Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5244 |
|---|---|
| ensemblid | ENSG00000005471.19 |
| hgncid | 45 |
| symbol | ABCB4 |
| name | ATP binding cassette subfamily B member 4 |
| refseq_nuc | NM_000443.4 |
| refseq_prot | NP_000434.1 |
| ensembl_nuc | ENST00000649586.2 |
| ensembl_prot | ENSP00000496956.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 87401696 |
| end | 87475680 |
| strand | - |
| ver | v1.2 |
| region | chr7:87401696-87475680 |
| region5000 | chr7:87396696-87480680 |
| regionname0 | ABCB4_chr7_87401696_87475680 |
| regionname5000 | ABCB4_chr7_87396696_87480680 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1279 | 225 | 37 | 41 | 113 | 8 | 24 | 92 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002 | 0/0 | 1279 | 46 | 31 | 7 | 3 | 2 | 3 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0003 | 0/0 | 1279 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0004 | 0/0 | 1279 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0005 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0006 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0007 | 0/0 | 1279 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0008 | 0/0 | 1279 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0009 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0010 | 0/0 | 1279 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0011 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3840 | 74 | 18 | 16 | 34 | 2 | 3 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0002 | 0/0 | 3840 | 67 | 8 | 10 | 38 | 4 | 7 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0003 | 0/1 | 3840 | 65 | 0 | 14 | 35 | 1 | 14 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0004 | 0/0 | 3840 | 18 | 17 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0005 | 0/0 | 3840 | 12 | 2 | 4 | 3 | 1 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0006 | 0/0 | 3840 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0007 | 0/0 | 3840 | 6 | 0 | 1 | 4 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0008 | 0/0 | 3840 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0009 | 0/0 | 3840 | 5 | 2 | 1 | 0 | 1 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0010 | 0/0 | 3840 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0011 | 0/0 | 3840 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0012 | 0/0 | 3840 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0013 | 0/0 | 3840 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0014 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0015 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0016 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0017 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0018 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0019 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0020 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0021 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0022 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0023 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0024 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0025 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0026 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0027 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0028 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0029 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| c0030 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 454 | 288 | 81 | 50 | 118 | 10 | 27 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| t0002 | 0/0 | 454 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| t0003 | 0/0 | 454 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3840 | 74 | 18 | 16 | 34 | 2 | 3 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0002 | 0/0 | 3840 | 67 | 8 | 10 | 38 | 4 | 7 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0003 | 0/1 | 3840 | 65 | 0 | 14 | 35 | 1 | 14 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0006 | 0/0 | 3840 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0007 | 0/0 | 3840 | 6 | 0 | 1 | 4 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0015 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0019 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0026 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0029 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0004 | 0/0 | 3840 | 18 | 17 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0005 | 0/0 | 3840 | 12 | 2 | 4 | 3 | 1 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0009 | 0/0 | 3840 | 5 | 2 | 1 | 0 | 1 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0010 | 0/0 | 3840 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0012 | 0/0 | 3840 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0017 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0021 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0023 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0024 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0027 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0003c0008 | 0/0 | 3840 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0003c0011 | 0/0 | 3840 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0003c0022 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0004c0013 | 0/0 | 3840 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0005c0030 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0006c0028 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0007c0018 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0008c0025 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0009c0016 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0010c0014 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0011c0020 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4293 | 73 | 17 | 16 | 34 | 2 | 3 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0001t0002 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0002t0001 | 0/0 | 4293 | 66 | 8 | 10 | 38 | 4 | 6 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0002t0003 | 0/0 | 4293 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0003t0001 | 0/1 | 4293 | 65 | 0 | 14 | 35 | 1 | 14 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0006t0001 | 0/0 | 4293 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0007t0001 | 0/0 | 4293 | 6 | 0 | 1 | 4 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0015t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0019t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0026t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0001c0029t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0004t0001 | 0/0 | 4293 | 18 | 17 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0005t0001 | 0/0 | 4293 | 12 | 2 | 4 | 3 | 1 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0009t0001 | 0/0 | 4293 | 5 | 2 | 1 | 0 | 1 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0010t0001 | 0/0 | 4293 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0012t0001 | 0/0 | 4293 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0017t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0021t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0023t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0024t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0002c0027t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0003c0008t0001 | 0/0 | 4293 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0003c0011t0001 | 0/0 | 4293 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0003c0022t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0004c0013t0001 | 0/0 | 4293 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0005c0030t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0006c0028t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0007c0018t0001 | 0/0 | 4293 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0008c0025t0001 | 0/0 | 4293 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0009c0016t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0010c0014t0001 | 0/0 | 4293 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| a0011c0020t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | copy fasta | chr7 | 87396696 | 87480680 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0015t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0019t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0026t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0029t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0010t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0010t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0010t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0010t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0012t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0012t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0017t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0021t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0023t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0024t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0027t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0011t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0011t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0011t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0011t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0022t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0004c0013t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0004c0013t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0005c0030t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0006c0028t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0007c0018t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0008c0025t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0009c0016t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0010c0014t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0011c0020t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0103 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00140 | hp1 | a0002 | c0009 | t0001 | g0222 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00140 | hp2 | a0001 | c0007 | t0001 | g0037 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0123 | EUR | FIN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00323 | hp1 | a0002 | c0005 | t0001 | g0056 | EUR | FIN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0104 | EUR | FIN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00735 | hp2 | a0002 | c0005 | t0001 | g0054 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0128 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0157 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01109 | hp1 | a0008 | c0025 | t0001 | g0091 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0161 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0126 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01192 | hp1 | a0002 | c0012 | t0001 | g0152 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01243 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0133 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01256 | hp1 | a0010 | c0014 | t0001 | g0162 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0131 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0105 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01934 | hp2 | a0002 | c0005 | t0001 | g0055 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01943 | hp1 | a0002 | c0005 | t0001 | g0035 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0132 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02004 | hp1 | a0002 | c0005 | t0001 | g0036 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02040 | hp2 | a0001 | c0007 | t0001 | g0050 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02055 | hp1 | a0002 | c0005 | t0001 | g0169 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0044 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02135 | hp2 | a0001 | c0015 | t0001 | g0178 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02145 | hp1 | a0003 | c0008 | t0001 | g0170 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02148 | hp2 | a0002 | c0009 | t0001 | g0214 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CDX | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02155 | hp2 | a0002 | c0005 | t0001 | g0042 | EAS | CDX | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02257 | hp1 | a0002 | c0010 | t0001 | g0172 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02258 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02273 | hp1 | a0001 | c0007 | t0001 | g0034 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02451 | hp1 | a0002 | c0010 | t0001 | g0174 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02451 | hp2 | a0002 | c0004 | t0001 | g0045 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02615 | hp1 | a0003 | c0022 | t0001 | g0248 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02615 | hp2 | a0005 | c0030 | t0001 | g0239 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02622 | hp2 | a0001 | c0029 | t0001 | g0115 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02630 | hp1 | a0003 | c0008 | t0001 | g0223 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02630 | hp2 | a0002 | c0009 | t0001 | g0193 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0043 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02647 | hp2 | a0002 | c0004 | t0001 | g0058 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0140 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02683 | hp2 | a0002 | c0005 | t0001 | g0053 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02717 | hp1 | a0002 | c0010 | t0001 | g0175 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02717 | hp2 | a0002 | c0023 | t0001 | g0250 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02723 | hp1 | a0002 | c0004 | t0001 | g0253 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02723 | hp2 | a0002 | c0005 | t0001 | g0168 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0146 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0031 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0154 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0030 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02818 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02886 | hp1 | a0004 | c0013 | t0001 | g0100 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02886 | hp2 | a0002 | c0012 | t0001 | g0136 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0244 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02896 | hp2 | a0009 | c0016 | t0001 | g0232 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02922 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02965 | hp1 | a0003 | c0011 | t0001 | g0111 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0243 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02970 | hp2 | a0002 | c0004 | t0001 | g0038 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03017 | hp1 | a0002 | c0009 | t0001 | g0237 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03041 | hp1 | a0002 | c0027 | t0001 | g0256 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03041 | hp2 | a0002 | c0017 | t0001 | g0196 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0242 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03130 | hp2 | a0002 | c0004 | t0001 | g0057 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03139 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03195 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03195 | hp2 | a0003 | c0008 | t0001 | g0025 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03209 | hp1 | a0002 | c0021 | t0001 | g0107 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0247 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0159 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0153 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03453 | hp1 | a0002 | c0009 | t0001 | g0241 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0145 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03492 | hp1 | a0007 | c0018 | t0001 | g0122 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03516 | hp1 | a0003 | c0008 | t0001 | g0024 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03516 | hp2 | a0002 | c0004 | t0001 | g0041 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03540 | hp2 | a0002 | c0004 | t0001 | g0008 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0156 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0155 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03942 | hp2 | a0002 | c0005 | t0001 | g0046 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | STU | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0033 | SAS | STU | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18747 | hp1 | a0001 | c0007 | t0001 | g0048 | EAS | CHB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18906 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | YRI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18906 | hp2 | a0003 | c0008 | t0001 | g0171 | AFR | YRI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18943 | hp1 | a0001 | c0026 | t0001 | g0082 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18999 | hp2 | a0011 | c0020 | t0001 | g0189 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19011 | hp1 | a0001 | c0007 | t0001 | g0049 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19043 | hp1 | a0002 | c0004 | t0001 | g0095 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19058 | hp1 | a0002 | c0005 | t0001 | g0051 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19065 | hp2 | a0006 | c0028 | t0001 | g0068 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19072 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19086 | hp1 | a0002 | c0005 | t0001 | g0052 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19087 | hp2 | a0001 | c0007 | t0001 | g0047 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | YRI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20129 | hp1 | a0002 | c0010 | t0001 | g0173 | AFR | ASW | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20129 | hp2 | a0001 | c0006 | t0001 | g0245 | AFR | ASW | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0102 | EUR | TSI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0092 | EUR | TSI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0127 | SAS | GIH | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02109 | hp1 | a0004 | c0013 | t0001 | g0101 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02109 | hp2 | a0003 | c0011 | t0001 | g0114 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02486 | hp1 | a0002 | c0024 | t0001 | g0039 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0246 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03471 | hp2 | a0001 | c0006 | t0001 | g0249 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG06807 | hp2 | a0002 | c0004 | t0001 | g0008 | AFR | USA | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | USA | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20300 | hp2 | a0003 | c0011 | t0001 | g0113 | AFR | USA | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA21309 | hp1 | a0001 | c0019 | t0001 | g0023 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA21309 | hp2 | a0003 | c0011 | t0001 | g0112 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0129 | REF | REF | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0149 | REF | REF | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87409304
|
C | T | 1 | a0009 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.3013G>A | p.Ala1005Thr | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 24/28 | 3066/4293 | 3013/3840 | 1005/1279 | chr7 | 87409304 | ||
| chr7:87412017
|
C | T | 1 | a0004 | 2 | HG02109.hp1 HG02886.hp1 |
missense_variant | MODERATE | c.2800G>A | p.Ala934Thr | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/28 | 2853/4293 | 2800/3840 | 934/1279 | chr7 | 87412017 | ||
| chr7:87420029
|
C | T | 1 | a0003 | 10 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(7): Show |
missense_variant | MODERATE | c.2363G>A | p.Arg788Gln | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/28 | 2416/4293 | 2363/3840 | 788/1279 | chr7 | 87420029 | ||
| chr7:87426860
|
T | C | 2 | a0002a0004 | 48 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(45): Show |
missense_variant | MODERATE | c.1954A>G | p.Arg652Gly | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/28 | 2007/4293 | 1954/3840 | 652/1279 | chr7 | 87426860 | ||
| chr7:87431528
|
C | T | 1 | a0008 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1769G>A | p.Arg590Gln | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/28 | 1822/4293 | 1769/3840 | 590/1279 | chr7 | 87431528 | ||
| chr7:87452957
|
T | C | 1 | a0007 | 1 | HG03492.hp1 | missense_variant | MODERATE | c.523A>G | p.Thr175Ala | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/28 | 576/4293 | 523/3840 | 175/1279 | chr7 | 87452957 | ||
| chr7:87453082
|
A | G | 1 | a0010 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.398T>C | p.Ile133Thr | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/28 | 451/4293 | 398/3840 | 133/1279 | chr7 | 87453082 | ||
| chr7:87454577
|
G | A | 1 | a0006 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.302C>T | p.Ser101Leu | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/28 | 355/4293 | 302/3840 | 101/1279 | chr7 | 87454577 | ||
| chr7:87462818
|
T | C | 1 | a0011 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.226A>G | p.Ile76Val | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/28 | 279/4293 | 226/3840 | 76/1279 | chr7 | 87462818 | ||
| chr7:87472655
|
G | A | 1 | a0005 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.101C>T | p.Thr34Met | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/28 | 154/4293 | 101/3840 | 34/1279 | chr7 | 87472655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87409365
|
T | C | 1 | a0002c0027 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2952A>G | p.Ala984Ala | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 24/28 | 3005/4293 | 2952/3840 | 984/1279 | chr7 | 87409365 | ||
| chr7:87417459
|
A | G | 1 | a0001c0015 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.2535T>C | p.Gly845Gly | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/28 | 2588/4293 | 2535/3840 | 845/1279 | chr7 | 87417459 | ||
| chr7:87420067
|
C | G | 1 | a0002c0010 | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.2325G>C | p.Thr775Thr | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/28 | 2378/4293 | 2325/3840 | 775/1279 | chr7 | 87420067 | ||
| chr7:87423930
|
T | G | 1 | a0001c0026 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.2187A>C | p.Ser729Ser | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/28 | 2240/4293 | 2187/3840 | 729/1279 | chr7 | 87423930 | ||
| chr7:87423939
|
C | T | 1 | a0002c0017 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.2178G>A | p.Pro726Pro | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/28 | 2231/4293 | 2178/3840 | 726/1279 | chr7 | 87423939 | ||
| chr7:87440382
|
A | G | 1 | a0002c0024 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1377T>C | p.Asp459Asp | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 13/28 | 1430/4293 | 1377/3840 | 459/1279 | chr7 | 87440382 | ||
| chr7:87450090
|
T | A | 12 | a0001c0002a0001c0007a0001c0019others(9): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
splice_region_variant&synonymous_variant | LOW | c.711A>T | p.Ile237Ile | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/28 | 764/4293 | 711/3840 | 237/1279 | chr7 | 87450090 | ||
| chr7:87452976
|
G | A | 4 | a0001c0003a0002c0012a0007c0018others(1): Show | 69 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(66): Show |
synonymous_variant | LOW | c.504C>T | p.Asn168Asn | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/28 | 557/4293 | 504/3840 | 168/1279 | chr7 | 87452976 | ||
| chr7:87453021
|
A | G | 2 | a0001c0029a0004c0013 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.459T>C | p.Phe153Phe | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/28 | 512/4293 | 459/3840 | 153/1279 | chr7 | 87453021 | ||
| chr7:87453024
|
C | T | 1 | a0002c0021 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.456G>A | p.Lys152Lys | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/28 | 509/4293 | 456/3840 | 152/1279 | chr7 | 87453024 | ||
| chr7:87453114
|
T | C | 1 | a0001c0019 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.366A>G | p.Gly122Gly | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/28 | 419/4293 | 366/3840 | 122/1279 | chr7 | 87453114 | ||
| chr7:87462869
|
G | A | 14 | a0001c0002a0001c0006a0001c0026others(11): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
synonymous_variant | LOW | c.175C>T | p.Leu59Leu | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/28 | 228/4293 | 175/3840 | 59/1279 | chr7 | 87462869 | ||
| chr7:87462897
|
G | A | 2 | a0001c0029a0004c0013 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.147C>T | p.Ser49Ser | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/28 | 200/4293 | 147/3840 | 49/1279 | chr7 | 87462897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87401721
|
C | A | 1 | a0001c0002t0003 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*375G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 28/28 | 375 | chr7 | 87401721 | |||||
| chr7:87475466
|
C | T | 1 | a0001c0001t0002 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/28 | 1 | chr7 | 87475466 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87402374
|
A | G | 41 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(38): Show | 45 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3634-72T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402374 | ||||||
| chr7:87402493
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(132): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3634-191T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402493 | ||||||
| chr7:87402513
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3634-211A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402513 | ||||||
| chr7:87402530
|
T | G | 7 | a0003c0008t0001g0024a0003c0008t0001g0025a0003c0011t0001g0111others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3634-228A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402530 | ||||||
| chr7:87402625
|
A | G | 1 | a0001c0003t0001g0005 | 3 | NA18966.hp2 NA18984.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3634-323T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402625 | ||||||
| chr7:87402642
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3634-340A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402642 | ||||||
| chr7:87402678
|
A | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0185 | 2 | NA18963.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.3634-376T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402678 | ||||||
| chr7:87402935
|
G | T | 41 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(38): Show | 45 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3633+200C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87402935 | ||||||
| chr7:87403051
|
T | C | 4 | a0001c0003t0001g0015a0001c0003t0001g0137a0001c0003t0001g0138others(1): Show | 5 | NA18948.hp2 NA18950.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.3633+84A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87403051 | ||||||
| chr7:87403066
|
C | T | 1 | a0001c0015t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3633+69G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 27/27 | chr7 | 87403066 | ||||||
| chr7:87403297
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(194): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.3487-16T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87403297 | ||||||
| chr7:87403763
|
G | T | 3 | a0001c0001t0001g0197a0001c0003t0001g0133a0001c0003t0001g0153 | 3 | HG01106.hp1 HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.3487-482C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87403763 | ||||||
| chr7:87403846
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0216a0001c0003t0001g0128 | 4 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3487-565C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87403846 | ||||||
| chr7:87404190
|
G | T | 2 | a0004c0013t0001g0100a0004c0013t0001g0101 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3487-909C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87404190 | ||||||
| chr7:87404245
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(130): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.3487-964G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87404245 | ||||||
| chr7:87404632
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(132): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3487-1351A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87404632 | ||||||
| chr7:87404647
|
C | A | 1 | a0001c0007t0001g0049 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3487-1366G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87404647 | ||||||
| chr7:87404704
|
C | CA | 4 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3487-1424dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87404704 | ||||||
| chr7:87404826
|
C | T | 1 | a0001c0003t0001g0118 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3486+1462G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87404826 | ||||||
| chr7:87405015
|
G | A | 10 | a0001c0001t0001g0026a0001c0001t0001g0231a0001c0006t0001g0022others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.3486+1273C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405015 | ||||||
| chr7:87405427
|
C | CT | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(130): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.3486+860dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405427 | ||||||
| chr7:87405448
|
A | T | 1 | a0002c0004t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3486+840T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405448 | ||||||
| chr7:87405449
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(131): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.3486+839G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405449 | ||||||
| chr7:87405466
|
G | A | 1 | a0002c0005t0001g0035 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3486+822C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405466 | ||||||
| chr7:87405486
|
G | T | 1 | a0001c0003t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3486+802C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405486 | ||||||
| chr7:87405513
|
G | A | 1 | a0001c0003t0001g0127 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3486+775C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405513 | ||||||
| chr7:87405529
|
C | T | 41 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(38): Show | 45 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3486+759G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405529 | ||||||
| chr7:87406549
|
A | C | 1 | a0001c0003t0001g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3280-55T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87406549 | ||||||
| chr7:87406584
|
G | GCAT | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.3280-93_3280-91dup others(3): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87406584 | ||||||
| chr7:87406599
|
C | G | 1 | a0002c0004t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3280-105G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87406599 | ||||||
| chr7:87406789
|
G | A | 18 | a0001c0001t0001g0195a0001c0002t0001g0062a0001c0002t0003g0033others(15): Show | 18 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3280-295C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87406789 | ||||||
| chr7:87406909
|
A | T | 1 | a0002c0004t0001g0095 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3280-415T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87406909 | ||||||
| chr7:87406911
|
C | T | 31 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(28): Show | 35 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.3280-417G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87406911 | ||||||
| chr7:87406959
|
T | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0001t0001g0206 | 3 | HG00099.hp2 HG01069.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3280-465A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87406959 | ||||||
| chr7:87407626
|
G | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(171): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3279+411C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87407626 | ||||||
| chr7:87407663
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3279+374G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87407663 | ||||||
| chr7:87407700
|
G | A | 1 | a0001c0003t0001g0140 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3279+337C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87407700 | ||||||
| chr7:87407842
|
G | C | 41 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(38): Show | 45 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3279+195C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 25/27 | chr7 | 87407842 | ||||||
| chr7:87408353
|
G | A | 14 | a0001c0001t0001g0026a0001c0001t0001g0231a0001c0006t0001g0022others(11): Show | 15 | HG02258.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.3082-119C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 24/27 | chr7 | 87408353 | ||||||
| chr7:87408724
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3082-490C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 24/27 | chr7 | 87408724 | ||||||
| chr7:87408758
|
A | G | 40 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(37): Show | 44 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3081+478T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 24/27 | chr7 | 87408758 | ||||||
| chr7:87408998
|
A | C | 1 | a0001c0001t0001g0207 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3081+238T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 24/27 | chr7 | 87408998 | ||||||
| chr7:87409462
|
G | T | 1 | a0001c0002t0001g0074 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2925-70C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87409462 | ||||||
| chr7:87409546
|
C | A | 2 | a0002c0004t0001g0105a0002c0027t0001g0256 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2925-154G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87409546 | ||||||
| chr7:87409825
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(175): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2925-433A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87409825 | ||||||
| chr7:87410622
|
A | T | 1 | a0002c0027t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2925-1230T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87410622 | ||||||
| chr7:87410712
|
G | A | 1 | a0001c0003t0001g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2924+1181C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87410712 | ||||||
| chr7:87410980
|
G | T | 30 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(27): Show | 34 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2924+913C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87410980 | ||||||
| chr7:87411020
|
A | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0179a0001c0001t0001g0181others(5): Show | 9 | HG01975.hp1 HG02148.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2924+873T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411020 | ||||||
| chr7:87411071
|
A | G | 16 | a0001c0001t0001g0195a0001c0002t0003g0033a0001c0003t0001g0155others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2924+822T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411071 | ||||||
| chr7:87411136
|
T | C | 1 | a0001c0003t0001g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2924+757A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411136 | ||||||
| chr7:87411174
|
A | C | 17 | a0001c0001t0001g0195a0001c0002t0003g0033a0001c0003t0001g0155others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2924+719T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411174 | ||||||
| chr7:87411215
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2924+678C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411215 | ||||||
| chr7:87411219
|
C | CA | 4 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2924+673dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411219 | ||||||
| chr7:87411313
|
C | T | 185 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(182): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.2924+580G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411313 | ||||||
| chr7:87411334
|
G | A | 2 | a0004c0013t0001g0100a0004c0013t0001g0101 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2924+559C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411334 | ||||||
| chr7:87411828
|
A | T | 14 | a0001c0001t0001g0026a0001c0001t0001g0231a0001c0006t0001g0022others(11): Show | 15 | HG02258.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2924+65T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 23/27 | chr7 | 87411828 | ||||||
| chr7:87412241
|
A | G | 7 | a0003c0008t0001g0024a0003c0008t0001g0025a0003c0011t0001g0111others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2784-208T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87412241 | ||||||
| chr7:87412532
|
A | G | 1 | a0002c0004t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2784-499T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87412532 | ||||||
| chr7:87412540
|
C | A | 41 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(38): Show | 45 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.2784-507G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87412540 | ||||||
| chr7:87412594
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2784-561T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87412594 | ||||||
| chr7:87412707
|
G | A | 1 | a0002c0027t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2784-674C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87412707 | ||||||
| chr7:87412878
|
A | G | 2 | a0002c0004t0001g0008a0002c0005t0001g0169 | 3 | HG02055.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2783+739T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87412878 | ||||||
| chr7:87413073
|
A | G | 1 | a0002c0017t0001g0196 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2783+544T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87413073 | ||||||
| chr7:87413583
|
C | G | 1 | a0002c0004t0001g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2783+34G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 22/27 | chr7 | 87413583 | ||||||
| chr7:87413885
|
C | A | 1 | a0001c0002t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2683-168G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87413885 | ||||||
| chr7:87413914
|
A | G | 17 | a0001c0001t0001g0195a0001c0002t0003g0033a0001c0003t0001g0155others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2683-197T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87413914 | ||||||
| chr7:87413919
|
A | G | 1 | a0001c0003t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2683-202T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87413919 | ||||||
| chr7:87414267
|
A | G | 42 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(39): Show | 46 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.2683-550T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87414267 | ||||||
| chr7:87414306
|
C | T | 1 | a0002c0004t0001g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2683-589G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87414306 | ||||||
| chr7:87414392
|
T | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(131): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.2683-675A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87414392 | ||||||
| chr7:87414584
|
T | C | 4 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-867A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87414584 | ||||||
| chr7:87414607
|
T | C | 1 | a0006c0028t0001g0068 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2683-890A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87414607 | ||||||
| chr7:87414685
|
T | TA | 27 | a0001c0001t0001g0019a0001c0001t0001g0179a0001c0001t0001g0181others(24): Show | 35 | HG01358.hp2 HG01496.hp2 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.2683-969dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87414685 | ||||||
| chr7:87415127
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(194): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2683-1410T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415127 | ||||||
| chr7:87415286
|
C | A | 1 | a0001c0003t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2683-1569G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415286 | ||||||
| chr7:87415348
|
T | TAAAC | 176 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(173): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2683-1632_2683-163 others(8): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415348 | ||||||
| chr7:87415350
|
G | A | 1 | a0001c0003t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2683-1633C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415350 | ||||||
| chr7:87415497
|
T | G | 1 | a0001c0007t0001g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2683-1780A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415497 | ||||||
| chr7:87415582
|
A | G | 1 | a0001c0003t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2682+1730T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415582 | ||||||
| chr7:87415677
|
G | A | 1 | a0002c0004t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2682+1635C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415677 | ||||||
| chr7:87415682
|
G | C | 2 | a0003c0008t0001g0024a0003c0008t0001g0025 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2682+1630C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415682 | ||||||
| chr7:87415691
|
C | T | 1 | a0002c0004t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2682+1621G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415691 | ||||||
| chr7:87415797
|
A | T | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2682+1515T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87415797 | ||||||
| chr7:87416001
|
G | A | 6 | a0001c0003t0001g0017a0001c0003t0001g0121a0001c0003t0001g0129others(3): Show | 7 | HG01106.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2682+1311C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416001 | ||||||
| chr7:87416003
|
T | A | 12 | a0001c0002t0001g0116a0002c0004t0001g0003a0002c0004t0001g0008others(9): Show | 16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2682+1309A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416003 | ||||||
| chr7:87416074
|
C | G | 17 | a0001c0001t0001g0195a0001c0002t0003g0033a0001c0003t0001g0155others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2682+1238G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416074 | ||||||
| chr7:87416249
|
G | A | 31 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(28): Show | 35 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.2682+1063C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416249 | ||||||
| chr7:87416268
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(165): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2682+1044T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416268 | ||||||
| chr7:87416521
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(250): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2682+791C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416521 | ||||||
| chr7:87416677
|
A | T | 2 | a0001c0003t0001g0134a0001c0003t0001g0139 | 2 | NA18957.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2682+635T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416677 | ||||||
| chr7:87416841
|
G | T | 2 | a0004c0013t0001g0100a0004c0013t0001g0101 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2682+471C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416841 | ||||||
| chr7:87416892
|
G | A | 1 | a0001c0006t0001g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2682+420C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416892 | ||||||
| chr7:87416937
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0185 | 2 | NA18963.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2682+375A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416937 | ||||||
| chr7:87417098
|
G | A | 1 | a0001c0002t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2682+214C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87417098 | ||||||
| chr7:87417154
|
A | G | 32 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(29): Show | 36 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2682+158T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87417154 | ||||||
| chr7:87417189
|
A | G | 1 | a0004c0013t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2682+123T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87417189 | ||||||
| chr7:87417580
|
GC | G | 30 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(27): Show | 34 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2479-66delG | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 20/27 | chr7 | 87417580 | ||||||
| chr7:87417723
|
C | T | 30 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(27): Show | 34 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2479-208G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 20/27 | chr7 | 87417723 | ||||||
| chr7:87418083
|
C | G | 1 | a0001c0002t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2478+454G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 20/27 | chr7 | 87418083 | ||||||
| chr7:87418117
|
C | T | 2 | a0001c0003t0001g0158a0001c0003t0001g0160 | 2 | HG01069.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2478+420G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 20/27 | chr7 | 87418117 | ||||||
| chr7:87418272
|
T | C | 10 | a0001c0001t0001g0026a0001c0001t0001g0231a0001c0006t0001g0022others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.2478+265A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 20/27 | chr7 | 87418272 | ||||||
| chr7:87418276
|
A | T | 1 | a0002c0004t0001g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2478+261T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 20/27 | chr7 | 87418276 | ||||||
| chr7:87418497
|
T | C | 31 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(28): Show | 35 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.2478+40A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 20/27 | chr7 | 87418497 | ||||||
| chr7:87418639
|
G | A | 2 | a0001c0006t0001g0242a0001c0029t0001g0115 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2395-19C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87418639 | ||||||
| chr7:87418675
|
A | C | 1 | a0002c0027t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2395-55T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87418675 | ||||||
| chr7:87418905
|
G | T | 1 | a0011c0020t0001g0189 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2395-285C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87418905 | ||||||
| chr7:87419214
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0202a0001c0001t0001g0205others(11): Show | 22 | HG00423.hp1 HG01106.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.2395-594T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419214 | ||||||
| chr7:87419421
|
T | C | 2 | a0001c0001t0001g0180a0002c0005t0001g0051 | 2 | NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2394+577A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419421 | ||||||
| chr7:87419423
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2394+575G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419423 | ||||||
| chr7:87419598
|
T | G | 2 | a0002c0004t0001g0105a0002c0027t0001g0256 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2394+400A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419598 | ||||||
| chr7:87419788
|
G | GA | 6 | a0001c0001t0001g0026a0001c0006t0001g0243a0001c0006t0001g0244others(3): Show | 6 | HG02895.hp1 HG02970.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2394+209dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419788 | ||||||
| chr7:87419796
|
AC | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(152): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2394+201delG | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419796 | ||||||
| chr7:87419797
|
C | A | 28 | a0001c0001t0001g0026a0001c0001t0001g0220a0001c0001t0001g0231others(25): Show | 30 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2394+201G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419797 | ||||||
| chr7:87419802
|
A | C | 24 | a0001c0002t0001g0116a0001c0003t0001g0016a0001c0003t0001g0120others(21): Show | 29 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2394+196T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419802 | ||||||
| chr7:87419803
|
C | A | 32 | a0001c0001t0001g0026a0001c0002t0001g0116a0001c0003t0001g0016others(29): Show | 38 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2394+195G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419803 | ||||||
| chr7:87419803
|
C | CA | 7 | a0001c0001t0001g0231a0001c0002t0001g0097a0002c0004t0001g0095others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2394+194dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419803 | ||||||
| chr7:87419813
|
A | C | 1 | a0001c0003t0001g0138 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2394+185T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419813 | ||||||
| chr7:87420130
|
C | G | 1 | a0001c0002t0001g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2317-55G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420130 | ||||||
| chr7:87420197
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0240 | 3 | HG00438.hp2 NA18983.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2317-122T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420197 | ||||||
| chr7:87420267
|
C | G | 35 | a0001c0001t0001g0195a0001c0002t0001g0116a0001c0002t0003g0033others(32): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2317-192G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420267 | ||||||
| chr7:87420323
|
A | T | 2 | a0001c0002t0001g0102a0001c0002t0001g0103 | 2 | HG00099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2317-248T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420323 | ||||||
| chr7:87420437
|
A | G | 1 | a0001c0002t0001g0104 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2317-362T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420437 | ||||||
| chr7:87420640
|
A | G | 7 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(4): Show | 7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2317-565T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420640 | ||||||
| chr7:87420815
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2317-740C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420815 | ||||||
| chr7:87420906
|
A | G | 1 | a0002c0004t0001g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2317-831T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420906 | ||||||
| chr7:87420926
|
T | C | 2 | a0001c0003t0001g0145a0001c0003t0001g0146 | 2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2317-851A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87420926 | ||||||
| chr7:87421260
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2316+861A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87421260 | ||||||
| chr7:87421558
|
T | C | 1 | a0001c0002t0001g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2316+563A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87421558 | ||||||
| chr7:87421605
|
C | A | 1 | a0001c0002t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2316+516G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87421605 | ||||||
| chr7:87421705
|
C | T | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2316+416G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87421705 | ||||||
| chr7:87422033
|
G | A | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2316+88C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 18/27 | chr7 | 87422033 | ||||||
| chr7:87422632
|
A | G | 4 | a0001c0003t0001g0013a0001c0003t0001g0118a0001c0003t0001g0167others(1): Show | 5 | HG01256.hp1 NA18971.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.2212-407T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87422632 | ||||||
| chr7:87422745
|
C | G | 1 | a0002c0005t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2212-520G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87422745 | ||||||
| chr7:87422854
|
A | G | 14 | a0001c0002t0001g0096a0002c0004t0001g0003a0002c0004t0001g0008others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2212-629T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87422854 | ||||||
| chr7:87422911
|
G | A | 1 | a0009c0016t0001g0232 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2212-686C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87422911 | ||||||
| chr7:87422952
|
C | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(155): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2212-727G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87422952 | ||||||
| chr7:87423092
|
C | T | 4 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+814G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423092 | ||||||
| chr7:87423163
|
T | C | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.2211+743A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423163 | ||||||
| chr7:87423289
|
A | G | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.2211+617T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423289 | ||||||
| chr7:87423321
|
A | G | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2211+585T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423321 | ||||||
| chr7:87423484
|
G | A | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2211+422C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423484 | ||||||
| chr7:87423695
|
T | C | 2 | a0001c0006t0001g0244a0001c0006t0001g0246 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2211+211A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423695 | ||||||
| chr7:87423834
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(143): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2211+72T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423834 | ||||||
| chr7:87423890
|
G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(193): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2211+16C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423890 | ||||||
| chr7:87424218
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2065-166T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87424218 | ||||||
| chr7:87424295
|
G | C | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.2065-243C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87424295 | ||||||
| chr7:87424380
|
T | A | 1 | a0007c0018t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2065-328A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87424380 | ||||||
| chr7:87424831
|
C | G | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2065-779G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87424831 | ||||||
| chr7:87424931
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(192): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2065-879T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87424931 | ||||||
| chr7:87425030
|
G | A | 2 | a0002c0005t0001g0168a0002c0017t0001g0196 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2065-978C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425030 | ||||||
| chr7:87425040
|
G | GT | 6 | a0001c0002t0001g0084a0002c0004t0001g0095a0002c0004t0001g0105others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2065-989dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425040 | ||||||
| chr7:87425055
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2065-1003G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425055 | ||||||
| chr7:87425139
|
C | A | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2065-1087G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425139 | ||||||
| chr7:87425392
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2065-1340A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425392 | ||||||
| chr7:87425401
|
C | T | 3 | a0002c0004t0001g0095a0002c0009t0001g0241a0002c0021t0001g0107 | 3 | HG03209.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2064+1349G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425401 | ||||||
| chr7:87425490
|
T | C | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2064+1260A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425490 | ||||||
| chr7:87425529
|
T | A | 5 | a0001c0002t0001g0106a0001c0002t0001g0251a0001c0002t0001g0252others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064+1221A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425529 | ||||||
| chr7:87425636
|
T | C | 3 | a0002c0004t0001g0095a0002c0009t0001g0241a0002c0021t0001g0107 | 3 | HG03209.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2064+1114A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425636 | ||||||
| chr7:87425736
|
T | A | 3 | a0002c0004t0001g0095a0002c0009t0001g0241a0002c0021t0001g0107 | 3 | HG03209.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2064+1014A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87425736 | ||||||
| chr7:87426026
|
C | CA | 21 | a0001c0002t0001g0096a0002c0005t0001g0035a0002c0005t0001g0036others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.2064+723dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426026 | ||||||
| chr7:87426026
|
CA | C | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2064+723delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426026 | ||||||
| chr7:87426034
|
A | T | 2 | a0002c0004t0001g0095a0002c0021t0001g0107 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2064+716T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426034 | ||||||
| chr7:87426281
|
T | C | 1 | a0001c0001t0001g0019 | 2 | HG01975.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2064+469A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426281 | ||||||
| chr7:87426319
|
G | T | 16 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2064+431C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426319 | ||||||
| chr7:87426365
|
C | T | 2 | a0001c0003t0001g0158a0001c0003t0001g0160 | 2 | HG01069.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2064+385G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426365 | ||||||
| chr7:87426405
|
T | G | 18 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0177others(15): Show | 20 | HG00438.hp1 HG00438.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.2064+345A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426405 | ||||||
| chr7:87426539
|
AT | A | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.2064+210delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426539 | ||||||
| chr7:87426610
|
T | C | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2064+140A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426610 | ||||||
| chr7:87426619
|
T | C | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2064+131A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426619 | ||||||
| chr7:87426695
|
T | C | 43 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(40): Show | 47 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.2064+55A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 16/27 | chr7 | 87426695 | ||||||
| chr7:87426944
|
A | AGT | 54 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(51): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1894-26_1894-25dup others(2): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426944
|
A | AGTGT | 64 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0197others(61): Show | 71 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1894-28_1894-25dup others(4): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426944
|
A | AGTGTGT | 21 | a0001c0001t0001g0026a0001c0001t0001g0180a0001c0001t0001g0235others(18): Show | 21 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1894-30_1894-25dup others(6): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426944
|
A | AGTGTGTG others(1): Show |
11 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0002t0001g0104others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1894-32_1894-25dup others(8): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426944
|
A | AGTGTGTG others(3): Show |
15 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(12): Show | 16 | HG00639.hp1 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1894-34_1894-25dup others(10): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426944
|
A | AGTGTGTG others(5): Show |
3 | a0001c0001t0001g0224a0001c0002t0001g0109a0001c0002t0001g0116 | 3 | HG01175.hp1 HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1894-36_1894-25dup others(12): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426944
|
AGT | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0177others(14): Show | 19 | HG00438.hp1 HG00438.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.1894-26_1894-25del others(2): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426944
|
AGTGTGTG others(1): Show |
A | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1894-32_1894-25del others(8): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426944 | ||||||
| chr7:87426979
|
G | A | 1 | a0001c0002t0001g0069 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1894-59C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87426979 | ||||||
| chr7:87427341
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1894-421G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87427341 | ||||||
| chr7:87427422
|
C | T | 1 | a0001c0002t0001g0063 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1894-502G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87427422 | ||||||
| chr7:87427425
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0236 | 2 | NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1894-505C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87427425 | ||||||
| chr7:87427439
|
G | C | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1894-519C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87427439 | ||||||
| chr7:87427498
|
G | A | 2 | a0002c0004t0001g0008a0002c0005t0001g0169 | 3 | HG02055.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1894-578C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87427498 | ||||||
| chr7:87427599
|
ACTATTAA others(4): Show |
A | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1894-690_1894-680d others(13): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87427599 | ||||||
| chr7:87427738
|
T | C | 1 | a0002c0004t0001g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1894-818A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87427738 | ||||||
| chr7:87428002
|
A | C | 3 | a0002c0004t0001g0253a0002c0017t0001g0196a0002c0027t0001g0256 | 3 | HG02723.hp1 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1894-1082T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87428002 | ||||||
| chr7:87428124
|
C | T | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1894-1204G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87428124 | ||||||
| chr7:87428383
|
G | A | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1894-1463C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87428383 | ||||||
| chr7:87428794
|
A | G | 6 | a0002c0004t0001g0095a0002c0004t0001g0105a0002c0009t0001g0241others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1894-1874T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87428794 | ||||||
| chr7:87428842
|
G | A | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1894-1922C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87428842 | ||||||
| chr7:87429102
|
G | A | 4 | a0002c0004t0001g0253a0002c0005t0001g0168a0002c0017t0001g0196others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1894-2182C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429102 | ||||||
| chr7:87429254
|
G | T | 16 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1893+2150C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429254 | ||||||
| chr7:87429410
|
C | T | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1893+1994G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429410 | ||||||
| chr7:87429697
|
G | A | 1 | a0001c0003t0001g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1893+1707C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429697 | ||||||
| chr7:87429848
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(126): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1893+1556C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429848 | ||||||
| chr7:87429903
|
CT | C | 24 | a0001c0001t0001g0204a0001c0001t0001g0219a0001c0003t0001g0142others(21): Show | 24 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1893+1500delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429903 | ||||||
| chr7:87429913
|
T | A | 19 | a0002c0005t0001g0036a0002c0005t0001g0042a0002c0005t0001g0046others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1893+1491A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429913 | ||||||
| chr7:87429914
|
T | A | 27 | a0001c0002t0001g0059a0001c0002t0001g0096a0001c0003t0001g0143others(24): Show | 27 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1893+1490A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429914 | ||||||
| chr7:87429914
|
TA | T | 29 | a0001c0001t0001g0026a0001c0001t0001g0200a0001c0001t0001g0224others(26): Show | 33 | HG00639.hp1 HG01243.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.1893+1489delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429914 | ||||||
| chr7:87429915
|
A | T | 3 | a0001c0001t0001g0211a0001c0003t0001g0133a0002c0004t0001g0105 | 3 | HG00639.hp2 HG01255.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1893+1489T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429915 | ||||||
| chr7:87429916
|
A | T | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1893+1488T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87429916 | ||||||
| chr7:87430087
|
G | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(126): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1893+1317C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430087 | ||||||
| chr7:87430143
|
T | G | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1893+1261A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430143 | ||||||
| chr7:87430179
|
G | A | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1893+1225C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430179 | ||||||
| chr7:87430234
|
A | G | 1 | a0003c0008t0001g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1893+1170T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430234 | ||||||
| chr7:87430313
|
A | G | 2 | a0002c0004t0001g0008a0002c0005t0001g0169 | 3 | HG02055.hp1 HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1893+1091T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430313 | ||||||
| chr7:87430383
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(126): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1893+1021G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430383 | ||||||
| chr7:87430384
|
G | A | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1893+1020C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430384 | ||||||
| chr7:87430765
|
G | T | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1893+639C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430765 | ||||||
| chr7:87430977
|
G | A | 1 | a0001c0002t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1893+427C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430977 | ||||||
| chr7:87430982
|
G | A | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1893+422C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87430982 | ||||||
| chr7:87431053
|
T | C | 1 | a0005c0030t0001g0239 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1893+351A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87431053 | ||||||
| chr7:87431126
|
C | T | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1893+278G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87431126 | ||||||
| chr7:87431205
|
G | T | 5 | a0001c0002t0001g0106a0001c0002t0001g0251a0001c0002t0001g0252others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1893+199C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87431205 | ||||||
| chr7:87431398
|
A | G | 2 | a0001c0003t0001g0145a0001c0003t0001g0146 | 2 | HG02735.hp1 HG03491.hp2 |
splice_region_variant&intron_variant | LOW | c.1893+6T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 15/27 | chr7 | 87431398 | ||||||
| chr7:87431918
|
C | T | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1732-353G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87431918 | ||||||
| chr7:87432065
|
C | T | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1732-500G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432065 | ||||||
| chr7:87432137
|
C | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0179a0001c0001t0001g0181 | 4 | HG01975.hp1 HG02148.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-572G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432137 | ||||||
| chr7:87432218
|
G | T | 43 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(40): Show | 47 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1732-653C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432218 | ||||||
| chr7:87432238
|
A | C | 1 | a0001c0001t0002g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1732-673T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432238 | ||||||
| chr7:87432376
|
G | A | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1732-811C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432376 | ||||||
| chr7:87432437
|
G | T | 16 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1732-872C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432437 | ||||||
| chr7:87432658
|
A | G | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1732-1093T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432658 | ||||||
| chr7:87432661
|
T | A | 1 | a0001c0001t0001g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1732-1096A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432661 | ||||||
| chr7:87432796
|
T | G | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1732-1231A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432796 | ||||||
| chr7:87432826
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1732-1261G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432826 | ||||||
| chr7:87432876
|
C | G | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1732-1311G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432876 | ||||||
| chr7:87432977
|
A | G | 17 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(14): Show | 18 | HG00639.hp1 HG02258.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1732-1412T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87432977 | ||||||
| chr7:87433089
|
C | T | 1 | a0001c0002t0001g0073 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1732-1524G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433089 | ||||||
| chr7:87433208
|
A | G | 1 | a0001c0002t0001g0079 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1732-1643T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433208 | ||||||
| chr7:87433660
|
C | G | 1 | a0002c0004t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1732-2095G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433660 | ||||||
| chr7:87433669
|
G | GTTTT | 9 | a0002c0005t0001g0042a0002c0005t0001g0051a0002c0005t0001g0052others(6): Show | 9 | HG00323.hp1 HG01934.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1732-2105_1732-210 others(8): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433669 | ||||||
| chr7:87433669
|
G | GTTTTT | 4 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0054others(1): Show | 4 | HG00735.hp2 HG01192.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-2105_1732-210 others(9): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433669 | ||||||
| chr7:87433670
|
TTG | T | 6 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0038others(3): Show | 9 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1732-2107_1732-210 others(6): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433670 | ||||||
| chr7:87433671
|
TG | T | 8 | a0002c0004t0001g0009a0002c0004t0001g0040a0002c0004t0001g0041others(5): Show | 9 | HG02055.hp2 HG02647.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1732-2107delC | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433671 | ||||||
| chr7:87433672
|
G | T | 20 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1732-2107C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433672 | ||||||
| chr7:87433675
|
G | T | 35 | a0001c0003t0001g0165a0002c0004t0001g0003a0002c0004t0001g0008others(32): Show | 39 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1732-2110C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433675 | ||||||
| chr7:87433678
|
T | G | 9 | a0001c0001t0001g0021a0001c0001t0001g0185a0001c0001t0001g0224others(6): Show | 10 | HG00438.hp2 HG00639.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1732-2113A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87433678 | ||||||
| chr7:87434095
|
A | AT | 21 | a0001c0001t0001g0199a0001c0002t0001g0096a0001c0003t0001g0126others(18): Show | 25 | HG01175.hp2 HG01243.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1732-2531dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87434095 | ||||||
| chr7:87434095
|
AT | A | 7 | a0001c0001t0001g0204a0001c0002t0001g0093a0001c0003t0001g0132others(4): Show | 7 | HG01167.hp1 HG01943.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1732-2531delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87434095 | ||||||
| chr7:87434471
|
C | T | 1 | a0002c0027t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1732-2906G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87434471 | ||||||
| chr7:87434574
|
C | T | 2 | a0001c0003t0001g0006a0001c0003t0001g0151 | 4 | HG02040.hp1 NA19001.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-3009G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87434574 | ||||||
| chr7:87434719
|
G | A | 2 | a0002c0004t0001g0038a0002c0004t0001g0041 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1732-3154C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87434719 | ||||||
| chr7:87434746
|
C | CA | 61 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(58): Show | 70 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1732-3182dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87434746 | ||||||
| chr7:87434781
|
T | C | 1 | a0001c0003t0001g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1732-3216A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87434781 | ||||||
| chr7:87435237
|
T | C | 1 | a0001c0002t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1732-3672A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87435237 | ||||||
| chr7:87435856
|
T | G | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1731+3811A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87435856 | ||||||
| chr7:87436016
|
T | C | 4 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1731+3651A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436016 | ||||||
| chr7:87436032
|
T | C | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1731+3635A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436032 | ||||||
| chr7:87436109
|
A | T | 8 | a0002c0004t0001g0003a0002c0004t0001g0009a0002c0004t0001g0038others(5): Show | 11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1731+3558T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436109 | ||||||
| chr7:87436137
|
A | G | 3 | a0002c0004t0001g0253a0002c0017t0001g0196a0002c0027t0001g0256 | 3 | HG02723.hp1 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1731+3530T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436137 | ||||||
| chr7:87436322
|
C | CA | 19 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0177others(16): Show | 21 | HG00438.hp1 HG00438.hp2 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.1731+3344dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436322 | ||||||
| chr7:87436371
|
G | A | 2 | a0001c0003t0001g0158a0001c0003t0001g0160 | 2 | HG01069.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1731+3296C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436371 | ||||||
| chr7:87436583
|
C | T | 3 | a0002c0004t0001g0095a0002c0009t0001g0241a0002c0021t0001g0107 | 3 | HG03209.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1731+3084G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436583 | ||||||
| chr7:87436684
|
TC | T | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1731+2982delG | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436684 | ||||||
| chr7:87436687
|
T | G | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1731+2980A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436687 | ||||||
| chr7:87436751
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1731+2916G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436751 | ||||||
| chr7:87436848
|
G | A | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1731+2819C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436848 | ||||||
| chr7:87436914
|
G | C | 1 | a0001c0002t0001g0104 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1731+2753C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87436914 | ||||||
| chr7:87437031
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1731+2636A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87437031 | ||||||
| chr7:87437476
|
T | C | 10 | a0001c0001t0001g0186a0001c0001t0001g0220a0001c0001t0001g0221others(7): Show | 10 | HG00438.hp1 HG02135.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1731+2191A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87437476 | ||||||
| chr7:87437498
|
T | A | 1 | a0002c0004t0001g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1731+2169A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87437498 | ||||||
| chr7:87437506
|
T | C | 1 | a0001c0007t0001g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1731+2161A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87437506 | ||||||
| chr7:87437514
|
C | T | 4 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1731+2153G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87437514 | ||||||
| chr7:87437726
|
G | C | 3 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0255 | 3 | HG02145.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1731+1941C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87437726 | ||||||
| chr7:87438311
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1731+1356T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438311 | ||||||
| chr7:87438324
|
C | G | 4 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1731+1343G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438324 | ||||||
| chr7:87438352
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1731+1315T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438352 | ||||||
| chr7:87438425
|
T | C | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1731+1242A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438425 | ||||||
| chr7:87438536
|
C | T | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1731+1131G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438536 | ||||||
| chr7:87438617
|
C | T | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1731+1050G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438617 | ||||||
| chr7:87438646
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1731+1021C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438646 | ||||||
| chr7:87438700
|
A | G | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1731+967T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438700 | ||||||
| chr7:87438707
|
C | T | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1731+960G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87438707 | ||||||
| chr7:87439092
|
G | A | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1731+575C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439092 | ||||||
| chr7:87439140
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1731+527A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439140 | ||||||
| chr7:87439148
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(128): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1731+519A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439148 | ||||||
| chr7:87439172
|
C | T | 3 | a0002c0004t0001g0095a0002c0009t0001g0241a0002c0021t0001g0107 | 3 | HG03209.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1731+495G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439172 | ||||||
| chr7:87439182
|
A | G | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1731+485T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439182 | ||||||
| chr7:87439231
|
T | C | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1731+436A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439231 | ||||||
| chr7:87439375
|
C | T | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1731+292G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439375 | ||||||
| chr7:87439557
|
T | C | 1 | a0002c0004t0001g0095 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1731+110A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439557 | ||||||
| chr7:87439572
|
T | C | 1 | a0001c0003t0001g0130 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1731+95A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 14/27 | chr7 | 87439572 | ||||||
| chr7:87440035
|
T | G | 4 | a0002c0004t0001g0105a0002c0023t0001g0250a0004c0013t0001g0100others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1560+164A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 13/27 | chr7 | 87440035 | ||||||
| chr7:87440115
|
A | G | 1 | a0001c0007t0001g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1560+84T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 13/27 | chr7 | 87440115 | ||||||
| chr7:87440193
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18944.hp1 | splice_region_variant&intron_variant | LOW | c.1560+6G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 13/27 | chr7 | 87440193 | ||||||
| chr7:87440419
|
T | C | 1 | a0002c0005t0001g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1357-17A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440419 | ||||||
| chr7:87440442
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(195): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1357-40A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440442 | ||||||
| chr7:87440450
|
T | C | 1 | a0001c0006t0001g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1357-48A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440450 | ||||||
| chr7:87440564
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(128): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1357-162A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440564 | ||||||
| chr7:87440607
|
G | A | 2 | a0002c0005t0001g0053a0002c0009t0001g0237 | 2 | HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1357-205C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440607 | ||||||
| chr7:87440773
|
G | A | 23 | a0002c0004t0001g0095a0002c0005t0001g0035a0002c0005t0001g0036others(20): Show | 23 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1357-371C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440773 | ||||||
| chr7:87440780
|
C | T | 16 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0042others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1357-378G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440780 | ||||||
| chr7:87440786
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1357-384C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440786 | ||||||
| chr7:87440931
|
G | A | 2 | a0001c0003t0001g0030a0001c0007t0001g0050 | 2 | HG02040.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1357-529C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440931 | ||||||
| chr7:87440982
|
G | A | 19 | a0002c0004t0001g0095a0002c0005t0001g0035a0002c0005t0001g0036others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1357-580C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440982 | ||||||
| chr7:87440985
|
C | T | 1 | a0001c0003t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1357-583G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87440985 | ||||||
| chr7:87441067
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1357-665T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441067 | ||||||
| chr7:87441178
|
A | G | 1 | a0002c0005t0001g0054 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1357-776T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441178 | ||||||
| chr7:87441241
|
A | G | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1357-839T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441241 | ||||||
| chr7:87441408
|
T | TATAA | 37 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(34): Show | 41 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1357-1010_1357-100 others(8): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441408 | ||||||
| chr7:87441431
|
AC | A | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1357-1030delG | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441431 | ||||||
| chr7:87441580
|
C | CT | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1357-1179dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441580 | ||||||
| chr7:87441592
|
T | A | 3 | a0002c0004t0001g0095a0002c0009t0001g0241a0002c0021t0001g0107 | 3 | HG03209.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1357-1190A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441592 | ||||||
| chr7:87441593
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1357-1191T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441593 | ||||||
| chr7:87441796
|
C | T | 4 | a0002c0004t0001g0253a0002c0005t0001g0168a0002c0017t0001g0196others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357-1394G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441796 | ||||||
| chr7:87441805
|
C | T | 13 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(10): Show | 17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1357-1403G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87441805 | ||||||
| chr7:87442214
|
T | G | 37 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(34): Show | 41 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1356+1105A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442214 | ||||||
| chr7:87442323
|
G | A | 37 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(34): Show | 41 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1356+996C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442323 | ||||||
| chr7:87442459
|
A | C | 1 | a0002c0010t0001g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1356+860T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442459 | ||||||
| chr7:87442466
|
C | G | 1 | a0001c0003t0001g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1356+853G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442466 | ||||||
| chr7:87442471
|
C | T | 3 | a0002c0004t0001g0105a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG01884.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1356+848G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442471 | ||||||
| chr7:87442824
|
T | C | 40 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(37): Show | 44 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1356+495A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442824 | ||||||
| chr7:87442880
|
C | A | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1356+439G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442880 | ||||||
| chr7:87442882
|
C | T | 2 | a0001c0001t0001g0238a0001c0002t0001g0096 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1356+437G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442882 | ||||||
| chr7:87442910
|
C | T | 37 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(34): Show | 41 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1356+409G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442910 | ||||||
| chr7:87442959
|
C | A | 4 | a0001c0003t0001g0013a0001c0003t0001g0118a0001c0003t0001g0167others(1): Show | 5 | HG01256.hp1 NA18971.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1356+360G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87442959 | ||||||
| chr7:87443189
|
C | A | 37 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(34): Show | 41 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1356+130G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87443189 | ||||||
| chr7:87443233
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1356+86G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87443233 | ||||||
| chr7:87443293
|
T | C | 2 | a0001c0001t0001g0238a0001c0002t0001g0096 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1356+26A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 12/27 | chr7 | 87443293 | ||||||
| chr7:87443514
|
T | C | 1 | a0002c0005t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1231-70A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 11/27 | chr7 | 87443514 | ||||||
| chr7:87443524
|
GA | G | 36 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(33): Show | 40 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1231-81delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 11/27 | chr7 | 87443524 | ||||||
| chr7:87443984
|
C | T | 2 | a0004c0013t0001g0100a0004c0013t0001g0101 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1120-211G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87443984 | ||||||
| chr7:87444066
|
T | C | 1 | a0002c0004t0001g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1120-293A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444066 | ||||||
| chr7:87444258
|
G | A | 1 | a0001c0002t0001g0059 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1120-485C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444258 | ||||||
| chr7:87444272
|
C | T | 6 | a0002c0004t0001g0095a0002c0004t0001g0253a0002c0005t0001g0168others(3): Show | 6 | HG02723.hp1 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120-499G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444272 | ||||||
| chr7:87444278
|
G | A | 71 | a0001c0001t0001g0026a0001c0001t0001g0176a0001c0001t0001g0183others(68): Show | 82 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1120-505C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444278 | ||||||
| chr7:87444368
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1119+494G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444368 | ||||||
| chr7:87444459
|
G | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(118): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1119+403C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444459 | ||||||
| chr7:87444502
|
G | A | 1 | a0001c0003t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1119+360C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444502 | ||||||
| chr7:87444584
|
C | T | 1 | a0001c0006t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1119+278G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 10/27 | chr7 | 87444584 | ||||||
| chr7:87445103
|
T | C | 116 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(113): Show | 132 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1006-128A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87445103 | ||||||
| chr7:87445545
|
C | T | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1006-570G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87445545 | ||||||
| chr7:87445620
|
G | GA | 88 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(85): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1006-646dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87445620 | ||||||
| chr7:87445648
|
T | C | 88 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(85): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1006-673A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87445648 | ||||||
| chr7:87445847
|
C | T | 1 | a0001c0015t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1006-872G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87445847 | ||||||
| chr7:87445902
|
G | A | 1 | a0001c0003t0001g0157 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1006-927C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87445902 | ||||||
| chr7:87445943
|
A | C | 8 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0104others(5): Show | 8 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-968T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87445943 | ||||||
| chr7:87446046
|
A | G | 119 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(116): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1005+988T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446046 | ||||||
| chr7:87446061
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1005+973G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446061 | ||||||
| chr7:87446065
|
T | C | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1005+969A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446065 | ||||||
| chr7:87446139
|
C | T | 19 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(16): Show | 23 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1005+895G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446139 | ||||||
| chr7:87446209
|
A | C | 2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1005+825T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446209 | ||||||
| chr7:87446303
|
T | C | 1 | a0001c0002t0001g0060 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1005+731A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446303 | ||||||
| chr7:87446419
|
A | T | 1 | a0001c0015t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1005+615T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446419 | ||||||
| chr7:87446424
|
T | C | 18 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(15): Show | 22 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1005+610A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446424 | ||||||
| chr7:87446450
|
C | T | 1 | a0007c0018t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1005+584G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446450 | ||||||
| chr7:87446487
|
G | C | 1 | a0001c0002t0001g0083 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1005+547C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446487 | ||||||
| chr7:87446487
|
G | T | 4 | a0003c0011t0001g0111a0003c0011t0001g0112a0003c0011t0001g0113others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+547C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446487 | ||||||
| chr7:87446566
|
G | C | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1005+468C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446566 | ||||||
| chr7:87446692
|
A | T | 9 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(6): Show | 10 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1005+342T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446692 | ||||||
| chr7:87446702
|
C | T | 1 | a0002c0004t0001g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1005+332G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446702 | ||||||
| chr7:87446828
|
C | T | 16 | a0001c0007t0001g0034a0001c0007t0001g0037a0001c0007t0001g0047others(13): Show | 16 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1005+206G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446828 | ||||||
| chr7:87446936
|
T | C | 4 | a0003c0011t0001g0111a0003c0011t0001g0112a0003c0011t0001g0113others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+98A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 9/27 | chr7 | 87446936 | ||||||
| chr7:87447271
|
C | A | 116 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(113): Show | 132 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.834-66G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87447271 | ||||||
| chr7:87447454
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.834-249C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87447454 | ||||||
| chr7:87447515
|
C | G | 1 | a0001c0003t0001g0005 | 3 | NA18966.hp2 NA18984.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.834-310G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87447515 | ||||||
| chr7:87447654
|
G | A | 1 | a0002c0004t0001g0008 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.834-449C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87447654 | ||||||
| chr7:87447725
|
T | C | 1 | a0001c0002t0001g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.834-520A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87447725 | ||||||
| chr7:87448233
|
C | A | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.834-1028G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448233 | ||||||
| chr7:87448281
|
C | CA | 8 | a0001c0002t0001g0063a0001c0002t0001g0071a0001c0002t0001g0073others(5): Show | 8 | HG02145.hp2 HG02155.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1077dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448281 | ||||||
| chr7:87448281
|
CA | C | 17 | a0001c0002t0001g0106a0001c0007t0001g0034a0001c0007t0001g0037others(14): Show | 17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.834-1077delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448281 | ||||||
| chr7:87448291
|
C | CA | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.834-1087dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448291 | ||||||
| chr7:87448390
|
T | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.834-1185A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448390 | ||||||
| chr7:87448507
|
G | C | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.834-1302C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448507 | ||||||
| chr7:87448539
|
G | A | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.834-1334C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448539 | ||||||
| chr7:87448663
|
T | C | 1 | a0001c0003t0001g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.833+1305A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448663 | ||||||
| chr7:87448680
|
A | G | 48 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(45): Show | 59 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.833+1288T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448680 | ||||||
| chr7:87448812
|
T | C | 1 | a0001c0003t0001g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.833+1156A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87448812 | ||||||
| chr7:87449048
|
C | G | 1 | a0001c0001t0001g0185 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.833+920G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87449048 | ||||||
| chr7:87449142
|
T | C | 1 | a0001c0003t0001g0123 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.833+826A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87449142 | ||||||
| chr7:87449231
|
G | T | 88 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(85): Show | 103 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.833+737C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87449231 | ||||||
| chr7:87449602
|
TA | T | 111 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(108): Show | 126 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.833+365delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87449602 | ||||||
| chr7:87449753
|
T | C | 111 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(108): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.833+215A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87449753 | ||||||
| chr7:87449787
|
T | A | 111 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(108): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.833+181A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 8/27 | chr7 | 87449787 | ||||||
| chr7:87450249
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.709-157C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450249 | ||||||
| chr7:87450286
|
G | C | 98 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(95): Show | 113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.709-194C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450286 | ||||||
| chr7:87450468
|
A | AT | 77 | a0001c0001t0001g0240a0001c0001t0002g0027a0001c0002t0001g0001others(74): Show | 92 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.709-377dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450468 | ||||||
| chr7:87450468
|
A | ATT | 9 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0086others(6): Show | 9 | HG01981.hp1 HG02109.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-378_709-377dup others(2): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450468 | ||||||
| chr7:87450468
|
A | ATTT | 11 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(8): Show | 12 | HG02055.hp1 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.709-379_709-377dup others(3): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450468 | ||||||
| chr7:87450468
|
AT | A | 10 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0236others(7): Show | 10 | HG00280.hp2 HG02083.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.709-377delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450468 | ||||||
| chr7:87450468
|
ATTTTT | A | 16 | a0001c0007t0001g0034a0001c0007t0001g0037a0001c0007t0001g0047others(13): Show | 16 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.709-381_709-377del others(5): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450468 | ||||||
| chr7:87450564
|
A | G | 111 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(108): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.709-472T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450564 | ||||||
| chr7:87450779
|
G | C | 1 | a0001c0002t0001g0085 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.709-687C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450779 | ||||||
| chr7:87450854
|
G | C | 5 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.709-762C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450854 | ||||||
| chr7:87450865
|
T | G | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): Show | 16 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.708+758A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450865 | ||||||
| chr7:87450941
|
A | G | 1 | a0001c0002t0001g0069 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.708+682T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450941 | ||||||
| chr7:87450970
|
C | G | 1 | a0002c0024t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.708+653G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87450970 | ||||||
| chr7:87451034
|
A | C | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.708+589T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87451034 | ||||||
| chr7:87451039
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.708+584G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87451039 | ||||||
| chr7:87451065
|
C | T | 2 | a0004c0013t0001g0100a0004c0013t0001g0101 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.708+558G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87451065 | ||||||
| chr7:87451139
|
A | ATTT | 20 | a0001c0002t0001g0099a0001c0007t0001g0034a0001c0007t0001g0037others(17): Show | 20 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.708+481_708+483dup others(3): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87451139 | ||||||
| chr7:87451139
|
A | ATTTT | 88 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(85): Show | 104 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.708+480_708+483dup others(4): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87451139 | ||||||
| chr7:87451166
|
T | C | 121 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(118): Show | 137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.708+457A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87451166 | ||||||
| chr7:87451382
|
T | C | 111 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(108): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.708+241A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 7/27 | chr7 | 87451382 | ||||||
| chr7:87451954
|
C | T | 4 | a0001c0001t0001g0191a0001c0029t0001g0115a0004c0013t0001g0100others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.537-160G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87451954 | ||||||
| chr7:87452033
|
A | G | 80 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.537-239T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452033 | ||||||
| chr7:87452116
|
A | C | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.537-322T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452116 | ||||||
| chr7:87452197
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.537-403C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452197 | ||||||
| chr7:87452197
|
G | T | 5 | a0001c0002t0001g0063a0001c0002t0001g0072a0001c0002t0001g0073others(2): Show | 5 | HG02155.hp1 NA18973.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.537-403C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452197 | ||||||
| chr7:87452348
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.537-554A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452348 | ||||||
| chr7:87452378
|
C | CT | 6 | a0001c0001t0001g0029a0001c0003t0001g0030a0001c0003t0001g0165others(3): Show | 6 | HG02132.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.536+565dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452378 | ||||||
| chr7:87452378
|
CT | C | 17 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0207others(14): Show | 18 | HG01123.hp1 HG01256.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.536+565delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452378 | ||||||
| chr7:87452378
|
CTT | C | 69 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(66): Show | 83 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.536+564_536+565del others(2): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452378 | ||||||
| chr7:87452378
|
CTTTT | C | 24 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(21): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.536+562_536+565del others(4): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452378 | ||||||
| chr7:87452544
|
G | A | 8 | a0001c0006t0001g0022a0001c0006t0001g0243a0001c0006t0001g0244others(5): Show | 9 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.536+400C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452544 | ||||||
| chr7:87452726
|
A | G | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.536+218T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 6/27 | chr7 | 87452726 | ||||||
| chr7:87453414
|
C | T | 1 | a0001c0006t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.345-279G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453414 | ||||||
| chr7:87453459
|
T | C | 1 | a0002c0021t0001g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-324A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453459 | ||||||
| chr7:87453552
|
A | T | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.345-417T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453552 | ||||||
| chr7:87453599
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.345-464G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453599 | ||||||
| chr7:87453659
|
A | G | 18 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(15): Show | 22 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-524T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453659 | ||||||
| chr7:87453841
|
C | A | 80 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.344+694G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453841 | ||||||
| chr7:87453944
|
TA | T | 65 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(62): Show | 75 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.344+590delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453944 | ||||||
| chr7:87454023
|
A | T | 111 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(108): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.344+512T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87454023 | ||||||
| chr7:87454180
|
C | G | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.344+355G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87454180 | ||||||
| chr7:87454261
|
T | G | 8 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0104others(5): Show | 8 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+274A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87454261 | ||||||
| chr7:87454377
|
G | A | 1 | a0002c0012t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.344+158C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87454377 | ||||||
| chr7:87454422
|
T | C | 111 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(108): Show | 127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.344+113A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87454422 | ||||||
| chr7:87454653
|
G | A | 1 | a0001c0003t0001g0017 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.287-61C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87454653 | ||||||
| chr7:87454957
|
A | C | 2 | a0004c0013t0001g0100a0004c0013t0001g0101 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.287-365T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87454957 | ||||||
| chr7:87454985
|
T | C | 3 | a0001c0001t0001g0026a0003c0008t0001g0024a0003c0008t0001g0025 | 3 | HG03195.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.287-393A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87454985 | ||||||
| chr7:87454995
|
A | AT | 15 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(12): Show | 15 | HG00639.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.287-404dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87454995 | ||||||
| chr7:87454995
|
AT | A | 11 | a0001c0003t0001g0153a0001c0006t0001g0022a0001c0006t0001g0242others(8): Show | 12 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.287-404delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87454995 | ||||||
| chr7:87455041
|
AT | A | 4 | a0003c0011t0001g0111a0003c0011t0001g0112a0003c0011t0001g0113others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-450delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455041 | ||||||
| chr7:87455087
|
A | G | 62 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(59): Show | 73 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.287-495T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455087 | ||||||
| chr7:87455456
|
T | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.287-864A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455456 | ||||||
| chr7:87455565
|
C | T | 1 | a0002c0009t0001g0222 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.287-973G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455565 | ||||||
| chr7:87455582
|
C | T | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-990G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455582 | ||||||
| chr7:87455801
|
GTCGTGTT others(1): Show |
G | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-1217_287-1210d others(10): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455801 | ||||||
| chr7:87455866
|
T | C | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-1274A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455866 | ||||||
| chr7:87455893
|
G | A | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-1301C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455893 | ||||||
| chr7:87455959
|
C | A | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.287-1367G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87455959 | ||||||
| chr7:87456063
|
C | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.287-1471G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456063 | ||||||
| chr7:87456123
|
G | A | 4 | a0003c0011t0001g0111a0003c0011t0001g0112a0003c0011t0001g0113others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-1531C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456123 | ||||||
| chr7:87456297
|
A | G | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.287-1705T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456297 | ||||||
| chr7:87456378
|
G | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.287-1786C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456378 | ||||||
| chr7:87456483
|
C | G | 4 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-1891G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456483 | ||||||
| chr7:87456723
|
A | C | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-2131T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456723 | ||||||
| chr7:87456725
|
G | A | 2 | a0001c0003t0001g0133a0001c0003t0001g0153 | 2 | HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.287-2133C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456725 | ||||||
| chr7:87456757
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0215a0001c0001t0001g0216 | 4 | HG00738.hp1 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-2165C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456757 | ||||||
| chr7:87456774
|
T | C | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-2182A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456774 | ||||||
| chr7:87456798
|
G | A | 18 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(15): Show | 22 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.287-2206C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456798 | ||||||
| chr7:87456824
|
C | T | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-2232G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456824 | ||||||
| chr7:87456828
|
G | A | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-2236C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456828 | ||||||
| chr7:87456902
|
T | C | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.287-2310A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456902 | ||||||
| chr7:87456935
|
G | C | 1 | a0001c0015t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287-2343C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87456935 | ||||||
| chr7:87457138
|
G | A | 2 | a0001c0002t0001g0060a0001c0002t0001g0085 | 2 | HG00597.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.287-2546C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457138 | ||||||
| chr7:87457234
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.287-2642G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457234 | ||||||
| chr7:87457371
|
C | G | 1 | a0001c0003t0001g0118 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.287-2779G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457371 | ||||||
| chr7:87457372
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.287-2780A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457372 | ||||||
| chr7:87457611
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.287-3019A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457611 | ||||||
| chr7:87457615
|
T | C | 89 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(86): Show | 105 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.287-3023A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457615 | ||||||
| chr7:87457638
|
C | G | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.287-3046G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457638 | ||||||
| chr7:87457709
|
A | G | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-3117T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457709 | ||||||
| chr7:87457819
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.287-3227A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457819 | ||||||
| chr7:87457823
|
C | G | 1 | a0002c0027t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.287-3231G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457823 | ||||||
| chr7:87457871
|
G | T | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-3279C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457871 | ||||||
| chr7:87457879
|
C | A | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.287-3287G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457879 | ||||||
| chr7:87457900
|
A | C | 1 | a0001c0002t0001g0065 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.287-3308T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457900 | ||||||
| chr7:87457925
|
T | A | 1 | a0001c0003t0001g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.287-3333A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457925 | ||||||
| chr7:87457967
|
A | G | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.287-3375T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87457967 | ||||||
| chr7:87458081
|
C | G | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-3489G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458081 | ||||||
| chr7:87458171
|
C | T | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.287-3579G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458171 | ||||||
| chr7:87458262
|
C | T | 4 | a0001c0003t0001g0125a0001c0003t0001g0128a0001c0003t0001g0132others(1): Show | 4 | HG00738.hp2 HG01943.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-3670G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458262 | ||||||
| chr7:87458263
|
G | A | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.287-3671C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458263 | ||||||
| chr7:87458415
|
G | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.287-3823C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458415 | ||||||
| chr7:87458518
|
A | T | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.287-3926T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458518 | ||||||
| chr7:87458752
|
T | C | 1 | a0001c0002t0001g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.286+4006A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458752 | ||||||
| chr7:87458857
|
G | A | 1 | a0002c0027t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286+3901C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458857 | ||||||
| chr7:87458870
|
T | C | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.286+3888A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458870 | ||||||
| chr7:87458985
|
G | GT | 85 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(82): Show | 101 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.286+3772dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458985 | ||||||
| chr7:87458987
|
T | TA | 23 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(20): Show | 23 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.286+3770dupT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458987 | ||||||
| chr7:87458987
|
T | TTA | 4 | a0001c0002t0001g0086a0002c0004t0001g0043a0002c0004t0001g0057others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+3770_286+3771i others(4): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458987 | ||||||
| chr7:87458988
|
A | T | 3 | a0001c0002t0001g0093a0001c0002t0001g0097a0003c0011t0001g0111 | 3 | HG02965.hp1 HG03654.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.286+3770T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87458988 | ||||||
| chr7:87459067
|
T | G | 1 | a0001c0003t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.286+3691A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459067 | ||||||
| chr7:87459174
|
C | T | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.286+3584G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459174 | ||||||
| chr7:87459456
|
A | G | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.286+3302T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459456 | ||||||
| chr7:87459520
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.286+3238G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459520 | ||||||
| chr7:87459689
|
A | G | 3 | a0001c0002t0001g0010a0001c0002t0001g0059a0001c0002t0001g0067 | 4 | HG00544.hp1 NA18747.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+3069T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459689 | ||||||
| chr7:87459731
|
T | C | 1 | a0001c0002t0001g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.286+3027A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459731 | ||||||
| chr7:87459845
|
A | T | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+2913T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459845 | ||||||
| chr7:87459911
|
G | A | 2 | a0001c0003t0001g0155a0001c0003t0001g0156 | 2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.286+2847C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87459911 | ||||||
| chr7:87460208
|
T | C | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.286+2550A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460208 | ||||||
| chr7:87460375
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.286+2383T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460375 | ||||||
| chr7:87460549
|
T | C | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+2209A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460549 | ||||||
| chr7:87460582
|
C | T | 80 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.286+2176G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460582 | ||||||
| chr7:87460611
|
G | A | 80 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.286+2147C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460611 | ||||||
| chr7:87460620
|
T | TTTTA | 15 | a0001c0007t0001g0034a0001c0007t0001g0037a0001c0007t0001g0047others(12): Show | 15 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+2137_286+2138i others(6): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460620 | ||||||
| chr7:87460622
|
G | GTATT | 26 | a0001c0001t0001g0179a0001c0001t0001g0194a0001c0001t0001g0211others(23): Show | 27 | HG00544.hp2 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.286+2132_286+2135d others(6): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460622 | ||||||
| chr7:87460622
|
G | GTATTTAT others(1): Show |
3 | a0001c0001t0001g0026a0003c0008t0001g0024a0003c0008t0001g0025 | 3 | HG03195.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.286+2128_286+2135d others(10): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460622 | ||||||
| chr7:87460622
|
G | T | 16 | a0001c0007t0001g0034a0001c0007t0001g0037a0001c0007t0001g0047others(13): Show | 16 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.286+2136C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460622 | ||||||
| chr7:87460622
|
GTATT | G | 29 | a0001c0001t0001g0210a0001c0001t0001g0217a0001c0002t0001g0087others(26): Show | 34 | HG01106.hp2 HG01243.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.286+2132_286+2135d others(6): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460622 | ||||||
| chr7:87460622
|
GTATTTAT others(1): Show |
G | 3 | a0001c0001t0001g0177a0001c0003t0001g0130a0001c0006t0001g0242 | 3 | HG03098.hp2 NA18943.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.286+2128_286+2135d others(10): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460622 | ||||||
| chr7:87460622
|
GTATTTAT others(5): Show |
G | 19 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(16): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.286+2124_286+2135d others(14): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460622 | ||||||
| chr7:87460626
|
T | G | 3 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0108 | 3 | NA18966.hp1 NA19072.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.286+2132A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460626 | ||||||
| chr7:87460690
|
G | A | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286+2068C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460690 | ||||||
| chr7:87460839
|
C | T | 5 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.286+1919G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460839 | ||||||
| chr7:87460985
|
C | T | 93 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(90): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.286+1773G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87460985 | ||||||
| chr7:87461164
|
C | T | 63 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(60): Show | 74 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.286+1594G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461164 | ||||||
| chr7:87461165
|
G | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.286+1593C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461165 | ||||||
| chr7:87461413
|
G | C | 1 | a0001c0003t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.286+1345C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461413 | ||||||
| chr7:87461541
|
A | G | 1 | a0001c0002t0001g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.286+1217T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461541 | ||||||
| chr7:87461610
|
T | C | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+1148A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461610 | ||||||
| chr7:87461830
|
A | C | 1 | a0001c0003t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286+928T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461830 | ||||||
| chr7:87461878
|
A | G | 2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.286+880T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461878 | ||||||
| chr7:87461994
|
G | A | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.286+764C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87461994 | ||||||
| chr7:87462045
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.286+713C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462045 | ||||||
| chr7:87462137
|
T | C | 1 | a0001c0006t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286+621A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462137 | ||||||
| chr7:87462227
|
T | C | 80 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.286+531A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462227 | ||||||
| chr7:87462276
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.286+482G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462276 | ||||||
| chr7:87462279
|
G | T | 1 | a0001c0002t0001g0065 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.286+479C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462279 | ||||||
| chr7:87462362
|
T | A | 1 | a0001c0003t0001g0016 | 2 | NA18973.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.286+396A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462362 | ||||||
| chr7:87462439
|
G | C | 1 | a0002c0009t0001g0214 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.286+319C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462439 | ||||||
| chr7:87462510
|
T | C | 80 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.286+248A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462510 | ||||||
| chr7:87462628
|
A | G | 80 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.286+130T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 4/27 | chr7 | 87462628 | ||||||
| chr7:87462982
|
G | A | 4 | a0003c0011t0001g0111a0003c0011t0001g0112a0003c0011t0001g0113others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-74C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87462982 | ||||||
| chr7:87462988
|
TA | T | 4 | a0003c0011t0001g0111a0003c0011t0001g0112a0003c0011t0001g0113others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-81delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87462988 | ||||||
| chr7:87463060
|
A | G | 121 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(118): Show | 137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.136-152T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463060 | ||||||
| chr7:87463184
|
T | A | 4 | a0001c0003t0001g0013a0001c0003t0001g0118a0001c0003t0001g0167others(1): Show | 5 | HG01256.hp1 NA18971.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-276A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463184 | ||||||
| chr7:87463222
|
G | A | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-314C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463222 | ||||||
| chr7:87463246
|
A | AAC | 5 | a0001c0001t0001g0231a0001c0003t0001g0129a0001c0003t0001g0130others(2): Show | 5 | HG00140.hp1 HG02896.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-340_136-339dup others(2): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463246 | ||||||
| chr7:87463246
|
AACAC | A | 20 | a0001c0001t0001g0026a0001c0001t0001g0190a0001c0001t0001g0224others(17): Show | 21 | HG00639.hp1 HG01123.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.136-342_136-339del others(4): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463246 | ||||||
| chr7:87463246
|
AACACAC | A | 102 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(99): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.136-344_136-339del others(6): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463246 | ||||||
| chr7:87463526
|
T | C | 9 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(6): Show | 10 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-618A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463526 | ||||||
| chr7:87463748
|
T | C | 4 | a0001c0002t0001g0004a0001c0002t0001g0090a0001c0002t0001g0092others(1): Show | 6 | HG01109.hp1 HG01167.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-840A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463748 | ||||||
| chr7:87463931
|
T | C | 34 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(31): Show | 38 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-1023A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87463931 | ||||||
| chr7:87464388
|
C | G | 1 | a0002c0005t0001g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.136-1480G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87464388 | ||||||
| chr7:87464743
|
A | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-1835T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87464743 | ||||||
| chr7:87464757
|
A | G | 2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.136-1849T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87464757 | ||||||
| chr7:87464925
|
C | G | 1 | a0002c0010t0001g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.136-2017G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87464925 | ||||||
| chr7:87464931
|
A | T | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.136-2023T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87464931 | ||||||
| chr7:87464958
|
T | C | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-2050A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87464958 | ||||||
| chr7:87464990
|
C | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.136-2082G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87464990 | ||||||
| chr7:87465017
|
G | A | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.136-2109C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465017 | ||||||
| chr7:87465146
|
C | T | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-2238G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465146 | ||||||
| chr7:87465172
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.136-2264G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465172 | ||||||
| chr7:87465175
|
C | T | 1 | a0001c0002t0001g0063 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.136-2267G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465175 | ||||||
| chr7:87465209
|
C | T | 2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.136-2301G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465209 | ||||||
| chr7:87465351
|
C | T | 1 | a0001c0015t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.136-2443G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465351 | ||||||
| chr7:87465402
|
C | T | 2 | a0002c0004t0001g0044a0002c0004t0001g0045 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.136-2494G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465402 | ||||||
| chr7:87465403
|
G | A | 3 | a0001c0001t0001g0026a0003c0008t0001g0024a0003c0008t0001g0025 | 3 | HG03195.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.136-2495C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465403 | ||||||
| chr7:87465417
|
T | A | 6 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-2509A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465417 | ||||||
| chr7:87465429
|
C | A | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.136-2521G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465429 | ||||||
| chr7:87465524
|
T | A | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.136-2616A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465524 | ||||||
| chr7:87465623
|
C | T | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-2715G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465623 | ||||||
| chr7:87465674
|
C | T | 1 | a0001c0003t0001g0120 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.136-2766G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465674 | ||||||
| chr7:87465720
|
G | T | 1 | a0001c0003t0001g0013 | 2 | NA18971.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.136-2812C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465720 | ||||||
| chr7:87465750
|
G | A | 2 | a0001c0003t0001g0163a0001c0003t0001g0164 | 2 | NA18951.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.136-2842C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465750 | ||||||
| chr7:87465767
|
G | A | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.136-2859C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465767 | ||||||
| chr7:87465796
|
G | A | 9 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(6): Show | 10 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-2888C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465796 | ||||||
| chr7:87465829
|
G | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.136-2921C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465829 | ||||||
| chr7:87465837
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0209a0001c0001t0001g0215others(1): Show | 5 | HG00738.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-2929C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465837 | ||||||
| chr7:87465894
|
T | C | 1 | a0001c0003t0001g0017 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.136-2986A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465894 | ||||||
| chr7:87465926
|
A | G | 2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.136-3018T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465926 | ||||||
| chr7:87465958
|
A | G | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.136-3050T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87465958 | ||||||
| chr7:87466111
|
C | G | 1 | a0001c0006t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136-3203G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466111 | ||||||
| chr7:87466146
|
C | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02965.hp2 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136-3238G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466146 | ||||||
| chr7:87466293
|
G | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(93): Show | 111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.136-3385C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466293 | ||||||
| chr7:87466635
|
A | C | 1 | a0001c0003t0001g0128 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.136-3727T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466635 | ||||||
| chr7:87466671
|
G | T | 1 | a0001c0002t0001g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.136-3763C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466671 | ||||||
| chr7:87466811
|
C | T | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.136-3903G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466811 | ||||||
| chr7:87466839
|
A | G | 3 | a0001c0019t0001g0023a0002c0005t0001g0168a0002c0005t0001g0169 | 3 | HG02055.hp1 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-3931T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466839 | ||||||
| chr7:87466842
|
C | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-3934G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466842 | ||||||
| chr7:87466849
|
TGA | T | 10 | a0002c0004t0001g0003a0002c0004t0001g0009a0002c0004t0001g0038others(7): Show | 13 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.136-3943_136-3942d others(4): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466849 | ||||||
| chr7:87466955
|
G | A | 62 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(59): Show | 73 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.136-4047C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87466955 | ||||||
| chr7:87467163
|
T | G | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.136-4255A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467163 | ||||||
| chr7:87467206
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.136-4298A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467206 | ||||||
| chr7:87467244
|
G | A | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.136-4336C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467244 | ||||||
| chr7:87467307
|
C | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(93): Show | 111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.136-4399G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467307 | ||||||
| chr7:87467324
|
C | T | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.136-4416G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467324 | ||||||
| chr7:87467458
|
G | C | 2 | a0001c0002t0001g0252a0001c0002t0001g0255 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.136-4550C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467458 | ||||||
| chr7:87467467
|
A | C | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-4559T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467467 | ||||||
| chr7:87467467
|
A | G | 120 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(117): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.136-4559T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467467 | ||||||
| chr7:87467515
|
G | A | 1 | a0001c0003t0001g0127 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.136-4607C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467515 | ||||||
| chr7:87467627
|
T | C | 1 | a0001c0002t0001g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-4719A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467627 | ||||||
| chr7:87467635
|
G | A | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.136-4727C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467635 | ||||||
| chr7:87467752
|
C | T | 1 | a0002c0004t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-4844G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467752 | ||||||
| chr7:87467814
|
G | T | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.135+4807C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467814 | ||||||
| chr7:87467830
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.135+4791T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87467830 | ||||||
| chr7:87468189
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.135+4432G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468189 | ||||||
| chr7:87468243
|
T | G | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.135+4378A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468243 | ||||||
| chr7:87468327
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.135+4294G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468327 | ||||||
| chr7:87468412
|
AG | A | 34 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(31): Show | 38 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.135+4208delC | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468412 | ||||||
| chr7:87468439
|
G | A | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.135+4182C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468439 | ||||||
| chr7:87468496
|
T | C | 4 | a0002c0010t0001g0172a0002c0010t0001g0173a0002c0010t0001g0174others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+4125A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468496 | ||||||
| chr7:87468506
|
A | C | 1 | a0001c0006t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.135+4115T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468506 | ||||||
| chr7:87468602
|
T | C | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.135+4019A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468602 | ||||||
| chr7:87468681
|
G | A | 1 | a0001c0003t0001g0018 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.135+3940C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468681 | ||||||
| chr7:87468788
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(192): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.135+3833T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468788 | ||||||
| chr7:87468791
|
C | T | 1 | a0001c0002t0001g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.135+3830G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468791 | ||||||
| chr7:87468792
|
G | A | 1 | a0001c0003t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.135+3829C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468792 | ||||||
| chr7:87468804
|
A | T | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.135+3817T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468804 | ||||||
| chr7:87468914
|
C | G | 8 | a0001c0006t0001g0022a0001c0006t0001g0243a0001c0006t0001g0244others(5): Show | 9 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+3707G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468914 | ||||||
| chr7:87468931
|
A | C | 1 | a0001c0002t0001g0098 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.135+3690T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468931 | ||||||
| chr7:87468941
|
T | TAAAATAA others(4): Show |
2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.135+3679_135+3680i others(13): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATA | 10 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0191others(7): Show | 14 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.135+3675_135+3679d others(7): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(13): Show |
1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.135+3660_135+3679d others(22): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(28): Show |
1 | a0002c0004t0001g0253 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.135+3679_135+3680i others(37): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(38): Show |
3 | a0001c0002t0001g0251a0001c0002t0001g0252a0002c0027t0001g0256 | 3 | HG02818.hp2 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.135+3679_135+3680i others(47): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(43): Show |
2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.135+3679_135+3680i others(52): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(23): Show |
11 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0006t0001g0022others(8): Show | 12 | HG00597.hp1 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.135+3679_135+3680i others(32): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(28): Show |
7 | a0001c0002t0001g0061a0001c0002t0001g0102a0001c0002t0001g0103others(4): Show | 7 | HG00099.hp1 HG00323.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+3679_135+3680i others(37): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(33): Show |
60 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(57): Show | 74 | HG00423.hp2 HG00544.hp1 HG01109.hp1 others(71): Show |
intron_variant | MODIFIER | c.135+3679_135+3680i others(42): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(38): Show |
18 | a0001c0002t0001g0093a0001c0002t0001g0094a0001c0006t0001g0242others(15): Show | 19 | HG01943.hp1 HG01978.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.135+3679_135+3680i others(47): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(43): Show |
6 | a0001c0007t0001g0037a0002c0005t0001g0052a0002c0005t0001g0053others(3): Show | 6 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+3679_135+3680i others(52): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
T | TAAATAAA others(43): Show |
1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.135+3679_135+3680i others(52): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468941
|
TAAATAAA others(3): Show |
T | 8 | a0001c0001t0001g0026a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+3670_135+3679d others(12): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468941 | ||||||
| chr7:87468951
|
A | T | 1 | a0001c0003t0001g0125 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.135+3670T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87468951 | ||||||
| chr7:87469035
|
G | A | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(93): Show | 111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.135+3586C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469035 | ||||||
| chr7:87469053
|
G | T | 8 | a0001c0006t0001g0022a0001c0006t0001g0243a0001c0006t0001g0244others(5): Show | 9 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+3568C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469053 | ||||||
| chr7:87469101
|
A | G | 1 | a0001c0003t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.135+3520T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469101 | ||||||
| chr7:87469122
|
C | A | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.135+3499G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469122 | ||||||
| chr7:87469204
|
G | C | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.135+3417C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469204 | ||||||
| chr7:87469491
|
G | A | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.135+3130C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469491 | ||||||
| chr7:87469684
|
G | A | 2 | a0002c0004t0001g0057a0002c0004t0001g0058 | 2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.135+2937C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469684 | ||||||
| chr7:87469708
|
G | A | 1 | a0001c0002t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.135+2913C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469708 | ||||||
| chr7:87469850
|
T | G | 9 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(6): Show | 10 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+2771A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469850 | ||||||
| chr7:87469905
|
T | C | 2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.135+2716A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87469905 | ||||||
| chr7:87470210
|
A | T | 2 | a0001c0003t0001g0032a0001c0003t0001g0124 | 2 | HG01192.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.135+2411T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470210 | ||||||
| chr7:87470409
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.135+2212C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470409 | ||||||
| chr7:87470420
|
T | C | 34 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(31): Show | 38 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.135+2201A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470420 | ||||||
| chr7:87470498
|
CT | C | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(2): Show | 5 | HG03834.hp1 NA18950.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2122delA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470498 | ||||||
| chr7:87470551
|
G | C | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.135+2070C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470551 | ||||||
| chr7:87470554
|
G | A | 1 | a0002c0009t0001g0222 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.135+2067C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470554 | ||||||
| chr7:87470609
|
A | G | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(93): Show | 111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.135+2012T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470609 | ||||||
| chr7:87470625
|
G | C | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.135+1996C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470625 | ||||||
| chr7:87470644
|
A | C | 28 | a0001c0007t0001g0034a0001c0007t0001g0037a0001c0007t0001g0047others(25): Show | 32 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.135+1977T>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470644 | ||||||
| chr7:87470763
|
A | G | 20 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0176others(17): Show | 22 | HG00438.hp1 HG00438.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.135+1858T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87470763 | ||||||
| chr7:87471091
|
C | T | 1 | a0001c0003t0001g0123 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.135+1530G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471091 | ||||||
| chr7:87471330
|
G | A | 1 | a0001c0002t0003g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.135+1291C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471330 | ||||||
| chr7:87471377
|
A | T | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.135+1244T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471377 | ||||||
| chr7:87471586
|
G | T | 1 | a0007c0018t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.135+1035C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471586 | ||||||
| chr7:87471608
|
A | G | 2 | a0002c0005t0001g0168a0002c0005t0001g0169 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.135+1013T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471608 | ||||||
| chr7:87471630
|
A | G | 13 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(10): Show | 14 | HG02109.hp1 HG02258.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.135+991T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471630 | ||||||
| chr7:87471658
|
C | T | 1 | a0001c0002t0001g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.135+963G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471658 | ||||||
| chr7:87471811
|
C | G | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+810G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471811 | ||||||
| chr7:87471858
|
C | T | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.135+763G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471858 | ||||||
| chr7:87471979
|
C | T | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.135+642G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87471979 | ||||||
| chr7:87472086
|
G | A | 1 | a0002c0009t0001g0222 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.135+535C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472086 | ||||||
| chr7:87472091
|
C | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(53): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.135+530G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472091 | ||||||
| chr7:87472153
|
A | G | 1 | a0001c0003t0001g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.135+468T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472153 | ||||||
| chr7:87472170
|
T | G | 112 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.135+451A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472170 | ||||||
| chr7:87472200
|
T | C | 1 | a0002c0023t0001g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.135+421A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472200 | ||||||
| chr7:87472227
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.135+394G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472227 | ||||||
| chr7:87472265
|
C | A | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+356G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472265 | ||||||
| chr7:87472334
|
C | A | 1 | a0001c0006t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.135+287G>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472334 | ||||||
| chr7:87472364
|
T | C | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+257A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472364 | ||||||
| chr7:87472382
|
A | T | 9 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(6): Show | 10 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+239T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472382 | ||||||
| chr7:87472450
|
T | C | 7 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0104others(4): Show | 7 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+171A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472450 | ||||||
| chr7:87472515
|
C | T | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.135+106G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472515 | ||||||
| chr7:87472516
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.135+105C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 3/27 | chr7 | 87472516 | ||||||
| chr7:87472745
|
T | C | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-70A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87472745 | ||||||
| chr7:87472921
|
GAAAGATA others(8): Show |
G | 2 | a0001c0002t0001g0098a0001c0002t0001g0099 | 2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.81-261_81-247delAG others(13): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87472921 | ||||||
| chr7:87472935
|
C | T | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(107): Show | 126 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.81-260G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87472935 | ||||||
| chr7:87472955
|
A | T | 1 | a0002c0004t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81-280T>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87472955 | ||||||
| chr7:87473135
|
G | T | 7 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0104others(4): Show | 7 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.81-460C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473135 | ||||||
| chr7:87473162
|
C | T | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.81-487G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473162 | ||||||
| chr7:87473166
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0240 | 3 | HG00438.hp2 NA18983.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.81-491A>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473166 | ||||||
| chr7:87473253
|
T | C | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-578A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473253 | ||||||
| chr7:87473649
|
A | G | 1 | a0001c0006t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.81-974T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473649 | ||||||
| chr7:87473678
|
A | G | 3 | a0001c0029t0001g0115a0004c0013t0001g0100a0004c0013t0001g0101 | 3 | HG02109.hp1 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.81-1003T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473678 | ||||||
| chr7:87473726
|
A | AGT | 30 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0104others(27): Show | 30 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-1053_81-1052dup others(2): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473726 | ||||||
| chr7:87473726
|
A | AGTGT | 77 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(74): Show | 92 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.81-1055_81-1052dup others(4): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473726 | ||||||
| chr7:87473726
|
AGT | A | 3 | a0001c0002t0001g0109a0001c0002t0001g0110a0002c0009t0001g0241 | 3 | HG01175.hp1 HG01255.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.81-1053_81-1052del others(2): Show |
ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473726 | ||||||
| chr7:87473760
|
T | C | 1 | a0001c0003t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.81-1085A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473760 | ||||||
| chr7:87473798
|
C | T | 4 | a0001c0007t0001g0034a0001c0007t0001g0037a0002c0005t0001g0035others(1): Show | 4 | HG00140.hp2 HG01943.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-1123G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473798 | ||||||
| chr7:87473947
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0019others(192): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.81-1272A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473947 | ||||||
| chr7:87473980
|
T | C | 4 | a0003c0011t0001g0111a0003c0011t0001g0112a0003c0011t0001g0113others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-1305A>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87473980 | ||||||
| chr7:87474066
|
G | C | 1 | a0001c0029t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80+1320C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474066 | ||||||
| chr7:87474106
|
C | T | 1 | a0001c0003t0001g0118 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.80+1280G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474106 | ||||||
| chr7:87474128
|
C | T | 1 | a0001c0002t0003g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.80+1258G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474128 | ||||||
| chr7:87474268
|
G | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.80+1118C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474268 | ||||||
| chr7:87474338
|
C | T | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80+1048G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474338 | ||||||
| chr7:87474354
|
C | G | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0010others(106): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.80+1032G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474354 | ||||||
| chr7:87474695
|
G | A | 10 | a0001c0006t0001g0022a0001c0006t0001g0242a0001c0006t0001g0243others(7): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.80+691C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474695 | ||||||
| chr7:87474826
|
G | T | 1 | a0001c0003t0001g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.80+560C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474826 | ||||||
| chr7:87474954
|
G | C | 1 | a0002c0027t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80+432C>G | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87474954 | ||||||
| chr7:87475134
|
A | G | 2 | a0001c0003t0001g0030a0001c0003t0001g0031 | 2 | HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.80+252T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87475134 | ||||||
| chr7:87475249
|
T | A | 6 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+137A>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87475249 | ||||||
| chr7:87475272
|
C | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG00280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.80+114G>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 2/27 | chr7 | 87475272 | ||||||
| chr7:87475475
|
A | G | 3 | a0001c0001t0001g0026a0003c0008t0001g0024a0003c0008t0001g0025 | 3 | HG03195.hp2 HG03453.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.-6-4T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 1/27 | chr7 | 87475475 | ||||||
| chr7:87475515
|
G | T | 1 | a0001c0019t0001g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-6-44C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 1/27 | chr7 | 87475515 |