Search by Gene
| geneid | 26154 |
|---|---|
| ensemblid | ENSG00000144452.15 |
| hgncid | 14637 |
| symbol | ABCA12 |
| name | ATP binding cassette subfamily A member 12 |
| refseq_nuc | NM_173076.3 |
| refseq_prot | NP_775099.2 |
| ensembl_nuc | ENST00000272895.12 |
| ensembl_prot | ENSP00000272895.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 214931542 |
| end | 215138626 |
| strand | - |
| ver | v1.2 |
| region | chr2:214931542-215138626 |
| region5000 | chr2:214926542-215143626 |
| regionname0 | ABCA12_chr2_214931542_215138626 |
| regionname5000 | ABCA12_chr2_214926542_215143626 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2595 | 130 | 36 | 28 | 47 | 4 | 14 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002 | 0/0 | 2595 | 26 | 25 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003 | 0/0 | 2595 | 10 | 10 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004 | 0/0 | 2595 | 6 | 5 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0005 | 0/0 | 2595 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0006 | 0/0 | 2595 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0007 | 0/0 | 2595 | 3 | 0 | 3 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0008 | 0/0 | 2595 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0009 | 0/0 | 2595 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0010 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0011 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0012 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0013 | 1/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0014 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0015 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0016 | 0/0 | 2481 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0017 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0018 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0019 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0020 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0021 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0022 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 7788 | 21 | 2 | 5 | 9 | 1 | 4 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0002 | 0/1 | 7788 | 18 | 1 | 1 | 10 | 1 | 4 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0003 | 0/0 | 7788 | 16 | 2 | 4 | 9 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0004 | 0/0 | 7788 | 14 | 1 | 5 | 6 | 1 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0005 | 0/0 | 7788 | 8 | 7 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0006 | 0/0 | 7788 | 7 | 1 | 2 | 4 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0007 | 0/0 | 7788 | 7 | 7 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0008 | 0/0 | 7788 | 6 | 6 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0009 | 0/0 | 7788 | 5 | 0 | 1 | 4 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0010 | 0/0 | 7788 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0011 | 0/0 | 7788 | 5 | 0 | 3 | 0 | 0 | 2 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0012 | 0/0 | 7788 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0013 | 0/0 | 7788 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0014 | 0/0 | 7788 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0015 | 0/0 | 7788 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0016 | 0/0 | 7788 | 3 | 0 | 3 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0017 | 0/0 | 7788 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0018 | 0/0 | 7788 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0019 | 0/0 | 7788 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0020 | 0/0 | 7788 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0021 | 0/0 | 7788 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0022 | 0/0 | 7788 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0023 | 0/0 | 7788 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0024 | 0/0 | 7788 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0025 | 0/0 | 7788 | 2 | 1 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0026 | 0/0 | 7788 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0027 | 0/0 | 7788 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0028 | 0/0 | 7788 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0029 | 0/0 | 7788 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0030 | 0/0 | 7788 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0031 | 0/0 | 7788 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0032 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0033 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0034 | 0/0 | 7788 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0035 | 0/0 | 7788 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0036 | 0/0 | 7788 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0037 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0038 | 0/0 | 7788 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0039 | 0/0 | 7788 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0040 | 0/0 | 7788 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0041 | 0/0 | 7788 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0042 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0043 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0044 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0045 | 0/0 | 7788 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0046 | 0/0 | 7788 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0047 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0048 | 0/0 | 7788 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0049 | 0/0 | 7788 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0050 | 1/0 | 7788 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0051 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0052 | 0/0 | 7788 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0053 | 0/0 | 7788 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0054 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0055 | 0/0 | 7788 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0056 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0057 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0058 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0059 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0060 | 0/0 | 7788 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0061 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0062 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0063 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0064 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0065 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0066 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0067 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| c0068 | 0/0 | 7788 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1511 | 54 | 9 | 14 | 20 | 2 | 7 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0002 | 0/0 | 1515 | 36 | 4 | 12 | 14 | 1 | 5 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0003 | 0/0 | 1511 | 23 | 13 | 6 | 3 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0004 | 0/0 | 1512 | 14 | 14 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0005 | 0/0 | 1511 | 14 | 7 | 4 | 0 | 1 | 2 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0006 | 0/0 | 1511 | 11 | 10 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0007 | 0/0 | 1511 | 7 | 7 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0008 | 0/0 | 1513 | 7 | 3 | 0 | 4 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0009 | 0/0 | 1510 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0010 | 0/0 | 1513 | 4 | 0 | 0 | 3 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0011 | 0/0 | 1515 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0012 | 0/0 | 1517 | 3 | 1 | 1 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0013 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0014 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0015 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0016 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0017 | 0/0 | 1514 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0018 | 0/0 | 1510 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0019 | 0/0 | 1511 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0020 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0021 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0022 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0023 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0024 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0025 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| t0026 | 0/0 | 1513 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/0 | 21 | 2 | 5 | 9 | 1 | 4 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/1 | 18 | 1 | 1 | 10 | 1 | 4 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 16 | 2 | 4 | 9 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 14 | 1 | 5 | 6 | 1 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0016 | a0001 | c0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0021 | a0001 | c0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0022 | a0001 | c0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0023 | a0001 | c0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0025 | a0001 | c0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0029 | a0001 | c0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0031 | a0001 | c0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0032 | a0001 | c0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0033 | a0001 | c0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0035 | a0001 | c0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0040 | a0001 | c0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0041 | a0001 | c0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0042 | a0001 | c0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0043 | a0001 | c0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0044 | a0001 | c0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0049 | a0001 | c0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0051 | a0001 | c0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0068 | a0001 | c0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0007 | a0002 | c0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0008 | a0002 | c0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0013 | a0002 | c0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0017 | a0002 | c0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0027 | a0002 | c0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0054 | a0002 | c0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0056 | a0002 | c0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0057 | a0002 | c0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0058 | a0002 | c0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0014 | a0003 | c0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0020 | a0003 | c0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0065 | a0003 | c0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0066 | a0003 | c0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0067 | a0003 | c0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0018 | a0004 | c0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0059 | a0004 | c0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0060 | a0004 | c0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0061 | a0004 | c0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0005c0062 | a0005 | c0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0005c0063 | a0005 | c0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0005c0064 | a0005 | c0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0006c0019 | a0006 | c0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0007c0024 | a0007 | c0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0007c0034 | a0007 | c0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0008c0028 | a0008 | c0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0009c0026 | a0009 | c0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0010c0055 | a0010 | c0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0011c0053 | a0011 | c0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0012c0052 | a0012 | c0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0013c0050 | a0013 | c0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0014c0038 | a0014 | c0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0015c0045 | a0015 | c0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0016c0039 | a0016 | c0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0017c0046 | a0017 | c0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0018c0048 | a0018 | c0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0019c0047 | a0019 | c0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0020c0036 | a0020 | c0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0021c0037 | a0021 | c0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0022c0030 | a0022 | c0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 17 | 0 | 5 | 7 | 1 | 4 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/1 | 15 | 1 | 1 | 9 | 1 | 2 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0002t0011 | a0001 | c0002 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0002t0022 | a0001 | c0002 | t0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0002t0024 | a0001 | c0002 | t0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 12 | 1 | 4 | 6 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0003t0002 | a0001 | c0003 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0003t0006 | a0001 | c0003 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0003t0011 | a0001 | c0003 | t0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 10 | 1 | 3 | 4 | 1 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0004t0002 | a0001 | c0004 | t0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0004t0003 | a0001 | c0004 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0004t0010 | a0001 | c0004 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0005t0003 | a0001 | c0005 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0005t0005 | a0001 | c0005 | t0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0006t0002 | a0001 | c0006 | t0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0006t0005 | a0001 | c0006 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0006t0023 | a0001 | c0006 | t0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0009t0003 | a0001 | c0009 | t0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0009t0008 | a0001 | c0009 | t0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0009t0010 | a0001 | c0009 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0010t0002 | a0001 | c0010 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0010t0003 | a0001 | c0010 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0010t0004 | a0001 | c0010 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0010t0009 | a0001 | c0010 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0011t0001 | a0001 | c0011 | t0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0011t0005 | a0001 | c0011 | t0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0012t0004 | a0001 | c0012 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0012t0014 | a0001 | c0012 | t0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0015t0007 | a0001 | c0015 | t0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0015t0009 | a0001 | c0015 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0016t0002 | a0001 | c0016 | t0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0016t0005 | a0001 | c0016 | t0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0021t0003 | a0001 | c0021 | t0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0021t0010 | a0001 | c0021 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0022t0006 | a0001 | c0022 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0022t0019 | a0001 | c0022 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0023t0003 | a0001 | c0023 | t0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0025t0003 | a0001 | c0025 | t0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0025t0015 | a0001 | c0025 | t0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0029t0002 | a0001 | c0029 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0031t0005 | a0001 | c0031 | t0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0032t0006 | a0001 | c0032 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0033t0026 | a0001 | c0033 | t0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0035t0002 | a0001 | c0035 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0040t0008 | a0001 | c0040 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0041t0003 | a0001 | c0041 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0042t0013 | a0001 | c0042 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0043t0006 | a0001 | c0043 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0044t0004 | a0001 | c0044 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0049t0002 | a0001 | c0049 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0051t0004 | a0001 | c0051 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0001c0068t0003 | a0001 | c0068 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0007t0002 | a0002 | c0007 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0007t0003 | a0002 | c0007 | t0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0007t0004 | a0002 | c0007 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0007t0006 | a0002 | c0007 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0007t0017 | a0002 | c0007 | t0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0008t0004 | a0002 | c0008 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0008t0007 | a0002 | c0008 | t0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0013t0003 | a0002 | c0013 | t0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0013t0008 | a0002 | c0013 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0013t0018 | a0002 | c0013 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0017t0009 | a0002 | c0017 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0017t0016 | a0002 | c0017 | t0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0027t0003 | a0002 | c0027 | t0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0054t0009 | a0002 | c0054 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0056t0004 | a0002 | c0056 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0057t0006 | a0002 | c0057 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0002c0058t0002 | a0002 | c0058 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0014t0002 | a0003 | c0014 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0014t0006 | a0003 | c0014 | t0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0020t0001 | a0003 | c0020 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0020t0003 | a0003 | c0020 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0020t0008 | a0003 | c0020 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0065t0001 | a0003 | c0065 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0066t0004 | a0003 | c0066 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0003c0067t0025 | a0003 | c0067 | t0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0018t0005 | a0004 | c0018 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0018t0008 | a0004 | c0018 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0018t0021 | a0004 | c0018 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0059t0004 | a0004 | c0059 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0060t0006 | a0004 | c0060 | t0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0004c0061t0015 | a0004 | c0061 | t0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0005c0062t0004 | a0005 | c0062 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0005c0063t0003 | a0005 | c0063 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0005c0064t0004 | a0005 | c0064 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0006c0019t0001 | a0006 | c0019 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0007c0024t0005 | a0007 | c0024 | t0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0007c0034t0005 | a0007 | c0034 | t0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0008c0028t0003 | a0008 | c0028 | t0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0009c0026t0003 | a0009 | c0026 | t0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0010c0055t0010 | a0010 | c0055 | t0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0011c0053t0002 | a0011 | c0053 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0012c0052t0001 | a0012 | c0052 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0013c0050t0001 | a0013 | c0050 | t0001 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0014c0038t0008 | a0014 | c0038 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0015c0045t0002 | a0015 | c0045 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0016c0039t0012 | a0016 | c0039 | t0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0017c0046t0001 | a0017 | c0046 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0018c0048t0001 | a0018 | c0048 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0019c0047t0003 | a0019 | c0047 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0020c0036t0001 | a0020 | c0036 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0021c0037t0004 | a0021 | c0037 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| a0022c0030t0001 | a0022 | c0030 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0025 | a0001 | c0001 | t0002 | g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0035 | a0001 | c0001 | t0002 | g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0130 | a0001 | c0001 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0140 | a0001 | c0001 | t0002 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0150 | a0001 | c0001 | t0002 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0154 | a0001 | c0001 | t0002 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0002g0170 | a0001 | c0001 | t0002 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0012g0191 | a0001 | c0001 | t0012 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0012g0192 | a0001 | c0001 | t0012 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0013g0040 | a0001 | c0001 | t0013 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0001t0020g0155 | a0001 | c0001 | t0020 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0027 | a0001 | c0002 | t0001 | g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0028 | a0001 | c0002 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0033 | a0001 | c0002 | t0001 | g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0043 | a0001 | c0002 | t0001 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0050 | a0001 | c0002 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0051 | a0001 | c0002 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0055 | a0001 | c0002 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0058 | a0001 | c0002 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0060 | a0001 | c0002 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0061 | a0001 | c0002 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0141 | a0001 | c0002 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0151 | a0001 | c0002 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0156 | a0001 | c0002 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0161 | a0001 | c0002 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0001g0163 | a0001 | c0002 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0011g0165 | a0001 | c0002 | t0011 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0022g0148 | a0001 | c0002 | t0022 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0002t0024g0178 | a0001 | c0002 | t0024 | g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0032 | a0001 | c0003 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0034 | a0001 | c0003 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0036 | a0001 | c0003 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0038 | a0001 | c0003 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0044 | a0001 | c0003 | t0001 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0122 | a0001 | c0003 | t0001 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0134 | a0001 | c0003 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0147 | a0001 | c0003 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0159 | a0001 | c0003 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0166 | a0001 | c0003 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0172 | a0001 | c0003 | t0001 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0001g0173 | a0001 | c0003 | t0001 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0002g0037 | a0001 | c0003 | t0002 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0006g0048 | a0001 | c0003 | t0006 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0011g0120 | a0001 | c0003 | t0011 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0003t0011g0139 | a0001 | c0003 | t0011 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0026 | a0001 | c0004 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0029 | a0001 | c0004 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0042 | a0001 | c0004 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0054 | a0001 | c0004 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0091 | a0001 | c0004 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0092 | a0001 | c0004 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0115 | a0001 | c0004 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0127 | a0001 | c0004 | t0001 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0133 | a0001 | c0004 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0001g0160 | a0001 | c0004 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0002g0137 | a0001 | c0004 | t0002 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0002g0138 | a0001 | c0004 | t0002 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0003g0062 | a0001 | c0004 | t0003 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0004t0010g0198 | a0001 | c0004 | t0010 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0001g0125 | a0001 | c0005 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0001g0145 | a0001 | c0005 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0003g0077 | a0001 | c0005 | t0003 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0005g0075 | a0001 | c0005 | t0005 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0005g0109 | a0001 | c0005 | t0005 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0005g0110 | a0001 | c0005 | t0005 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0005g0111 | a0001 | c0005 | t0005 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0005t0005g0167 | a0001 | c0005 | t0005 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0006t0002g0116 | a0001 | c0006 | t0002 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0006t0002g0124 | a0001 | c0006 | t0002 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0006t0002g0135 | a0001 | c0006 | t0002 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0006t0002g0142 | a0001 | c0006 | t0002 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0006t0002g0171 | a0001 | c0006 | t0002 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0006t0005g0152 | a0001 | c0006 | t0005 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0006t0023g0146 | a0001 | c0006 | t0023 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0009t0001g0136 | a0001 | c0009 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0009t0003g0157 | a0001 | c0009 | t0003 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0009t0008g0188 | a0001 | c0009 | t0008 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0009t0008g0189 | a0001 | c0009 | t0008 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0009t0010g0187 | a0001 | c0009 | t0010 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0010t0002g0168 | a0001 | c0010 | t0002 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0010t0003g0143 | a0001 | c0010 | t0003 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0010t0004g0113 | a0001 | c0010 | t0004 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0010t0004g0114 | a0001 | c0010 | t0004 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0010t0009g0001 | a0001 | c0010 | t0009 | g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0011t0001g0085 | a0001 | c0011 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0011t0001g0087 | a0001 | c0011 | t0001 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0011t0001g0126 | a0001 | c0011 | t0001 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0011t0005g0088 | a0001 | c0011 | t0005 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0011t0005g0089 | a0001 | c0011 | t0005 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0012t0004g0039 | a0001 | c0012 | t0004 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0012t0004g0065 | a0001 | c0012 | t0004 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0012t0014g0015 | a0001 | c0012 | t0014 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0012t0014g0097 | a0001 | c0012 | t0014 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0015t0007g0009 | a0001 | c0015 | t0007 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0015t0007g0013 | a0001 | c0015 | t0007 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0015t0009g0006 | a0001 | c0015 | t0009 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0016t0002g0086 | a0001 | c0016 | t0002 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0016t0002g0090 | a0001 | c0016 | t0002 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0016t0005g0063 | a0001 | c0016 | t0005 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0021t0003g0174 | a0001 | c0021 | t0003 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0021t0010g0194 | a0001 | c0021 | t0010 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0022t0006g0112 | a0001 | c0022 | t0006 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0022t0019g0014 | a0001 | c0022 | t0019 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0023t0003g0024 | a0001 | c0023 | t0003 | g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0023t0003g0153 | a0001 | c0023 | t0003 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0025t0003g0064 | a0001 | c0025 | t0003 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0025t0015g0182 | a0001 | c0025 | t0015 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0029t0002g0031 | a0001 | c0029 | t0002 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0031t0005g0158 | a0001 | c0031 | t0005 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0032t0006g0041 | a0001 | c0032 | t0006 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0033t0026g0193 | a0001 | c0033 | t0026 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0035t0002g0144 | a0001 | c0035 | t0002 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0040t0008g0186 | a0001 | c0040 | t0008 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0041t0003g0164 | a0001 | c0041 | t0003 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0042t0013g0045 | a0001 | c0042 | t0013 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0043t0006g0022 | a0001 | c0043 | t0006 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0044t0004g0067 | a0001 | c0044 | t0004 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0049t0002g0057 | a0001 | c0049 | t0002 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0051t0004g0076 | a0001 | c0051 | t0004 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0001c0068t0003g0016 | a0001 | c0068 | t0003 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0007t0002g0105 | a0002 | c0007 | t0002 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0007t0003g0017 | a0002 | c0007 | t0003 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0007t0003g0069 | a0002 | c0007 | t0003 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0007t0004g0149 | a0002 | c0007 | t0004 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0007t0006g0175 | a0002 | c0007 | t0006 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0007t0006g0176 | a0002 | c0007 | t0006 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0007t0017g0012 | a0002 | c0007 | t0017 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0008t0004g0021 | a0002 | c0008 | t0004 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0008t0007g0003 | a0002 | c0008 | t0007 | g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0008t0007g0005 | a0002 | c0008 | t0007 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0008t0007g0008 | a0002 | c0008 | t0007 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0008t0007g0010 | a0002 | c0008 | t0007 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0008t0007g0011 | a0002 | c0008 | t0007 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0013t0003g0018 | a0002 | c0013 | t0003 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0013t0003g0019 | a0002 | c0013 | t0003 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0013t0008g0190 | a0002 | c0013 | t0008 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0013t0018g0002 | a0002 | c0013 | t0018 | g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0017t0009g0007 | a0002 | c0017 | t0009 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0017t0016g0179 | a0002 | c0017 | t0016 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0017t0016g0180 | a0002 | c0017 | t0016 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0027t0003g0073 | a0002 | c0027 | t0003 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0027t0003g0074 | a0002 | c0027 | t0003 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0054t0009g0004 | a0002 | c0054 | t0009 | g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0056t0004g0020 | a0002 | c0056 | t0004 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0057t0006g0177 | a0002 | c0057 | t0006 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0002c0058t0002g0072 | a0002 | c0058 | t0002 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0014t0002g0101 | a0003 | c0014 | t0002 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0014t0006g0098 | a0003 | c0014 | t0006 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0014t0006g0102 | a0003 | c0014 | t0006 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0014t0006g0107 | a0003 | c0014 | t0006 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0020t0001g0106 | a0003 | c0020 | t0001 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0020t0003g0108 | a0003 | c0020 | t0003 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0020t0008g0197 | a0003 | c0020 | t0008 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0065t0001g0103 | a0003 | c0065 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0066t0004g0104 | a0003 | c0066 | t0004 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0003c0067t0025g0183 | a0003 | c0067 | t0025 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0004c0018t0005g0095 | a0004 | c0018 | t0005 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0004c0018t0008g0196 | a0004 | c0018 | t0008 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0004c0018t0021g0082 | a0004 | c0018 | t0021 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0004c0059t0004g0071 | a0004 | c0059 | t0004 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0004c0060t0006g0080 | a0004 | c0060 | t0006 | g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0004c0061t0015g0181 | a0004 | c0061 | t0015 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0005c0062t0004g0078 | a0005 | c0062 | t0004 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0005c0063t0003g0079 | a0005 | c0063 | t0003 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0005c0064t0004g0070 | a0005 | c0064 | t0004 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0006c0019t0001g0096 | a0006 | c0019 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0006c0019t0001g0099 | a0006 | c0019 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0006c0019t0001g0100 | a0006 | c0019 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0007c0024t0005g0093 | a0007 | c0024 | t0005 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0007c0024t0005g0094 | a0007 | c0024 | t0005 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0007c0034t0005g0169 | a0007 | c0034 | t0005 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0008c0028t0003g0081 | a0008 | c0028 | t0003 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0008c0028t0003g0083 | a0008 | c0028 | t0003 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0009c0026t0003g0053 | a0009 | c0026 | t0003 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0009c0026t0003g0056 | a0009 | c0026 | t0003 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0010c0055t0010g0184 | a0010 | c0055 | t0010 | g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0011c0053t0002g0129 | a0011 | c0053 | t0002 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0012c0052t0001g0128 | a0012 | c0052 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0013c0050t0001g0049 | a0013 | c0050 | t0001 | g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0014c0038t0008g0195 | a0014 | c0038 | t0008 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0015c0045t0002g0162 | a0015 | c0045 | t0002 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0016c0039t0012g0185 | a0016 | c0039 | t0012 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0017c0046t0001g0046 | a0017 | c0046 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0018c0048t0001g0068 | a0018 | c0048 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0019c0047t0003g0052 | a0019 | c0047 | t0003 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0020c0036t0001g0084 | a0020 | c0036 | t0001 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0021c0037t0004g0023 | a0021 | c0037 | t0004 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| a0022c0030t0001g0047 | a0022 | c0030 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA12_chr2_214926542_215143626 | ABCA12 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0091 | EUR | GBR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00423 | hp1 | a0015 | c0045 | t0002 | g0162 | EAS | CHS | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | CHS | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00438 | hp1 | a0001 | c0003 | t0011 | g0139 | EAS | CHS | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | CHS | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00735 | hp1 | a0001 | c0035 | t0002 | g0144 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00735 | hp2 | a0001 | c0023 | t0003 | g0024 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG00741 | hp2 | a0020 | c0036 | t0001 | g0084 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01070 | hp2 | a0009 | c0026 | t0003 | g0056 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01071 | hp1 | a0009 | c0026 | t0003 | g0053 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01074 | hp2 | a0001 | c0016 | t0005 | g0063 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01106 | hp1 | a0001 | c0006 | t0002 | g0142 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0125 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01243 | hp1 | a0004 | c0060 | t0006 | g0080 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01243 | hp2 | a0016 | c0039 | t0012 | g0185 | AMR | PUR | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01255 | hp1 | a0001 | c0009 | t0003 | g0157 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01255 | hp2 | a0007 | c0024 | t0005 | g0094 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01258 | hp1 | a0001 | c0011 | t0001 | g0087 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01346 | hp1 | a0022 | c0030 | t0001 | g0047 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0138 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01517 | hp1 | a0001 | c0031 | t0005 | g0158 | EUR | IBS | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0028 | EUR | IBS | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01884 | hp1 | a0001 | c0042 | t0013 | g0045 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01884 | hp2 | a0001 | c0010 | t0009 | g0001 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01891 | hp1 | a0003 | c0066 | t0004 | g0104 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0054 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01928 | hp1 | a0001 | c0011 | t0001 | g0126 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0172 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0092 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01934 | hp2 | a0001 | c0006 | t0002 | g0135 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01943 | hp1 | a0007 | c0024 | t0005 | g0093 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01943 | hp2 | a0001 | c0004 | t0002 | g0137 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0127 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01975 | hp2 | a0002 | c0027 | t0003 | g0073 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01978 | hp1 | a0001 | c0021 | t0003 | g0174 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0122 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01993 | hp2 | a0007 | c0034 | t0005 | g0169 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02004 | hp1 | a0001 | c0016 | t0002 | g0090 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0173 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0160 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02055 | hp1 | a0002 | c0007 | t0003 | g0017 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02055 | hp2 | a0003 | c0014 | t0006 | g0098 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02132 | hp1 | a0001 | c0021 | t0010 | g0194 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02132 | hp2 | a0001 | c0029 | t0002 | g0031 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02155 | hp1 | a0001 | c0004 | t0001 | g0115 | EAS | CDX | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02155 | hp2 | a0001 | c0004 | t0003 | g0062 | EAS | CDX | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02257 | hp1 | a0003 | c0014 | t0006 | g0107 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02257 | hp2 | a0001 | c0012 | t0014 | g0015 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02258 | hp1 | a0001 | c0032 | t0006 | g0041 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0192 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02280 | hp1 | a0001 | c0005 | t0003 | g0077 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02280 | hp2 | a0002 | c0013 | t0008 | g0190 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02293 | hp1 | a0001 | c0011 | t0001 | g0085 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0042 | AMR | PEL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02451 | hp1 | a0003 | c0020 | t0003 | g0108 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02451 | hp2 | a0004 | c0018 | t0021 | g0082 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02523 | hp1 | a0001 | c0001 | t0020 | g0155 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02523 | hp2 | a0001 | c0006 | t0002 | g0116 | EAS | KHV | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02572 | hp1 | a0002 | c0007 | t0002 | g0105 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02572 | hp2 | a0005 | c0063 | t0003 | g0079 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02615 | hp1 | a0001 | c0010 | t0004 | g0113 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02615 | hp2 | a0003 | c0067 | t0025 | g0183 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02622 | hp1 | a0002 | c0007 | t0004 | g0149 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02622 | hp2 | a0019 | c0047 | t0003 | g0052 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02630 | hp1 | a0005 | c0062 | t0004 | g0078 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02630 | hp2 | a0001 | c0010 | t0003 | g0143 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02647 | hp1 | a0002 | c0056 | t0004 | g0020 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02647 | hp2 | a0001 | c0044 | t0004 | g0067 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02717 | hp1 | a0001 | c0051 | t0004 | g0076 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02717 | hp2 | a0001 | c0025 | t0015 | g0182 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02723 | hp1 | a0001 | c0022 | t0019 | g0014 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02723 | hp2 | a0001 | c0043 | t0006 | g0022 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02738 | hp1 | a0001 | c0002 | t0024 | g0178 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02809 | hp1 | a0004 | c0018 | t0005 | g0095 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02818 | hp1 | a0003 | c0014 | t0002 | g0101 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02818 | hp2 | a0002 | c0007 | t0017 | g0012 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02886 | hp1 | a0002 | c0017 | t0009 | g0007 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02886 | hp2 | a0006 | c0019 | t0001 | g0099 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02895 | hp1 | a0002 | c0017 | t0016 | g0179 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02895 | hp2 | a0002 | c0007 | t0003 | g0069 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02896 | hp1 | a0002 | c0057 | t0006 | g0177 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02896 | hp2 | a0001 | c0005 | t0005 | g0111 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02897 | hp1 | a0001 | c0005 | t0005 | g0110 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02897 | hp2 | a0002 | c0017 | t0016 | g0180 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02922 | hp1 | a0001 | c0012 | t0014 | g0097 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02922 | hp2 | a0005 | c0064 | t0004 | g0070 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03041 | hp1 | a0002 | c0008 | t0007 | g0008 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03098 | hp1 | a0001 | c0010 | t0002 | g0168 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03098 | hp2 | a0001 | c0003 | t0006 | g0048 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03130 | hp1 | a0001 | c0068 | t0003 | g0016 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03130 | hp2 | a0006 | c0019 | t0001 | g0096 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03139 | hp1 | a0001 | c0012 | t0004 | g0065 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03139 | hp2 | a0002 | c0007 | t0006 | g0176 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03195 | hp1 | a0006 | c0019 | t0001 | g0100 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03195 | hp2 | a0002 | c0058 | t0002 | g0072 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03209 | hp1 | a0002 | c0013 | t0003 | g0018 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03209 | hp2 | a0001 | c0005 | t0005 | g0109 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03225 | hp1 | a0003 | c0020 | t0008 | g0197 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03225 | hp2 | a0002 | c0008 | t0007 | g0011 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03453 | hp1 | a0001 | c0006 | t0005 | g0152 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03453 | hp2 | a0002 | c0054 | t0009 | g0004 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03486 | hp1 | a0001 | c0005 | t0005 | g0075 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03486 | hp2 | a0001 | c0005 | t0005 | g0167 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03490 | hp1 | a0010 | c0055 | t0010 | g0184 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03490 | hp2 | a0001 | c0011 | t0005 | g0088 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03492 | hp1 | a0001 | c0011 | t0005 | g0089 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03492 | hp2 | a0001 | c0049 | t0002 | g0057 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03516 | hp1 | a0002 | c0007 | t0006 | g0175 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03516 | hp2 | a0004 | c0059 | t0004 | g0071 | AFR | ESN | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0040 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03540 | hp2 | a0001 | c0012 | t0004 | g0039 | AFR | GWD | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03579 | hp1 | a0002 | c0008 | t0007 | g0010 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03579 | hp2 | a0021 | c0037 | t0004 | g0023 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0029 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0166 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03669 | hp2 | a0018 | c0048 | t0001 | g0068 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03710 | hp1 | a0017 | c0046 | t0001 | g0046 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03710 | hp2 | a0001 | c0025 | t0003 | g0064 | SAS | PJL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | BEB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18522 | hp1 | a0001 | c0015 | t0007 | g0009 | AFR | YRI | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18522 | hp2 | a0003 | c0020 | t0001 | g0106 | AFR | YRI | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18906 | hp1 | a0004 | c0061 | t0015 | g0181 | AFR | YRI | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18906 | hp2 | a0003 | c0065 | t0001 | g0103 | AFR | YRI | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18951 | hp1 | a0001 | c0041 | t0003 | g0164 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18962 | hp2 | a0001 | c0009 | t0010 | g0187 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18971 | hp1 | a0014 | c0038 | t0008 | g0195 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18971 | hp2 | a0001 | c0006 | t0023 | g0146 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18981 | hp1 | a0001 | c0040 | t0008 | g0186 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18984 | hp1 | a0001 | c0006 | t0002 | g0124 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA18984 | hp2 | a0001 | c0009 | t0001 | g0136 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19000 | hp2 | a0001 | c0001 | t0012 | g0191 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19002 | hp2 | a0001 | c0004 | t0001 | g0026 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19007 | hp2 | a0001 | c0009 | t0008 | g0188 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19009 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19060 | hp2 | a0001 | c0003 | t0011 | g0120 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19070 | hp1 | a0001 | c0009 | t0008 | g0189 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19070 | hp2 | a0011 | c0053 | t0002 | g0129 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19088 | hp2 | a0001 | c0023 | t0003 | g0153 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19090 | hp1 | a0001 | c0006 | t0002 | g0171 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19090 | hp2 | a0001 | c0004 | t0010 | g0198 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19091 | hp2 | a0001 | c0002 | t0011 | g0165 | EAS | JPT | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19240 | hp1 | a0002 | c0013 | t0018 | g0002 | AFR | YRI | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA19240 | hp2 | a0008 | c0028 | t0003 | g0083 | AFR | YRI | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA20129 | hp1 | a0008 | c0028 | t0003 | g0081 | AFR | ASW | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA20129 | hp2 | a0002 | c0008 | t0004 | g0021 | AFR | ASW | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA20905 | hp1 | a0001 | c0002 | t0022 | g0148 | SAS | GIH | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA20905 | hp2 | a0012 | c0052 | t0001 | g0128 | SAS | GIH | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG01123 | hp2 | a0001 | c0016 | t0002 | g0086 | AMR | CLM | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02109 | hp1 | a0001 | c0033 | t0026 | g0193 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02109 | hp2 | a0001 | c0010 | t0004 | g0114 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02486 | hp1 | a0003 | c0014 | t0006 | g0102 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02486 | hp2 | a0002 | c0027 | t0003 | g0074 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02559 | hp1 | a0002 | c0008 | t0007 | g0003 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG02559 | hp2 | a0001 | c0022 | t0006 | g0112 | AFR | ACB | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03471 | hp1 | a0001 | c0015 | t0009 | g0006 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG03471 | hp2 | a0002 | c0013 | t0003 | g0019 | AFR | MSL | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG06807 | hp1 | a0004 | c0018 | t0008 | g0196 | AFR | USA | ABCA12_chr2_214926542_215143626 | ABCA12 |
| HG06807 | hp2 | a0001 | c0015 | t0007 | g0013 | AFR | USA | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | USA | ABCA12_chr2_214926542_215143626 | ABCA12 |
| NA20300 | hp2 | a0002 | c0008 | t0007 | g0005 | AFR | USA | ABCA12_chr2_214926542_215143626 | ABCA12 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0033 | REF | REF | ABCA12_chr2_214926542_215143626 | ABCA12 |
| homoSapiens_grch38 | hp1 | a0013 | c0050 | t0001 | g0049 | REF | REF | ABCA12_chr2_214926542_215143626 | ABCA12 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214934127
|
G | A | 1 | a0017 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.7631C>T | p.Thr2544Ile | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/53 | 8049/9298 | 7631/7788 | 2544/2595 | chr2 | 214934127 | ||
| chr2:214937608
|
G | A | 1 | a0016 | 1 | HG01243.hp2 | stop_gained | HIGH | c.7444C>T | p.Arg2482* | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/53 | 7862/9298 | 7444/7788 | 2482/2595 | chr2 | 214937608 | ||
| chr2:214948607
|
C | T | 2 | a0010a0018 | 2 | HG03490.hp1 HG03669.hp2 |
missense_variant | MODERATE | c.7093G>A | p.Asp2365Asn | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/53 | 7511/9298 | 7093/7788 | 2365/2595 | chr2 | 214948607 | ||
| chr2:214951083
|
C | A | 1 | a0007 | 3 | HG01255.hp2 HG01943.hp1 HG01993.hp2 |
missense_variant&splice_region_variant | MODERATE | c.6648G>T | p.Arg2216Ser | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/53 | 7066/9298 | 6648/7788 | 2216/2595 | chr2 | 214951083 | ||
| chr2:214958415
|
G | C | 2 | a0008a0019 | 3 | HG02622.hp2 NA19240.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.5979C>G | p.Ile1993Met | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/53 | 6397/9298 | 5979/7788 | 1993/2595 | chr2 | 214958415 | ||
| chr2:214978346
|
C | G | 1 | a0015 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.5098G>C | p.Val1700Leu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 33/53 | 5516/9298 | 5098/7788 | 1700/2595 | chr2 | 214978346 | ||
| chr2:214978874
|
C | T | 1 | a0014 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.4907G>A | p.Arg1636Gln | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 32/53 | 5325/9298 | 4907/7788 | 1636/2595 | chr2 | 214978874 | ||
| chr2:214983804
|
T | C | 1 | a0020 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.4225A>G | p.Ile1409Val | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 29/53 | 4643/9298 | 4225/7788 | 1409/2595 | chr2 | 214983804 | ||
| chr2:214990845
|
T | A | 1 | a0009 | 2 | HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.3481A>T | p.Met1161Leu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 24/53 | 3899/9298 | 3481/7788 | 1161/2595 | chr2 | 214990845 | ||
| chr2:215000938
|
T | G | 1 | a0021 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.2946A>C | p.Lys982Asn | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 22/53 | 3364/9298 | 2946/7788 | 982/2595 | chr2 | 215000938 | ||
| chr2:215011442
|
A | T | 21 | a0001a0002a0003others(18): Show | 197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
missense_variant | MODERATE | c.2329T>A | p.Ser777Thr | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 17/53 | 2747/9298 | 2329/7788 | 777/2595 | chr2 | 215011442 | ||
| chr2:215012125
|
G | A | 1 | a0012 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1967C>T | p.Pro656Leu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 16/53 | 2385/9298 | 1967/7788 | 656/2595 | chr2 | 215012125 | ||
| chr2:215018025
|
G | T | 1 | a0022 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1765C>A | p.Pro589Thr | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 14/53 | 2183/9298 | 1765/7788 | 589/2595 | chr2 | 215018025 | ||
| chr2:215019344
|
T | C | 2 | a0003a0005 | 13 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
missense_variant | MODERATE | c.1649A>G | p.Glu550Gly | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 13/53 | 2067/9298 | 1649/7788 | 550/2595 | chr2 | 215019344 | ||
| chr2:215025738
|
A | G | 1 | a0009 | 2 | HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.1222T>C | p.Ser408Pro | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 11/53 | 1640/9298 | 1222/7788 | 408/2595 | chr2 | 215025738 | ||
| chr2:215036964
|
G | A | 1 | a0011 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.974C>T | p.Ser325Phe | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 8/53 | 1392/9298 | 974/7788 | 325/2595 | chr2 | 215036964 | ||
| chr2:215045850
|
G | C | 2 | a0003a0006 | 13 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
missense_variant | MODERATE | c.859C>G | p.Arg287Gly | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 7/53 | 1277/9298 | 859/7788 | 287/2595 | chr2 | 215045850 | ||
| chr2:215045888
|
T | C | 2 | a0003a0006 | 13 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
missense_variant | MODERATE | c.821A>G | p.Gln274Arg | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 7/53 | 1239/9298 | 821/7788 | 274/2595 | chr2 | 215045888 | ||
| chr2:215046000
|
T | G | 8 | a0002a0003a0004others(5): Show | 53 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(50): Show |
missense_variant | MODERATE | c.709A>C | p.Asn237His | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 7/53 | 1127/9298 | 709/7788 | 237/2595 | chr2 | 215046000 | ||
| chr2:215049722
|
C | G | 5 | a0003a0004a0005others(2): Show | 24 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
missense_variant | MODERATE | c.597G>C | p.Trp199Cys | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 6/53 | 1015/9298 | 597/7788 | 199/2595 | chr2 | 215049722 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214950912
|
T | C | 1 | a0002c0056 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.6819A>G | p.Val2273Val | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/53 | 7237/9298 | 6819/7788 | 2273/2595 | chr2 | 214950912 | ||
| chr2:214955289
|
G | A | 22 | a0001c0001a0001c0006a0001c0012others(19): Show | 57 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(54): Show |
synonymous_variant | LOW | c.6306C>T | p.Tyr2102Tyr | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/53 | 6724/9298 | 6306/7788 | 2102/2595 | chr2 | 214955289 | ||
| chr2:214959038
|
G | A | 4 | a0001c0022a0001c0032a0002c0057others(1): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
synonymous_variant | LOW | c.5925C>T | p.Asp1975Asp | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 40/53 | 6343/9298 | 5925/7788 | 1975/2595 | chr2 | 214959038 | ||
| chr2:214970344
|
T | A | 1 | a0001c0035 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.5619A>T | p.Val1873Val | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 37/53 | 6037/9298 | 5619/7788 | 1873/2595 | chr2 | 214970344 | ||
| chr2:214974840
|
T | C | 1 | a0011c0053 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.5406A>G | p.Ala1802Ala | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 35/53 | 5824/9298 | 5406/7788 | 1802/2595 | chr2 | 214974840 | ||
| chr2:214974846
|
C | T | 20 | a0001c0009a0001c0022a0001c0023others(17): Show | 39 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
synonymous_variant | LOW | c.5400G>A | p.Thr1800Thr | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 35/53 | 5818/9298 | 5400/7788 | 1800/2595 | chr2 | 214974846 | ||
| chr2:214975805
|
G | A | 2 | a0005c0063a0005c0064 | 2 | HG02572.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.5361C>T | p.Ser1787Ser | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 34/53 | 5779/9298 | 5361/7788 | 1787/2595 | chr2 | 214975805 | ||
| chr2:214978840
|
G | A | 1 | a0003c0066 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.4941C>T | p.Ile1647Ile | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 32/53 | 5359/9298 | 4941/7788 | 1647/2595 | chr2 | 214978840 | ||
| chr2:214983661
|
G | A | 1 | a0002c0058 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.4368C>T | p.His1456His | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 29/53 | 4786/9298 | 4368/7788 | 1456/2595 | chr2 | 214983661 | ||
| chr2:214986579
|
A | G | 27 | a0001c0005a0001c0009a0001c0010others(24): Show | 64 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(61): Show |
synonymous_variant | LOW | c.4126T>C | p.Leu1376Leu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 28/53 | 4544/9298 | 4126/7788 | 1376/2595 | chr2 | 214986579 | ||
| chr2:214989432
|
C | T | 7 | a0001c0011a0001c0016a0001c0031others(4): Show | 15 | HG01074.hp2 HG01123.hp2 HG01255.hp2 others(12): Show |
synonymous_variant | LOW | c.3726G>A | p.Pro1242Pro | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 26/53 | 4144/9298 | 3726/7788 | 1242/2595 | chr2 | 214989432 | ||
| chr2:214989568
|
G | A | 1 | a0001c0068 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.3678C>T | p.Tyr1226Tyr | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 25/53 | 4096/9298 | 3678/7788 | 1226/2595 | chr2 | 214989568 | ||
| chr2:215000851
|
T | C | 7 | a0001c0002a0001c0021a0001c0023others(4): Show | 26 | HG00438.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
synonymous_variant | LOW | c.3033A>G | p.Pro1011Pro | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 22/53 | 3451/9298 | 3033/7788 | 1011/2595 | chr2 | 215000851 | ||
| chr2:215011476
|
C | T | 2 | a0001c0051a0002c0008 | 7 | HG02559.hp1 HG02717.hp1 HG03041.hp1 others(4): Show |
synonymous_variant | LOW | c.2295G>A | p.Glu765Glu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 17/53 | 2713/9298 | 2295/7788 | 765/2595 | chr2 | 215011476 | ||
| chr2:215011647
|
T | C | 37 | a0001c0005a0001c0009a0001c0010others(34): Show | 89 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(86): Show |
splice_region_variant&synonymous_variant | LOW | c.2124A>G | p.Ala708Ala | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 17/53 | 2542/9298 | 2124/7788 | 708/2595 | chr2 | 215011647 | ||
| chr2:215019656
|
C | T | 4 | a0001c0012a0001c0015a0001c0022others(1): Show | 10 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
synonymous_variant | LOW | c.1428G>A | p.Ala476Ala | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 12/53 | 1846/9298 | 1428/7788 | 476/2595 | chr2 | 215019656 | ||
| chr2:215026868
|
A | G | 1 | a0004c0059 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1132T>C | p.Leu378Leu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 10/53 | 1550/9298 | 1132/7788 | 378/2595 | chr2 | 215026868 | ||
| chr2:215037050
|
C | T | 17 | a0001c0003a0001c0006a0001c0009others(14): Show | 47 | HG00423.hp2 HG00438.hp1 HG00735.hp1 others(44): Show |
synonymous_variant | LOW | c.888G>A | p.Val296Val | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 8/53 | 1306/9298 | 888/7788 | 296/2595 | chr2 | 215037050 | ||
| chr2:215049767
|
T | C | 14 | a0003c0014a0003c0020a0003c0065others(11): Show | 24 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
synonymous_variant | LOW | c.552A>G | p.Leu184Leu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 6/53 | 970/9298 | 552/7788 | 184/2595 | chr2 | 215049767 | ||
| chr2:215049770
|
T | C | 1 | a0001c0068 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.549A>G | p.Glu183Glu | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 6/53 | 967/9298 | 549/7788 | 183/2595 | chr2 | 215049770 | ||
| chr2:215052568
|
A | G | 1 | a0001c0029 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.426T>C | p.Ser142Ser | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 5/53 | 844/9298 | 426/7788 | 142/2595 | chr2 | 215052568 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214931578
|
G | GACAA | 21 | a0001c0001t0002a0001c0001t0012a0001c0002t0011others(18): Show | 45 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1052_*1055dupTTGT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 1055 | chr2 | 214931578 | |||||
| chr2:214931753
|
A | G | 13 | a0001c0003t0006a0001c0012t0014a0001c0022t0006others(10): Show | 17 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 881 | chr2 | 214931753 | |||||
| chr2:214931762
|
T | C | 1 | a0004c0018t0021 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 872 | chr2 | 214931762 | |||||
| chr2:214931844
|
T | C | 88 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(85): Show | 137 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*790A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 790 | chr2 | 214931844 | |||||
| chr2:214932094
|
A | AC | 18 | a0001c0001t0013a0001c0010t0004a0001c0012t0004others(15): Show | 26 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*539dupG | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 539 | chr2 | 214932094 | |||||
| chr2:214932149
|
A | G | 2 | a0001c0001t0013a0001c0042t0013 | 2 | HG01884.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*485T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 485 | chr2 | 214932149 | |||||
| chr2:214932608
|
C | T | 48 | a0001c0001t0002a0001c0001t0012a0001c0001t0020others(45): Show | 78 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 26 | chr2 | 214932608 | |||||
| chr2:214932627
|
G | GGAAGTGT others(29): Show |
1 | a0001c0006t0023 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6_*7insTCAGAGATGT others(26): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 53/53 | 6 | chr2 | 214932627 | |||||
| chr2:215138242
|
C | G | 1 | a0001c0022t0019 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34G>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 1/53 | 34 | chr2 | 215138242 | |||||
| chr2:215138559
|
G | GA | 5 | a0001c0002t0024a0001c0025t0015a0002c0017t0016others(2): Show | 6 | HG02615.hp2 HG02717.hp2 HG02738.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-352dupT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 1/53 | 352 | chr2 | 215138559 | |||||
| chr2:215138559
|
G | GAA | 13 | a0001c0001t0012a0001c0004t0010a0001c0009t0008others(10): Show | 15 | HG01243.hp2 HG02109.hp1 HG02132.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-353_-352dupTT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 1/53 | 352 | chr2 | 215138559 | |||||
| chr2:215138559
|
GA | G | 8 | a0001c0010t0009a0001c0015t0007a0001c0015t0009others(5): Show | 13 | HG01884.hp2 HG02559.hp1 HG02818.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-352delT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 1/53 | 352 | chr2 | 215138559 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:214932803
|
AATTC | A | 50 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.7681-66_7681-63del others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214932803 | ||||||
| chr2:214932830
|
C | T | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7681-89G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214932830 | ||||||
| chr2:214932939
|
G | GGGGCTTG others(10): Show |
1 | a0001c0006t0023g0146 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7681-215_7681-199d others(19): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214932939 | ||||||
| chr2:214933317
|
T | A | 1 | a0006c0019t0001g0100 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.7681-576A>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933317 | ||||||
| chr2:214933385
|
G | T | 8 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.7681-644C>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933385 | ||||||
| chr2:214933425
|
A | C | 197 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.7680+653T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933425 | ||||||
| chr2:214933507
|
A | G | 1 | a0001c0004t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.7680+571T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933507 | ||||||
| chr2:214933619
|
GT | G | 122 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(119): Show | 122 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.7680+458delA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933619 | ||||||
| chr2:214933626
|
G | A | 3 | a0008c0028t0003g0081a0008c0028t0003g0083a0019c0047t0003g0052 | 3 | HG02622.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.7680+452C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933626 | ||||||
| chr2:214933684
|
A | G | 116 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(113): Show | 116 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(113): Show |
intron_variant | MODIFIER | c.7680+394T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933684 | ||||||
| chr2:214933778
|
G | A | 65 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0033others(62): Show | 65 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.7680+300C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933778 | ||||||
| chr2:214933817
|
G | GT | 6 | a0001c0006t0005g0152a0001c0016t0005g0063a0001c0031t0005g0158others(3): Show | 6 | HG01074.hp2 HG01517.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7680+260dupA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933817 | ||||||
| chr2:214933911
|
C | T | 1 | a0019c0047t0003g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7680+167G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214933911 | ||||||
| chr2:214934000
|
A | C | 79 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(76): Show | 79 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.7680+78T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214934000 | ||||||
| chr2:214934046
|
G | A | 3 | a0001c0010t0004g0113a0001c0010t0004g0114a0002c0007t0004g0149 | 3 | HG02109.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.7680+32C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 52/52 | chr2 | 214934046 | ||||||
| chr2:214934373
|
T | C | 1 | a0010c0055t0010g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.7543-158A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214934373 | ||||||
| chr2:214934420
|
T | A | 1 | a0005c0064t0004g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7543-205A>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214934420 | ||||||
| chr2:214934605
|
G | A | 1 | a0001c0003t0001g0038 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.7543-390C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214934605 | ||||||
| chr2:214934718
|
A | G | 3 | a0001c0002t0001g0161a0001c0009t0010g0187a0001c0021t0010g0194 | 3 | HG02074.hp2 HG02132.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.7543-503T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214934718 | ||||||
| chr2:214934737
|
C | T | 1 | a0001c0003t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7543-522G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214934737 | ||||||
| chr2:214934913
|
A | ATTAG | 12 | a0001c0010t0004g0113a0001c0010t0004g0114a0001c0044t0004g0067others(9): Show | 12 | HG02109.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.7543-702_7543-699d others(6): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214934913 | ||||||
| chr2:214935004
|
CT | C | 2 | a0001c0001t0013g0040a0001c0042t0013g0045 | 2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.7543-790delA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935004 | ||||||
| chr2:214935029
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.7543-814T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935029 | ||||||
| chr2:214935056
|
T | C | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7543-841A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935056 | ||||||
| chr2:214935128
|
G | A | 122 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(119): Show | 122 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.7543-913C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935128 | ||||||
| chr2:214935272
|
G | A | 2 | a0009c0026t0003g0053a0009c0026t0003g0056 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.7543-1057C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935272 | ||||||
| chr2:214935532
|
C | T | 9 | a0001c0012t0004g0039a0001c0012t0004g0065a0001c0012t0014g0015others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.7543-1317G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935532 | ||||||
| chr2:214935779
|
A | G | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7543-1564T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935779 | ||||||
| chr2:214935805
|
A | T | 3 | a0005c0062t0004g0078a0005c0064t0004g0070a0021c0037t0004g0023 | 3 | HG02630.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.7543-1590T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935805 | ||||||
| chr2:214935806
|
A | T | 118 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(115): Show | 118 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.7543-1591T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935806 | ||||||
| chr2:214935875
|
C | G | 5 | a0001c0006t0005g0152a0001c0016t0005g0063a0001c0031t0005g0158others(2): Show | 5 | HG01074.hp2 HG01517.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.7542+1635G>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935875 | ||||||
| chr2:214935879
|
G | A | 1 | a0001c0002t0022g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7542+1631C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935879 | ||||||
| chr2:214935910
|
A | C | 2 | a0002c0013t0003g0018a0002c0013t0003g0019 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.7542+1600T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935910 | ||||||
| chr2:214935986
|
G | A | 39 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(36): Show | 39 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.7542+1524C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214935986 | ||||||
| chr2:214936148
|
C | T | 1 | a0002c0054t0009g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7542+1362G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936148 | ||||||
| chr2:214936208
|
G | A | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7542+1302C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936208 | ||||||
| chr2:214936245
|
A | G | 2 | a0001c0005t0005g0075a0004c0018t0005g0095 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7542+1265T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936245 | ||||||
| chr2:214936267
|
T | A | 5 | a0001c0006t0005g0152a0001c0016t0005g0063a0001c0031t0005g0158others(2): Show | 5 | HG01074.hp2 HG01517.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.7542+1243A>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936267 | ||||||
| chr2:214936309
|
G | A | 1 | a0001c0002t0001g0061 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.7542+1201C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936309 | ||||||
| chr2:214936464
|
A | G | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7542+1046T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936464 | ||||||
| chr2:214936567
|
T | C | 1 | a0001c0003t0006g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7542+943A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936567 | ||||||
| chr2:214936755
|
A | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7542+755T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936755 | ||||||
| chr2:214936873
|
A | G | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7542+637T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936873 | ||||||
| chr2:214936938
|
G | GAA | 38 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(35): Show | 38 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.7542+570_7542+571d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936938 | ||||||
| chr2:214936938
|
G | GAAA | 11 | a0001c0004t0002g0137a0001c0004t0002g0138a0001c0012t0004g0039others(8): Show | 11 | HG01346.hp2 HG01891.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.7542+569_7542+571d others(5): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936938 | ||||||
| chr2:214936938
|
G | GAAAA | 12 | a0001c0010t0004g0113a0001c0010t0004g0114a0001c0044t0004g0067others(9): Show | 12 | HG02109.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.7542+568_7542+571d others(6): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936938 | ||||||
| chr2:214936938
|
GA | G | 6 | a0001c0004t0001g0091a0001c0009t0008g0188a0001c0009t0008g0189others(3): Show | 6 | HG00140.hp2 HG02886.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.7542+571delT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936938 | ||||||
| chr2:214936940
|
A | AG | 2 | a0001c0033t0026g0193a0003c0020t0003g0108 | 2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.7542+569_7542+570i others(3): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214936940 | ||||||
| chr2:214937189
|
GTTTGTT | G | 2 | a0003c0020t0003g0108a0003c0065t0001g0103 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7542+315_7542+320d others(8): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214937189 | ||||||
| chr2:214937222
|
A | G | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7542+288T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214937222 | ||||||
| chr2:214937388
|
G | A | 64 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(61): Show | 64 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.7542+122C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 51/52 | chr2 | 214937388 | ||||||
| chr2:214937863
|
AAACAT | A | 8 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.7437-253_7437-249d others(7): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214937863 | ||||||
| chr2:214937889
|
T | C | 40 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(37): Show | 40 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.7437-274A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214937889 | ||||||
| chr2:214938471
|
G | T | 72 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(69): Show | 72 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.7437-856C>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938471 | ||||||
| chr2:214938485
|
T | C | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7437-870A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938485 | ||||||
| chr2:214938577
|
G | A | 6 | a0001c0003t0006g0048a0001c0005t0005g0109a0001c0005t0005g0110others(3): Show | 6 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.7437-962C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938577 | ||||||
| chr2:214938723
|
A | C | 67 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(64): Show | 67 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.7437-1108T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938723 | ||||||
| chr2:214938778
|
A | C | 1 | a0001c0002t0001g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.7437-1163T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938778 | ||||||
| chr2:214938788
|
A | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7437-1173T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938788 | ||||||
| chr2:214938852
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.7437-1237A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938852 | ||||||
| chr2:214938878
|
T | C | 13 | a0001c0010t0004g0113a0001c0010t0004g0114a0001c0033t0026g0193others(10): Show | 13 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.7437-1263A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214938878 | ||||||
| chr2:214939041
|
G | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7437-1426C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214939041 | ||||||
| chr2:214939050
|
G | A | 1 | a0001c0011t0001g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.7437-1435C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214939050 | ||||||
| chr2:214939553
|
A | G | 4 | a0001c0015t0007g0009a0001c0015t0007g0013a0004c0018t0021g0082others(1): Show | 4 | HG02451.hp2 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.7437-1938T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214939553 | ||||||
| chr2:214939892
|
G | A | 121 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(118): Show | 121 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(118): Show |
intron_variant | MODIFIER | c.7437-2277C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214939892 | ||||||
| chr2:214940315
|
G | A | 1 | a0001c0016t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7436+2610C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214940315 | ||||||
| chr2:214940358
|
C | T | 8 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.7436+2567G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214940358 | ||||||
| chr2:214940645
|
A | G | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7436+2280T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214940645 | ||||||
| chr2:214940755
|
T | TAGA | 4 | a0001c0015t0009g0006a0008c0028t0003g0081a0008c0028t0003g0083others(1): Show | 4 | HG02622.hp2 HG03471.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.7436+2167_7436+216 others(7): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214940755 | ||||||
| chr2:214940763
|
T | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7436+2162A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214940763 | ||||||
| chr2:214940948
|
C | T | 39 | a0001c0004t0003g0062a0001c0005t0003g0077a0001c0009t0003g0157others(36): Show | 39 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.7436+1977G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214940948 | ||||||
| chr2:214941063
|
G | T | 4 | a0003c0014t0002g0101a0003c0014t0006g0098a0003c0014t0006g0102others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7436+1862C>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941063 | ||||||
| chr2:214941269
|
C | T | 39 | a0001c0004t0003g0062a0001c0005t0003g0077a0001c0009t0003g0157others(36): Show | 39 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.7436+1656G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941269 | ||||||
| chr2:214941437
|
T | C | 1 | a0001c0015t0007g0009 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7436+1488A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941437 | ||||||
| chr2:214941445
|
T | C | 11 | a0001c0001t0013g0040a0001c0012t0004g0039a0001c0012t0004g0065others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.7436+1480A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941445 | ||||||
| chr2:214941568
|
G | T | 2 | a0001c0005t0001g0125a0012c0052t0001g0128 | 2 | HG01106.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.7436+1357C>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941568 | ||||||
| chr2:214941736
|
T | C | 26 | a0001c0004t0003g0062a0001c0009t0003g0157a0001c0009t0008g0188others(23): Show | 26 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.7436+1189A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941736 | ||||||
| chr2:214941781
|
C | CT | 44 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(41): Show | 44 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.7436+1143dupA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941781 | ||||||
| chr2:214941800
|
G | A | 1 | a0002c0058t0002g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7436+1125C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214941800 | ||||||
| chr2:214942046
|
C | T | 1 | a0001c0001t0013g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.7436+879G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214942046 | ||||||
| chr2:214942195
|
A | G | 65 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(62): Show | 65 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.7436+730T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214942195 | ||||||
| chr2:214942236
|
A | G | 26 | a0001c0004t0003g0062a0001c0009t0003g0157a0001c0009t0008g0188others(23): Show | 26 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.7436+689T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214942236 | ||||||
| chr2:214942433
|
G | A | 40 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(37): Show | 40 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.7436+492C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214942433 | ||||||
| chr2:214942637
|
C | T | 127 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(124): Show | 127 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(124): Show |
intron_variant | MODIFIER | c.7436+288G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214942637 | ||||||
| chr2:214942819
|
A | G | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7436+106T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214942819 | ||||||
| chr2:214942910
|
G | A | 1 | a0001c0002t0024g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.7436+15C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 50/52 | chr2 | 214942910 | ||||||
| chr2:214943089
|
C | T | 1 | a0004c0059t0004g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7344-72G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214943089 | ||||||
| chr2:214943157
|
A | AGAT | 57 | a0001c0004t0003g0062a0001c0005t0003g0077a0001c0009t0003g0157others(54): Show | 57 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.7344-143_7344-141d others(5): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214943157 | ||||||
| chr2:214943164
|
G | T | 64 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(61): Show | 64 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.7344-147C>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214943164 | ||||||
| chr2:214943315
|
AT | A | 7 | a0001c0051t0004g0076a0002c0008t0004g0021a0002c0008t0007g0003others(4): Show | 7 | HG02559.hp1 HG02717.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.7344-299delA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214943315 | ||||||
| chr2:214943359
|
G | A | 77 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(74): Show | 77 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.7344-342C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214943359 | ||||||
| chr2:214943393
|
C | T | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7344-376G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214943393 | ||||||
| chr2:214943492
|
C | A | 1 | a0001c0001t0002g0030 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.7344-475G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214943492 | ||||||
| chr2:214944065
|
G | A | 1 | a0001c0004t0003g0062 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.7343+936C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944065 | ||||||
| chr2:214944182
|
G | GT | 129 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(126): Show | 129 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(126): Show |
intron_variant | MODIFIER | c.7343+818_7343+819i others(3): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944182 | ||||||
| chr2:214944336
|
C | T | 2 | a0001c0002t0001g0033a0001c0003t0001g0166 | 2 | HG03654.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.7343+665G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944336 | ||||||
| chr2:214944415
|
A | T | 2 | a0001c0005t0005g0075a0004c0018t0005g0095 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7343+586T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944415 | ||||||
| chr2:214944431
|
T | TA | 68 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(65): Show | 68 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.7343+569dupT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944431 | ||||||
| chr2:214944485
|
A | G | 1 | a0001c0010t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7343+516T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944485 | ||||||
| chr2:214944538
|
A | T | 1 | a0001c0001t0013g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.7343+463T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944538 | ||||||
| chr2:214944552
|
G | C | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7343+449C>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944552 | ||||||
| chr2:214944592
|
T | C | 1 | a0022c0030t0001g0047 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.7343+409A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944592 | ||||||
| chr2:214944682
|
A | C | 1 | a0001c0002t0001g0163 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7343+319T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944682 | ||||||
| chr2:214944873
|
G | GTA | 66 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(63): Show | 66 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.7343+126_7343+127d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944873 | ||||||
| chr2:214944886
|
T | C | 1 | a0001c0004t0001g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.7343+115A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 49/52 | chr2 | 214944886 | ||||||
| chr2:214945249
|
T | C | 1 | a0001c0003t0001g0032 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.7240-145A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214945249 | ||||||
| chr2:214945304
|
C | T | 8 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.7240-200G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214945304 | ||||||
| chr2:214945579
|
C | T | 117 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(114): Show | 117 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.7240-475G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214945579 | ||||||
| chr2:214945932
|
C | T | 8 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.7240-828G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214945932 | ||||||
| chr2:214946006
|
G | A | 1 | a0001c0004t0001g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.7240-902C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214946006 | ||||||
| chr2:214946514
|
C | T | 8 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.7239+908G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214946514 | ||||||
| chr2:214946544
|
T | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7239+878A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214946544 | ||||||
| chr2:214946577
|
C | T | 1 | a0005c0064t0004g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7239+845G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214946577 | ||||||
| chr2:214946609
|
T | C | 2 | a0001c0016t0002g0086a0001c0016t0002g0090 | 2 | HG01123.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.7239+813A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214946609 | ||||||
| chr2:214946677
|
C | A | 1 | a0001c0001t0002g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7239+745G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214946677 | ||||||
| chr2:214947015
|
A | T | 1 | a0001c0002t0024g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.7239+407T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214947015 | ||||||
| chr2:214947181
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7239+241G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214947181 | ||||||
| chr2:214947315
|
G | A | 1 | a0005c0062t0004g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7239+107C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 48/52 | chr2 | 214947315 | ||||||
| chr2:214947573
|
G | A | 121 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(118): Show | 121 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(118): Show |
intron_variant | MODIFIER | c.7105-17C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214947573 | ||||||
| chr2:214947884
|
A | C | 2 | a0001c0025t0015g0182a0001c0043t0006g0022 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.7105-328T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214947884 | ||||||
| chr2:214947899
|
G | A | 3 | a0002c0008t0004g0021a0002c0008t0007g0003a0002c0008t0007g0005 | 3 | HG02559.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7105-343C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214947899 | ||||||
| chr2:214947925
|
G | A | 1 | a0001c0009t0010g0187 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.7105-369C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214947925 | ||||||
| chr2:214947936
|
C | T | 121 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(118): Show | 121 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(118): Show |
intron_variant | MODIFIER | c.7105-380G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214947936 | ||||||
| chr2:214948082
|
T | C | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7104+514A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214948082 | ||||||
| chr2:214948090
|
A | G | 1 | a0001c0004t0001g0115 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.7104+506T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214948090 | ||||||
| chr2:214948196
|
A | G | 13 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.7104+400T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214948196 | ||||||
| chr2:214948283
|
C | A | 9 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.7104+313G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 47/52 | chr2 | 214948283 | ||||||
| chr2:214949176
|
T | A | 51 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(48): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.6853-27A>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949176 | ||||||
| chr2:214949357
|
A | AAT | 9 | a0001c0001t0002g0118a0001c0006t0002g0116a0001c0015t0007g0009others(6): Show | 9 | HG02129.hp1 HG02451.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.6853-210_6853-209d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949357 | ||||||
| chr2:214949371
|
T | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6853-222A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949371 | ||||||
| chr2:214949373
|
T | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6853-224A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949373 | ||||||
| chr2:214949373
|
T | TACACAC | 7 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.6853-225_6853-224i others(8): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949373 | ||||||
| chr2:214949375
|
T | C | 17 | a0001c0004t0001g0054a0001c0011t0005g0088a0001c0011t0005g0089others(14): Show | 17 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.6853-226A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949375 | ||||||
| chr2:214949375
|
T | TAC | 10 | a0001c0009t0003g0157a0001c0010t0004g0113a0001c0010t0004g0114others(7): Show | 10 | HG00735.hp2 HG01255.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.6853-227_6853-226i others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949375 | ||||||
| chr2:214949375
|
T | TACACACA others(1): Show |
6 | a0001c0032t0006g0041a0002c0057t0006g0177a0003c0014t0002g0101others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.6853-227_6853-226i others(10): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949375 | ||||||
| chr2:214949375
|
T | TACACACA others(3): Show |
4 | a0002c0007t0006g0175a0002c0007t0006g0176a0002c0013t0018g0002others(1): Show | 4 | HG01243.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6853-227_6853-226i others(12): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949375 | ||||||
| chr2:214949377
|
T | C | 72 | a0001c0003t0001g0147a0001c0003t0006g0048a0001c0004t0001g0054others(69): Show | 72 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.6853-228A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949377 | ||||||
| chr2:214949377
|
T | TAC | 2 | a0001c0001t0013g0040a0003c0065t0001g0103 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6853-230_6853-229d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949377 | ||||||
| chr2:214949377
|
T | TACACACA others(3): Show |
1 | a0003c0014t0006g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6853-238_6853-229d others(12): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949377 | ||||||
| chr2:214949377
|
TAC | T | 2 | a0001c0022t0006g0112a0001c0022t0019g0014 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.6853-230_6853-229d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949377 | ||||||
| chr2:214949379
|
C | T | 63 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.6853-230G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949379 | ||||||
| chr2:214949555
|
G | A | 3 | a0005c0062t0004g0078a0005c0064t0004g0070a0021c0037t0004g0023 | 3 | HG02630.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6853-406C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949555 | ||||||
| chr2:214949671
|
C | A | 1 | a0001c0003t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6853-522G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949671 | ||||||
| chr2:214949721
|
C | A | 12 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6853-572G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214949721 | ||||||
| chr2:214950053
|
G | A | 2 | a0001c0005t0001g0125a0012c0052t0001g0128 | 2 | HG01106.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.6852+826C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950053 | ||||||
| chr2:214950102
|
C | T | 2 | a0001c0003t0011g0120a0001c0033t0026g0193 | 2 | HG02109.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.6852+777G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950102 | ||||||
| chr2:214950119
|
A | G | 1 | a0002c0056t0004g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6852+760T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950119 | ||||||
| chr2:214950295
|
C | T | 1 | a0001c0015t0009g0006 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6852+584G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950295 | ||||||
| chr2:214950350
|
G | A | 1 | a0001c0029t0002g0031 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6852+529C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950350 | ||||||
| chr2:214950354
|
A | G | 12 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6852+525T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950354 | ||||||
| chr2:214950364
|
A | G | 50 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.6852+515T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950364 | ||||||
| chr2:214950372
|
G | GTA | 13 | a0001c0016t0005g0063a0001c0022t0006g0112a0001c0022t0019g0014others(10): Show | 13 | HG01074.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.6852+505_6852+506d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950372 | ||||||
| chr2:214950380
|
A | C | 50 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.6852+499T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950380 | ||||||
| chr2:214950382
|
A | C | 8 | a0001c0015t0007g0009a0001c0015t0007g0013a0001c0015t0009g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.6852+497T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950382 | ||||||
| chr2:214950382
|
ATCTGTGT others(1): Show |
A | 39 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(36): Show | 39 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.6852+489_6852+496d others(10): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950382 | ||||||
| chr2:214950382
|
ATCTGTGT others(3): Show |
A | 2 | a0001c0042t0013g0045a0003c0066t0004g0104 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.6852+487_6852+496d others(12): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950382 | ||||||
| chr2:214950382
|
ATCTGTGT others(5): Show |
A | 6 | a0001c0001t0013g0040a0001c0012t0004g0039a0001c0012t0004g0065others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.6852+485_6852+496d others(14): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950382 | ||||||
| chr2:214950382
|
ATCTGTGT others(7): Show |
A | 3 | a0005c0062t0004g0078a0005c0064t0004g0070a0021c0037t0004g0023 | 3 | HG02630.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6852+483_6852+496d others(16): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950382 | ||||||
| chr2:214950384
|
C | A | 2 | a0001c0006t0005g0152a0001c0031t0005g0158 | 2 | HG01517.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6852+495G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
C | CTG | 43 | a0001c0002t0001g0027a0001c0002t0001g0033a0001c0002t0001g0055others(40): Show | 43 | HG00140.hp2 HG00438.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.6852+493_6852+494d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
C | CTGTG | 9 | a0001c0002t0001g0051a0001c0002t0001g0151a0001c0003t0001g0032others(6): Show | 9 | HG02809.hp1 HG02809.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.6852+491_6852+494d others(6): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
C | CTGTGTG | 5 | a0001c0011t0005g0088a0001c0011t0005g0089a0007c0024t0005g0093others(2): Show | 5 | HG01255.hp2 HG01943.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.6852+489_6852+494d others(8): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
CTG | C | 10 | a0001c0002t0001g0043a0001c0003t0006g0048a0001c0005t0005g0109others(7): Show | 10 | HG00741.hp1 HG01074.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.6852+493_6852+494d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
CTGTG | C | 8 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(5): Show | 8 | HG02559.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.6852+491_6852+494d others(6): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
CTGTGTG | C | 2 | a0003c0020t0001g0106a0005c0063t0003g0079 | 2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6852+489_6852+494d others(8): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
CTGTGTGT others(1): Show |
C | 5 | a0001c0015t0007g0009a0001c0015t0007g0013a0001c0015t0009g0006others(2): Show | 5 | HG02451.hp2 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.6852+487_6852+494d others(10): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
CTGTGTGT others(3): Show |
C | 26 | a0001c0009t0003g0157a0001c0009t0008g0188a0001c0009t0008g0189others(23): Show | 26 | HG00735.hp2 HG01255.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.6852+485_6852+494d others(12): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
CTGTGTGT others(5): Show |
C | 1 | a0003c0020t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6852+483_6852+494d others(14): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950384
|
CTGTGTGT others(7): Show |
C | 9 | a0001c0005t0003g0077a0001c0010t0002g0168a0001c0010t0009g0001others(6): Show | 9 | HG01884.hp2 HG01975.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.6852+481_6852+494d others(16): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950384 | ||||||
| chr2:214950386
|
G | C | 2 | a0001c0006t0005g0152a0001c0031t0005g0158 | 2 | HG01517.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6852+493C>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950386 | ||||||
| chr2:214950412
|
GTGTGTGT others(3): Show |
G | 2 | a0009c0026t0003g0053a0009c0026t0003g0056 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.6852+457_6852+466d others(12): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950412 | ||||||
| chr2:214950414
|
GTGTGTGT others(1): Show |
G | 3 | a0008c0028t0003g0081a0008c0028t0003g0083a0019c0047t0003g0052 | 3 | HG02622.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6852+457_6852+464d others(10): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950414 | ||||||
| chr2:214950416
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6852+463C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950416 | ||||||
| chr2:214950418
|
G | A | 46 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(43): Show | 46 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.6852+461C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950418 | ||||||
| chr2:214950418
|
GTGTA | G | 2 | a0001c0022t0006g0112a0001c0022t0019g0014 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.6852+457_6852+460d others(6): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950418 | ||||||
| chr2:214950420
|
G | A | 63 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.6852+459C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950420 | ||||||
| chr2:214950420
|
GTA | G | 6 | a0001c0032t0006g0041a0002c0007t0006g0175a0002c0007t0006g0176others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.6852+457_6852+458d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950420 | ||||||
| chr2:214950422
|
A | G | 7 | a0001c0003t0001g0044a0001c0004t0001g0029a0001c0004t0001g0133others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.6852+457T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950422 | ||||||
| chr2:214950483
|
G | GA | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6852+395dupT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950483 | ||||||
| chr2:214950510
|
A | AT | 141 | a0001c0001t0002g0150a0001c0002t0001g0027a0001c0002t0001g0028others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.6852+368dupA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950510 | ||||||
| chr2:214950510
|
A | ATT | 48 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(45): Show | 48 | HG00423.hp1 HG00735.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.6852+367_6852+368d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950510 | ||||||
| chr2:214950608
|
T | G | 59 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(56): Show | 59 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.6852+271A>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950608 | ||||||
| chr2:214950670
|
A | T | 1 | a0001c0009t0003g0157 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.6852+209T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950670 | ||||||
| chr2:214950684
|
C | T | 115 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(112): Show | 115 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(112): Show |
intron_variant | MODIFIER | c.6852+195G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950684 | ||||||
| chr2:214950699
|
T | C | 13 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(10): Show | 13 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.6852+180A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950699 | ||||||
| chr2:214950722
|
C | A | 1 | a0001c0004t0001g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.6852+157G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 45/52 | chr2 | 214950722 | ||||||
| chr2:214951208
|
T | TGA | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-126_6648-125i others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951208 | ||||||
| chr2:214951211
|
A | AGCAT | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-129_6648-128i others(6): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951211 | ||||||
| chr2:214951212
|
A | T | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-129T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951212 | ||||||
| chr2:214951485
|
A | G | 189 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.6648-402T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951485 | ||||||
| chr2:214951513
|
A | G | 7 | a0001c0001t0013g0040a0001c0012t0004g0039a0001c0012t0004g0065others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.6648-430T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951513 | ||||||
| chr2:214951531
|
C | A | 8 | a0001c0015t0007g0009a0001c0015t0007g0013a0001c0015t0009g0006others(5): Show | 8 | HG02451.hp2 HG02622.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.6648-448G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951531 | ||||||
| chr2:214951628
|
A | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6648-545T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951628 | ||||||
| chr2:214951689
|
A | G | 52 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.6648-606T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951689 | ||||||
| chr2:214951752
|
G | A | 8 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(5): Show | 8 | HG02559.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.6648-669C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951752 | ||||||
| chr2:214951866
|
T | C | 49 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.6648-783A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214951866 | ||||||
| chr2:214952055
|
AC | A | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-973delG | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952055 | ||||||
| chr2:214952057
|
C | CA | 7 | a0001c0025t0015g0182a0001c0043t0006g0022a0002c0056t0004g0020others(4): Show | 7 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.6648-975dupT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952057 | ||||||
| chr2:214952063
|
A | C | 13 | a0001c0009t0003g0157a0001c0009t0008g0188a0001c0009t0008g0189others(10): Show | 13 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.6648-980T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952063 | ||||||
| chr2:214952085
|
A | G | 1 | a0002c0057t0006g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.6648-1002T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952085 | ||||||
| chr2:214952105
|
G | A | 1 | a0001c0002t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6648-1022C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952105 | ||||||
| chr2:214952210
|
C | CT | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-1128dupA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952210 | ||||||
| chr2:214952222
|
GT | G | 93 | a0001c0001t0002g0119a0001c0001t0012g0192a0001c0001t0013g0040others(90): Show | 93 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.6648-1140delA | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952222 | ||||||
| chr2:214952222
|
GTT | G | 93 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(90): Show | 93 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.6648-1141_6648-114 others(6): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952222 | ||||||
| chr2:214952224
|
T | G | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-1141A>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952224 | ||||||
| chr2:214952230
|
T | C | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6648-1147A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952230 | ||||||
| chr2:214952252
|
G | A | 8 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(5): Show | 8 | HG02559.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.6648-1169C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952252 | ||||||
| chr2:214952289
|
C | T | 1 | a0002c0007t0017g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6648-1206G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952289 | ||||||
| chr2:214952346
|
G | A | 2 | a0001c0006t0002g0116a0001c0006t0002g0124 | 2 | HG02523.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.6648-1263C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952346 | ||||||
| chr2:214952367
|
C | T | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-1284G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952367 | ||||||
| chr2:214952369
|
T | C | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6648-1286A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952369 | ||||||
| chr2:214952686
|
C | G | 46 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(43): Show | 46 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.6647+1168G>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952686 | ||||||
| chr2:214952865
|
T | A | 1 | a0021c0037t0004g0023 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6647+989A>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952865 | ||||||
| chr2:214952890
|
T | C | 1 | a0005c0062t0004g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6647+964A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214952890 | ||||||
| chr2:214953250
|
G | A | 1 | a0003c0020t0001g0106 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6647+604C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214953250 | ||||||
| chr2:214953332
|
A | G | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6647+522T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214953332 | ||||||
| chr2:214953403
|
G | T | 5 | a0001c0009t0008g0188a0001c0009t0008g0189a0001c0009t0010g0187others(2): Show | 5 | NA18962.hp2 NA18971.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.6647+451C>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214953403 | ||||||
| chr2:214953540
|
A | T | 2 | a0002c0013t0003g0018a0002c0013t0003g0019 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.6647+314T>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 44/52 | chr2 | 214953540 | ||||||
| chr2:214954374
|
A | G | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6394-267T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/52 | chr2 | 214954374 | ||||||
| chr2:214954440
|
C | G | 37 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.6394-333G>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/52 | chr2 | 214954440 | ||||||
| chr2:214954550
|
G | A | 1 | a0001c0002t0001g0161 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.6394-443C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/52 | chr2 | 214954550 | ||||||
| chr2:214954779
|
T | C | 9 | a0001c0044t0004g0067a0001c0051t0004g0076a0002c0008t0004g0021others(6): Show | 9 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6393+423A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/52 | chr2 | 214954779 | ||||||
| chr2:214954786
|
T | C | 4 | a0003c0014t0002g0101a0003c0014t0006g0098a0003c0014t0006g0102others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6393+416A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/52 | chr2 | 214954786 | ||||||
| chr2:214955083
|
C | A | 7 | a0001c0025t0015g0182a0001c0043t0006g0022a0001c0068t0003g0016others(4): Show | 7 | HG01243.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.6393+119G>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/52 | chr2 | 214955083 | ||||||
| chr2:214955129
|
T | C | 64 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(61): Show | 64 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.6393+73A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 43/52 | chr2 | 214955129 | ||||||
| chr2:214955406
|
G | C | 4 | a0002c0056t0004g0020a0005c0062t0004g0078a0005c0064t0004g0070others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.6234-45C>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 42/52 | chr2 | 214955406 | ||||||
| chr2:214955836
|
T | G | 73 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(70): Show | 73 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.6234-475A>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 42/52 | chr2 | 214955836 | ||||||
| chr2:214956197
|
G | A | 110 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(107): Show | 110 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.6233+466C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 42/52 | chr2 | 214956197 | ||||||
| chr2:214956325
|
CAA | C | 8 | a0001c0022t0006g0112a0001c0022t0019g0014a0001c0032t0006g0041others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.6233+336_6233+337d others(4): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 42/52 | chr2 | 214956325 | ||||||
| chr2:214956490
|
GTAT | G | 34 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(31): Show | 34 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.6233+170_6233+172d others(5): Show |
ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 42/52 | chr2 | 214956490 | ||||||
| chr2:214956552
|
A | C | 7 | a0001c0003t0001g0122a0001c0003t0001g0134a0001c0004t0001g0092others(4): Show | 7 | HG01123.hp1 HG01258.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.6233+111T>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 42/52 | chr2 | 214956552 | ||||||
| chr2:214956825
|
CA | C | 58 | a0001c0001t0002g0132a0001c0005t0003g0077a0001c0009t0003g0157others(55): Show | 58 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.6118-48delT | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214956825 | ||||||
| chr2:214956842
|
A | G | 1 | a0001c0002t0001g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.6118-64T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214956842 | ||||||
| chr2:214956846
|
C | G | 1 | a0001c0033t0026g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6118-68G>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214956846 | ||||||
| chr2:214956856
|
T | C | 41 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(38): Show | 41 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.6118-78A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214956856 | ||||||
| chr2:214957101
|
G | A | 59 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(56): Show | 59 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.6118-323C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214957101 | ||||||
| chr2:214957160
|
T | C | 68 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(65): Show | 68 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.6118-382A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214957160 | ||||||
| chr2:214957667
|
C | T | 1 | a0001c0031t0005g0158 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.6117+610G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214957667 | ||||||
| chr2:214957783
|
A | G | 7 | a0001c0001t0013g0040a0001c0012t0004g0039a0001c0012t0004g0065others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.6117+494T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214957783 | ||||||
| chr2:214957906
|
T | C | 68 | a0001c0005t0003g0077a0001c0009t0003g0157a0001c0009t0008g0188others(65): Show | 68 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.6117+371A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214957906 | ||||||
| chr2:214958094
|
G | A | 1 | a0001c0003t0002g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6117+183C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214958094 | ||||||
| chr2:214958128
|
A | G | 1 | a0003c0067t0025g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6117+149T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 41/52 | chr2 | 214958128 | ||||||
| chr2:214958610
|
C | T | 36 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(33): Show | 36 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.5940-156G>A | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 40/52 | chr2 | 214958610 | ||||||
| chr2:214958622
|
A | G | 118 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(115): Show | 118 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.5940-168T>C | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 40/52 | chr2 | 214958622 | ||||||
| chr2:214958667
|
G | A | 2 | a0001c0004t0002g0137a0001c0004t0002g0138 | 2 | HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.5940-213C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 40/52 | chr2 | 214958667 | ||||||
| chr2:214958726
|
T | C | 5 | a0001c0012t0004g0039a0001c0012t0004g0065a0001c0012t0014g0015others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5940-272A>G | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 40/52 | chr2 | 214958726 | ||||||
| chr2:214958811
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5939+213C>T | ABCA12 | ENSG00000144452.15 | transcript | ENST00000272895.12 | protein_coding | 40/52 | chr2 | 214958811 | ||||||
| chr2:214959258
|
T | C | 45 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0035others(42): Show |