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(24): Show | 27 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+1028A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888074 | ||||||
| chr9:104888076
|
T | G | 3 | a0001c0005t0002g0123a0001c0005t0002g0129a0002c0011t0004g0263 | 3 | HG02155.hp2 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.160+1026A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888076 | ||||||
| chr9:104888141
|
G | A | 1 | a0001c0001t0011g0085 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.160+961C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888141 | ||||||
| chr9:104888149
|
A | G | 49 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(46): Show | 49 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+953T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888149 | ||||||
| chr9:104888174
|
C | T | 1 | a0002c0037t0011g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.160+928G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888174 | ||||||
| chr9:104888232
|
C | T | 5 | a0001c0035t0004g0011a0004c0064t0007g0175a0005c0016t0001g0009others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+870G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888232 | ||||||
| chr9:104888252
|
G | A | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.160+850C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888252 | ||||||
| chr9:104888294
|
T | C | 167 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(164): Show | 167 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.160+808A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888294 | ||||||
| chr9:104888297
|
G | C | 60 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0102others(57): Show | 60 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.160+805C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888297 | ||||||
| chr9:104888383
|
C | G | 1 | a0004c0098t0005g0303 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+719G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888383 | ||||||
| chr9:104888395
|
A | G | 2 | a0006c0012t0001g0090a0006c0012t0001g0212 | 2 | HG01243.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.160+707T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888395 | ||||||
| chr9:104888539
|
C | T | 25 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(22): Show | 25 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.160+563G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888539 | ||||||
| chr9:104888547
|
C | T | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.160+555G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888547 | ||||||
| chr9:104888562
|
C | T | 176 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(173): Show | 176 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.160+540G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888562 | ||||||
| chr9:104888711
|
G | A | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.160+391C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888711 | ||||||
| chr9:104888714
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0003g0089 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.160+388C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888714 | ||||||
| chr9:104888749
|
G | T | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.160+353C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888749 | ||||||
| chr9:104888883
|
T | C | 2 | a0002c0017t0026g0276a0002c0085t0008g0142 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.160+219A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888883 | ||||||
| chr9:104888893
|
T | C | 22 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(19): Show | 22 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.160+209A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888893 | ||||||
| chr9:104888931
|
T | C | 39 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(36): Show | 39 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+171A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888931 | ||||||
| chr9:104888951
|
T | C | 13 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(10): Show | 13 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+151A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104888951 | ||||||
| chr9:104889010
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.160+92T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104889010 | ||||||
| chr9:104889046
|
T | C | 2 | a0002c0025t0008g0285a0011c0010t0005g0286 | 2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.160+56A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104889046 | ||||||
| chr9:104889067
|
T | C | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104889067 | ||||||
| chr9:104889076
|
C | T | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.160+26G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104889076 | ||||||
| chr9:104889080
|
G | A | 1 | a0003c0002t0002g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.160+22C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 3/49 | chr9 | 104889080 | ||||||
| chr9:104889245
|
A | G | 56 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0003g0297others(53): Show | 56 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.67-50T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104889245 | ||||||
| chr9:104889253
|
C | T | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-58G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104889253 | ||||||
| chr9:104889425
|
G | A | 2 | a0008c0006t0003g0187a0012c0102t0007g0188 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.67-230C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104889425 | ||||||
| chr9:104889592
|
G | C | 1 | a0014c0053t0002g0146 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.67-397C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104889592 | ||||||
| chr9:104889664
|
T | C | 176 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(173): Show | 176 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-469A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104889664 | ||||||
| chr9:104889686
|
A | G | 2 | a0002c0074t0027g0290a0005c0052t0001g0281 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67-491T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104889686 | ||||||
| chr9:104889859
|
A | G | 1 | a0004c0008t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67-664T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104889859 | ||||||
| chr9:104890008
|
C | T | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67-813G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890008 | ||||||
| chr9:104890060
|
G | C | 19 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(16): Show | 19 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.67-865C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890060 | ||||||
| chr9:104890178
|
C | T | 3 | a0003c0009t0003g0178a0006c0004t0042g0265a0016c0019t0018g0177 | 3 | NA18964.hp2 NA18979.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.67-983G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890178 | ||||||
| chr9:104890193
|
C | A | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-998G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890193 | ||||||
| chr9:104890211
|
C | T | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1016G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890211 | ||||||
| chr9:104890557
|
G | A | 1 | a0018c0080t0004g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.67-1362C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890557 | ||||||
| chr9:104890590
|
C | CA | 13 | a0001c0001t0003g0211a0002c0031t0001g0152a0003c0002t0003g0127others(10): Show | 13 | HG01891.hp2 HG02083.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-1396dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890590 | ||||||
| chr9:104890594
|
A | C | 3 | a0002c0074t0027g0290a0005c0052t0001g0281a0011c0010t0005g0287 | 3 | HG02886.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67-1399T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890594 | ||||||
| chr9:104890648
|
C | T | 1 | a0006c0012t0002g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.67-1453G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890648 | ||||||
| chr9:104890681
|
G | A | 2 | a0009c0018t0004g0292a0021c0060t0001g0078 | 2 | HG00741.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.67-1486C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890681 | ||||||
| chr9:104890699
|
A | G | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1504T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890699 | ||||||
| chr9:104890773
|
A | G | 1 | a0009c0021t0004g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67-1578T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890773 | ||||||
| chr9:104890973
|
A | C | 1 | a0001c0001t0043g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67-1778T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890973 | ||||||
| chr9:104890983
|
C | T | 1 | a0011c0010t0005g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.67-1788G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104890983 | ||||||
| chr9:104891145
|
G | A | 50 | a0001c0001t0006g0047a0001c0001t0006g0058a0001c0001t0006g0214others(47): Show | 50 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.67-1950C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891145 | ||||||
| chr9:104891334
|
C | T | 1 | a0002c0011t0004g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.67-2139G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891334 | ||||||
| chr9:104891396
|
C | T | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-2201G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891396 | ||||||
| chr9:104891577
|
G | A | 3 | a0002c0033t0002g0301a0004c0114t0005g0304a0005c0051t0019g0164 | 3 | HG02622.hp2 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.67-2382C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891577 | ||||||
| chr9:104891676
|
C | G | 15 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(12): Show | 15 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-2481G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891676 | ||||||
| chr9:104891725
|
C | T | 6 | a0002c0031t0001g0152a0002c0078t0001g0216a0011c0010t0005g0255others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-2530G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891725 | ||||||
| chr9:104891741
|
G | A | 2 | a0001c0001t0004g0021a0004c0096t0007g0020 | 2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.67-2546C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891741 | ||||||
| chr9:104891822
|
G | A | 15 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(12): Show | 15 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-2627C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891822 | ||||||
| chr9:104891891
|
G | A | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67-2696C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891891 | ||||||
| chr9:104891897
|
G | A | 1 | a0001c0001t0049g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.67-2702C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891897 | ||||||
| chr9:104891944
|
G | A | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-2749C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891944 | ||||||
| chr9:104891966
|
T | TA | 29 | a0001c0001t0001g0102a0001c0001t0001g0196a0001c0001t0002g0233others(26): Show | 29 | HG00609.hp2 HG01168.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.67-2772dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891966 | ||||||
| chr9:104891966
|
TA | T | 45 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(42): Show | 45 | HG01099.hp1 HG01106.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.67-2772delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891966 | ||||||
| chr9:104891966
|
TAA | T | 95 | a0001c0001t0003g0089a0001c0001t0004g0194a0001c0001t0006g0047others(92): Show | 95 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.67-2773_67-2772del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891966 | ||||||
| chr9:104891966
|
TAAA | T | 23 | a0001c0001t0001g0088a0001c0001t0049g0034a0002c0011t0004g0213others(20): Show | 23 | HG01070.hp1 HG01169.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.67-2774_67-2772del others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891966 | ||||||
| chr9:104891966
|
TAAAA | T | 11 | a0002c0024t0008g0008a0002c0031t0001g0278a0002c0037t0001g0275others(8): Show | 11 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.67-2775_67-2772del others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891966 | ||||||
| chr9:104891966
|
TAAAAAAA others(5): Show |
T | 1 | a0010c0030t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.67-2783_67-2772del others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891966 | ||||||
| chr9:104891966
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67-2784_67-2772del others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104891966 | ||||||
| chr9:104892012
|
C | T | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-2817G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892012 | ||||||
| chr9:104892077
|
ACT | A | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-2884_67-2883del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892077 | ||||||
| chr9:104892107
|
T | G | 1 | a0009c0021t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67-2912A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892107 | ||||||
| chr9:104892115
|
C | T | 1 | a0009c0027t0006g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-2920G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892115 | ||||||
| chr9:104892379
|
T | C | 1 | a0009c0021t0004g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67-3184A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892379 | ||||||
| chr9:104892484
|
G | A | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3289C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892484 | ||||||
| chr9:104892529
|
C | T | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3334G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892529 | ||||||
| chr9:104892675
|
A | G | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3480T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892675 | ||||||
| chr9:104892727
|
GT | G | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3533delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892727 | ||||||
| chr9:104892868
|
A | T | 9 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-3673T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892868 | ||||||
| chr9:104892873
|
T | C | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-3678A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892873 | ||||||
| chr9:104892910
|
T | C | 1 | a0001c0005t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.67-3715A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892910 | ||||||
| chr9:104892918
|
T | C | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.67-3723A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892918 | ||||||
| chr9:104892938
|
A | G | 3 | a0002c0011t0004g0112a0008c0006t0007g0111a0008c0049t0004g0103 | 3 | HG01257.hp2 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.67-3743T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892938 | ||||||
| chr9:104892954
|
A | G | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67-3759T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104892954 | ||||||
| chr9:104893067
|
A | T | 2 | a0004c0087t0009g0118a0008c0006t0047g0056 | 2 | HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.67-3872T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893067 | ||||||
| chr9:104893145
|
G | T | 33 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(30): Show | 33 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.67-3950C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893145 | ||||||
| chr9:104893259
|
G | A | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-4064C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893259 | ||||||
| chr9:104893283
|
A | G | 1 | a0003c0009t0006g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.67-4088T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893283 | ||||||
| chr9:104893315
|
G | A | 4 | a0001c0001t0002g0074a0001c0001t0052g0318a0002c0011t0007g0119others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-4120C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893315 | ||||||
| chr9:104893399
|
G | A | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-4204C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893399 | ||||||
| chr9:104893421
|
C | CA | 78 | a0001c0001t0001g0026a0001c0001t0001g0196a0001c0001t0002g0233others(75): Show | 78 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.67-4227dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
C | CAA | 22 | a0001c0001t0002g0074a0001c0001t0003g0210a0001c0001t0006g0239others(19): Show | 22 | HG00621.hp2 HG00673.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-4228_67-4227dup others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
C | CAAA | 9 | a0001c0005t0002g0254a0002c0017t0015g0101a0006c0004t0006g0249others(6): Show | 9 | HG00741.hp2 HG01099.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-4229_67-4227dup others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
C | CAAAAAAA | 7 | a0002c0074t0027g0290a0004c0044t0007g0302a0004c0107t0002g0236others(4): Show | 7 | HG02451.hp1 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-4233_67-4227dup others(7): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
C | CAAAAAAA others(12): Show |
1 | a0004c0066t0008g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-4245_67-4227dup others(19): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
CA | C | 38 | a0001c0001t0001g0088a0001c0001t0001g0176a0001c0001t0003g0089others(35): Show | 38 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.67-4227delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
CAAAAAAA others(2): Show |
C | 7 | a0002c0015t0002g0315a0002c0015t0013g0305a0002c0015t0013g0306others(4): Show | 7 | HG01952.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-4235_67-4227del others(9): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
CAAAAAAA others(5): Show |
C | 1 | a0003c0002t0002g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.67-4238_67-4227del others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
CAAAAAAA others(13): Show |
C | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-4246_67-4227del others(20): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893421
|
CAAAAAAA others(16): Show |
C | 21 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(18): Show | 21 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.67-4249_67-4227del others(23): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893421 | ||||||
| chr9:104893438
|
A | G | 1 | a0004c0008t0016g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.67-4243T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893438 | ||||||
| chr9:104893493
|
C | G | 2 | a0002c0011t0007g0119a0002c0011t0007g0247 | 2 | HG02027.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.67-4298G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893493 | ||||||
| chr9:104893567
|
T | C | 89 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(86): Show | 89 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.67-4372A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893567 | ||||||
| chr9:104893672
|
T | C | 1 | a0002c0031t0001g0278 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.67-4477A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893672 | ||||||
| chr9:104893733
|
C | A | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-4538G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893733 | ||||||
| chr9:104893744
|
T | C | 3 | a0002c0033t0002g0301a0004c0114t0005g0304a0005c0051t0019g0164 | 3 | HG02622.hp2 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.67-4549A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893744 | ||||||
| chr9:104893841
|
A | C | 67 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0003g0297others(64): Show | 67 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.67-4646T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893841 | ||||||
| chr9:104893869
|
G | C | 176 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(173): Show | 176 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-4674C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104893869 | ||||||
| chr9:104894012
|
C | T | 9 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-4817G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894012 | ||||||
| chr9:104894069
|
C | A | 5 | a0002c0015t0002g0315a0002c0015t0013g0305a0002c0015t0013g0306others(2): Show | 5 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-4874G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894069 | ||||||
| chr9:104894128
|
GC | G | 47 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(44): Show | 47 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.67-4934delG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894128 | ||||||
| chr9:104894167
|
A | G | 1 | a0010c0030t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.67-4972T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894167 | ||||||
| chr9:104894292
|
G | A | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-5097C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894292 | ||||||
| chr9:104894342
|
T | C | 2 | a0009c0028t0009g0092a0009c0028t0009g0093 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.67-5147A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894342 | ||||||
| chr9:104894414
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.67-5219C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894414 | ||||||
| chr9:104894467
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.67-5272C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894467 | ||||||
| chr9:104894485
|
G | A | 1 | a0010c0030t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.67-5290C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894485 | ||||||
| chr9:104894502
|
C | T | 6 | a0002c0017t0026g0276a0002c0024t0008g0003a0002c0024t0008g0008others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-5307G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894502 | ||||||
| chr9:104894789
|
G | A | 38 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(35): Show | 38 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.67-5594C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894789 | ||||||
| chr9:104894838
|
A | G | 1 | a0008c0069t0008g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.67-5643T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894838 | ||||||
| chr9:104894972
|
G | C | 78 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0003g0297others(75): Show | 78 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.67-5777C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104894972 | ||||||
| chr9:104895075
|
A | G | 33 | a0002c0015t0004g0004a0002c0017t0015g0101a0002c0017t0026g0163others(30): Show | 33 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.67-5880T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895075 | ||||||
| chr9:104895101
|
T | C | 2 | a0014c0054t0010g0251a0016c0019t0006g0250 | 2 | NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.67-5906A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895101 | ||||||
| chr9:104895366
|
T | C | 1 | a0001c0001t0043g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67-6171A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895366 | ||||||
| chr9:104895421
|
C | A | 2 | a0014c0023t0017g0105a0014c0023t0036g0104 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.67-6226G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895421 | ||||||
| chr9:104895544
|
C | T | 176 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(173): Show | 176 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-6349G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895544 | ||||||
| chr9:104895670
|
T | C | 2 | a0005c0039t0017g0018a0005c0039t0017g0019 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.67-6475A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895670 | ||||||
| chr9:104895705
|
A | C | 16 | a0002c0017t0026g0276a0002c0057t0001g0148a0002c0081t0013g0277others(13): Show | 16 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.67-6510T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895705 | ||||||
| chr9:104895709
|
T | C | 5 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-6514A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895709 | ||||||
| chr9:104895967
|
C | T | 109 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(106): Show | 109 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-6772G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104895967 | ||||||
| chr9:104896058
|
T | C | 13 | a0002c0057t0001g0148a0002c0081t0013g0277a0004c0044t0013g0280others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-6863A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896058 | ||||||
| chr9:104896104
|
G | A | 174 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(171): Show | 174 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.67-6909C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896104 | ||||||
| chr9:104896442
|
C | T | 7 | a0001c0035t0004g0011a0004c0064t0007g0175a0005c0016t0001g0009others(4): Show | 7 | HG00642.hp1 HG01175.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+7172G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896442 | ||||||
| chr9:104896629
|
C | A | 52 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(49): Show | 52 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.66+6985G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896629 | ||||||
| chr9:104896711
|
C | CT | 55 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(52): Show | 55 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.66+6902dupA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTT | 30 | a0001c0001t0001g0196a0001c0001t0002g0074a0001c0001t0003g0210others(27): Show | 30 | HG00544.hp2 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.66+6901_66+6902dup others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTTT | 17 | a0001c0001t0001g0082a0001c0001t0001g0102a0001c0001t0003g0211others(14): Show | 17 | HG00741.hp1 HG01934.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.66+6900_66+6902dup others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTTTT | 8 | a0001c0005t0001g0050a0002c0011t0004g0263a0003c0002t0014g0066others(5): Show | 8 | HG00423.hp2 HG01099.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+6899_66+6902dup others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTTTTT | 10 | a0001c0001t0004g0021a0002c0032t0001g0025a0002c0057t0001g0148others(7): Show | 10 | HG01192.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+6898_66+6902dup others(5): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTTTTTT | 8 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0025t0015g0283others(5): Show | 8 | HG01255.hp2 HG01993.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+6897_66+6902dup others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTTTTTTT others(4): Show |
2 | a0005c0026t0024g0157a0012c0041t0001g0274 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66+6892_66+6902dup others(11): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTTTTTTT others(9): Show |
1 | a0002c0037t0001g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.66+6887_66+6902dup others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
C | CTTTTTTT others(14): Show |
2 | a0015c0020t0001g0006a0015c0020t0004g0005 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.66+6882_66+6902dup others(21): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
CT | C | 7 | a0001c0005t0002g0192a0002c0032t0001g0317a0004c0008t0016g0266others(4): Show | 7 | HG02723.hp2 HG02922.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+6902delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
CTTTTTT | C | 6 | a0004c0042t0008g0083a0004c0044t0007g0302a0004c0107t0002g0236others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+6897_66+6902del others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
CTTTTTTT others(5): Show |
C | 21 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0006g0047others(18): Show | 21 | HG00621.hp2 HG01070.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+6891_66+6902del others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
CTTTTTTT others(6): Show |
C | 79 | a0001c0001t0004g0194a0001c0001t0006g0214a0001c0001t0006g0225others(76): Show | 79 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.66+6890_66+6902del others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
CTTTTTTT others(7): Show |
C | 10 | a0002c0017t0002g0271a0002c0085t0008g0142a0004c0029t0001g0099others(7): Show | 10 | HG01081.hp2 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+6889_66+6902del others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.66+6888_66+6902del others(15): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896711
|
CTTTTTTT others(9): Show |
C | 3 | a0003c0002t0002g0122a0006c0004t0004g0227a0013c0013t0003g0120 | 3 | HG00609.hp2 NA19066.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.66+6887_66+6902del others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896711 | ||||||
| chr9:104896719
|
T | TA | 10 | a0002c0031t0001g0152a0002c0078t0001g0216a0005c0070t0001g0316others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+6894_66+6895ins others(1): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896719 | ||||||
| chr9:104896732
|
T | A | 6 | a0002c0031t0001g0152a0002c0078t0001g0216a0011c0010t0005g0255others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+6882A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896732 | ||||||
| chr9:104896785
|
C | T | 1 | a0005c0014t0006g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.66+6829G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896785 | ||||||
| chr9:104896803
|
T | A | 12 | a0002c0031t0001g0152a0002c0078t0001g0216a0004c0043t0003g0128others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+6811A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896803 | ||||||
| chr9:104896812
|
C | T | 92 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(89): Show | 92 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.66+6802G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896812 | ||||||
| chr9:104896824
|
G | A | 161 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(158): Show | 161 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.66+6790C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896824 | ||||||
| chr9:104896998
|
G | A | 11 | a0001c0001t0007g0183a0002c0011t0020g0171a0003c0002t0002g0044others(8): Show | 11 | NA18942.hp2 NA18978.hp1 NA18978.hp2 others(8): Show |
intron_variant | MODIFIER | c.66+6616C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104896998 | ||||||
| chr9:104897128
|
GA | G | 4 | a0002c0032t0001g0025a0002c0037t0001g0275a0002c0046t0002g0154others(1): Show | 4 | HG01109.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6485delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104897128 | ||||||
| chr9:104898153
|
T | G | 4 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+5461A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898153 | ||||||
| chr9:104898267
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.66+5347G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898267 | ||||||
| chr9:104898289
|
G | A | 2 | a0006c0012t0001g0090a0006c0012t0001g0212 | 2 | HG01243.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.66+5325C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898289 | ||||||
| chr9:104898499
|
A | T | 174 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(171): Show | 174 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.66+5115T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898499 | ||||||
| chr9:104898549
|
A | AAAAT | 13 | a0001c0001t0001g0195a0001c0097t0001g0106a0003c0002t0002g0044others(10): Show | 13 | HG00408.hp2 HG01071.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+5061_66+5064dup others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898549 | ||||||
| chr9:104898549
|
AAAAT | A | 40 | a0001c0001t0001g0121a0001c0001t0001g0218a0001c0001t0001g0291others(37): Show | 40 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.66+5061_66+5064del others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898549 | ||||||
| chr9:104898549
|
AAAATAAA others(1): Show |
A | 73 | a0001c0001t0006g0047a0001c0001t0006g0054a0001c0001t0006g0058others(70): Show | 73 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.66+5057_66+5064del others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898549 | ||||||
| chr9:104898549
|
AAAATAAA others(5): Show |
A | 25 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(22): Show | 25 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.66+5053_66+5064del others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898549 | ||||||
| chr9:104898549
|
AAAATAAA others(9): Show |
A | 48 | a0001c0001t0001g0088a0001c0001t0001g0208a0001c0001t0003g0089others(45): Show | 48 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.66+5049_66+5064del others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898549 | ||||||
| chr9:104898657
|
T | C | 13 | a0002c0015t0002g0315a0002c0015t0013g0305a0002c0015t0013g0306others(10): Show | 13 | HG01255.hp2 HG01952.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+4957A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898657 | ||||||
| chr9:104898670
|
C | T | 2 | a0002c0059t0001g0235a0019c0106t0001g0094 | 2 | HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.66+4944G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898670 | ||||||
| chr9:104898768
|
C | T | 1 | a0010c0007t0002g0012 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.66+4846G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898768 | ||||||
| chr9:104898778
|
A | G | 174 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(171): Show | 174 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.66+4836T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898778 | ||||||
| chr9:104898805
|
T | C | 11 | a0002c0057t0001g0148a0004c0044t0013g0280a0005c0022t0002g0284others(8): Show | 11 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.66+4809A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898805 | ||||||
| chr9:104898841
|
A | G | 175 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(172): Show | 175 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.66+4773T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898841 | ||||||
| chr9:104898848
|
C | A | 53 | a0001c0001t0006g0047a0001c0001t0006g0054a0001c0001t0006g0058others(50): Show | 53 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.66+4766G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898848 | ||||||
| chr9:104898869
|
C | A | 48 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(45): Show | 48 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.66+4745G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898869 | ||||||
| chr9:104898888
|
A | T | 2 | a0014c0054t0010g0251a0016c0019t0006g0250 | 2 | NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.66+4726T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104898888 | ||||||
| chr9:104899215
|
ATTGGAAT others(17): Show |
A | 1 | a0012c0041t0002g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.66+4375_66+4398del others(24): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899215 | ||||||
| chr9:104899239
|
G | GA | 3 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278 | 3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.66+4374_66+4375ins others(1): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899239 | ||||||
| chr9:104899280
|
C | G | 186 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0088others(183): Show | 186 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.66+4334G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899280 | ||||||
| chr9:104899410
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.66+4204G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899410 | ||||||
| chr9:104899454
|
A | G | 186 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(183): Show | 186 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.66+4160T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899454 | ||||||
| chr9:104899461
|
A | C | 122 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(119): Show | 122 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.66+4153T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899461 | ||||||
| chr9:104899586
|
C | T | 1 | a0001c0001t0043g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.66+4028G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899586 | ||||||
| chr9:104899672
|
C | T | 12 | a0002c0017t0002g0271a0002c0017t0026g0276a0002c0085t0008g0142others(9): Show | 12 | HG01081.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+3942G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899672 | ||||||
| chr9:104899881
|
T | C | 2 | a0001c0005t0002g0192a0008c0006t0022g0135 | 2 | NA18969.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.66+3733A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104899881 | ||||||
| chr9:104900023
|
G | C | 22 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(19): Show | 22 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.66+3591C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900023 | ||||||
| chr9:104900024
|
C | G | 22 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(19): Show | 22 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.66+3590G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900024 | ||||||
| chr9:104900069
|
G | A | 1 | a0021c0060t0001g0078 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.66+3545C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900069 | ||||||
| chr9:104900103
|
C | T | 1 | a0003c0002t0002g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.66+3511G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900103 | ||||||
| chr9:104900213
|
G | A | 168 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(165): Show | 168 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.66+3401C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900213 | ||||||
| chr9:104900410
|
T | C | 173 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(170): Show | 173 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.66+3204A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900410 | ||||||
| chr9:104900420
|
A | G | 173 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(170): Show | 173 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.66+3194T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900420 | ||||||
| chr9:104900424
|
A | G | 173 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(170): Show | 173 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.66+3190T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900424 | ||||||
| chr9:104900427
|
C | T | 173 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(170): Show | 173 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.66+3187G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900427 | ||||||
| chr9:104900531
|
A | G | 40 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(37): Show | 40 | HG00609.hp1 HG01070.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.66+3083T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900531 | ||||||
| chr9:104900758
|
C | T | 173 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(170): Show | 173 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.66+2856G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900758 | ||||||
| chr9:104900784
|
C | G | 173 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(170): Show | 173 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.66+2830G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900784 | ||||||
| chr9:104900813
|
C | T | 173 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0003g0089others(170): Show | 173 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.66+2801G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104900813 | ||||||
| chr9:104901071
|
G | C | 1 | a0018c0080t0004g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.66+2543C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901071 | ||||||
| chr9:104901363
|
C | T | 3 | a0005c0071t0041g0311a0015c0020t0001g0160a0035c0091t0008g0161 | 3 | HG01891.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+2251G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901363 | ||||||
| chr9:104901364
|
G | A | 1 | a0018c0079t0004g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.66+2250C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901364 | ||||||
| chr9:104901480
|
C | T | 1 | a0011c0010t0005g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.66+2134G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901480 | ||||||
| chr9:104901481
|
G | A | 14 | a0001c0001t0003g0297a0002c0032t0001g0025a0002c0037t0001g0275others(11): Show | 14 | HG01109.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+2133C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901481 | ||||||
| chr9:104901612
|
C | A | 1 | a0002c0015t0004g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.66+2002G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901612 | ||||||
| chr9:104901864
|
C | T | 1 | a0010c0030t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.66+1750G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901864 | ||||||
| chr9:104901959
|
A | G | 5 | a0003c0009t0051g0145a0006c0004t0006g0249a0007c0003t0009g0156others(2): Show | 5 | HG00558.hp1 HG01346.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+1655T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104901959 | ||||||
| chr9:104902020
|
C | T | 116 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(113): Show | 116 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+1594G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902020 | ||||||
| chr9:104902092
|
C | T | 20 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0004g0194others(17): Show | 20 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+1522G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902092 | ||||||
| chr9:104902194
|
A | T | 3 | a0002c0025t0008g0285a0004c0066t0008g0007a0011c0010t0005g0286 | 3 | HG03098.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+1420T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902194 | ||||||
| chr9:104902362
|
A | G | 6 | a0002c0025t0015g0283a0003c0056t0001g0288a0011c0010t0005g0097others(3): Show | 6 | HG01255.hp2 HG01952.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+1252T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902362 | ||||||
| chr9:104902410
|
T | C | 1 | a0001c0001t0002g0137 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.66+1204A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902410 | ||||||
| chr9:104902430
|
A | T | 1 | a0004c0008t0016g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.66+1184T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902430 | ||||||
| chr9:104902534
|
T | C | 110 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0102others(107): Show | 110 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.66+1080A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902534 | ||||||
| chr9:104902680
|
A | G | 241 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(238): Show | 241 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.66+934T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902680 | ||||||
| chr9:104902780
|
A | G | 1 | a0006c0004t0003g0190 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.66+834T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902780 | ||||||
| chr9:104902786
|
G | T | 1 | a0012c0040t0040g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.66+828C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902786 | ||||||
| chr9:104902880
|
A | G | 2 | a0001c0005t0002g0192a0008c0006t0022g0135 | 2 | NA18969.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.66+734T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104902880 | ||||||
| chr9:104903178
|
G | A | 1 | a0004c0114t0005g0304 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.66+436C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104903178 | ||||||
| chr9:104903230
|
C | T | 199 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(196): Show | 199 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.66+384G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104903230 | ||||||
| chr9:104903333
|
C | T | 8 | a0002c0025t0015g0283a0002c0074t0027g0290a0003c0056t0001g0288others(5): Show | 8 | HG01255.hp2 HG01952.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+281G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104903333 | ||||||
| chr9:104903458
|
G | A | 93 | a0001c0001t0001g0082a0001c0001t0003g0211a0001c0001t0004g0021others(90): Show | 93 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.66+156C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104903458 | ||||||
| chr9:104903466
|
C | T | 1 | a0010c0030t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.66+148G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104903466 | ||||||
| chr9:104903470
|
C | T | 38 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0238others(35): Show | 38 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.66+144G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104903470 | ||||||
| chr9:104903591
|
G | A | 6 | a0002c0025t0015g0283a0003c0056t0001g0288a0011c0010t0005g0097others(3): Show | 6 | HG01255.hp2 HG01952.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+23C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 2/49 | chr9 | 104903591 | ||||||
| chr9:104903957
|
G | A | 2 | a0002c0017t0026g0163a0017c0034t0001g0300 | 2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-92-186C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104903957 | ||||||
| chr9:104903987
|
A | G | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-92-216T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104903987 | ||||||
| chr9:104904064
|
C | T | 5 | a0001c0035t0004g0011a0004c0064t0007g0175a0005c0016t0001g0009others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-293G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904064 | ||||||
| chr9:104904072
|
G | C | 1 | a0004c0044t0013g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-92-301C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904072 | ||||||
| chr9:104904133
|
T | C | 209 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(206): Show | 209 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.-92-362A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904133 | ||||||
| chr9:104904232
|
T | G | 219 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(216): Show | 219 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.-92-461A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904232 | ||||||
| chr9:104904274
|
T | C | 1 | a0013c0013t0003g0256 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-92-503A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904274 | ||||||
| chr9:104904296
|
G | A | 1 | a0019c0086t0003g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-92-525C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904296 | ||||||
| chr9:104904405
|
T | C | 2 | a0013c0013t0025g0032a0013c0013t0025g0033 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-92-634A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904405 | ||||||
| chr9:104904410
|
A | G | 1 | a0007c0003t0011g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-92-639T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904410 | ||||||
| chr9:104904491
|
T | C | 241 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(238): Show | 241 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.-92-720A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904491 | ||||||
| chr9:104904543
|
C | T | 1 | a0001c0001t0003g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-92-772G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904543 | ||||||
| chr9:104904564
|
C | CA | 14 | a0002c0031t0001g0278a0003c0009t0003g0178a0004c0042t0008g0083others(11): Show | 14 | HG01891.hp2 HG02257.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-794dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904564 | ||||||
| chr9:104904564
|
CA | C | 64 | a0001c0001t0001g0026a0001c0001t0006g0047a0001c0001t0006g0054others(61): Show | 64 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-92-794delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904564 | ||||||
| chr9:104904564
|
CAA | C | 9 | a0002c0025t0015g0283a0002c0074t0027g0290a0003c0056t0001g0288others(6): Show | 9 | HG01255.hp2 HG01952.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-92-795_-92-794del others(2): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904564 | ||||||
| chr9:104904665
|
C | T | 1 | a0006c0012t0010g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-92-894G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904665 | ||||||
| chr9:104904701
|
C | T | 1 | a0019c0106t0001g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-92-930G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904701 | ||||||
| chr9:104904780
|
C | T | 1 | a0009c0021t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-92-1009G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904780 | ||||||
| chr9:104904798
|
T | C | 241 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(238): Show | 241 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.-92-1027A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904798 | ||||||
| chr9:104904856
|
C | T | 11 | a0002c0025t0015g0283a0002c0032t0001g0025a0002c0046t0002g0154others(8): Show | 11 | HG01109.hp1 HG01255.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-92-1085G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904856 | ||||||
| chr9:104904866
|
T | C | 72 | a0001c0001t0001g0026a0001c0001t0006g0047a0001c0001t0006g0054others(69): Show | 72 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-92-1095A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904866 | ||||||
| chr9:104904934
|
A | AAGGG | 11 | a0002c0031t0001g0152a0002c0078t0001g0216a0004c0043t0003g0128others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.-92-1167_-92-1164d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904934 | ||||||
| chr9:104904934
|
A | C | 11 | a0002c0025t0015g0283a0002c0032t0001g0025a0002c0046t0002g0154others(8): Show | 11 | HG01109.hp1 HG01255.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-92-1163T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104904934 | ||||||
| chr9:104905240
|
G | A | 1 | a0011c0010t0005g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-92-1469C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104905240 | ||||||
| chr9:104905420
|
A | G | 3 | a0002c0032t0001g0025a0002c0046t0002g0154a0018c0079t0004g0314 | 3 | HG01109.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-92-1649T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104905420 | ||||||
| chr9:104905783
|
G | C | 128 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0088others(125): Show | 128 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-92-2012C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104905783 | ||||||
| chr9:104905786
|
C | T | 7 | a0004c0042t0008g0083a0004c0042t0008g0158a0004c0044t0007g0302others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-2015G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104905786 | ||||||
| chr9:104905965
|
AG | A | 3 | a0002c0017t0026g0276a0002c0085t0008g0142a0012c0041t0001g0274 | 3 | HG02257.hp2 HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-92-2195delC | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104905965 | ||||||
| chr9:104906284
|
A | G | 2 | a0011c0010t0005g0097a0018c0080t0004g0107 | 2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-92-2513T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906284 | ||||||
| chr9:104906306
|
A | G | 1 | a0010c0007t0010g0185 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-92-2535T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906306 | ||||||
| chr9:104906436
|
T | C | 1 | a0002c0037t0011g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-92-2665A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906436 | ||||||
| chr9:104906544
|
G | C | 236 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(233): Show | 236 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.-92-2773C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906544 | ||||||
| chr9:104906605
|
A | T | 234 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(231): Show | 234 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.-92-2834T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906605 | ||||||
| chr9:104906749
|
TC | T | 9 | a0002c0017t0026g0276a0002c0025t0008g0285a0002c0025t0015g0283others(6): Show | 9 | HG01255.hp2 HG01952.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-92-2979delG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906749 | ||||||
| chr9:104906750
|
C | A | 2 | a0003c0056t0001g0288a0022c0050t0001g0166 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-92-2979G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906750 | ||||||
| chr9:104906750
|
C | CA | 39 | a0001c0001t0001g0082a0001c0001t0001g0102a0001c0001t0004g0021others(36): Show | 39 | HG00741.hp1 HG01106.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.-92-2980dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906750 | ||||||
| chr9:104906750
|
CA | C | 28 | a0001c0001t0001g0176a0001c0001t0001g0203a0001c0001t0004g0193others(25): Show | 28 | HG00558.hp2 HG00642.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-92-2980delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906750 | ||||||
| chr9:104906792
|
T | C | 33 | a0001c0001t0001g0082a0001c0001t0004g0021a0001c0005t0001g0050others(30): Show | 33 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.-92-3021A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906792 | ||||||
| chr9:104906927
|
C | G | 2 | a0002c0017t0026g0276a0012c0041t0001g0274 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-92-3156G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906927 | ||||||
| chr9:104906960
|
T | C | 22 | a0001c0001t0001g0082a0001c0001t0004g0021a0001c0005t0001g0050others(19): Show | 22 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-92-3189A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104906960 | ||||||
| chr9:104907018
|
G | C | 13 | a0002c0031t0001g0152a0002c0078t0001g0216a0004c0043t0003g0128others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.-92-3247C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907018 | ||||||
| chr9:104907065
|
G | C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-92-3294C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907065 | ||||||
| chr9:104907143
|
C | G | 1 | a0004c0008t0004g0264 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-92-3372G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907143 | ||||||
| chr9:104907329
|
G | A | 9 | a0004c0029t0001g0099a0004c0029t0005g0162a0004c0099t0001g0110others(6): Show | 9 | HG01081.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-92-3558C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907329 | ||||||
| chr9:104907451
|
A | G | 13 | a0002c0031t0001g0152a0002c0078t0001g0216a0004c0043t0003g0128others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.-92-3680T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907451 | ||||||
| chr9:104907545
|
C | T | 1 | a0005c0052t0001g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-92-3774G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907545 | ||||||
| chr9:104907621
|
G | T | 1 | a0001c0005t0001g0050 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-92-3850C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907621 | ||||||
| chr9:104907700
|
C | T | 1 | a0002c0037t0001g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-92-3929G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907700 | ||||||
| chr9:104907790
|
G | A | 1 | a0002c0011t0007g0119 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-92-4019C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907790 | ||||||
| chr9:104907834
|
C | T | 10 | a0002c0015t0031g0084a0002c0081t0013g0277a0002c0085t0008g0142others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-92-4063G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907834 | ||||||
| chr9:104907849
|
A | G | 1 | a0005c0014t0005g0245 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-92-4078T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907849 | ||||||
| chr9:104907861
|
A | C | 1 | a0005c0082t0002g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-92-4090T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907861 | ||||||
| chr9:104907886
|
G | A | 1 | a0011c0010t0005g0287 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-92-4115C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907886 | ||||||
| chr9:104907928
|
T | C | 1 | a0005c0082t0002g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-92-4157A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907928 | ||||||
| chr9:104907941
|
T | A | 2 | a0014c0054t0010g0251a0016c0019t0006g0250 | 2 | NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-92-4170A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104907941 | ||||||
| chr9:104908036
|
C | T | 2 | a0002c0017t0026g0276a0012c0041t0001g0274 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-92-4265G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104908036 | ||||||
| chr9:104908154
|
G | C | 1 | a0018c0079t0004g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-92-4383C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104908154 | ||||||
| chr9:104908167
|
GACACTGG others(8): Show |
G | 13 | a0002c0017t0015g0101a0002c0024t0008g0003a0002c0024t0008g0008others(10): Show | 13 | HG02486.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-92-4411_-92-4397d others(17): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104908167 | ||||||
| chr9:104908393
|
A | G | 50 | a0001c0001t0001g0088a0001c0001t0003g0089a0001c0001t0011g0085others(47): Show | 50 | HG00609.hp1 HG01070.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-92-4622T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104908393 | ||||||
| chr9:104908585
|
T | C | 5 | a0002c0017t0026g0276a0002c0025t0008g0285a0004c0066t0008g0007others(2): Show | 5 | HG02257.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-4814A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104908585 | ||||||
| chr9:104908730
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0003g0089a0004c0008t0003g0289others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-4959G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104908730 | ||||||
| chr9:104908834
|
G | A | 1 | a0002c0037t0011g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-92-5063C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104908834 | ||||||
| chr9:104909378
|
T | C | 100 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(97): Show | 100 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-92-5607A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909378 | ||||||
| chr9:104909607
|
T | TAC | 19 | a0001c0001t0003g0210a0001c0001t0043g0002a0001c0097t0001g0106others(16): Show | 19 | HG00738.hp1 HG01071.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-92-5838_-92-5837d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TAC | T | 32 | a0001c0001t0001g0195a0001c0001t0001g0208a0001c0001t0004g0194others(29): Show | 32 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-92-5838_-92-5837d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TACAC | T | 40 | a0001c0001t0003g0211a0001c0001t0006g0047a0001c0001t0006g0058others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.-92-5840_-92-5837d others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TACACAC | T | 33 | a0001c0001t0004g0193a0001c0001t0006g0225a0001c0001t0012g0039others(30): Show | 33 | HG00642.hp1 HG01081.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.-92-5842_-92-5837d others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TACACACA others(1): Show |
T | 18 | a0001c0001t0001g0291a0002c0011t0004g0263a0002c0017t0026g0276others(15): Show | 18 | HG01978.hp2 HG02155.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-92-5844_-92-5837d others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TACACACA others(3): Show |
T | 76 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(73): Show | 76 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-92-5846_-92-5837d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TACACACA others(5): Show |
T | 2 | a0002c0032t0001g0317a0023c0072t0001g0309 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-92-5848_-92-5837d others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TACACACA others(7): Show |
T | 7 | a0002c0025t0015g0283a0003c0056t0001g0288a0005c0052t0001g0281others(4): Show | 7 | HG01255.hp2 HG01952.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-5850_-92-5837d others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909607
|
TACACACA others(9): Show |
T | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-5852_-92-5837d others(18): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909607 | ||||||
| chr9:104909649
|
C | T | 1 | a0010c0030t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-92-5878G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909649 | ||||||
| chr9:104909654
|
A | ACACACAC others(3): Show |
1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-92-5884_-92-5883i others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909654
|
A | ACACACAC others(7): Show |
1 | a0005c0082t0002g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-92-5884_-92-5883i others(16): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909654
|
A | ACACACAC others(1): Show |
3 | a0002c0024t0008g0003a0002c0024t0008g0008a0002c0031t0001g0278 | 3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-92-5884_-92-5883i others(10): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909654
|
A | ACACACAT others(5): Show |
1 | a0018c0080t0004g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-92-5884_-92-5883i others(14): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909654
|
A | ACACACG | 3 | a0001c0001t0001g0088a0001c0001t0003g0089a0004c0008t0003g0289 | 3 | HG01168.hp1 HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-92-5884_-92-5883i others(8): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909654
|
A | ACACG | 5 | a0005c0016t0001g0049a0005c0039t0017g0018a0005c0039t0017g0019others(2): Show | 5 | HG02055.hp1 HG03471.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-5884_-92-5883i others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909654
|
A | ACG | 21 | a0001c0001t0011g0085a0001c0005t0002g0031a0002c0011t0004g0112others(18): Show | 21 | HG01070.hp2 HG01257.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.-92-5884_-92-5883i others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909654
|
A | G | 139 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(136): Show | 139 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.-92-5883T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909654 | ||||||
| chr9:104909710
|
C | T | 1 | a0009c0021t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-92-5939G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909710 | ||||||
| chr9:104909805
|
G | T | 4 | a0003c0002t0003g0127a0006c0004t0011g0269a0009c0018t0003g0253others(1): Show | 4 | NA18955.hp2 NA18999.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-6034C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104909805 | ||||||
| chr9:104910084
|
G | A | 44 | a0001c0001t0003g0211a0001c0001t0006g0047a0001c0001t0006g0058others(41): Show | 44 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.-92-6313C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104910084 | ||||||
| chr9:104910169
|
C | G | 1 | a0007c0003t0033g0035 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-92-6398G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104910169 | ||||||
| chr9:104910217
|
G | A | 91 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(88): Show | 91 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-92-6446C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104910217 | ||||||
| chr9:104910245
|
T | G | 20 | a0001c0001t0001g0082a0001c0001t0004g0021a0001c0005t0001g0050others(17): Show | 20 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-6474A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104910245 | ||||||
| chr9:104910595
|
T | C | 1 | a0004c0008t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-92-6824A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104910595 | ||||||
| chr9:104910606
|
G | C | 1 | a0004c0008t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-92-6835C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104910606 | ||||||
| chr9:104910865
|
C | T | 1 | a0018c0079t0004g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-92-7094G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104910865 | ||||||
| chr9:104911028
|
T | C | 2 | a0027c0062t0001g0310a0033c0101t0001g0308 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-92-7257A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911028 | ||||||
| chr9:104911133
|
A | G | 1 | a0001c0005t0002g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-92-7362T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911133 | ||||||
| chr9:104911251
|
C | T | 1 | a0026c0111t0002g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-92-7480G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911251 | ||||||
| chr9:104911357
|
A | G | 1 | a0001c0005t0004g0167 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-92-7586T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911357 | ||||||
| chr9:104911359
|
T | C | 42 | a0002c0015t0031g0084a0002c0017t0015g0101a0002c0024t0008g0003others(39): Show | 42 | HG01109.hp1 HG01243.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.-92-7588A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911359 | ||||||
| chr9:104911373
|
T | C | 1 | a0001c0001t0006g0225 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-92-7602A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911373 | ||||||
| chr9:104911617
|
T | C | 6 | a0002c0025t0015g0283a0002c0032t0001g0025a0003c0056t0001g0288others(3): Show | 6 | HG01255.hp2 HG01952.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-7846A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911617 | ||||||
| chr9:104911687
|
A | G | 2 | a0002c0025t0015g0283a0012c0093t0001g0108 | 2 | HG01255.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-92-7916T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911687 | ||||||
| chr9:104911833
|
G | T | 36 | a0002c0015t0031g0084a0002c0024t0008g0003a0002c0024t0008g0008others(33): Show | 36 | HG01109.hp1 HG01255.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.-92-8062C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911833 | ||||||
| chr9:104911888
|
G | A | 13 | a0002c0017t0015g0101a0002c0024t0008g0003a0002c0024t0008g0008others(10): Show | 13 | HG02486.hp2 HG02615.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-92-8117C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911888 | ||||||
| chr9:104911946
|
G | A | 1 | a0002c0011t0004g0213 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-92-8175C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104911946 | ||||||
| chr9:104912044
|
A | T | 1 | a0007c0003t0004g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-92-8273T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912044 | ||||||
| chr9:104912152
|
A | T | 5 | a0002c0017t0026g0276a0002c0025t0008g0285a0004c0066t0008g0007others(2): Show | 5 | HG02257.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-8381T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912152 | ||||||
| chr9:104912429
|
C | A | 5 | a0002c0017t0026g0276a0002c0025t0008g0285a0004c0066t0008g0007others(2): Show | 5 | HG02257.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-8658G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912429 | ||||||
| chr9:104912609
|
A | G | 23 | a0002c0015t0031g0084a0002c0032t0001g0025a0002c0046t0002g0154others(20): Show | 23 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-92-8838T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912609 | ||||||
| chr9:104912747
|
G | C | 1 | a0033c0101t0001g0308 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-92-8976C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912747 | ||||||
| chr9:104912821
|
G | GA | 133 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(130): Show | 133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-92-9051dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912821 | ||||||
| chr9:104912833
|
AT | A | 6 | a0002c0057t0001g0148a0005c0022t0002g0284a0005c0022t0021g0141others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-9063delA | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912833 | ||||||
| chr9:104912895
|
A | T | 9 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0015t0031g0084others(6): Show | 9 | HG01243.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-92-9124T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912895 | ||||||
| chr9:104912910
|
G | A | 2 | a0005c0022t0021g0141a0005c0022t0021g0147 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-92-9139C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104912910 | ||||||
| chr9:104913002
|
G | A | 1 | a0001c0001t0003g0211 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-92-9231C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913002 | ||||||
| chr9:104913089
|
T | C | 4 | a0002c0033t0002g0301a0004c0114t0005g0304a0005c0051t0019g0164others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-9318A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913089 | ||||||
| chr9:104913141
|
G | C | 28 | a0001c0001t0006g0054a0001c0005t0002g0031a0002c0011t0004g0112others(25): Show | 28 | HG00609.hp1 HG01257.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.-92-9370C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913141 | ||||||
| chr9:104913223
|
T | C | 1 | a0018c0079t0004g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-92-9452A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913223 | ||||||
| chr9:104913243
|
C | G | 6 | a0001c0001t0001g0026a0001c0001t0002g0074a0001c0001t0052g0318others(3): Show | 6 | HG00099.hp1 HG01106.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-9472G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913243 | ||||||
| chr9:104913338
|
T | C | 1 | a0004c0098t0005g0303 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-92-9567A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913338 | ||||||
| chr9:104913342
|
C | T | 2 | a0001c0001t0043g0002a0002c0015t0002g0315 | 2 | HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-92-9571G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913342 | ||||||
| chr9:104913377
|
T | A | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-9606A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913377 | ||||||
| chr9:104913745
|
C | T | 43 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0006g0047others(40): Show | 43 | HG00099.hp2 HG00558.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.-92-9974G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913745 | ||||||
| chr9:104913776
|
TTTTTA | T | 25 | a0001c0001t0001g0016a0001c0001t0039g0246a0001c0005t0002g0017others(22): Show | 25 | HG00621.hp1 HG01106.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.-92-10010_-92-1000 others(9): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913776 | ||||||
| chr9:104913826
|
G | C | 1 | a0001c0005t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-92-10055C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913826 | ||||||
| chr9:104913835
|
G | C | 2 | a0002c0032t0001g0317a0005c0070t0001g0316 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-92-10064C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913835 | ||||||
| chr9:104913877
|
G | C | 1 | a0007c0090t0007g0046 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-92-10106C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913877 | ||||||
| chr9:104913943
|
C | G | 1 | a0001c0001t0003g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-92-10172G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913943 | ||||||
| chr9:104913948
|
T | C | 3 | a0001c0001t0001g0208a0001c0001t0003g0086a0001c0001t0049g0034 | 3 | HG01109.hp2 HG01515.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-92-10177A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913948 | ||||||
| chr9:104913953
|
A | C | 1 | a0001c0001t0003g0086 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-92-10182T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913953 | ||||||
| chr9:104913956
|
CGCCCG | C | 88 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-92-10190_-92-1018 others(9): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913956 | ||||||
| chr9:104913961
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-92-10190C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913961 | ||||||
| chr9:104913993
|
G | A | 3 | a0002c0011t0020g0171a0003c0009t0003g0138a0007c0003t0004g0170 | 3 | HG02132.hp2 NA18942.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-92-10222C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104913993 | ||||||
| chr9:104914014
|
T | G | 28 | a0001c0001t0001g0218a0001c0001t0006g0225a0001c0001t0012g0039others(25): Show | 28 | HG00609.hp2 HG00738.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-92-10243A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914014 | ||||||
| chr9:104914188
|
T | C | 2 | a0001c0097t0001g0106a0003c0009t0001g0279 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-92-10417A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914188 | ||||||
| chr9:104914296
|
A | C | 48 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(45): Show | 48 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-92-10525T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914296 | ||||||
| chr9:104914425
|
G | A | 63 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0176others(60): Show | 63 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-92-10654C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914425 | ||||||
| chr9:104914477
|
A | G | 244 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.-92-10706T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914477 | ||||||
| chr9:104914500
|
TA | T | 11 | a0001c0001t0006g0047a0002c0024t0008g0003a0002c0059t0001g0235others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.-92-10730delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914500 | ||||||
| chr9:104914514
|
A | G | 4 | a0004c0044t0013g0280a0005c0052t0001g0281a0014c0054t0010g0251others(1): Show | 4 | HG03195.hp2 NA18964.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-10743T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914514 | ||||||
| chr9:104914575
|
A | C | 1 | a0018c0079t0004g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-92-10804T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914575 | ||||||
| chr9:104914659
|
A | G | 41 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(38): Show | 41 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-92-10888T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914659 | ||||||
| chr9:104914768
|
T | G | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-10997A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914768 | ||||||
| chr9:104914930
|
G | C | 49 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0121others(46): Show | 49 | HG00099.hp1 HG00673.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.-92-11159C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914930 | ||||||
| chr9:104914995
|
G | A | 1 | a0001c0001t0052g0318 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-92-11224C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104914995 | ||||||
| chr9:104915008
|
A | G | 49 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0121others(46): Show | 49 | HG00099.hp1 HG00673.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.-92-11237T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915008 | ||||||
| chr9:104915052
|
A | T | 4 | a0002c0046t0002g0154a0002c0074t0027g0290a0004c0029t0005g0023others(1): Show | 4 | HG01109.hp1 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-11281T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915052 | ||||||
| chr9:104915072
|
C | T | 5 | a0002c0017t0026g0276a0002c0037t0001g0275a0005c0036t0001g0273others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-11301G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915072 | ||||||
| chr9:104915201
|
G | A | 29 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(26): Show | 29 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.-92-11430C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915201 | ||||||
| chr9:104915231
|
G | C | 23 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(20): Show | 23 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-92-11460C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915231 | ||||||
| chr9:104915292
|
G | A | 1 | a0001c0001t0049g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-92-11521C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915292 | ||||||
| chr9:104915308
|
G | A | 1 | a0017c0034t0001g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-92-11537C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915308 | ||||||
| chr9:104915651
|
A | T | 40 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(37): Show | 40 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-92-11880T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915651 | ||||||
| chr9:104915654
|
T | C | 31 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(28): Show | 31 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-92-11883A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915654 | ||||||
| chr9:104915657
|
A | G | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-11886T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915657 | ||||||
| chr9:104915660
|
A | G | 2 | a0013c0013t0025g0032a0013c0013t0025g0033 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-92-11889T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915660 | ||||||
| chr9:104915730
|
T | G | 31 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(28): Show | 31 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-92-11959A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915730 | ||||||
| chr9:104915939
|
C | G | 2 | a0005c0022t0021g0141a0005c0022t0021g0147 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-93+11996G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915939 | ||||||
| chr9:104915977
|
G | A | 5 | a0001c0035t0004g0011a0005c0016t0001g0009a0005c0016t0001g0010others(2): Show | 5 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+11958C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915977 | ||||||
| chr9:104915997
|
C | T | 43 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(40): Show | 43 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-93+11938G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104915997 | ||||||
| chr9:104916165
|
G | A | 31 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(28): Show | 31 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-93+11770C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916165 | ||||||
| chr9:104916329
|
C | G | 2 | a0005c0026t0024g0157a0005c0051t0019g0164 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-93+11606G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916329 | ||||||
| chr9:104916359
|
G | T | 31 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(28): Show | 31 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-93+11576C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916359 | ||||||
| chr9:104916393
|
C | T | 8 | a0001c0001t0043g0002a0002c0031t0001g0152a0002c0057t0001g0148others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+11542G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916393 | ||||||
| chr9:104916495
|
C | T | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+11440G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916495 | ||||||
| chr9:104916516
|
C | T | 69 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.-93+11419G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916516 | ||||||
| chr9:104916554
|
G | A | 1 | a0002c0031t0001g0278 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-93+11381C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916554 | ||||||
| chr9:104916635
|
T | C | 40 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(37): Show | 40 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-93+11300A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916635 | ||||||
| chr9:104916742
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-93+11193G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916742 | ||||||
| chr9:104916834
|
C | T | 1 | a0028c0095t0002g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-93+11101G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916834 | ||||||
| chr9:104916847
|
AAAATATG others(14): Show |
A | 15 | a0001c0097t0001g0106a0002c0015t0002g0315a0002c0015t0013g0305others(12): Show | 15 | HG00738.hp1 HG01071.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-93+11067_-93+1108 others(25): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916847 | ||||||
| chr9:104916860
|
T | C | 40 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(37): Show | 40 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-93+11075A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916860 | ||||||
| chr9:104916919
|
G | T | 40 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(37): Show | 40 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-93+11016C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104916919 | ||||||
| chr9:104917034
|
G | A | 16 | a0001c0097t0001g0106a0002c0015t0002g0315a0002c0015t0013g0305others(13): Show | 16 | HG00738.hp1 HG01071.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+10901C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917034 | ||||||
| chr9:104917144
|
T | G | 16 | a0001c0001t0039g0246a0002c0017t0026g0276a0002c0024t0008g0109others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+10791A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917144 | ||||||
| chr9:104917179
|
G | A | 1 | a0008c0049t0004g0103 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-93+10756C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917179 | ||||||
| chr9:104917219
|
C | A | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+10716G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917219 | ||||||
| chr9:104917437
|
CTA | C | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+10496_-93+1049 others(6): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917437 | ||||||
| chr9:104917477
|
G | A | 1 | a0007c0003t0020g0179 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-93+10458C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917477 | ||||||
| chr9:104917493
|
A | G | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+10442T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917493 | ||||||
| chr9:104917568
|
A | G | 14 | a0001c0001t0039g0246a0002c0017t0026g0276a0002c0024t0008g0109others(11): Show | 14 | HG01081.hp2 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-93+10367T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917568 | ||||||
| chr9:104917573
|
G | A | 40 | a0001c0001t0002g0233a0001c0001t0007g0183a0001c0001t0012g0144others(37): Show | 40 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-93+10362C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917573 | ||||||
| chr9:104917576
|
G | GA | 242 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(239): Show | 242 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.-93+10358dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917576 | ||||||
| chr9:104917584
|
T | C | 2 | a0002c0033t0032g0024a0011c0010t0005g0287 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93+10351A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917584 | ||||||
| chr9:104917589
|
G | A | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+10346C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917589 | ||||||
| chr9:104917605
|
T | C | 2 | a0004c0029t0005g0023a0018c0079t0004g0314 | 2 | HG01109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-93+10330A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917605 | ||||||
| chr9:104917623
|
A | G | 30 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(27): Show | 30 | HG01081.hp1 HG01257.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+10312T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917623 | ||||||
| chr9:104917669
|
G | A | 1 | a0006c0089t0003g0180 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-93+10266C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917669 | ||||||
| chr9:104917673
|
G | A | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+10262C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917673 | ||||||
| chr9:104917716
|
T | G | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+10219A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917716 | ||||||
| chr9:104917724
|
A | G | 6 | a0001c0108t0002g0113a0002c0011t0020g0171a0003c0002t0002g0044others(3): Show | 6 | HG00544.hp2 NA18942.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+10211T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917724 | ||||||
| chr9:104917832
|
G | C | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+10103C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917832 | ||||||
| chr9:104917858
|
G | A | 1 | a0002c0074t0027g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-93+10077C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917858 | ||||||
| chr9:104917891
|
A | G | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+10044T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917891 | ||||||
| chr9:104917963
|
T | C | 3 | a0002c0024t0008g0109a0002c0074t0027g0290a0019c0106t0001g0094 | 3 | HG03471.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-93+9972A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104917963 | ||||||
| chr9:104918026
|
T | G | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+9909A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918026 | ||||||
| chr9:104918074
|
T | A | 16 | a0001c0001t0039g0246a0002c0017t0026g0276a0002c0024t0008g0109others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+9861A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918074 | ||||||
| chr9:104918160
|
T | TA | 172 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(169): Show | 172 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-93+9774dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918160 | ||||||
| chr9:104918177
|
C | T | 245 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(242): Show | 245 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.-93+9758G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918177 | ||||||
| chr9:104918272
|
G | A | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+9663C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918272 | ||||||
| chr9:104918358
|
T | G | 25 | a0001c0001t0001g0016a0001c0001t0004g0021a0001c0005t0002g0017others(22): Show | 25 | HG01099.hp1 HG01192.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.-93+9577A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918358 | ||||||
| chr9:104918410
|
G | C | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+9525C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918410 | ||||||
| chr9:104918447
|
C | T | 2 | a0002c0033t0032g0024a0011c0010t0005g0287 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93+9488G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918447 | ||||||
| chr9:104918449
|
G | A | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+9486C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918449 | ||||||
| chr9:104918627
|
T | C | 2 | a0001c0001t0007g0183a0003c0002t0002g0184 | 2 | NA19002.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-93+9308A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918627 | ||||||
| chr9:104918634
|
A | G | 172 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(169): Show | 172 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-93+9301T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918634 | ||||||
| chr9:104918672
|
C | A | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+9263G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918672 | ||||||
| chr9:104918753
|
T | A | 1 | a0003c0002t0002g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-93+9182A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918753 | ||||||
| chr9:104918913
|
G | C | 25 | a0001c0001t0001g0016a0001c0001t0004g0021a0001c0005t0002g0017others(22): Show | 25 | HG01099.hp1 HG01192.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.-93+9022C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104918913 | ||||||
| chr9:104919144
|
G | C | 45 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(42): Show | 45 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-93+8791C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919144 | ||||||
| chr9:104919218
|
G | A | 1 | a0002c0025t0007g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-93+8717C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919218 | ||||||
| chr9:104919263
|
A | C | 1 | a0003c0009t0006g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-93+8672T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919263 | ||||||
| chr9:104919333
|
C | T | 21 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(18): Show | 21 | HG01081.hp1 HG01255.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93+8602G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919333 | ||||||
| chr9:104919407
|
A | C | 92 | a0001c0001t0001g0102a0001c0001t0003g0297a0001c0001t0011g0085others(89): Show | 92 | HG00099.hp1 HG00673.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.-93+8528T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919407 | ||||||
| chr9:104919412
|
C | A | 17 | a0001c0097t0001g0106a0002c0015t0002g0315a0002c0015t0013g0305others(14): Show | 17 | HG00738.hp1 HG01071.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+8523G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919412 | ||||||
| chr9:104919436
|
C | A | 29 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(26): Show | 29 | HG01081.hp1 HG01255.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.-93+8499G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919436 | ||||||
| chr9:104919482
|
T | C | 46 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(43): Show | 46 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.-93+8453A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919482 | ||||||
| chr9:104919568
|
C | T | 1 | a0012c0065t0007g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-93+8367G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919568 | ||||||
| chr9:104919569
|
G | A | 8 | a0002c0015t0004g0004a0002c0024t0008g0003a0002c0024t0008g0008others(5): Show | 8 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+8366C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919569 | ||||||
| chr9:104919594
|
A | G | 1 | a0010c0007t0010g0185 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-93+8341T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919594 | ||||||
| chr9:104919611
|
C | CA | 52 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(49): Show | 52 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.-93+8323dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919611 | ||||||
| chr9:104919692
|
G | A | 14 | a0001c0001t0039g0246a0002c0017t0002g0271a0002c0017t0026g0276others(11): Show | 14 | HG01081.hp2 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-93+8243C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919692 | ||||||
| chr9:104919714
|
A | G | 245 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(242): Show | 245 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.-93+8221T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919714 | ||||||
| chr9:104919731
|
T | G | 29 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(26): Show | 29 | HG01081.hp1 HG01255.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.-93+8204A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919731 | ||||||
| chr9:104919871
|
C | T | 1 | a0005c0026t0004g0042 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-93+8064G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919871 | ||||||
| chr9:104919913
|
C | G | 45 | a0001c0001t0002g0233a0001c0001t0012g0144a0001c0005t0002g0123others(42): Show | 45 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-93+8022G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919913 | ||||||
| chr9:104919919
|
C | T | 2 | a0004c0029t0005g0023a0018c0079t0004g0314 | 2 | HG01109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-93+8016G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919919 | ||||||
| chr9:104919940
|
T | C | 21 | a0001c0097t0001g0106a0002c0015t0002g0315a0002c0015t0013g0305others(18): Show | 21 | HG00738.hp1 HG01071.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.-93+7995A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104919940 | ||||||
| chr9:104920077
|
C | G | 1 | a0003c0002t0002g0041 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-93+7858G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920077 | ||||||
| chr9:104920096
|
T | A | 5 | a0001c0001t0001g0088a0001c0001t0003g0086a0001c0001t0003g0089others(2): Show | 5 | HG01070.hp2 HG01109.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+7839A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920096 | ||||||
| chr9:104920116
|
C | T | 2 | a0003c0077t0005g0312a0025c0083t0001g0313 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-93+7819G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920116 | ||||||
| chr9:104920236
|
T | C | 272 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-93+7699A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920236 | ||||||
| chr9:104920296
|
T | C | 1 | a0002c0046t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-93+7639A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920296 | ||||||
| chr9:104920560
|
T | C | 1 | a0001c0109t0001g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-93+7375A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920560 | ||||||
| chr9:104920589
|
G | A | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+7346C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920589 | ||||||
| chr9:104920604
|
T | C | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+7331A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920604 | ||||||
| chr9:104920614
|
C | T | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+7321G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920614 | ||||||
| chr9:104920652
|
C | T | 1 | a0003c0002t0002g0040 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-93+7283G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920652 | ||||||
| chr9:104920701
|
G | A | 1 | a0001c0005t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-93+7234C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920701 | ||||||
| chr9:104920796
|
C | T | 1 | a0011c0010t0037g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-93+7139G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920796 | ||||||
| chr9:104920841
|
T | G | 74 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(71): Show | 74 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-93+7094A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920841 | ||||||
| chr9:104920843
|
G | A | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+7092C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920843 | ||||||
| chr9:104920891
|
A | G | 21 | a0001c0097t0001g0106a0002c0015t0002g0315a0002c0015t0013g0305others(18): Show | 21 | HG00738.hp1 HG01071.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.-93+7044T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920891 | ||||||
| chr9:104920916
|
T | G | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+7019A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920916 | ||||||
| chr9:104920976
|
A | T | 13 | a0002c0025t0007g0237a0002c0025t0008g0285a0002c0025t0015g0283others(10): Show | 13 | HG01255.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+6959T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104920976 | ||||||
| chr9:104921018
|
G | A | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-93+6917C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921018 | ||||||
| chr9:104921096
|
A | AG | 272 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-93+6838dupC | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921096 | ||||||
| chr9:104921184
|
A | G | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+6751T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921184 | ||||||
| chr9:104921243
|
T | C | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+6692A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921243 | ||||||
| chr9:104921246
|
T | C | 1 | a0002c0075t0027g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-93+6689A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921246 | ||||||
| chr9:104921313
|
C | A | 23 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(20): Show | 23 | HG01081.hp1 HG01255.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93+6622G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921313 | ||||||
| chr9:104921355
|
T | C | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+6580A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921355 | ||||||
| chr9:104921411
|
G | C | 272 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-93+6524C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921411 | ||||||
| chr9:104921470
|
C | A | 2 | a0001c0005t0004g0167a0006c0012t0002g0140 | 2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-93+6465G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921470 | ||||||
| chr9:104921560
|
A | T | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+6375T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921560 | ||||||
| chr9:104921949
|
T | G | 85 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(82): Show | 85 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-93+5986A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921949 | ||||||
| chr9:104921972
|
G | A | 75 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0203others(72): Show | 75 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-93+5963C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921972 | ||||||
| chr9:104921978
|
G | C | 1 | a0007c0003t0011g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-93+5957C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921978 | ||||||
| chr9:104921995
|
T | C | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+5940A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104921995 | ||||||
| chr9:104922005
|
A | G | 68 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0203others(65): Show | 68 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-93+5930T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922005 | ||||||
| chr9:104922016
|
C | T | 2 | a0004c0044t0007g0302a0033c0101t0001g0308 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+5919G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922016 | ||||||
| chr9:104922037
|
A | C | 85 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(82): Show | 85 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-93+5898T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922037 | ||||||
| chr9:104922067
|
T | C | 2 | a0002c0011t0007g0119a0006c0063t0003g0151 | 2 | NA18978.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-93+5868A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922067 | ||||||
| chr9:104922111
|
G | A | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+5824C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922111 | ||||||
| chr9:104922124
|
G | A | 50 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(47): Show | 50 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+5811C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922124 | ||||||
| chr9:104922138
|
T | C | 16 | a0001c0001t0001g0088a0001c0001t0001g0238a0001c0001t0001g0291others(13): Show | 16 | HG00741.hp1 HG01070.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+5797A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922138 | ||||||
| chr9:104922207
|
A | G | 8 | a0001c0001t0043g0002a0002c0031t0001g0152a0002c0057t0001g0148others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+5728T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922207 | ||||||
| chr9:104922251
|
G | C | 1 | a0003c0038t0003g0293 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-93+5684C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922251 | ||||||
| chr9:104922338
|
C | T | 2 | a0002c0011t0007g0119a0006c0063t0003g0151 | 2 | NA18978.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-93+5597G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922338 | ||||||
| chr9:104922345
|
C | A | 11 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(8): Show | 11 | HG01081.hp1 HG01257.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-93+5590G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922345 | ||||||
| chr9:104922435
|
G | A | 1 | a0005c0026t0009g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+5500C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922435 | ||||||
| chr9:104922462
|
C | T | 1 | a0001c0001t0049g0034 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-93+5473G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922462 | ||||||
| chr9:104922567
|
G | A | 41 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(38): Show | 41 | HG01081.hp1 HG01257.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.-93+5368C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922567 | ||||||
| chr9:104922626
|
C | T | 11 | a0002c0015t0013g0305a0002c0015t0013g0306a0003c0038t0005g0307others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-93+5309G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922626 | ||||||
| chr9:104922662
|
T | C | 41 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(38): Show | 41 | HG01081.hp1 HG01257.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.-93+5273A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922662 | ||||||
| chr9:104922735
|
G | A | 41 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(38): Show | 41 | HG01081.hp1 HG01257.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.-93+5200C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922735 | ||||||
| chr9:104922863
|
CCCA | C | 3 | a0001c0001t0012g0039a0007c0003t0002g0037a0007c0003t0002g0038 | 3 | NA18985.hp1 NA18990.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-93+5069_-93+5071d others(5): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922863 | ||||||
| chr9:104922874
|
G | A | 24 | a0001c0001t0043g0002a0002c0015t0013g0305a0002c0015t0013g0306others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-93+5061C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922874 | ||||||
| chr9:104922875
|
C | T | 31 | a0001c0001t0043g0002a0002c0015t0002g0315a0002c0015t0013g0305others(28): Show | 31 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-93+5060G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922875 | ||||||
| chr9:104922919
|
A | G | 43 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(40): Show | 43 | HG01081.hp1 HG01257.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.-93+5016T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104922919 | ||||||
| chr9:104923106
|
G | A | 38 | a0002c0015t0002g0315a0002c0015t0013g0305a0002c0015t0013g0306others(35): Show | 38 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.-93+4829C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923106 | ||||||
| chr9:104923145
|
C | T | 1 | a0004c0087t0009g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-93+4790G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923145 | ||||||
| chr9:104923261
|
G | T | 142 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(139): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-93+4674C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923261 | ||||||
| chr9:104923287
|
T | C | 53 | a0001c0001t0001g0102a0001c0001t0039g0246a0001c0005t0002g0031others(50): Show | 53 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.-93+4648A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923287 | ||||||
| chr9:104923296
|
C | A | 66 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(63): Show | 66 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.-93+4639G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923296 | ||||||
| chr9:104923308
|
T | C | 83 | a0001c0001t0001g0121a0001c0001t0002g0137a0001c0001t0012g0144others(80): Show | 83 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.-93+4627A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923308 | ||||||
| chr9:104923486
|
T | C | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-93+4449A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923486 | ||||||
| chr9:104923797
|
T | C | 3 | a0002c0015t0002g0315a0002c0032t0001g0317a0005c0070t0001g0316 | 3 | HG02723.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-93+4138A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923797 | ||||||
| chr9:104923850
|
A | G | 152 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(149): Show | 152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-93+4085T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923850 | ||||||
| chr9:104923867
|
T | C | 2 | a0003c0077t0005g0312a0025c0083t0001g0313 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-93+4068A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923867 | ||||||
| chr9:104923913
|
G | A | 1 | a0002c0033t0032g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-93+4022C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923913 | ||||||
| chr9:104923960
|
T | C | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+3975A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104923960 | ||||||
| chr9:104924011
|
C | T | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+3924G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924011 | ||||||
| chr9:104924073
|
A | G | 48 | a0001c0001t0001g0102a0001c0001t0039g0246a0001c0005t0002g0031others(45): Show | 48 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.-93+3862T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924073 | ||||||
| chr9:104924124
|
C | T | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+3811G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924124 | ||||||
| chr9:104924311
|
T | TA | 84 | a0001c0001t0001g0121a0001c0001t0001g0291a0001c0001t0002g0137others(81): Show | 84 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.-93+3623dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924311 | ||||||
| chr9:104924467
|
G | A | 1 | a0034c0103t0007g0240 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-93+3468C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924467 | ||||||
| chr9:104924471
|
G | A | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+3464C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924471 | ||||||
| chr9:104924542
|
G | A | 84 | a0001c0001t0001g0121a0001c0001t0001g0291a0001c0001t0002g0137others(81): Show | 84 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.-93+3393C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924542 | ||||||
| chr9:104924611
|
G | GA | 13 | a0001c0001t0001g0016a0001c0001t0004g0021a0001c0005t0002g0017others(10): Show | 13 | HG01099.hp1 HG01192.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+3323dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924611 | ||||||
| chr9:104924624
|
AAG | A | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+3309_-93+3310d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924624 | ||||||
| chr9:104924736
|
T | A | 4 | a0004c0042t0008g0158a0004c0113t0002g0159a0008c0006t0015g0095others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+3199A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924736 | ||||||
| chr9:104924752
|
C | G | 151 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(148): Show | 151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-93+3183G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924752 | ||||||
| chr9:104924823
|
C | T | 151 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(148): Show | 151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-93+3112G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924823 | ||||||
| chr9:104924854
|
T | A | 1 | a0009c0028t0048g0241 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-93+3081A>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924854 | ||||||
| chr9:104924870
|
C | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0003g0086others(29): Show | 32 | HG01070.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+3065G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924870 | ||||||
| chr9:104924912
|
A | C | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+3023T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924912 | ||||||
| chr9:104924941
|
G | A | 1 | a0002c0033t0032g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-93+2994C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924941 | ||||||
| chr9:104924980
|
G | A | 32 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0003g0086others(29): Show | 32 | HG01070.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+2955C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104924980 | ||||||
| chr9:104925144
|
C | T | 68 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-93+2791G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925144 | ||||||
| chr9:104925215
|
G | A | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+2720C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925215 | ||||||
| chr9:104925325
|
C | CG | 151 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(148): Show | 151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-93+2609_-93+2610i others(3): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925325 | ||||||
| chr9:104925375
|
C | CAAAAAAA others(3): Show |
57 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0002g0074others(54): Show | 57 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-93+2550_-93+2559d others(12): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925375 | ||||||
| chr9:104925375
|
C | CAAAAAAA others(4): Show |
8 | a0001c0001t0001g0077a0003c0002t0002g0172a0008c0006t0012g0081others(5): Show | 8 | HG01243.hp2 HG01261.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+2549_-93+2559d others(13): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925375 | ||||||
| chr9:104925417
|
A | T | 50 | a0001c0001t0001g0102a0001c0001t0039g0246a0001c0005t0002g0031others(47): Show | 50 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.-93+2518T>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925417 | ||||||
| chr9:104925430
|
C | T | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+2505G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925430 | ||||||
| chr9:104925500
|
A | G | 1 | a0007c0003t0004g0170 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-93+2435T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925500 | ||||||
| chr9:104925615
|
C | G | 3 | a0011c0010t0005g0169a0028c0095t0002g0114a0032c0104t0005g0168 | 3 | HG02280.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-93+2320G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925615 | ||||||
| chr9:104925625
|
G | T | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+2310C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925625 | ||||||
| chr9:104925778
|
G | A | 67 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-93+2157C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104925778 | ||||||
| chr9:104926016
|
T | TA | 84 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0088others(81): Show | 84 | HG00673.hp1 HG00738.hp1 HG01070.hp2 others(81): Show |
intron_variant | MODIFIER | c.-93+1918dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926016 | ||||||
| chr9:104926016
|
T | TAA | 87 | a0001c0001t0001g0121a0001c0001t0001g0291a0001c0001t0002g0137others(84): Show | 87 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.-93+1917_-93+1918d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926016 | ||||||
| chr9:104926206
|
C | G | 1 | a0017c0034t0001g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93+1729G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926206 | ||||||
| chr9:104926348
|
A | C | 171 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0102others(168): Show | 171 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(168): Show |
intron_variant | MODIFIER | c.-93+1587T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926348 | ||||||
| chr9:104926436
|
G | A | 2 | a0004c0043t0003g0128a0004c0043t0003g0136 | 2 | HG01952.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-93+1499C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926436 | ||||||
| chr9:104926441
|
C | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0003g0086others(27): Show | 30 | HG01070.hp2 HG01099.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+1494G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926441 | ||||||
| chr9:104926449
|
CA | C | 71 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-93+1485delT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926449 | ||||||
| chr9:104926449
|
CAA | C | 160 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0102others(157): Show | 160 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(157): Show |
intron_variant | MODIFIER | c.-93+1484_-93+1485d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926449 | ||||||
| chr9:104926459
|
AAC | A | 9 | a0001c0001t0001g0291a0002c0017t0026g0163a0003c0038t0003g0293others(6): Show | 9 | HG00741.hp1 HG01346.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-93+1474_-93+1475d others(4): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926459 | ||||||
| chr9:104926460
|
A | C | 1 | a0017c0034t0001g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93+1475T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926460 | ||||||
| chr9:104926470
|
C | CA | 32 | a0001c0001t0003g0297a0001c0001t0023g0295a0001c0001t0023g0296others(29): Show | 32 | HG00558.hp1 HG01081.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+1464dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926470 | ||||||
| chr9:104926474
|
A | C | 18 | a0001c0001t0001g0016a0001c0001t0004g0021a0001c0001t0043g0002others(15): Show | 18 | HG01099.hp1 HG01192.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+1461T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926474 | ||||||
| chr9:104926475
|
A | C | 54 | a0001c0001t0001g0102a0001c0001t0039g0246a0001c0005t0002g0031others(51): Show | 54 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.-93+1460T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926475 | ||||||
| chr9:104926477
|
A | C | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1458T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926477 | ||||||
| chr9:104926478
|
A | C | 1 | a0001c0001t0043g0002 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-93+1457T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926478 | ||||||
| chr9:104926479
|
A | C | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1456T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926479 | ||||||
| chr9:104926480
|
A | G | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1455T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926480 | ||||||
| chr9:104926481
|
A | C | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1454T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926481 | ||||||
| chr9:104926482
|
A | G | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1453T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926482 | ||||||
| chr9:104926483
|
AC | A | 11 | a0001c0001t0001g0016a0001c0001t0004g0021a0001c0005t0002g0017others(8): Show | 11 | HG01099.hp1 HG01192.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-93+1451delG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926483 | ||||||
| chr9:104926484
|
C | A | 159 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0121others(156): Show | 159 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(156): Show |
intron_variant | MODIFIER | c.-93+1451G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926484 | ||||||
| chr9:104926484
|
C | G | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1451G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926484 | ||||||
| chr9:104926486
|
A | C | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1449T>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926486 | ||||||
| chr9:104926488
|
A | G | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1447T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926488 | ||||||
| chr9:104926489
|
C | A | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1446G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926489 | ||||||
| chr9:104926489
|
C | T | 50 | a0001c0001t0001g0102a0001c0001t0039g0246a0001c0005t0002g0031others(47): Show | 50 | HG00673.hp1 HG00738.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.-93+1446G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926489 | ||||||
| chr9:104926490
|
G | T | 1 | a0007c0003t0014g0030 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-93+1445C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926490 | ||||||
| chr9:104926611
|
C | T | 46 | a0001c0001t0001g0121a0001c0001t0002g0137a0001c0001t0012g0144others(43): Show | 46 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-93+1324G>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926611 | ||||||
| chr9:104926635
|
C | CG | 27 | a0001c0001t0001g0121a0001c0005t0002g0123a0001c0005t0002g0129others(24): Show | 27 | HG00642.hp1 HG00673.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-93+1299dupC | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926635 | ||||||
| chr9:104926739
|
T | C | 3 | a0002c0033t0032g0024a0004c0029t0005g0023a0008c0048t0030g0022 | 3 | HG01081.hp2 HG02896.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-93+1196A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926739 | ||||||
| chr9:104926754
|
G | T | 47 | a0001c0001t0001g0121a0001c0001t0002g0137a0001c0001t0012g0144others(44): Show | 47 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-93+1181C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926754 | ||||||
| chr9:104926758
|
C | G | 1 | a0012c0093t0001g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-93+1177G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926758 | ||||||
| chr9:104926761
|
C | A | 172 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0102others(169): Show | 172 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(169): Show |
intron_variant | MODIFIER | c.-93+1174G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926761 | ||||||
| chr9:104926782
|
T | G | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-93+1153A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926782 | ||||||
| chr9:104926969
|
G | T | 172 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0102others(169): Show | 172 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(169): Show |
intron_variant | MODIFIER | c.-93+966C>A | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104926969 | ||||||
| chr9:104927008
|
T | G | 12 | a0001c0001t0001g0291a0001c0001t0003g0297a0001c0001t0023g0295others(9): Show | 12 | HG00741.hp1 HG01081.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93+927A>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927008 | ||||||
| chr9:104927019
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-93+916G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927019 | ||||||
| chr9:104927071
|
A | G | 172 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0102others(169): Show | 172 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(169): Show |
intron_variant | MODIFIER | c.-93+864T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927071 | ||||||
| chr9:104927145
|
G | A | 4 | a0002c0015t0002g0315a0002c0032t0001g0317a0005c0070t0001g0316others(1): Show | 4 | HG01109.hp1 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+790C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927145 | ||||||
| chr9:104927212
|
G | GA | 62 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.-93+722dupT | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927212 | ||||||
| chr9:104927220
|
AG | A | 36 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0003g0086others(33): Show | 36 | HG00642.hp1 HG01070.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.-93+714delC | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927220 | ||||||
| chr9:104927221
|
G | A | 118 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0102others(115): Show | 118 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-93+714C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927221 | ||||||
| chr9:104927223
|
A | G | 16 | a0001c0001t0001g0088a0001c0001t0003g0086a0001c0001t0003g0089others(13): Show | 16 | HG01070.hp2 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-93+712T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927223 | ||||||
| chr9:104927232
|
G | C | 1 | a0002c0032t0001g0317 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-93+703C>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927232 | ||||||
| chr9:104927247
|
C | A | 14 | a0002c0015t0013g0305a0002c0015t0013g0306a0002c0033t0002g0301others(11): Show | 14 | HG01891.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+688G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927247 | ||||||
| chr9:104927309
|
C | A | 1 | a0028c0095t0002g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-93+626G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927309 | ||||||
| chr9:104927429
|
C | G | 59 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0082others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-93+506G>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927429 | ||||||
| chr9:104927521
|
T | C | 1 | a0002c0032t0001g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-93+414A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927521 | ||||||
| chr9:104927534
|
A | AC | 30 | a0001c0001t0001g0016a0001c0001t0004g0021a0001c0001t0043g0002others(27): Show | 30 | HG00642.hp1 HG01081.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-93+400dupG | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927534 | ||||||
| chr9:104927548
|
T | C | 2 | a0003c0077t0005g0312a0025c0083t0001g0313 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-93+387A>G | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927548 | ||||||
| chr9:104927584
|
G | A | 2 | a0002c0024t0008g0109a0012c0093t0001g0108 | 2 | HG01952.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-93+351C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927584 | ||||||
| chr9:104927675
|
GGGTCTCC others(19): Show |
G | 3 | a0002c0011t0004g0112a0004c0099t0001g0110a0008c0006t0007g0111 | 3 | HG02818.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-93+234_-93+259del others(26): Show |
ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927675 | ||||||
| chr9:104927758
|
G | A | 2 | a0002c0024t0008g0109a0012c0093t0001g0108 | 2 | HG01952.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-93+177C>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927758 | ||||||
| chr9:104927776
|
C | A | 112 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(109): Show | 112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-93+159G>T | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927776 | ||||||
| chr9:104927843
|
A | G | 108 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0077others(105): Show | 108 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-93+92T>C | ABCA1 | ENSG00000165029.17 | transcript | ENST00000374736.8 | protein_coding | 1/49 | chr9 | 104927843 |