Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 225 |
|---|---|
| ensemblid | ENSG00000173208.4 |
| hgncid | 66 |
| symbol | ABCD2 |
| name | ATP binding cassette subfamily D member 2 |
| refseq_nuc | NM_005164.4 |
| refseq_prot | NP_005155.1 |
| ensembl_nuc | ENST00000308666.4 |
| ensembl_prot | ENSP00000310688.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 39550033 |
| end | 39619803 |
| strand | - |
| ver | v1.2 |
| region | chr12:39550033-39619803 |
| region5000 | chr12:39545033-39624803 |
| regionname0 | ABCD2_chr12_39550033_39619803 |
| regionname5000 | ABCD2_chr12_39545033_39624803 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 740 | 324 | 81 | 52 | 145 | 6 | 38 | 114 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0002 | 0/0 | 740 | 11 | 0 | 6 | 5 | 0 | 0 | 4 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0003 | 0/0 | 740 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0004 | 0/0 | 740 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2223 | 318 | 78 | 50 | 145 | 6 | 37 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0002 | 0/0 | 2223 | 11 | 0 | 6 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0003 | 0/0 | 2223 | 3 | 0 | 2 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0004 | 0/0 | 2223 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0005 | 0/0 | 2223 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0006 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0007 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0008 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| c0009 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4068 | 160 | 32 | 27 | 80 | 2 | 17 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0002 | 0/0 | 4068 | 56 | 0 | 8 | 35 | 1 | 12 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0003 | 0/0 | 4068 | 24 | 0 | 3 | 20 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0004 | 0/0 | 4068 | 18 | 5 | 6 | 6 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0005 | 0/0 | 4068 | 17 | 17 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0006 | 0/0 | 4068 | 15 | 3 | 4 | 3 | 1 | 4 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0007 | 0/0 | 4068 | 7 | 7 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0008 | 0/0 | 4068 | 6 | 0 | 6 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0009 | 0/0 | 4068 | 5 | 3 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0010 | 0/0 | 4068 | 4 | 4 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0011 | 0/0 | 4068 | 4 | 2 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0012 | 0/0 | 4063 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0013 | 0/0 | 4068 | 2 | 0 | 0 | 0 | 2 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0014 | 0/0 | 4068 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0015 | 0/0 | 4068 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0016 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0017 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0018 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0019 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0020 | 0/0 | 4068 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0021 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0022 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0023 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0024 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0025 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0026 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0027 | 0/0 | 4068 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0028 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0029 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| t0030 | 0/0 | 4068 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2223 | 318 | 78 | 50 | 145 | 6 | 37 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0003 | 0/0 | 2223 | 3 | 0 | 2 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0006 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0007 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0008 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0002c0002 | 0/0 | 2223 | 11 | 0 | 6 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0003c0005 | 0/0 | 2223 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0003c0009 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0004c0004 | 0/0 | 2223 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6290 | 158 | 32 | 26 | 80 | 2 | 16 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0002 | 0/0 | 6290 | 56 | 0 | 8 | 35 | 1 | 12 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0003 | 0/0 | 6290 | 24 | 0 | 3 | 20 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0004 | 0/0 | 6290 | 7 | 5 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0005 | 0/0 | 6290 | 17 | 17 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0006 | 0/0 | 6290 | 14 | 2 | 4 | 3 | 1 | 4 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0007 | 0/0 | 6290 | 6 | 6 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0008 | 0/0 | 6290 | 6 | 0 | 6 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0009 | 0/0 | 6290 | 5 | 3 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0010 | 0/0 | 6290 | 4 | 4 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0011 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0012 | 0/0 | 6285 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0013 | 0/0 | 6290 | 2 | 0 | 0 | 0 | 2 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0014 | 0/0 | 6290 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0015 | 0/0 | 6290 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0016 | 0/0 | 6290 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0017 | 0/0 | 6290 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0018 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0019 | 0/0 | 6285 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0020 | 0/0 | 6290 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0021 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0022 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0023 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0025 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0027 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0028 | 0/0 | 6290 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0029 | 0/0 | 6290 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0001t0030 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0003t0001 | 0/0 | 6290 | 2 | 0 | 1 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0003t0026 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0006t0024 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0007t0007 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0001c0008t0006 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0002c0002t0004 | 0/0 | 6290 | 11 | 0 | 6 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0003c0005t0011 | 0/0 | 6290 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0003c0009t0011 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| a0004c0004t0012 | 0/0 | 6285 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | copy fasta | chr12 | 39545033 | 39624803 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0001 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0010g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0013g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0016g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0017g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0018g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0019g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0020g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0021g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0022g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0023g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0025g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0027g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0028g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0029g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0030g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0003t0026g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0006t0024g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0007t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0008t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0003c0005t0011g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0003c0009t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0004c0004t0012g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0010 | EUR | FIN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | FIN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00639 | hp1 | a0002 | c0002 | t0004 | g0288 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00733 | hp2 | a0001 | c0001 | t0023 | g0080 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0208 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01070 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01071 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01074 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01106 | hp1 | a0001 | c0003 | t0026 | g0210 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0108 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0262 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01167 | hp1 | a0003 | c0005 | t0011 | g0027 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01168 | hp1 | a0002 | c0002 | t0004 | g0289 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01169 | hp1 | a0003 | c0005 | t0011 | g0027 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01169 | hp2 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01192 | hp2 | a0001 | c0001 | t0018 | g0073 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0053 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0060 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01515 | hp2 | a0001 | c0001 | t0013 | g0032 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01517 | hp2 | a0001 | c0001 | t0013 | g0031 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01891 | hp2 | a0001 | c0006 | t0024 | g0030 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01934 | hp1 | a0001 | c0001 | t0030 | g0291 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0261 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0260 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0216 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0234 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02056 | hp1 | a0002 | c0002 | t0004 | g0287 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0062 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0082 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02155 | hp1 | a0001 | c0001 | t0017 | g0215 | EAS | CDX | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | CDX | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0072 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0094 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0076 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0207 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0085 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0088 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0077 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0206 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0071 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0033 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0089 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0011 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0081 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03239 | hp1 | a0001 | c0001 | t0028 | g0035 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03453 | hp1 | a0001 | c0001 | t0022 | g0075 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03453 | hp2 | a0001 | c0001 | t0025 | g0143 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0054 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0093 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03516 | hp2 | a0003 | c0009 | t0011 | g0285 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03579 | hp1 | a0001 | c0007 | t0007 | g0083 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0056 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0013 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0050 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0061 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0209 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04204 | hp1 | a0001 | c0001 | t0029 | g0264 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18939 | hp2 | a0004 | c0004 | t0012 | g0017 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18950 | hp2 | a0001 | c0001 | t0012 | g0142 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18957 | hp1 | a0004 | c0004 | t0012 | g0017 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18960 | hp1 | a0001 | c0001 | t0019 | g0139 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18969 | hp1 | a0001 | c0001 | t0016 | g0029 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0028 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18979 | hp2 | a0001 | c0001 | t0020 | g0225 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0290 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19002 | hp2 | a0002 | c0002 | t0004 | g0286 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0059 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19085 | hp1 | a0002 | c0002 | t0004 | g0028 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | ASW | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | ASW | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | GIH | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | GIH | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02109 | hp2 | a0001 | c0008 | t0006 | g0058 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0039 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03471 | hp2 | a0001 | c0001 | t0021 | g0202 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0175 | REF | REF | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39554040
|
C | G | 1 | a0004 | 2 | NA18939.hp2 NA18957.hp1 |
missense_variant | MODERATE | c.2095G>C | p.Glu699Gln | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2283/6290 | 2095/2223 | 699/740 | chr12 | 39554040 | ||
| chr12:39619428
|
G | C | 1 | a0003 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.188C>G | p.Thr63Arg | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 376/6290 | 188/2223 | 63/740 | chr12 | 39619428 | ||
| chr12:39619590
|
G | C | 1 | a0002 | 11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
missense_variant | MODERATE | c.26C>G | p.Ala9Gly | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 214/6290 | 26/2223 | 9/740 | chr12 | 39619590 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39553936
|
A | G | 1 | a0001c0007 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.2199T>C | p.Ile733Ile | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2387/6290 | 2199/2223 | 733/740 | chr12 | 39553936 | ||
| chr12:39554083
|
G | A | 1 | a0001c0008 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2052C>T | p.Arg684Arg | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2240/6290 | 2052/2223 | 684/740 | chr12 | 39554083 | ||
| chr12:39586261
|
G | T | 1 | a0001c0006 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1683C>A | p.Val561Val | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/10 | 1871/6290 | 1683/2223 | 561/740 | chr12 | 39586261 | ||
| chr12:39617061
|
C | T | 1 | a0001c0003 | 3 | HG00738.hp2 HG01106.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1047G>A | p.Lys349Lys | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/10 | 1235/6290 | 1047/2223 | 349/740 | chr12 | 39617061 | ||
| chr12:39619351
|
G | A | 1 | a0003c0009 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.265C>T | p.Leu89Leu | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 453/6290 | 265/2223 | 89/740 | chr12 | 39619351 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39550042
|
G | C | 3 | a0001c0001t0011a0003c0005t0011a0003c0009t0011 | 4 | HG01167.hp1 HG01169.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3870C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3870 | chr12 | 39550042 | |||||
| chr12:39550117
|
A | G | 1 | a0001c0001t0020 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3795T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3795 | chr12 | 39550117 | |||||
| chr12:39550488
|
C | A | 1 | a0001c0001t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3424G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3424 | chr12 | 39550488 | |||||
| chr12:39550501
|
A | G | 2 | a0001c0001t0002a0001c0001t0029 | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3411T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3411 | chr12 | 39550501 | |||||
| chr12:39550892
|
T | C | 1 | a0001c0001t0014 | 2 | HG02717.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3020A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3020 | chr12 | 39550892 | |||||
| chr12:39551200
|
A | G | 1 | a0001c0001t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2712T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2712 | chr12 | 39551200 | |||||
| chr12:39551251
|
T | G | 3 | a0001c0001t0010a0001c0001t0018a0001c0001t0022 | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2661A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2661 | chr12 | 39551251 | |||||
| chr12:39551442
|
A | G | 1 | a0001c0001t0019 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2470T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2470 | chr12 | 39551442 | |||||
| chr12:39551451
|
G | A | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(4): Show | 40 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2461C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2461 | chr12 | 39551451 | |||||
| chr12:39551930
|
GTTAAC | G | 3 | a0001c0001t0012a0001c0001t0019a0004c0004t0012 | 4 | NA18939.hp2 NA18950.hp2 NA18957.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1977_*1981delGTTA others(1): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1977 | chr12 | 39551930 | |||||
| chr12:39552139
|
G | T | 1 | a0001c0003t0026 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1773C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1773 | chr12 | 39552139 | |||||
| chr12:39552326
|
A | G | 1 | a0001c0001t0028 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1586T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1586 | chr12 | 39552326 | |||||
| chr12:39552552
|
C | A | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | 162 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1360G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1360 | chr12 | 39552552 | |||||
| chr12:39552671
|
C | T | 1 | a0001c0001t0005 | 17 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1241G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1241 | chr12 | 39552671 | |||||
| chr12:39552672
|
G | A | 1 | a0001c0001t0023 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1240C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1240 | chr12 | 39552672 | |||||
| chr12:39552779
|
G | A | 1 | a0001c0001t0008 | 6 | HG01106.hp2 HG01109.hp2 HG01934.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1133C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1133 | chr12 | 39552779 | |||||
| chr12:39552851
|
T | G | 2 | a0001c0001t0003a0001c0001t0028 | 25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1061A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1061 | chr12 | 39552851 | |||||
| chr12:39552894
|
G | A | 1 | a0001c0001t0029 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1018C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1018 | chr12 | 39552894 | |||||
| chr12:39552908
|
C | T | 1 | a0001c0001t0018 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1004 | chr12 | 39552908 | |||||
| chr12:39553225
|
C | T | 1 | a0001c0001t0017 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*687G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 687 | chr12 | 39553225 | |||||
| chr12:39553338
|
T | C | 1 | a0001c0006t0024 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*574A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 574 | chr12 | 39553338 | |||||
| chr12:39553437
|
T | C | 1 | a0001c0001t0025 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 475 | chr12 | 39553437 | |||||
| chr12:39553506
|
G | A | 7 | a0001c0001t0003a0001c0001t0006a0001c0001t0013others(4): Show | 44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*406C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 406 | chr12 | 39553506 | |||||
| chr12:39553523
|
T | C | 2 | a0001c0001t0002a0001c0001t0029 | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*389A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 389 | chr12 | 39553523 | |||||
| chr12:39553557
|
A | C | 1 | a0001c0001t0013 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*355T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 355 | chr12 | 39553557 | |||||
| chr12:39553603
|
A | G | 2 | a0001c0001t0007a0001c0007t0007 | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*309T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 309 | chr12 | 39553603 | |||||
| chr12:39553892
|
T | G | 1 | a0001c0001t0015 | 2 | HG02280.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 20 | chr12 | 39553892 | |||||
| chr12:39619626
|
A | G | 1 | a0001c0001t0030 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 11 | chr12 | 39619626 | |||||
| chr12:39619627
|
C | A | 1 | a0001c0001t0030 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 12 | chr12 | 39619627 | |||||
| chr12:39619753
|
A | G | 1 | a0001c0001t0016 | 1 | NA18969.hp1 | 5_prime_UTR_variant | MODIFIER | c.-138T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 138 | chr12 | 39619753 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39554162
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2004-31C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554162 | ||||||
| chr12:39554239
|
C | T | 1 | a0001c0001t0011g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2004-108G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554239 | ||||||
| chr12:39554275
|
G | C | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2004-144C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554275 | ||||||
| chr12:39554327
|
G | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(38): Show | 50 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2004-196C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554327 | ||||||
| chr12:39554464
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2004-333C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554464 | ||||||
| chr12:39554653
|
G | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(47): Show | 59 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2004-522C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554653 | ||||||
| chr12:39554791
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2004-660A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554791 | ||||||
| chr12:39554806
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2004-675C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554806 | ||||||
| chr12:39554809
|
G | A | 2 | a0001c0001t0010g0011a0001c0001t0010g0074 | 3 | HG02109.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2004-678C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554809 | ||||||
| chr12:39554820
|
G | A | 1 | a0001c0001t0025g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2004-689C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554820 | ||||||
| chr12:39554852
|
G | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0249 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2004-721C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554852 | ||||||
| chr12:39555004
|
C | G | 18 | a0001c0001t0006g0010a0001c0001t0006g0050a0001c0001t0006g0052others(15): Show | 19 | HG00280.hp1 HG01106.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.2004-873G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555004 | ||||||
| chr12:39555081
|
G | A | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-950C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555081 | ||||||
| chr12:39555242
|
C | A | 1 | a0001c0001t0001g0280 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2004-1111G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555242 | ||||||
| chr12:39555244
|
A | G | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2004-1113T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555244 | ||||||
| chr12:39555345
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 338 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(335): Show |
intron_variant | MODIFIER | c.2004-1214T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555345 | ||||||
| chr12:39555491
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0273 | 3 | HG02257.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2004-1360T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555491 | ||||||
| chr12:39555593
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2004-1462G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555593 | ||||||
| chr12:39555656
|
C | T | 1 | a0001c0001t0006g0077 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2004-1525G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555656 | ||||||
| chr12:39555798
|
A | G | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2004-1667T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555798 | ||||||
| chr12:39555805
|
C | T | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2004-1674G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555805 | ||||||
| chr12:39555852
|
G | C | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-1721C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555852 | ||||||
| chr12:39555853
|
C | A | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-1722G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555853 | ||||||
| chr12:39555921
|
A | G | 2 | a0002c0002t0004g0287a0002c0002t0004g0290 | 2 | HG02056.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.2004-1790T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555921 | ||||||
| chr12:39555943
|
T | C | 2 | a0001c0001t0003g0043a0001c0001t0003g0048 | 2 | NA18947.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2004-1812A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555943 | ||||||
| chr12:39556207
|
C | T | 1 | a0001c0001t0011g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2004-2076G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556207 | ||||||
| chr12:39556250
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0231a0001c0001t0001g0248 | 3 | HG01975.hp1 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2004-2119T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556250 | ||||||
| chr12:39556368
|
G | A | 2 | a0001c0003t0001g0208a0001c0003t0001g0209 | 2 | HG00738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2004-2237C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556368 | ||||||
| chr12:39556605
|
A | G | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2004-2474T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556605 | ||||||
| chr12:39556615
|
C | T | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-2484G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556615 | ||||||
| chr12:39556639
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2004-2508C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556639 | ||||||
| chr12:39556649
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2004-2518G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556649 | ||||||
| chr12:39556680
|
T | C | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2004-2549A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556680 | ||||||
| chr12:39556758
|
A | T | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2004-2627T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556758 | ||||||
| chr12:39556982
|
C | CA | 115 | a0001c0001t0001g0101a0001c0001t0001g0154a0001c0001t0002g0002others(112): Show | 145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2004-2852dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556982 | ||||||
| chr12:39557034
|
T | C | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-2903A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557034 | ||||||
| chr12:39557114
|
T | C | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2004-2983A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557114 | ||||||
| chr12:39557189
|
G | A | 36 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004-3058C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557189 | ||||||
| chr12:39557251
|
C | T | 49 | a0001c0001t0002g0002a0001c0001t0002g0019a0001c0001t0002g0021others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2004-3120G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557251 | ||||||
| chr12:39557332
|
A | G | 14 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(11): Show | 20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2004-3201T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557332 | ||||||
| chr12:39557529
|
A | C | 5 | a0001c0001t0009g0033a0001c0001t0009g0038a0001c0001t0009g0039others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-3398T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557529 | ||||||
| chr12:39557675
|
T | C | 26 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(23): Show | 39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-3544A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557675 | ||||||
| chr12:39557717
|
C | T | 3 | a0001c0001t0006g0062a0001c0001t0006g0063a0001c0001t0006g0064 | 3 | HG02129.hp2 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2004-3586G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557717 | ||||||
| chr12:39557718
|
C | G | 36 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004-3587G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557718 | ||||||
| chr12:39557749
|
G | T | 1 | a0001c0001t0003g0141 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2004-3618C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557749 | ||||||
| chr12:39557761
|
G | A | 124 | a0001c0001t0002g0002a0001c0001t0002g0019a0001c0001t0002g0021others(121): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2004-3630C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557761 | ||||||
| chr12:39558127
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2004-3996G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558127 | ||||||
| chr12:39558216
|
G | A | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2004-4085C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558216 | ||||||
| chr12:39558263
|
G | C | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-4132C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558263 | ||||||
| chr12:39558507
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2004-4376C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558507 | ||||||
| chr12:39558585
|
A | C | 1 | a0001c0001t0006g0063 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2004-4454T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558585 | ||||||
| chr12:39558610
|
T | C | 124 | a0001c0001t0002g0002a0001c0001t0002g0019a0001c0001t0002g0021others(121): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2004-4479A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558610 | ||||||
| chr12:39558611
|
G | A | 1 | a0001c0001t0006g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2004-4480C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558611 | ||||||
| chr12:39558615
|
T | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0019a0001c0001t0002g0021others(87): Show | 107 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.2004-4484A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558615 | ||||||
| chr12:39558684
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2004-4553G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558684 | ||||||
| chr12:39558754
|
A | G | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2004-4623T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558754 | ||||||
| chr12:39558907
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0131a0001c0001t0001g0273 | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004-4776C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558907 | ||||||
| chr12:39558935
|
G | T | 10 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | NA18944.hp2 NA18959.hp1 NA19000.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004-4804C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558935 | ||||||
| chr12:39558936
|
C | T | 26 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(23): Show | 39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-4805G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558936 | ||||||
| chr12:39559145
|
G | A | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-5014C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559145 | ||||||
| chr12:39559149
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0068 | 4 | HG01884.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004-5018C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559149 | ||||||
| chr12:39559183
|
A | G | 2 | a0002c0002t0004g0287a0002c0002t0004g0290 | 2 | HG02056.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.2004-5052T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559183 | ||||||
| chr12:39559261
|
A | G | 2 | a0001c0001t0015g0093a0001c0001t0015g0094 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2004-5130T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559261 | ||||||
| chr12:39559308
|
C | T | 1 | a0001c0008t0006g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2004-5177G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559308 | ||||||
| chr12:39559309
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0019a0001c0001t0002g0021others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2004-5178C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559309 | ||||||
| chr12:39559331
|
C | T | 36 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(33): Show | 44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004-5200G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559331 | ||||||
| chr12:39559378
|
C | CA | 68 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0105others(65): Show | 78 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2004-5248dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | ||||||
| chr12:39559378
|
C | CAA | 7 | a0001c0001t0001g0193a0001c0001t0002g0042a0001c0001t0002g0121others(4): Show | 7 | HG00423.hp2 HG00741.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-5249_2004-524 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | ||||||
| chr12:39559378
|
CA | C | 11 | a0001c0001t0001g0132a0001c0001t0001g0203a0001c0001t0001g0252others(8): Show | 12 | HG01167.hp2 HG01192.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.2004-5248delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | ||||||
| chr12:39559378
|
CAAAAAAA others(5): Show |
C | 26 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(23): Show | 39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-5259_2004-524 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | ||||||
| chr12:39559400
|
A | G | 26 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(23): Show | 39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-5269T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559400 | ||||||
| chr12:39559571
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0169 | 7 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-5440G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559571 | ||||||
| chr12:39559727
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2004-5596G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559727 | ||||||
| chr12:39560072
|
A | G | 1 | a0001c0001t0003g0047 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2004-5941T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560072 | ||||||
| chr12:39560147
|
C | T | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-6016G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560147 | ||||||
| chr12:39560162
|
G | T | 1 | a0001c0001t0014g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2004-6031C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560162 | ||||||
| chr12:39560191
|
T | A | 1 | a0001c0001t0022g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2004-6060A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560191 | ||||||
| chr12:39560289
|
C | T | 3 | a0001c0001t0002g0119a0001c0001t0002g0161a0001c0001t0002g0163 | 3 | HG03491.hp2 HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2004-6158G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560289 | ||||||
| chr12:39560471
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2004-6340T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560471 | ||||||
| chr12:39560508
|
C | G | 1 | a0001c0001t0002g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2004-6377G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560508 | ||||||
| chr12:39560905
|
G | A | 5 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-6774C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560905 | ||||||
| chr12:39560938
|
A | G | 1 | a0001c0001t0003g0006 | 3 | NA18939.hp1 NA18997.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2004-6807T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560938 | ||||||
| chr12:39561115
|
G | A | 1 | a0001c0001t0005g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2004-6984C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561115 | ||||||
| chr12:39561233
|
T | TAA | 18 | a0001c0001t0006g0010a0001c0001t0006g0050a0001c0001t0006g0052others(15): Show | 19 | HG00280.hp1 HG01106.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.2004-7104_2004-710 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561233 | ||||||
| chr12:39561233
|
T | TAAA | 96 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0002others(93): Show | 118 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2004-7105_2004-710 others(7): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561233 | ||||||
| chr12:39561283
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2004-7152G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561283 | ||||||
| chr12:39561391
|
C | CA | 34 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0178others(31): Show | 43 | HG00741.hp1 HG01192.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.2004-7261dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561391 | ||||||
| chr12:39561391
|
CA | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0132a0001c0001t0001g0213others(3): Show | 6 | HG01168.hp1 HG01943.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-7261delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561391 | ||||||
| chr12:39561428
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2004-7297T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561428 | ||||||
| chr12:39561446
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(38): Show | 50 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2004-7315G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561446 | ||||||
| chr12:39561480
|
A | T | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2004-7349T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561480 | ||||||
| chr12:39561624
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2004-7493T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561624 | ||||||
| chr12:39561653
|
T | G | 10 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(7): Show | 10 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004-7522A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561653 | ||||||
| chr12:39561707
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0248 | 2 | HG01975.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2004-7576T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561707 | ||||||
| chr12:39561937
|
T | C | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2004-7806A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561937 | ||||||
| chr12:39562000
|
T | C | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2004-7869A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562000 | ||||||
| chr12:39562084
|
GT | G | 11 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(8): Show | 18 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2004-7954delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562084 | ||||||
| chr12:39562089
|
C | A | 1 | a0001c0001t0027g0059 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2004-7958G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562089 | ||||||
| chr12:39562132
|
T | A | 1 | a0001c0001t0025g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2004-8001A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562132 | ||||||
| chr12:39562306
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2004-8175G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562306 | ||||||
| chr12:39562374
|
A | C | 1 | a0001c0001t0028g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2004-8243T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562374 | ||||||
| chr12:39562458
|
A | G | 1 | a0001c0001t0017g0215 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2004-8327T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562458 | ||||||
| chr12:39562541
|
G | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0186 | 2 | HG01168.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2004-8410C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562541 | ||||||
| chr12:39562587
|
A | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-8456T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562587 | ||||||
| chr12:39562607
|
C | T | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-8476G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562607 | ||||||
| chr12:39562732
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2004-8601T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562732 | ||||||
| chr12:39563141
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2004-9010T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563141 | ||||||
| chr12:39563146
|
T | C | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2004-9015A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563146 | ||||||
| chr12:39563180
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2004-9049T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563180 | ||||||
| chr12:39563582
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0200 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2004-9451A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563582 | ||||||
| chr12:39563645
|
C | CT | 35 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(32): Show | 43 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2004-9515dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563645 | ||||||
| chr12:39563709
|
T | C | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-9578A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563709 | ||||||
| chr12:39563782
|
T | A | 35 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(32): Show | 43 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2004-9651A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563782 | ||||||
| chr12:39563947
|
A | G | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+9769T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563947 | ||||||
| chr12:39564202
|
C | A | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+9514G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564202 | ||||||
| chr12:39564257
|
G | A | 3 | a0001c0001t0003g0006a0001c0001t0003g0040a0001c0001t0003g0041 | 5 | NA18939.hp1 NA18941.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003+9459C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564257 | ||||||
| chr12:39564273
|
A | G | 15 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(12): Show | 20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+9443T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564273 | ||||||
| chr12:39564286
|
C | T | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+9430G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564286 | ||||||
| chr12:39564310
|
A | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | NA19062.hp1 NA19080.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.2003+9406T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564310 | ||||||
| chr12:39564324
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2003+9392G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564324 | ||||||
| chr12:39564348
|
T | C | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+9368A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564348 | ||||||
| chr12:39564379
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG00609.hp2 NA18747.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+9337T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564379 | ||||||
| chr12:39564464
|
T | G | 1 | a0001c0001t0005g0088 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2003+9252A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564464 | ||||||
| chr12:39564582
|
C | T | 2 | a0001c0001t0015g0093a0001c0001t0015g0094 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2003+9134G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564582 | ||||||
| chr12:39564593
|
A | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+9123T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564593 | ||||||
| chr12:39564713
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2003+9003C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564713 | ||||||
| chr12:39564797
|
A | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0203others(1): Show | 5 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003+8919T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564797 | ||||||
| chr12:39565031
|
G | C | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003+8685C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565031 | ||||||
| chr12:39565036
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2003+8680C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565036 | ||||||
| chr12:39565362
|
T | C | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2003+8354A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565362 | ||||||
| chr12:39565482
|
A | G | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2003+8234T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565482 | ||||||
| chr12:39565556
|
T | A | 113 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(110): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2003+8160A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565556 | ||||||
| chr12:39565679
|
G | A | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+8037C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565679 | ||||||
| chr12:39565686
|
A | G | 1 | a0001c0001t0002g0278 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2003+8030T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565686 | ||||||
| chr12:39565726
|
C | T | 2 | a0001c0001t0006g0010a0001c0001t0006g0053 | 3 | HG00280.hp1 HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2003+7990G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565726 | ||||||
| chr12:39565840
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2003+7876C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565840 | ||||||
| chr12:39566164
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2003+7552G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566164 | ||||||
| chr12:39566207
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2003+7509G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566207 | ||||||
| chr12:39566211
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0135a0001c0001t0001g0172 | 4 | HG02922.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2003+7505A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566211 | ||||||
| chr12:39566317
|
G | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG00609.hp2 NA18747.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+7399C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566317 | ||||||
| chr12:39566349
|
T | G | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+7367A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566349 | ||||||
| chr12:39566370
|
G | T | 16 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(13): Show | 24 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2003+7346C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566370 | ||||||
| chr12:39566373
|
G | A | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+7343C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566373 | ||||||
| chr12:39566435
|
T | C | 113 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(110): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2003+7281A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566435 | ||||||
| chr12:39566490
|
T | C | 1 | a0001c0001t0017g0215 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2003+7226A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566490 | ||||||
| chr12:39566511
|
C | A | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+7205G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566511 | ||||||
| chr12:39566545
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2003+7171C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566545 | ||||||
| chr12:39566581
|
C | T | 2 | a0001c0001t0006g0052a0001c0001t0006g0055 | 2 | HG01175.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2003+7135G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566581 | ||||||
| chr12:39566606
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 6 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003+7110T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566606 | ||||||
| chr12:39566736
|
T | G | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+6980A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566736 | ||||||
| chr12:39566741
|
C | A | 21 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132others(18): Show | 22 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.2003+6975G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566741 | ||||||
| chr12:39566755
|
G | C | 1 | a0001c0001t0003g0036 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2003+6961C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566755 | ||||||
| chr12:39566933
|
T | G | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+6783A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566933 | ||||||
| chr12:39567220
|
C | T | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+6496G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567220 | ||||||
| chr12:39567221
|
G | A | 15 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(12): Show | 20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+6495C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567221 | ||||||
| chr12:39567260
|
G | A | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2003+6456C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567260 | ||||||
| chr12:39567322
|
G | T | 4 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(1): Show | 5 | HG02809.hp1 HG03041.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003+6394C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567322 | ||||||
| chr12:39567341
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2003+6375T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567341 | ||||||
| chr12:39567342
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2003+6374A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567342 | ||||||
| chr12:39567422
|
A | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0251 | 2 | NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2003+6294T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567422 | ||||||
| chr12:39567492
|
C | T | 2 | a0001c0001t0004g0016a0001c0001t0004g0134 | 3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2003+6224G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567492 | ||||||
| chr12:39567511
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2003+6205T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567511 | ||||||
| chr12:39567516
|
A | G | 15 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(12): Show | 20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+6200T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567516 | ||||||
| chr12:39567532
|
A | G | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+6184T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567532 | ||||||
| chr12:39567561
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2003+6155A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567561 | ||||||
| chr12:39567562
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2003+6154C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567562 | ||||||
| chr12:39567644
|
T | TTGTTA | 237 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(234): Show | 282 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.2003+6071_2003+607 others(9): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567644 | ||||||
| chr12:39567654
|
T | A | 1 | a0001c0001t0002g0170 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2003+6062A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567654 | ||||||
| chr12:39567786
|
G | C | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+5930C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567786 | ||||||
| chr12:39567957
|
A | C | 11 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(8): Show | 16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2003+5759T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567957 | ||||||
| chr12:39567988
|
T | G | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+5728A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567988 | ||||||
| chr12:39568010
|
G | C | 1 | a0001c0001t0002g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2003+5706C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568010 | ||||||
| chr12:39568011
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2003+5705C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568011 | ||||||
| chr12:39568032
|
C | G | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+5684G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568032 | ||||||
| chr12:39568302
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2003+5414A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568302 | ||||||
| chr12:39568442
|
C | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0203others(1): Show | 5 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003+5274G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568442 | ||||||
| chr12:39568450
|
A | G | 235 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(232): Show | 280 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.2003+5266T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568450 | ||||||
| chr12:39568455
|
C | T | 30 | a0001c0001t0001g0015a0001c0001t0001g0111a0001c0001t0001g0114others(27): Show | 31 | HG01175.hp2 HG01255.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.2003+5261G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568455 | ||||||
| chr12:39568526
|
G | A | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2003+5190C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568526 | ||||||
| chr12:39568569
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 6 | HG00741.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003+5147G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568569 | ||||||
| chr12:39568589
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2003+5127C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568589 | ||||||
| chr12:39568627
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2003+5089G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568627 | ||||||
| chr12:39568649
|
G | A | 13 | a0001c0001t0002g0026a0001c0001t0002g0128a0001c0001t0002g0160others(10): Show | 14 | HG00438.hp2 HG02040.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.2003+5067C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568649 | ||||||
| chr12:39568678
|
G | A | 38 | a0001c0001t0002g0119a0001c0001t0002g0161a0001c0001t0002g0163others(35): Show | 46 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.2003+5038C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568678 | ||||||
| chr12:39568760
|
A | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0251others(1): Show | 4 | HG02071.hp1 NA18956.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+4956T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568760 | ||||||
| chr12:39568919
|
G | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(11): Show | 21 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2003+4797C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568919 | ||||||
| chr12:39568961
|
T | C | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+4755A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568961 | ||||||
| chr12:39569040
|
T | G | 98 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(95): Show | 116 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.2003+4676A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569040 | ||||||
| chr12:39569055
|
G | C | 1 | a0001c0001t0008g0261 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2003+4661C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569055 | ||||||
| chr12:39569131
|
A | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+4585T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569131 | ||||||
| chr12:39569150
|
A | G | 18 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(15): Show | 25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2003+4566T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569150 | ||||||
| chr12:39569294
|
C | T | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+4422G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569294 | ||||||
| chr12:39569295
|
G | A | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+4421C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569295 | ||||||
| chr12:39569332
|
A | G | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+4384T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569332 | ||||||
| chr12:39569338
|
C | A | 40 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(37): Show | 49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.2003+4378G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569338 | ||||||
| chr12:39569411
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0117a0001c0001t0001g0125others(1): Show | 4 | HG01106.hp2 HG01433.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2003+4305T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569411 | ||||||
| chr12:39569421
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0266 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.2003+4295C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569421 | ||||||
| chr12:39569459
|
G | C | 1 | a0001c0001t0002g0162 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2003+4257C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569459 | ||||||
| chr12:39569460
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2003+4256G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569460 | ||||||
| chr12:39569559
|
A | T | 13 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(10): Show | 20 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+4157T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569559 | ||||||
| chr12:39569608
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2003+4108G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569608 | ||||||
| chr12:39569612
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA19005.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2003+4104G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569612 | ||||||
| chr12:39569641
|
G | A | 3 | a0001c0001t0002g0188a0001c0001t0009g0013a0002c0002t0004g0286 | 4 | HG02129.hp1 HG03710.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+4075C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569641 | ||||||
| chr12:39569672
|
G | A | 6 | a0001c0001t0001g0111a0001c0001t0010g0011a0001c0001t0010g0074others(3): Show | 7 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+4044C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569672 | ||||||
| chr12:39569863
|
T | G | 1 | a0001c0001t0003g0141 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2003+3853A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569863 | ||||||
| chr12:39569885
|
A | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+3831T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569885 | ||||||
| chr12:39569917
|
A | T | 1 | a0001c0001t0009g0013 | 2 | HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+3799T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569917 | ||||||
| chr12:39570204
|
A | G | 91 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(88): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.2003+3512T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570204 | ||||||
| chr12:39570310
|
C | T | 1 | a0001c0001t0018g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2003+3406G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570310 | ||||||
| chr12:39570573
|
A | C | 50 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(47): Show | 59 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2003+3143T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570573 | ||||||
| chr12:39570661
|
G | C | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+3055C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570661 | ||||||
| chr12:39570697
|
C | A | 14 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(11): Show | 21 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2003+3019G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570697 | ||||||
| chr12:39570728
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2003+2988G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570728 | ||||||
| chr12:39570878
|
A | T | 1 | a0001c0001t0001g0283 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2003+2838T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570878 | ||||||
| chr12:39571010
|
AATC | A | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+2703_2003+270 others(7): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571010 | ||||||
| chr12:39571069
|
A | T | 1 | a0001c0001t0001g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2003+2647T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571069 | ||||||
| chr12:39571130
|
A | AATTAGTA others(5): Show |
1 | a0001c0001t0001g0146 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2003+2574_2003+258 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571130 | ||||||
| chr12:39571135
|
G | A | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2003+2581C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571135 | ||||||
| chr12:39571406
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2003+2310C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571406 | ||||||
| chr12:39571471
|
A | T | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+2245T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571471 | ||||||
| chr12:39571476
|
A | G | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+2240T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571476 | ||||||
| chr12:39571516
|
T | C | 1 | a0001c0001t0006g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2003+2200A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571516 | ||||||
| chr12:39571580
|
A | G | 23 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(20): Show | 30 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.2003+2136T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571580 | ||||||
| chr12:39571639
|
C | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 338 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(335): Show |
intron_variant | MODIFIER | c.2003+2077G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571639 | ||||||
| chr12:39571812
|
A | C | 1 | a0001c0001t0001g0271 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2003+1904T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571812 | ||||||
| chr12:39571835
|
T | A | 18 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(15): Show | 25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2003+1881A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571835 | ||||||
| chr12:39572113
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2003+1603A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572113 | ||||||
| chr12:39572120
|
G | A | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003+1596C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572120 | ||||||
| chr12:39572140
|
G | C | 1 | a0001c0001t0010g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2003+1576C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572140 | ||||||
| chr12:39572197
|
T | C | 18 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(15): Show | 25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2003+1519A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572197 | ||||||
| chr12:39572514
|
T | A | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+1202A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572514 | ||||||
| chr12:39572522
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2003+1194A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572522 | ||||||
| chr12:39572527
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2003+1189T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572527 | ||||||
| chr12:39572608
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2003+1108T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572608 | ||||||
| chr12:39572924
|
A | G | 1 | a0001c0001t0005g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2003+792T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572924 | ||||||
| chr12:39573141
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2003+575A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573141 | ||||||
| chr12:39573211
|
T | C | 1 | a0001c0001t0003g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2003+505A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573211 | ||||||
| chr12:39573332
|
G | A | 126 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(123): Show | 156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.2003+384C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573332 | ||||||
| chr12:39573621
|
T | A | 1 | a0001c0001t0003g0044 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2003+95A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573621 | ||||||
| chr12:39573677
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2003+39T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573677 | ||||||
| chr12:39573708
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | splice_region_variant&intron_variant | LOW | c.2003+8T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573708 | ||||||
| chr12:39573859
|
C | G | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1878-18G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39573859 | ||||||
| chr12:39573954
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1878-113C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39573954 | ||||||
| chr12:39573998
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1878-157G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39573998 | ||||||
| chr12:39574052
|
C | T | 61 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(58): Show | 74 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1878-211G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574052 | ||||||
| chr12:39574096
|
G | T | 9 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(6): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1878-255C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574096 | ||||||
| chr12:39574181
|
G | C | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1878-340C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574181 | ||||||
| chr12:39574184
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1878-343A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574184 | ||||||
| chr12:39574330
|
C | T | 1 | a0001c0001t0003g0046 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1878-489G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574330 | ||||||
| chr12:39574485
|
C | T | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1878-644G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574485 | ||||||
| chr12:39575144
|
A | G | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1878-1303T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575144 | ||||||
| chr12:39575305
|
T | G | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1878-1464A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575305 | ||||||
| chr12:39575567
|
T | C | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1878-1726A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575567 | ||||||
| chr12:39575910
|
T | C | 1 | a0001c0001t0008g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1878-2069A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575910 | ||||||
| chr12:39576198
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0221a0001c0001t0002g0226 | 4 | HG00438.hp1 NA19011.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878-2357A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576198 | ||||||
| chr12:39576268
|
C | T | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1878-2427G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576268 | ||||||
| chr12:39576269
|
G | C | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1878-2428C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576269 | ||||||
| chr12:39576471
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG00408.hp1 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1878-2630C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576471 | ||||||
| chr12:39576514
|
C | A | 7 | a0002c0002t0004g0005a0002c0002t0004g0028a0002c0002t0004g0286others(4): Show | 11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1878-2673G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576514 | ||||||
| chr12:39576552
|
T | C | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1878-2711A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576552 | ||||||
| chr12:39576917
|
C | T | 1 | a0001c0001t0015g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1877+2618G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576917 | ||||||
| chr12:39577026
|
A | G | 2 | a0001c0001t0004g0016a0001c0001t0004g0134 | 3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1877+2509T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577026 | ||||||
| chr12:39577412
|
C | G | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+2123G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577412 | ||||||
| chr12:39577438
|
T | C | 40 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(37): Show | 49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1877+2097A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577438 | ||||||
| chr12:39577475
|
T | A | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1877+2060A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577475 | ||||||
| chr12:39577557
|
T | A | 48 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(45): Show | 56 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1877+1978A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577557 | ||||||
| chr12:39577708
|
G | T | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+1827C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577708 | ||||||
| chr12:39577779
|
T | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0194a0001c0001t0001g0227others(3): Show | 7 | NA18951.hp2 NA18957.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1877+1756A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577779 | ||||||
| chr12:39577840
|
C | G | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+1695G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577840 | ||||||
| chr12:39577990
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 6 | HG00741.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1877+1545T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577990 | ||||||
| chr12:39578019
|
C | G | 129 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(126): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1877+1516G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578019 | ||||||
| chr12:39578078
|
T | C | 1 | a0001c0008t0006g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1877+1457A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578078 | ||||||
| chr12:39578196
|
C | T | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+1339G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578196 | ||||||
| chr12:39578212
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1877+1323G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578212 | ||||||
| chr12:39578240
|
C | T | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1877+1295G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578240 | ||||||
| chr12:39578290
|
C | T | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1877+1245G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578290 | ||||||
| chr12:39578473
|
C | CA | 21 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0102others(18): Show | 29 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1877+1061dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578473 | ||||||
| chr12:39578473
|
CA | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(101): Show | 121 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1877+1061delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578473 | ||||||
| chr12:39578517
|
C | T | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1877+1018G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578517 | ||||||
| chr12:39578748
|
A | T | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1877+787T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578748 | ||||||
| chr12:39579137
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1877+398C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579137 | ||||||
| chr12:39579137
|
G | T | 1 | a0001c0001t0009g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1877+398C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579137 | ||||||
| chr12:39579154
|
G | A | 1 | a0001c0001t0027g0059 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1877+381C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579154 | ||||||
| chr12:39579402
|
A | G | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+133T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579402 | ||||||
| chr12:39579636
|
A | T | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1793-17T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39579636 | ||||||
| chr12:39579733
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1793-114A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39579733 | ||||||
| chr12:39580017
|
C | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1793-398G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580017 | ||||||
| chr12:39580231
|
A | G | 246 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 293 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.1793-612T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580231 | ||||||
| chr12:39580359
|
T | G | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1793-740A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580359 | ||||||
| chr12:39580540
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1793-921T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580540 | ||||||
| chr12:39580579
|
C | A | 9 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(6): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-960G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580579 | ||||||
| chr12:39580658
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1793-1039G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580658 | ||||||
| chr12:39580776
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1793-1157A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580776 | ||||||
| chr12:39580800
|
C | A | 33 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0036others(30): Show | 40 | HG00280.hp1 HG00642.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1793-1181G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580800 | ||||||
| chr12:39580804
|
G | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0199 | 2 | NA19064.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1793-1185C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580804 | ||||||
| chr12:39581084
|
C | G | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793-1465G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581084 | ||||||
| chr12:39581432
|
A | G | 2 | a0001c0001t0004g0016a0001c0001t0004g0134 | 3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1793-1813T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581432 | ||||||
| chr12:39581435
|
T | A | 9 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(6): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-1816A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581435 | ||||||
| chr12:39581517
|
A | T | 1 | a0001c0001t0002g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1793-1898T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581517 | ||||||
| chr12:39581594
|
T | C | 1 | a0001c0001t0005g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1793-1975A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581594 | ||||||
| chr12:39581694
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1793-2075C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581694 | ||||||
| chr12:39581700
|
A | C | 9 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(6): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-2081T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581700 | ||||||
| chr12:39581846
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1793-2227G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581846 | ||||||
| chr12:39581900
|
T | C | 50 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(47): Show | 59 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1793-2281A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581900 | ||||||
| chr12:39581929
|
G | A | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1793-2310C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581929 | ||||||
| chr12:39582084
|
G | C | 1 | a0001c0001t0002g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1793-2465C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582084 | ||||||
| chr12:39582174
|
T | C | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1793-2555A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582174 | ||||||
| chr12:39582188
|
AG | A | 1 | a0001c0001t0003g0006 | 3 | NA18939.hp1 NA18997.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1793-2570delC | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582188 | ||||||
| chr12:39582389
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1793-2770T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582389 | ||||||
| chr12:39582648
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1793-3029T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582648 | ||||||
| chr12:39582663
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1793-3044A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582663 | ||||||
| chr12:39582880
|
A | G | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1793-3261T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582880 | ||||||
| chr12:39583020
|
C | G | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1792+3132G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583020 | ||||||
| chr12:39583136
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792+3016T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583136 | ||||||
| chr12:39583207
|
A | C | 3 | a0001c0001t0002g0042a0001c0001t0002g0188a0001c0001t0002g0276 | 3 | HG00423.hp2 NA18952.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1792+2945T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583207 | ||||||
| chr12:39583224
|
C | T | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1792+2928G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583224 | ||||||
| chr12:39583410
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1792+2742T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583410 | ||||||
| chr12:39583821
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1792+2331G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583821 | ||||||
| chr12:39583848
|
T | G | 1 | a0001c0001t0006g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1792+2304A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583848 | ||||||
| chr12:39583972
|
T | G | 1 | a0001c0001t0001g0280 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1792+2180A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583972 | ||||||
| chr12:39583990
|
T | C | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1792+2162A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583990 | ||||||
| chr12:39584081
|
A | G | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1792+2071T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584081 | ||||||
| chr12:39584098
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(48): Show | 60 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1792+2054G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584098 | ||||||
| chr12:39584111
|
G | T | 2 | a0001c0001t0015g0093a0001c0001t0015g0094 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1792+2041C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584111 | ||||||
| chr12:39584237
|
G | A | 2 | a0001c0001t0002g0128a0001c0001t0002g0228 | 2 | HG02056.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1792+1915C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584237 | ||||||
| chr12:39584258
|
C | G | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1792+1894G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584258 | ||||||
| chr12:39584430
|
T | C | 40 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(37): Show | 49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1792+1722A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584430 | ||||||
| chr12:39584434
|
T | G | 1 | a0001c0001t0025g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1792+1718A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584434 | ||||||
| chr12:39584477
|
C | G | 1 | a0001c0001t0006g0062 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1792+1675G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584477 | ||||||
| chr12:39584541
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1792+1611A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584541 | ||||||
| chr12:39584602
|
T | C | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+1550A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584602 | ||||||
| chr12:39584785
|
C | T | 2 | a0001c0001t0006g0054a0001c0001t0006g0077 | 2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1792+1367G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584785 | ||||||
| chr12:39584927
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1792+1225T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584927 | ||||||
| chr12:39585018
|
A | G | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1792+1134T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585018 | ||||||
| chr12:39585034
|
G | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0179a0001c0001t0001g0187 | 3 | HG01070.hp2 HG01433.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1792+1118C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585034 | ||||||
| chr12:39585060
|
G | A | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1792+1092C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585060 | ||||||
| chr12:39585167
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1792+985G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585167 | ||||||
| chr12:39585265
|
T | C | 1 | a0001c0001t0006g0077 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1792+887A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585265 | ||||||
| chr12:39585270
|
T | C | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1792+882A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585270 | ||||||
| chr12:39585294
|
C | G | 1 | a0001c0001t0003g0037 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1792+858G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585294 | ||||||
| chr12:39585314
|
G | A | 40 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(37): Show | 49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1792+838C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585314 | ||||||
| chr12:39585590
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1792+562T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585590 | ||||||
| chr12:39585615
|
A | G | 1 | a0001c0001t0011g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1792+537T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585615 | ||||||
| chr12:39585642
|
C | T | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1792+510G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585642 | ||||||
| chr12:39585732
|
C | T | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1792+420G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585732 | ||||||
| chr12:39585756
|
C | T | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792+396G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585756 | ||||||
| chr12:39585889
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1792+263G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585889 | ||||||
| chr12:39586014
|
A | T | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1792+138T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586014 | ||||||
| chr12:39586037
|
T | C | 40 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(37): Show | 49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1792+115A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586037 | ||||||
| chr12:39586050
|
G | A | 11 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(8): Show | 16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1792+102C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586050 | ||||||
| chr12:39586098
|
G | C | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1792+54C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586098 | ||||||
| chr12:39586109
|
A | T | 7 | a0002c0002t0004g0005a0002c0002t0004g0028a0002c0002t0004g0286others(4): Show | 11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1792+43T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586109 | ||||||
| chr12:39586332
|
A | G | 1 | a0001c0001t0006g0062 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1647-35T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586332 | ||||||
| chr12:39586422
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0169 | 7 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647-125A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586422 | ||||||
| chr12:39586446
|
C | A | 1 | a0001c0001t0001g0238 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1647-149G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586446 | ||||||
| chr12:39586456
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1647-159C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586456 | ||||||
| chr12:39586554
|
A | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0259 | 2 | HG01069.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1647-257T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586554 | ||||||
| chr12:39586684
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1647-387A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586684 | ||||||
| chr12:39586721
|
T | C | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1647-424A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586721 | ||||||
| chr12:39586735
|
T | A | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1647-438A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586735 | ||||||
| chr12:39586815
|
G | A | 35 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(32): Show | 43 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1647-518C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586815 | ||||||
| chr12:39586904
|
A | G | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1647-607T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586904 | ||||||
| chr12:39587169
|
C | A | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1647-872G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587169 | ||||||
| chr12:39587202
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1647-905A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587202 | ||||||
| chr12:39587741
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0125 | 2 | HG01433.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1647-1444A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587741 | ||||||
| chr12:39587928
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1647-1631T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587928 | ||||||
| chr12:39587932
|
T | C | 2 | a0001c0001t0015g0093a0001c0001t0015g0094 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1647-1635A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587932 | ||||||
| chr12:39587937
|
C | T | 9 | a0001c0001t0001g0229a0001c0001t0001g0239a0001c0001t0007g0070others(6): Show | 9 | HG00639.hp2 HG01081.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1647-1640G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587937 | ||||||
| chr12:39588031
|
C | T | 13 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(10): Show | 18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1647-1734G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588031 | ||||||
| chr12:39588118
|
G | A | 1 | a0001c0001t0005g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1647-1821C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588118 | ||||||
| chr12:39588176
|
T | A | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1647-1879A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588176 | ||||||
| chr12:39588494
|
C | T | 17 | a0001c0001t0006g0010a0001c0001t0006g0050a0001c0001t0006g0052others(14): Show | 18 | HG00280.hp1 HG01175.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1647-2197G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588494 | ||||||
| chr12:39588528
|
A | C | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-2231T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588528 | ||||||
| chr12:39588611
|
A | G | 49 | a0001c0001t0001g0185a0001c0001t0002g0002a0001c0001t0002g0019others(46): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1647-2314T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588611 | ||||||
| chr12:39588751
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1647-2454C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588751 | ||||||
| chr12:39589080
|
G | A | 80 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0009others(77): Show | 103 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1647-2783C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589080 | ||||||
| chr12:39589149
|
A | G | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647-2852T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589149 | ||||||
| chr12:39589200
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1647-2903T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589200 | ||||||
| chr12:39589202
|
C | T | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1647-2905G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589202 | ||||||
| chr12:39589209
|
T | G | 11 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(8): Show | 16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1647-2912A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589209 | ||||||
| chr12:39589350
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0200 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1647-3053T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589350 | ||||||
| chr12:39589384
|
G | GT | 33 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0110others(30): Show | 34 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1647-3088dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589384 | ||||||
| chr12:39589384
|
GT | G | 51 | a0001c0001t0001g0129a0001c0001t0001g0282a0001c0001t0003g0004others(48): Show | 64 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1647-3088delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589384 | ||||||
| chr12:39589417
|
C | T | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1647-3120G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589417 | ||||||
| chr12:39589509
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0236others(1): Show | 4 | HG02071.hp2 NA18942.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647-3212A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589509 | ||||||
| chr12:39589600
|
G | A | 17 | a0001c0001t0006g0010a0001c0001t0006g0050a0001c0001t0006g0052others(14): Show | 18 | HG00280.hp1 HG01175.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1647-3303C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589600 | ||||||
| chr12:39589623
|
G | A | 11 | a0001c0001t0004g0016a0001c0001t0004g0051a0001c0001t0004g0061others(8): Show | 16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1647-3326C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589623 | ||||||
| chr12:39589629
|
C | T | 16 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(13): Show | 24 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1647-3332G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589629 | ||||||
| chr12:39589630
|
G | A | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1647-3333C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589630 | ||||||
| chr12:39589660
|
T | C | 9 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(6): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1647-3363A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589660 | ||||||
| chr12:39589676
|
C | T | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-3379G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589676 | ||||||
| chr12:39589681
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1647-3384G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589681 | ||||||
| chr12:39589896
|
T | C | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1647-3599A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589896 | ||||||
| chr12:39589960
|
T | A | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1647-3663A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589960 | ||||||
| chr12:39590222
|
C | T | 14 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(11): Show | 21 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1647-3925G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590222 | ||||||
| chr12:39590590
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1647-4293A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590590 | ||||||
| chr12:39590756
|
A | AT | 10 | a0001c0001t0001g0157a0001c0001t0001g0185a0001c0001t0005g0092others(7): Show | 10 | HG01175.hp1 HG01255.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1647-4460dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590756 | ||||||
| chr12:39590889
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0154others(1): Show | 4 | HG00738.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647-4592T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590889 | ||||||
| chr12:39590967
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1647-4670T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590967 | ||||||
| chr12:39591026
|
CAA | C | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-4731_1647-473 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591026 | ||||||
| chr12:39591110
|
A | G | 1 | a0001c0007t0007g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1647-4813T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591110 | ||||||
| chr12:39591183
|
A | G | 2 | a0001c0001t0009g0013a0001c0001t0023g0080 | 3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-4886T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591183 | ||||||
| chr12:39591255
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1647-4958A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591255 | ||||||
| chr12:39591404
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(49): Show | 61 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1647-5107T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591404 | ||||||
| chr12:39591570
|
G | T | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1647-5273C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591570 | ||||||
| chr12:39591987
|
A | G | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1647-5690T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591987 | ||||||
| chr12:39592124
|
C | T | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647-5827G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592124 | ||||||
| chr12:39592191
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1647-5894G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592191 | ||||||
| chr12:39592290
|
C | A | 1 | a0001c0001t0018g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1647-5993G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592290 | ||||||
| chr12:39592302
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1647-6005C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592302 | ||||||
| chr12:39592457
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1647-6160T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592457 | ||||||
| chr12:39592576
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1647-6279T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592576 | ||||||
| chr12:39592646
|
C | T | 3 | a0001c0001t0006g0062a0001c0001t0006g0063a0001c0001t0006g0064 | 3 | HG02129.hp2 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1647-6349G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592646 | ||||||
| chr12:39592664
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1647-6367C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592664 | ||||||
| chr12:39592880
|
A | G | 1 | a0001c0001t0004g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1647-6583T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592880 | ||||||
| chr12:39593105
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1647-6808G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593105 | ||||||
| chr12:39593126
|
G | A | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647-6829C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593126 | ||||||
| chr12:39593238
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1647-6941T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593238 | ||||||
| chr12:39593562
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1646+7009A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593562 | ||||||
| chr12:39593825
|
C | A | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+6746G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593825 | ||||||
| chr12:39593853
|
A | G | 9 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1646+6718T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593853 | ||||||
| chr12:39593896
|
A | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(81): Show | 109 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.1646+6675T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593896 | ||||||
| chr12:39593968
|
C | T | 13 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(10): Show | 20 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1646+6603G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593968 | ||||||
| chr12:39594042
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1646+6529A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594042 | ||||||
| chr12:39594105
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1646+6466G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594105 | ||||||
| chr12:39594260
|
T | G | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1646+6311A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594260 | ||||||
| chr12:39594348
|
T | TATA | 2 | a0001c0001t0004g0016a0001c0001t0004g0134 | 3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1646+6220_1646+622 others(7): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594348 | ||||||
| chr12:39594348
|
T | TATATA | 80 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(77): Show | 103 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1646+6218_1646+622 others(9): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594348 | ||||||
| chr12:39594381
|
T | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1646+6190A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594381 | ||||||
| chr12:39594426
|
A | G | 11 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(8): Show | 18 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1646+6145T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594426 | ||||||
| chr12:39594434
|
T | C | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+6137A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594434 | ||||||
| chr12:39594713
|
T | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(81): Show | 108 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1646+5858A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594713 | ||||||
| chr12:39594761
|
G | T | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1646+5810C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594761 | ||||||
| chr12:39594837
|
C | G | 84 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(81): Show | 108 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1646+5734G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594837 | ||||||
| chr12:39594847
|
G | A | 3 | a0001c0001t0009g0033a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1646+5724C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594847 | ||||||
| chr12:39595169
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(68): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1646+5402C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595169 | ||||||
| chr12:39595225
|
G | C | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+5346C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595225 | ||||||
| chr12:39595370
|
A | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(75): Show | 101 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1646+5201T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595370 | ||||||
| chr12:39595685
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0259 | 2 | HG01069.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1646+4886A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595685 | ||||||
| chr12:39595818
|
T | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1646+4753A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595818 | ||||||
| chr12:39596274
|
T | A | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+4297A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596274 | ||||||
| chr12:39596447
|
G | T | 1 | a0002c0002t0004g0290 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1646+4124C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596447 | ||||||
| chr12:39596463
|
C | T | 3 | a0001c0001t0002g0034a0001c0001t0009g0013a0001c0001t0023g0080 | 4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646+4108G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596463 | ||||||
| chr12:39596476
|
TCC | T | 2 | a0001c0001t0006g0010a0001c0001t0006g0053 | 3 | HG00280.hp1 HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1646+4093_1646+409 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596476 | ||||||
| chr12:39596477
|
C | A | 1 | a0001c0001t0001g0233 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1646+4094G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596477 | ||||||
| chr12:39596507
|
A | T | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+4064T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596507 | ||||||
| chr12:39596775
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1646+3796G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596775 | ||||||
| chr12:39596797
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1646+3774A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596797 | ||||||
| chr12:39596802
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1646+3769C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596802 | ||||||
| chr12:39597227
|
C | T | 17 | a0001c0001t0002g0034a0001c0001t0004g0078a0001c0001t0004g0079others(14): Show | 23 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1646+3344G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597227 | ||||||
| chr12:39597234
|
T | A | 17 | a0001c0001t0002g0034a0001c0001t0004g0078a0001c0001t0004g0079others(14): Show | 23 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1646+3337A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597234 | ||||||
| chr12:39597238
|
T | A | 1 | a0001c0001t0007g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1646+3333A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597238 | ||||||
| chr12:39597695
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1646+2876T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597695 | ||||||
| chr12:39597760
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1646+2811A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597760 | ||||||
| chr12:39597800
|
T | C | 3 | a0001c0001t0011g0081a0001c0006t0024g0030a0003c0009t0011g0285 | 3 | HG01891.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1646+2771A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597800 | ||||||
| chr12:39598156
|
A | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1646+2415T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598156 | ||||||
| chr12:39598185
|
T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 9 | HG00741.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1646+2386A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598185 | ||||||
| chr12:39598307
|
C | A | 2 | a0001c0001t0011g0081a0003c0009t0011g0285 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1646+2264G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598307 | ||||||
| chr12:39598476
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1646+2095G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598476 | ||||||
| chr12:39598479
|
C | T | 1 | a0001c0001t0002g0021 | 2 | NA18956.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1646+2092G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598479 | ||||||
| chr12:39598486
|
T | C | 213 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(210): Show | 252 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1646+2085A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598486 | ||||||
| chr12:39598487
|
G | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0091 | 3 | HG02895.hp1 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1646+2084C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598487 | ||||||
| chr12:39598562
|
G | A | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1646+2009C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598562 | ||||||
| chr12:39599071
|
G | T | 1 | a0001c0001t0011g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1646+1500C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599071 | ||||||
| chr12:39599073
|
T | G | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+1498A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599073 | ||||||
| chr12:39599135
|
G | A | 1 | a0001c0001t0008g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1646+1436C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599135 | ||||||
| chr12:39599271
|
T | C | 5 | a0001c0001t0010g0011a0001c0001t0010g0074a0001c0001t0010g0076others(2): Show | 6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1646+1300A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599271 | ||||||
| chr12:39599307
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1646+1264T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599307 | ||||||
| chr12:39599335
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1646+1236G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599335 | ||||||
| chr12:39599456
|
G | A | 1 | a0002c0002t0004g0290 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1646+1115C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599456 | ||||||
| chr12:39599658
|
C | T | 15 | a0001c0001t0001g0012a0001c0001t0004g0078a0001c0001t0004g0079others(12): Show | 21 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1646+913G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599658 | ||||||
| chr12:39600192
|
T | TA | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1646+378_1646+379i others(3): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39600192 | ||||||
| chr12:39600229
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1646+342C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39600229 | ||||||
| chr12:39600872
|
T | C | 21 | a0001c0001t0002g0042a0001c0001t0003g0004a0001c0001t0003g0006others(18): Show | 28 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1501-156A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39600872 | ||||||
| chr12:39601160
|
A | G | 1 | a0001c0001t0016g0029 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1501-444T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601160 | ||||||
| chr12:39601388
|
AAT | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 9 | HG00741.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1501-674_1501-673d others(4): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601388 | ||||||
| chr12:39601421
|
GTTAT | G | 6 | a0001c0001t0008g0216a0001c0001t0008g0234a0001c0001t0008g0260others(3): Show | 6 | HG00733.hp2 HG01109.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1501-709_1501-706d others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601421 | ||||||
| chr12:39601544
|
T | C | 3 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0192 | 3 | HG02132.hp1 NA18947.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1501-828A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601544 | ||||||
| chr12:39601559
|
G | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG00609.hp2 HG02080.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1501-843C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601559 | ||||||
| chr12:39601571
|
C | A | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501-855G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601571 | ||||||
| chr12:39601729
|
G | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0249 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1501-1013C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601729 | ||||||
| chr12:39601757
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1501-1041C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601757 | ||||||
| chr12:39601766
|
T | C | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1501-1050A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601766 | ||||||
| chr12:39602127
|
T | TTTTA | 39 | a0001c0001t0001g0024a0001c0001t0001g0095a0001c0001t0001g0103others(36): Show | 46 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1501-1415_1501-141 others(8): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | ||||||
| chr12:39602127
|
T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0239a0001c0001t0010g0074a0001c0001t0018g0073others(1): Show | 4 | HG00639.hp2 HG01192.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501-1419_1501-141 others(12): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | ||||||
| chr12:39602127
|
T | TTTTATTT others(5): Show |
4 | a0001c0001t0001g0012a0001c0001t0010g0011a0001c0001t0010g0076others(1): Show | 6 | HG01891.hp2 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1501-1423_1501-141 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | ||||||
| chr12:39602127
|
TTTTA | T | 19 | a0001c0001t0001g0120a0001c0001t0001g0131a0001c0001t0001g0133others(16): Show | 21 | HG00544.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1501-1415_1501-141 others(8): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | ||||||
| chr12:39602127
|
TTTTATTT others(1): Show |
T | 57 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(54): Show | 74 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1501-1419_1501-141 others(12): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | ||||||
| chr12:39602127
|
TTTTATTT others(5): Show |
T | 2 | a0001c0001t0001g0069a0001c0001t0006g0052 | 2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1501-1423_1501-141 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | ||||||
| chr12:39602256
|
G | T | 1 | a0001c0001t0009g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1501-1540C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602256 | ||||||
| chr12:39602296
|
G | T | 7 | a0002c0002t0004g0005a0002c0002t0004g0028a0002c0002t0004g0286others(4): Show | 11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1501-1580C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602296 | ||||||
| chr12:39602341
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0268 | 3 | HG01257.hp1 HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1500+1571T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602341 | ||||||
| chr12:39602345
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1500+1567C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602345 | ||||||
| chr12:39602445
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1500+1467G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602445 | ||||||
| chr12:39602643
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1500+1269A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602643 | ||||||
| chr12:39602671
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1500+1241A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602671 | ||||||
| chr12:39602684
|
CTGAG | C | 4 | a0001c0001t0002g0034a0001c0001t0009g0013a0001c0001t0023g0080others(1): Show | 5 | HG00733.hp2 HG01891.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1500+1224_1500+122 others(8): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602684 | ||||||
| chr12:39602708
|
T | A | 1 | a0001c0001t0025g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1500+1204A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602708 | ||||||
| chr12:39602857
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1500+1055G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602857 | ||||||
| chr12:39602891
|
A | T | 15 | a0001c0001t0001g0012a0001c0001t0004g0078a0001c0001t0004g0079others(12): Show | 21 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1500+1021T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602891 | ||||||
| chr12:39602931
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0267others(1): Show | 4 | NA18988.hp1 NA18989.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500+981C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602931 | ||||||
| chr12:39603259
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0002g0184a0001c0001t0002g0186 | 3 | HG01168.hp2 HG01255.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1500+653C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603259 | ||||||
| chr12:39603353
|
A | G | 18 | a0001c0001t0001g0012a0001c0001t0004g0078a0001c0001t0004g0079others(15): Show | 24 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1500+559T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603353 | ||||||
| chr12:39603381
|
T | G | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1500+531A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603381 | ||||||
| chr12:39603388
|
A | T | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1500+524T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603388 | ||||||
| chr12:39603645
|
C | G | 84 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0067others(81): Show | 109 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1500+267G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603645 | ||||||
| chr12:39603692
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1500+220A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603692 | ||||||
| chr12:39603796
|
C | T | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0249others(2): Show | 5 | HG02602.hp1 HG02735.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1500+116G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603796 | ||||||
| chr12:39603844
|
C | T | 9 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(6): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1500+68G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603844 | ||||||
| chr12:39604065
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1406-59C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604065 | ||||||
| chr12:39604065
|
G | T | 83 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0067others(80): Show | 107 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.1406-59C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604065 | ||||||
| chr12:39604067
|
A | T | 1 | a0001c0001t0003g0036 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1406-61T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604067 | ||||||
| chr12:39604195
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1406-189T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604195 | ||||||
| chr12:39604296
|
C | G | 3 | a0001c0001t0002g0034a0001c0001t0009g0013a0001c0001t0023g0080 | 4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-290G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604296 | ||||||
| chr12:39604342
|
T | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(41): Show | 54 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1406-336A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604342 | ||||||
| chr12:39604371
|
G | T | 1 | a0002c0002t0004g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1406-365C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604371 | ||||||
| chr12:39604468
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1405+294A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604468 | ||||||
| chr12:39604965
|
T | C | 9 | a0001c0001t0002g0021a0001c0001t0002g0188a0001c0001t0002g0189others(6): Show | 10 | HG00621.hp1 HG02132.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237-35A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39604965 | ||||||
| chr12:39605006
|
A | T | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1237-76T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605006 | ||||||
| chr12:39605031
|
T | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(60): Show | 82 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1237-101A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605031 | ||||||
| chr12:39605344
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1237-414G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605344 | ||||||
| chr12:39605523
|
C | T | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1237-593G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605523 | ||||||
| chr12:39605535
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1237-605A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605535 | ||||||
| chr12:39605550
|
A | G | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1237-620T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605550 | ||||||
| chr12:39605585
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1237-655T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605585 | ||||||
| chr12:39605613
|
C | G | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-683G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605613 | ||||||
| chr12:39605623
|
C | T | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-693G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605623 | ||||||
| chr12:39605761
|
T | C | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1237-831A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605761 | ||||||
| chr12:39605796
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1237-866A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605796 | ||||||
| chr12:39605834
|
TACA | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0146others(5): Show | 8 | HG00597.hp2 HG00621.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-907_1237-905d others(5): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605834 | ||||||
| chr12:39605885
|
A | G | 1 | a0001c0001t0009g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1237-955T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605885 | ||||||
| chr12:39605933
|
C | G | 1 | a0001c0001t0008g0216 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1237-1003G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605933 | ||||||
| chr12:39605983
|
T | C | 1 | a0001c0001t0003g0066 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1237-1053A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605983 | ||||||
| chr12:39606200
|
G | A | 1 | a0001c0001t0023g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1237-1270C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606200 | ||||||
| chr12:39606282
|
C | A | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+1317G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606282 | ||||||
| chr12:39606348
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0008g0108 | 2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1236+1251A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606348 | ||||||
| chr12:39606651
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1236+948A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606651 | ||||||
| chr12:39606989
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1236+610C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606989 | ||||||
| chr12:39607200
|
A | G | 1 | a0001c0001t0002g0278 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1236+399T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39607200 | ||||||
| chr12:39607282
|
A | G | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+317T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39607282 | ||||||
| chr12:39607745
|
G | GT | 15 | a0001c0001t0001g0110a0001c0001t0001g0149a0001c0001t0001g0154others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1121-32dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607745 | ||||||
| chr12:39607745
|
GT | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0067others(56): Show | 80 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.1121-32delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607745 | ||||||
| chr12:39607745
|
GTT | G | 6 | a0001c0001t0004g0051a0001c0001t0004g0061a0001c0001t0005g0092others(3): Show | 6 | HG00733.hp2 HG01515.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-33_1121-32del others(2): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607745 | ||||||
| chr12:39607812
|
A | C | 1 | a0001c0001t0004g0051 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1121-98T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607812 | ||||||
| chr12:39608023
|
C | T | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1121-309G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608023 | ||||||
| chr12:39608180
|
G | A | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121-466C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608180 | ||||||
| chr12:39608327
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG00609.hp2 NA18747.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121-613T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608327 | ||||||
| chr12:39608405
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0037 | 3 | HG00741.hp2 HG01243.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1121-691C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608405 | ||||||
| chr12:39608469
|
T | G | 4 | a0001c0001t0007g0082a0001c0001t0007g0084a0001c0001t0007g0085others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121-755A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608469 | ||||||
| chr12:39608533
|
C | T | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1121-819G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608533 | ||||||
| chr12:39608551
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0268 | 3 | HG01257.hp1 HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1121-837C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608551 | ||||||
| chr12:39608618
|
G | A | 3 | a0001c0001t0009g0033a0001c0001t0009g0038a0001c0001t0009g0039 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1121-904C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608618 | ||||||
| chr12:39608741
|
C | A | 1 | a0001c0001t0004g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121-1027G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608741 | ||||||
| chr12:39608853
|
T | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1121-1139A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608853 | ||||||
| chr12:39609089
|
CTG | C | 3 | a0001c0001t0002g0034a0001c0001t0009g0013a0001c0001t0023g0080 | 4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121-1377_1121-137 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609089 | ||||||
| chr12:39609395
|
G | A | 2 | a0001c0001t0007g0071a0001c0001t0007g0072 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1121-1681C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609395 | ||||||
| chr12:39609570
|
T | A | 1 | a0002c0002t0004g0028 | 2 | NA18971.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1121-1856A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609570 | ||||||
| chr12:39609633
|
A | G | 19 | a0001c0001t0002g0042a0001c0001t0003g0004a0001c0001t0003g0006others(16): Show | 26 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1121-1919T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609633 | ||||||
| chr12:39609740
|
C | T | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1121-2026G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609740 | ||||||
| chr12:39609927
|
C | T | 2 | a0001c0001t0010g0011a0001c0001t0010g0074 | 3 | HG02109.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1121-2213G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609927 | ||||||
| chr12:39610049
|
G | A | 1 | a0001c0001t0009g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1121-2335C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610049 | ||||||
| chr12:39610150
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1121-2436G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610150 | ||||||
| chr12:39610235
|
C | A | 1 | a0001c0001t0002g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1121-2521G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610235 | ||||||
| chr12:39610773
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0008g0108 | 2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1121-3059G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610773 | ||||||
| chr12:39610932
|
CCTAAAAT others(22): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1121-3247_1121-321 others(33): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610932 | ||||||
| chr12:39610986
|
T | C | 62 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(59): Show | 81 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1121-3272A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610986 | ||||||
| chr12:39610987
|
G | A | 2 | a0001c0001t0015g0093a0001c0001t0015g0094 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1121-3273C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610987 | ||||||
| chr12:39611048
|
C | T | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1121-3334G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611048 | ||||||
| chr12:39611066
|
A | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(60): Show | 82 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1121-3352T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611066 | ||||||
| chr12:39611103
|
T | C | 3 | a0001c0001t0006g0062a0001c0001t0006g0063a0001c0001t0006g0064 | 3 | HG02129.hp2 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1121-3389A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611103 | ||||||
| chr12:39611104
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0014g0206a0001c0001t0014g0207 | 3 | HG02717.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1121-3390A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611104 | ||||||
| chr12:39611842
|
G | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG00408.hp1 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1121-4128C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611842 | ||||||
| chr12:39611929
|
G | A | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1121-4215C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611929 | ||||||
| chr12:39611947
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1121-4233G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611947 | ||||||
| chr12:39612335
|
A | T | 1 | a0001c0001t0018g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1121-4621T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612335 | ||||||
| chr12:39612375
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(67): Show | 81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1120+4613C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612375 | ||||||
| chr12:39612439
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1120+4549T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612439 | ||||||
| chr12:39612599
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 6 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+4389G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612599 | ||||||
| chr12:39612664
|
C | T | 1 | a0001c0001t0004g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1120+4324G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612664 | ||||||
| chr12:39612822
|
T | C | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1120+4166A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612822 | ||||||
| chr12:39613041
|
C | T | 1 | a0002c0002t0004g0286 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1120+3947G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613041 | ||||||
| chr12:39613087
|
TAAAGAAT others(320): Show |
T | 80 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0067others(77): Show | 105 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1120+3574_1120+390 others(4): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613087 | ||||||
| chr12:39613164
|
A | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1120+3824T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613164 | ||||||
| chr12:39613242
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1120+3746G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613242 | ||||||
| chr12:39613385
|
C | CA | 23 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(20): Show | 23 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1120+3602dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613385 | ||||||
| chr12:39613385
|
CA | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0022others(75): Show | 88 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1120+3602delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613385 | ||||||
| chr12:39613711
|
C | T | 3 | a0001c0001t0002g0034a0001c0001t0009g0013a0001c0001t0023g0080 | 4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+3277G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613711 | ||||||
| chr12:39613901
|
T | A | 2 | a0001c0001t0002g0034a0001c0001t0023g0080 | 2 | HG00733.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1120+3087A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613901 | ||||||
| chr12:39614154
|
G | T | 19 | a0001c0001t0002g0042a0001c0001t0003g0004a0001c0001t0003g0006others(16): Show | 26 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1120+2834C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614154 | ||||||
| chr12:39614422
|
G | A | 1 | a0003c0009t0011g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1120+2566C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614422 | ||||||
| chr12:39614498
|
C | G | 1 | a0001c0001t0002g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1120+2490G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614498 | ||||||
| chr12:39614552
|
C | CT | 35 | a0001c0001t0002g0042a0001c0001t0003g0004a0001c0001t0003g0006others(32): Show | 43 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1120+2435dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614552 | ||||||
| chr12:39614571
|
A | G | 16 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(13): Show | 23 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1120+2417T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614571 | ||||||
| chr12:39615051
|
GTGGGATT others(2): Show |
G | 44 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(41): Show | 54 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1120+1928_1120+193 others(13): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615051 | ||||||
| chr12:39615074
|
T | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(57): Show | 77 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1120+1914A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615074 | ||||||
| chr12:39615198
|
C | CCCCCCCC others(22): Show |
1 | a0001c0001t0001g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1789_1120+179 others(33): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615198 | ||||||
| chr12:39615200
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1788T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615200 | ||||||
| chr12:39615201
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1787C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615201 | ||||||
| chr12:39615202
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1786C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615202 | ||||||
| chr12:39615203
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1785C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615203 | ||||||
| chr12:39615204
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1784A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615204 | ||||||
| chr12:39615290
|
T | C | 3 | a0001c0001t0002g0034a0001c0001t0009g0013a0001c0001t0023g0080 | 4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1698A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615290 | ||||||
| chr12:39615293
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1120+1695T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615293 | ||||||
| chr12:39615392
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1120+1596A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615392 | ||||||
| chr12:39615597
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 5 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+1391G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615597 | ||||||
| chr12:39615728
|
A | G | 3 | a0001c0001t0002g0034a0001c0001t0009g0013a0001c0001t0023g0080 | 4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1260T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615728 | ||||||
| chr12:39615809
|
T | C | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1120+1179A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615809 | ||||||
| chr12:39615950
|
C | G | 1 | a0001c0001t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1120+1038G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615950 | ||||||
| chr12:39615954
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1120+1034T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615954 | ||||||
| chr12:39616024
|
C | T | 23 | a0001c0001t0001g0015a0001c0001t0001g0109a0001c0001t0001g0110others(20): Show | 24 | HG00280.hp2 HG01106.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1120+964G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616024 | ||||||
| chr12:39616468
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0010g0011a0001c0001t0010g0074others(3): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+520C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616468 | ||||||
| chr12:39616601
|
G | T | 10 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | NA18944.hp2 NA18959.hp1 NA19000.hp2 others(7): Show |
intron_variant | MODIFIER | c.1120+387C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616601 | ||||||
| chr12:39616619
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1120+369A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616619 | ||||||
| chr12:39616623
|
T | C | 2 | a0001c0006t0024g0030a0003c0005t0011g0027 | 3 | HG01167.hp1 HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1120+365A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616623 | ||||||
| chr12:39616707
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1120+281T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616707 | ||||||
| chr12:39616780
|
T | G | 1 | a0001c0001t0006g0077 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1120+208A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616780 | ||||||
| chr12:39616794
|
G | A | 9 | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0086others(6): Show | 16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1120+194C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616794 | ||||||
| chr12:39616893
|
C | T | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1120+95G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616893 | ||||||
| chr12:39616914
|
A | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | NA19062.hp1 NA19080.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1120+74T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616914 | ||||||
| chr12:39616980
|
G | A | 2 | a0001c0001t0014g0206a0001c0001t0014g0207 | 2 | HG02717.hp1 HG02809.hp2 |
splice_region_variant&intron_variant | LOW | c.1120+8C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616980 | ||||||
| chr12:39617223
|
CT | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(68): Show | 82 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.940-56delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617223 | ||||||
| chr12:39617346
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940-178C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617346 | ||||||
| chr12:39617524
|
T | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | NA18944.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.940-356A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617524 | ||||||
| chr12:39617722
|
G | A | 8 | a0001c0001t0004g0078a0001c0001t0004g0079a0002c0002t0004g0005others(5): Show | 12 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.940-554C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617722 | ||||||
| chr12:39617931
|
A | G | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.939+746T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617931 | ||||||
| chr12:39618025
|
CT | C | 32 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(29): Show | 41 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.939+651delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618025 | ||||||
| chr12:39618234
|
C | A | 2 | a0001c0001t0015g0093a0001c0001t0015g0094 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.939+443G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618234 | ||||||
| chr12:39618235
|
C | G | 1 | a0003c0005t0011g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.939+442G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618235 | ||||||
| chr12:39618323
|
A | G | 1 | a0001c0006t0024g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.939+354T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618323 | ||||||
| chr12:39618495
|
C | T | 83 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0067others(80): Show | 108 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.939+182G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618495 |