Search by Gene
| Item | Value |
|---|---|
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1279 | 225 | 37 | 41 | 113 | 8 | 24 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0002 | 0/0 | 1279 | 46 | 31 | 7 | 3 | 2 | 3 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0003 | 0/0 | 1279 | 10 | 10 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0004 | 0/0 | 1279 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0005 | 0/0 | 1279 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0006 | 0/0 | 1279 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0007 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0008 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0009 | 0/0 | 1279 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0010 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| a0011 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | MDLEA others(1274): Show |
chr7 | 87396696 | 87480680 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3837 | 74 | 18 | 16 | 34 | 2 | 3 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0002 | 0/0 | 3837 | 67 | 8 | 10 | 38 | 4 | 7 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0003 | 0/1 | 3837 | 65 | 0 | 14 | 35 | 1 | 14 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0006 | 0/0 | 3837 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0007 | 0/0 | 3837 | 6 | 0 | 1 | 4 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0015 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0019 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0026 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0001c0029 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0004 | 0/0 | 3837 | 18 | 17 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0005 | 0/0 | 3837 | 12 | 2 | 4 | 3 | 1 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0009 | 0/0 | 3837 | 5 | 2 | 1 | 0 | 1 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0010 | 0/0 | 3837 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0012 | 0/0 | 3837 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0017 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0021 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0023 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0024 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0002c0027 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0003c0008 | 0/0 | 3837 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0003c0011 | 0/0 | 3837 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0003c0022 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0004c0013 | 0/0 | 3837 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0005c0025 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0006c0014 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0007c0030 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0008c0016 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0009c0018 | 0/0 | 3837 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0010c0020 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 | ||
| a0011c0028 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | ATGGA others(3832): Show |
chr7 | 87396696 | 87480680 |
| acthapid | grch38/chm13v2 | 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 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0001t0002 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0002t0001 | 0/0 | 4293 | 66 | 8 | 10 | 38 | 4 | 6 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0002t0003 | 0/0 | 4293 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0003t0001 | 0/1 | 4293 | 65 | 0 | 14 | 35 | 1 | 14 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0006t0001 | 0/0 | 4293 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0007t0001 | 0/0 | 4293 | 6 | 0 | 1 | 4 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0015t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0019t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0026t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0001c0029t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0004t0001 | 0/0 | 4293 | 18 | 17 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0005t0001 | 0/0 | 4293 | 12 | 2 | 4 | 3 | 1 | 2 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0009t0001 | 0/0 | 4293 | 5 | 2 | 1 | 0 | 1 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0010t0001 | 0/0 | 4293 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0012t0001 | 0/0 | 4293 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0017t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0021t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0023t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0024t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0002c0027t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0003c0008t0001 | 0/0 | 4293 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0003c0011t0001 | 0/0 | 4293 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0003c0022t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0004c0013t0001 | 0/0 | 4293 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0005c0025t0001 | 0/0 | 4293 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0006c0014t0001 | 0/0 | 4293 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0007c0030t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0008c0016t0001 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0009c0018t0001 | 0/0 | 4293 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0010c0020t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
chr7 | 87396696 | 87480680 |
| a0011c0028t0001 | 0/0 | 4293 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | AGCGC others(4288): Show |
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 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 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 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0175 | 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 |
| a0001c0001t0001g0178 | 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 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0001 | 0/0 | 8 | 0 | 1 | 7 | 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 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0013 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0001g0082 | 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 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0002t0001g0249 | 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 |
| a0001c0002t0003g0035 | 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 |
| a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | 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 | 0 | 2 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | 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 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0133 | 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 |
| a0001c0003t0001g0136 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0006t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0006t0001g0241 | 0/0 | 1 | 1 | 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 |
| a0001c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0007t0001g0039 | 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 |
| a0001c0015t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0019t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0026t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0001c0029t0001g0114 | 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 |
| a0002c0004t0001g0010 | 0/0 | 2 | 2 | 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 |
| a0002c0004t0001g0042 | 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 |
| 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 |
| a0002c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0044 | 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 |
| a0002c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0009t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0010t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0010t0001g0171 | 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 |
| a0002c0012t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0012t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0017t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0021t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0023t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0024t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0002c0027t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0008t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0003c0011t0001g0110 | 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 |
| a0003c0022t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0004c0013t0001g0099 | 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 |
| a0005c0025t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0006c0014t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0007c0030t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0008c0016t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0009c0018t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0010c0020t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| a0011c0028t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0102 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00140 | hp1 | a0002 | c0009 | t0001 | g0219 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00140 | hp2 | a0001 | c0007 | t0001 | g0039 | EUR | GBR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0122 | EUR | FIN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0030 | 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 | g0103 | EUR | FIN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0118 | 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 | g0210 | EAS | CHS | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0119 | 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 | g0212 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0127 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0159 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0155 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01109 | hp1 | a0005 | c0025 | t0001 | g0090 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0160 | 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 | g0108 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01192 | hp1 | a0002 | c0012 | t0001 | g0150 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0123 | 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 | g0229 | AMR | PUR | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0131 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01256 | hp1 | a0006 | c0014 | t0001 | g0161 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0129 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0089 | 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 | g0251 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0104 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | 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 | g0037 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0130 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0012 | 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 | g0093 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02004 | hp1 | a0002 | c0005 | t0001 | g0038 | 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 | g0174 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0164 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02135 | hp2 | a0001 | c0015 | t0001 | g0177 | EAS | KHV | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02145 | hp1 | a0003 | c0008 | t0001 | g0168 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02148 | hp2 | a0002 | c0009 | t0001 | g0211 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CDX | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02155 | hp2 | a0002 | c0005 | t0001 | g0044 | EAS | CDX | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02257 | hp1 | a0002 | c0010 | t0001 | g0170 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02258 | hp1 | a0001 | c0006 | t0001 | g0024 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02273 | hp1 | a0001 | c0007 | t0001 | g0036 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02451 | hp1 | a0002 | c0010 | t0001 | g0172 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02451 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02615 | hp1 | a0003 | c0022 | t0001 | g0245 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02615 | hp2 | a0007 | c0030 | t0001 | g0236 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02622 | hp2 | a0001 | c0029 | t0001 | g0114 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02630 | hp1 | a0003 | c0008 | t0001 | g0220 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02630 | hp2 | a0002 | c0009 | t0001 | g0190 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0045 | 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 | g0138 | 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 | g0173 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02717 | hp2 | a0002 | c0023 | t0001 | g0247 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02723 | hp1 | a0002 | c0004 | t0001 | g0250 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02723 | hp2 | a0002 | c0005 | t0001 | g0167 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0144 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0033 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0152 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0032 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02818 | hp1 | a0002 | c0004 | t0001 | g0010 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02886 | hp1 | a0004 | c0013 | t0001 | g0099 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02886 | hp2 | a0002 | c0012 | t0001 | g0134 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0241 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02896 | hp2 | a0008 | c0016 | t0001 | g0234 | 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 | g0206 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02965 | hp1 | a0003 | c0011 | t0001 | g0110 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0240 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02970 | hp2 | a0002 | c0004 | t0001 | g0040 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03017 | hp1 | a0002 | c0009 | t0001 | g0232 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0015 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03041 | hp1 | a0002 | c0027 | t0001 | g0253 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03041 | hp2 | a0002 | c0017 | t0001 | g0193 | AFR | GWD | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0239 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0226 | 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 | g0010 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0221 | 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 | g0027 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03209 | hp1 | a0002 | c0021 | t0001 | g0106 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0244 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0158 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0151 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03453 | hp1 | a0002 | c0009 | t0001 | g0238 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0028 | 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 | g0143 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03492 | hp1 | a0009 | c0018 | t0001 | g0121 | 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 | g0026 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03516 | hp2 | a0002 | c0004 | t0001 | g0043 | AFR | ESN | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0024 | 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 | g0096 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0154 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0120 | SAS | PJL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0215 | 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 | g0013 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0153 | SAS | BEB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0088 | 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 | g0034 | SAS | STU | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0035 | SAS | STU | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0078 | 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 | g0011 | EAS | CHB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18906 | hp1 | a0002 | c0004 | t0001 | g0042 | AFR | YRI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18906 | hp2 | a0003 | c0008 | t0001 | g0169 | 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 | g0083 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0188 | 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 | g0098 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0163 | 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 | g0132 | 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 | g0183 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0107 | 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 | g0087 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0166 | 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 | g0228 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18999 | hp2 | a0010 | c0020 | t0001 | g0187 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0097 | 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 | g0231 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19043 | hp1 | a0002 | c0004 | t0001 | g0094 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0201 | 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 | g0218 | 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 | g0178 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19065 | hp2 | a0011 | c0028 | t0001 | g0068 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0142 | 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 | g0117 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19072 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0023 | 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 | g0070 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0082 | 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 | g0148 | 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 | g0185 | 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 | g0001 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | YRI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20129 | hp1 | a0002 | c0010 | t0001 | g0171 | AFR | ASW | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20129 | hp2 | a0001 | c0006 | t0001 | g0242 | AFR | ASW | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0101 | EUR | TSI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0091 | EUR | TSI | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0126 | SAS | GIH | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0157 | AMR | CLM | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02109 | hp1 | a0004 | c0013 | t0001 | g0100 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02109 | hp2 | a0003 | c0011 | t0001 | g0113 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02486 | hp1 | a0002 | c0024 | t0001 | g0041 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0243 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG03471 | hp2 | a0001 | c0006 | t0001 | g0246 | AFR | MSL | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | 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 | g0186 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | USA | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA20300 | hp2 | a0003 | c0011 | t0001 | g0112 | AFR | USA | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA21309 | hp1 | a0001 | c0019 | t0001 | g0025 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| NA21309 | hp2 | a0003 | c0011 | t0001 | g0111 | AFR | LWK | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0128 | REF | REF | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0147 | REF | REF | ABCB4_chr7_87396696_87480680 | ABCB4 | chr7 | 87396696 | 87480680 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87409304 | C | T | 1 | a0008 | 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 | a0005 | 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 | a0009 | 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 | a0006 | 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 | a0011 | 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 | a0010 | 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 | a0007 | 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 |
| view | chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0003a0002c0012a0006c0014others(1): Show | 68 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(65): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87402374 | A | G | 40 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(37): 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 | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(131): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): 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 | a0001c0001t0001g0230 | 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 | a0003c0008t0001g0026a0003c0008t0001g0027a0003c0011t0001g0110others(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 | a0001c0002t0001g0103 | 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 | a0001c0001t0001g0181a0001c0001t0001g0183 | 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 | 40 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(37): 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 | a0001c0003t0001g0016a0001c0003t0001g0135a0001c0003t0001g0136others(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 | a0001c0015t0001g0177 | 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 | 195 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(192): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): 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 | a0001c0001t0001g0194a0001c0003t0001g0131a0001c0003t0001g0151 | 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 | a0001c0001t0001g0022a0001c0001t0001g0213a0001c0003t0001g0127 | 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 | a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | 132 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(129): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.3487-964G>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87404245 | |||||||
| chr7:87404632 | T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(131): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | a0001c0003t0001g0117 | 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 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0006t0001g0024others(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 | 132 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(129): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.3486+860dupA | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 26/27 | chr7 | 87405427 | |||||||
| chr7:87405448 | A | T | 1 | a0002c0004t0001g0104 | 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 | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(130): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): 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 | a0002c0005t0001g0037 | 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 | a0001c0003t0001g0166 | 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 | a0001c0003t0001g0126 | 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 | 40 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(37): 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 | a0001c0003t0001g0131 | 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 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0002c0004t0001g0104 | 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 | a0001c0001t0001g0192a0001c0002t0001g0062a0001c0002t0003g0035others(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 | a0002c0004t0001g0094 | 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 | 30 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(27): 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 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0203 | 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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(169): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): 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 | a0001c0001t0001g0176 | 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 | a0001c0003t0001g0138 | 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 | 40 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(37): 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 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0006t0001g0024others(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 | a0001c0001t0001g0222 | 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 | 39 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(36): 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 | a0001c0001t0001g0204 | 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 | a0001c0002t0001g0075 | 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 | a0002c0004t0001g0104a0002c0027t0001g0253 | 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 | 176 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(173): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): 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 | a0002c0027t0001g0253 | 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 | a0001c0003t0001g0032 | 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 | 29 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(26): 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 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0180others(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 | a0001c0001t0001g0192a0001c0002t0003g0035a0001c0003t0001g0153others(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 | a0001c0003t0001g0120 | 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 | a0001c0001t0001g0192a0001c0002t0003g0035a0001c0003t0001g0153others(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 | a0001c0001t0001g0200 | 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | 183 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(180): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0006t0001g0024others(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 | a0003c0008t0001g0026a0003c0008t0001g0027a0003c0011t0001g0110others(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 | 40 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(37): 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 | a0001c0001t0001g0148 | 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 | a0002c0027t0001g0253 | 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 | a0002c0004t0001g0008a0002c0005t0001g0174 | 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 | a0002c0017t0001g0193 | 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 | a0002c0004t0001g0250 | 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 | a0001c0002t0001g0116 | 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 | a0001c0001t0001g0192a0001c0002t0003g0035a0001c0003t0001g0153others(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 | a0001c0003t0001g0132 | 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 | 41 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(38): 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 | a0002c0004t0001g0250 | 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 | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(130): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): 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 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(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 | a0011c0028t0001g0068 | 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 | 25 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0178others(22): 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 | 195 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(192): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): 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 | a0001c0003t0001g0158 | 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 | 174 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(171): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): 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 | a0001c0003t0001g0164 | 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 | a0001c0003t0001g0154 | 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 | a0002c0004t0001g0104 | 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 | a0003c0008t0001g0026a0003c0008t0001g0027 | 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 | a0002c0004t0001g0104 | 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 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(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 | 5 | a0001c0003t0001g0018a0001c0003t0001g0120a0001c0003t0001g0143others(2): Show | 6 | HG01106.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2682+1311C>T | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416001 | |||||||
| chr7:87416003 | T | A | 11 | a0001c0002t0001g0115a0002c0004t0001g0003a0002c0004t0001g0008others(8): 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 | a0001c0001t0001g0192a0001c0002t0003g0035a0001c0003t0001g0153others(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 | 30 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(27): 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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(163): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2682+1044T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 21/27 | chr7 | 87416268 | |||||||
| chr7:87416521 | G | A | 249 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(246): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): 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 | a0001c0003t0001g0132a0001c0003t0001g0137 | 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 | a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0006t0001g0244 | 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 | a0001c0001t0001g0181a0001c0001t0001g0183 | 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 | a0001c0002t0001g0095 | 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 | 31 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(28): 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 | a0004c0013t0001g0099 | 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 | 29 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(26): 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 | 29 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(26): 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 | a0001c0002t0001g0088 | 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 | a0001c0003t0001g0157a0001c0003t0001g0159 | 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 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0006t0001g0024others(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 | 30 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(27): 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 | a0001c0006t0001g0239a0001c0029t0001g0114 | 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 | a0002c0027t0001g0253 | 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 | a0010c0020t0001g0187 | 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 | 13 | a0001c0001t0001g0002a0001c0001t0001g0199a0001c0001t0001g0202others(10): Show | 21 | HG00423.hp1 HG01106.hp2 HG01256.hp2 others(18): 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 | a0001c0001t0001g0179a0002c0005t0001g0051 | 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 | a0001c0001t0001g0206 | 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 | a0002c0004t0001g0104a0002c0027t0001g0253 | 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 | a0001c0001t0001g0028a0001c0006t0001g0240a0001c0006t0001g0241others(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 | 153 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(150): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2394+201delG | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 19/27 | chr7 | 87419796 | |||||||
| chr7:87419797 | C | A | 28 | a0001c0001t0001g0028a0001c0001t0001g0217a0001c0001t0001g0233others(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 | 23 | a0001c0002t0001g0115a0001c0003t0001g0017a0001c0003t0001g0119others(20): 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 | 31 | a0001c0001t0001g0028a0001c0002t0001g0115a0001c0003t0001g0017others(28): 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 | a0001c0001t0001g0233a0001c0002t0001g0096a0002c0004t0001g0094others(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 | a0001c0003t0001g0136 | 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 | a0001c0002t0001g0071 | 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 | a0001c0001t0001g0023a0001c0001t0001g0237 | 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 | 34 | a0001c0001t0001g0192a0001c0002t0001g0115a0001c0002t0003g0035others(31): 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 | a0001c0002t0001g0101a0001c0002t0001g0102 | 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 | a0001c0002t0001g0103 | 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 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0001t0001g0222 | 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 | a0002c0004t0001g0250 | 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 | a0001c0003t0001g0143a0001c0003t0001g0144 | 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 | a0001c0001t0001g0230 | 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 | a0001c0002t0001g0248 | 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 | a0001c0002t0001g0082 | 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 | a0002c0023t0001g0247 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0003t0001g0014a0001c0003t0001g0117a0001c0003t0001g0166others(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 | a0002c0005t0001g0044 | 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 | 13 | a0001c0002t0001g0095a0002c0004t0001g0003a0002c0004t0001g0008others(10): 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 | a0008c0016t0001g0234 | 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 | 156 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(153): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0002c0023t0001g0247 | 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 | a0002c0023t0001g0247 | 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 | a0001c0006t0001g0241a0001c0006t0001g0243 | 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 | 145 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(142): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.2211+72T>C | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 17/27 | chr7 | 87423834 | |||||||
| chr7:87423890 | G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(191): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): 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 | a0001c0001t0001g0206 | 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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0009c0018t0001g0121 | 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | 193 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(190): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): 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 | a0002c0005t0001g0167a0002c0017t0001g0193 | 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 | a0001c0002t0001g0085a0002c0004t0001g0094a0002c0004t0001g0104others(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 | a0001c0001t0001g0182 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0179 | 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 | a0002c0004t0001g0094a0002c0009t0001g0238a0002c0021t0001g0106 | 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 | a0002c0005t0001g0167 | 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 | a0001c0002t0001g0105a0001c0002t0001g0248a0001c0002t0001g0249others(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 | a0002c0004t0001g0094a0002c0009t0001g0238a0002c0021t0001g0106 | 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 | a0002c0004t0001g0094a0002c0009t0001g0238a0002c0021t0001g0106 | 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 | a0001c0002t0001g0095a0002c0005t0001g0037a0002c0005t0001g0038others(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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0002c0004t0001g0094a0002c0021t0001g0106 | 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 | a0001c0001t0001g0020 | 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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0001c0003t0001g0157a0001c0003t0001g0159 | 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 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0176others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | 42 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(39): 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 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0022others(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 | 63 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0194others(60): Show | 70 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(67): 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 | a0001c0001t0001g0028a0001c0001t0001g0179a0001c0001t0001g0230others(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 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0002t0001g0103others(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 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(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 | a0001c0001t0001g0221a0001c0002t0001g0108a0001c0002t0001g0115 | 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 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0176others(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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0001c0002t0001g0070 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0228a0001c0001t0001g0231 | 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0002c0004t0001g0008a0002c0005t0001g0174 | 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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0002c0004t0001g0045 | 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 | a0002c0004t0001g0250a0002c0017t0001g0193a0002c0027t0001g0253 | 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 | a0001c0019t0001g0025 | 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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0002c0004t0001g0094a0002c0004t0001g0104a0002c0009t0001g0238others(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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0002c0004t0001g0250a0002c0005t0001g0167a0002c0017t0001g0193others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0003t0001g0120 | 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 | 128 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(125): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): 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 | a0001c0001t0001g0201a0001c0001t0001g0216a0001c0003t0001g0140others(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 | a0002c0005t0001g0038a0002c0005t0001g0044a0002c0005t0001g0046others(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 | a0001c0002t0001g0059a0001c0002t0001g0095a0001c0003t0001g0141others(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 | 28 | a0001c0001t0001g0028a0001c0001t0001g0197a0001c0001t0001g0221others(25): 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 | a0001c0001t0001g0208a0001c0003t0001g0131a0002c0004t0001g0104 | 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | 128 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(125): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): 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 | a0002c0005t0001g0167 | 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0003c0008t0001g0220 | 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 | a0002c0004t0001g0008a0002c0005t0001g0174 | 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 | 128 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(125): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): 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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0001c0029t0001g0114 | 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 | a0001c0002t0001g0116 | 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 | a0002c0023t0001g0247 | 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 | a0007c0030t0001g0236 | 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0001c0002t0001g0105a0001c0002t0001g0248a0001c0002t0001g0249others(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 | a0001c0003t0001g0143a0001c0003t0001g0144 | 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 | a0002c0005t0001g0167 | 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 | a0002c0023t0001g0247 | 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 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0180 | 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 | 42 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(39): 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 | a0001c0001t0002g0029 | 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0001c0001t0001g0178 | 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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0001c0001t0001g0205 | 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 | a0002c0023t0001g0247 | 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0001c0002t0001g0074 | 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 | a0001c0002t0001g0080 | 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 | a0002c0004t0001g0104 | 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 | a0002c0005t0001g0044a0002c0005t0001g0051a0002c0005t0001g0052others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0054others(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 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(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 | a0002c0004t0001g0009a0002c0004t0001g0010a0002c0004t0001g0042others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | 34 | a0001c0003t0001g0164a0002c0004t0001g0003a0002c0004t0001g0008others(31): 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 | a0001c0001t0001g0023a0001c0001t0001g0183a0001c0001t0001g0221others(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 | 20 | a0001c0001t0001g0196a0001c0002t0001g0095a0001c0003t0001g0125others(17): 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 | a0001c0001t0001g0201a0001c0002t0001g0092a0001c0003t0001g0130others(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 | a0002c0027t0001g0253 | 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 | a0001c0003t0001g0006a0001c0003t0001g0149 | 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 | a0002c0004t0001g0040a0002c0004t0001g0043 | 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 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(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 | a0001c0003t0001g0152 | 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 | a0001c0002t0001g0096 | 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 | a0002c0005t0001g0167 | 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | a0002c0005t0001g0167 | 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 | 7 | a0002c0004t0001g0003a0002c0004t0001g0009a0002c0004t0001g0010others(4): 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 | a0002c0004t0001g0250a0002c0017t0001g0193a0002c0027t0001g0253 | 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 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0176others(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 | a0001c0003t0001g0157a0001c0003t0001g0159 | 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 | a0002c0004t0001g0094a0002c0009t0001g0238a0002c0021t0001g0106 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0185 | 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 | a0002c0023t0001g0247 | 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 | a0001c0002t0001g0103 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0184a0001c0001t0001g0217a0001c0001t0001g0218others(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 | a0002c0004t0001g0045 | 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0252 | 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 | a0001c0001t0001g0195 | 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | a0001c0001t0001g0231 | 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 | a0002c0005t0001g0167 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0002c0023t0001g0247 | 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 | a0001c0001t0001g0208 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0002c0005t0001g0167 | 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 | a0002c0023t0001g0247 | 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 | a0001c0001t0001g0214 | 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 | 130 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(127): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): 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 | a0002c0004t0001g0094a0002c0009t0001g0238a0002c0021t0001g0106 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0003t0001g0125a0001c0003t0001g0126 | 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 | a0002c0004t0001g0094 | 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 | a0001c0003t0001g0156 | 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 | a0002c0004t0001g0104a0002c0023t0001g0247a0004c0013t0001g0099others(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 | a0001c0001t0001g0188 | 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 | 196 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(193): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): 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 | a0001c0006t0001g0244 | 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 | 130 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(127): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): 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 | a0002c0005t0001g0053a0002c0009t0001g0232 | 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 | a0002c0004t0001g0094a0002c0005t0001g0037a0002c0005t0001g0038others(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 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0005t0001g0044others(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 | a0001c0001t0001g0194 | 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 | a0001c0003t0001g0032a0001c0007t0001g0050 | 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 | a0002c0004t0001g0094a0002c0005t0001g0037a0002c0005t0001g0038others(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 | a0001c0003t0001g0118 | 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 | a0001c0001t0001g0231 | 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | 36 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(33): 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | a0002c0004t0001g0094a0002c0009t0001g0238a0002c0021t0001g0106 | 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 | a0001c0001t0001g0194 | 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 | a0002c0004t0001g0250a0002c0005t0001g0167a0002c0017t0001g0193others(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 | 12 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(9): 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 | 36 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(33): 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 | 36 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(33): 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 | a0002c0010t0001g0170 | 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 | a0001c0003t0001g0157 | 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 | a0002c0004t0001g0104a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | 39 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(36): 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 | a0002c0023t0001g0247 | 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 | a0001c0001t0001g0235a0001c0002t0001g0095 | 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 | 36 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(33): 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 | a0001c0003t0001g0014a0001c0003t0001g0117a0001c0003t0001g0166others(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 | 36 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(33): 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0235a0001c0002t0001g0095 | 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 | a0002c0005t0001g0167 | 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 | 35 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(32): 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 | a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0002c0004t0001g0045 | 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 | a0002c0004t0001g0094a0002c0004t0001g0250a0002c0005t0001g0167others(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 | 69 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0175others(66): 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 | a0001c0001t0001g0207 | 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 | 120 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(117): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): 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 | a0001c0003t0001g0154 | 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 | a0001c0006t0001g0239 | 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 | 114 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(111): 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | 87 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(84): 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 | 87 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(84): 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 | a0001c0015t0001g0177 | 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 | a0001c0003t0001g0155 | 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 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(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 | 117 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(114): 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 | a0001c0001t0001g0205 | 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 | a0001c0019t0001g0025 | 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 | 18 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(15): 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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0001c0015t0001g0177 | 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 | 17 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(14): 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 | a0009c0018t0001g0121 | 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 | a0001c0002t0001g0084 | 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 | a0003c0011t0001g0110a0003c0011t0001g0111a0003c0011t0001g0112others(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 | a0001c0019t0001g0025 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0002c0004t0001g0250 | 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 | a0001c0007t0001g0036a0001c0007t0001g0039a0001c0007t0001g0047others(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 | a0003c0011t0001g0110a0003c0011t0001g0111a0003c0011t0001g0112others(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 | 114 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(111): 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 | a0001c0001t0001g0183 | 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 | a0001c0002t0001g0073 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0002t0001g0063a0001c0002t0001g0072a0001c0002t0001g0074others(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 | a0001c0002t0001g0105a0001c0007t0001g0036a0001c0007t0001g0039others(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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0001c0029t0001g0114 | 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 | a0002c0023t0001g0247 | 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 | a0001c0003t0001g0034 | 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 | 47 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(44): 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 | a0001c0003t0001g0120 | 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 | a0001c0001t0001g0183 | 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 | a0001c0003t0001g0122 | 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 | 86 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(83): 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 | 109 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(106): 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 | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(106): 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 | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(106): 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 | a0001c0001t0001g0182 | 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 | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(93): 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 | 75 | a0001c0001t0001g0237a0001c0001t0002g0029a0001c0002t0001g0001others(72): 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 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0087others(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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0231others(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 | a0001c0007t0001g0036a0001c0007t0001g0039a0001c0007t0001g0047others(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 | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(106): 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 | a0001c0002t0001g0086 | 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 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(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 | 11 | a0002c0004t0001g0003a0002c0004t0001g0008a0002c0004t0001g0009others(8): 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 | a0001c0002t0001g0070 | 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 | a0002c0024t0001g0041 | 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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0002t0001g0098a0001c0007t0001g0036a0001c0007t0001g0039others(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 | 86 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(83): 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 | 119 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(116): 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 | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(106): 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 | a0001c0001t0001g0188a0001c0029t0001g0114a0004c0013t0001g0099others(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 | 78 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(75): 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0183 | 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 | a0001c0002t0001g0063a0001c0002t0001g0073a0001c0002t0001g0074others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0031a0001c0003t0001g0032a0001c0003t0001g0164others(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 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0204others(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 | 67 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(64): 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0006t0001g0024a0001c0006t0001g0240a0001c0006t0001g0241others(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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0006t0001g0239 | 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 | a0002c0021t0001g0106 | 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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0001t0001g0235 | 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 | 17 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(14): 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 | 78 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(75): 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 | 64 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(61): Show | 74 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.344+590delT | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 5/27 | chr7 | 87453944 | |||||||
| chr7:87454023 | A | T | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(106): 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 | a0001c0019t0001g0025 | 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 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(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 | a0002c0012t0001g0150 | 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 | 109 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(106): 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 | a0001c0003t0001g0018 | 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 | a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0028a0003c0008t0001g0026a0003c0008t0001g0027 | 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0001c0003t0001g0151a0001c0006t0001g0024a0001c0006t0001g0239others(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 | a0003c0011t0001g0110a0003c0011t0001g0111a0003c0011t0001g0112others(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 | 61 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(58): 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0002c0009t0001g0219 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0002c0023t0001g0247 | 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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0003c0011t0001g0110a0003c0011t0001g0111a0003c0011t0001g0112others(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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0002t0001g0115a0001c0002t0001g0116 | 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 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0001c0003t0001g0131a0001c0003t0001g0151 | 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 | a0001c0001t0001g0022a0001c0001t0001g0212a0001c0001t0001g0213 | 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | 17 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(14): 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0015t0001g0177 | 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 | a0001c0002t0001g0060a0001c0002t0001g0086 | 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 | a0001c0001t0001g0207 | 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 | a0001c0003t0001g0117 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0192 | 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 | 87 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(84): 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 | a0002c0023t0001g0247 | 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0001c0001t0001g0205 | 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 | a0002c0027t0001g0253 | 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0001c0019t0001g0025 | 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 | a0001c0002t0001g0064 | 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 | a0001c0003t0001g0152 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0001c0019t0001g0025 | 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 | a0001c0003t0001g0124a0001c0003t0001g0127a0001c0003t0001g0130others(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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0001c0002t0001g0091 | 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 | a0002c0027t0001g0253 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | 83 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(80): 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 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0002t0001g0087a0002c0004t0001g0045a0002c0004t0001g0057others(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 | a0001c0002t0001g0092a0001c0002t0001g0096a0003c0011t0001g0110 | 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 | a0001c0003t0001g0118 | 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 | a0002c0023t0001g0247 | 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0001c0001t0001g0192 | 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 | a0001c0002t0001g0011a0001c0002t0001g0059a0001c0002t0001g0066 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0003t0001g0153a0001c0003t0001g0154 | 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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | a0001c0001t0001g0206 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | 78 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(75): 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 | 78 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(75): 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 | a0001c0007t0001g0036a0001c0007t0001g0039a0001c0007t0001g0047others(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 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0208others(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 | a0001c0001t0001g0028a0003c0008t0001g0026a0003c0008t0001g0027 | 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 | a0001c0007t0001g0036a0001c0007t0001g0039a0001c0007t0001g0047others(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 | 28 | a0001c0001t0001g0207a0001c0001t0001g0214a0001c0002t0001g0088others(25): 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 | a0001c0001t0001g0176a0001c0003t0001g0156a0001c0006t0001g0239 | 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 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0002t0001g0001a0001c0002t0001g0069a0001c0002t0001g0107 | 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 | a0001c0029t0001g0114 | 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 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(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 | 91 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(88): 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 | 62 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(59): 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0001c0003t0001g0164 | 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 | a0001c0002t0001g0065 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0003t0001g0129 | 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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0001t0001g0205 | 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 | a0001c0006t0001g0239 | 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 | 78 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(75): 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 | a0001c0001t0001g0189 | 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 | a0001c0002t0001g0064 | 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 | a0001c0003t0001g0017 | 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 | a0002c0009t0001g0211 | 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 | 78 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(75): 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 | 78 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(75): 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 | a0003c0011t0001g0110a0003c0011t0001g0111a0003c0011t0001g0112others(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 | a0003c0011t0001g0110a0003c0011t0001g0111a0003c0011t0001g0112others(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 | 119 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(116): 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 | a0001c0003t0001g0014a0001c0003t0001g0117a0001c0003t0001g0166others(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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | 4 | a0001c0001t0001g0233a0001c0003t0001g0156a0002c0009t0001g0219others(1): Show | 4 | HG00140.hp1 HG02896.hp2 NA19005.hp2 others(1): 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 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0221others(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 | 100 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(97): 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0002t0001g0004a0001c0002t0001g0089a0001c0002t0001g0091others(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 | 33 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(30): 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 | a0002c0005t0001g0174 | 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0002c0010t0001g0170 | 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0019t0001g0025 | 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 | a0001c0001t0001g0214 | 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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0001c0015t0001g0177 | 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 | 1 | a0002c0004t0001g0009 | 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 | a0001c0001t0001g0028a0003c0008t0001g0026a0003c0008t0001g0027 | 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0029t0001g0114 | 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 | a0001c0019t0001g0025 | 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 | a0001c0003t0001g0119 | 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 | a0001c0003t0001g0014 | 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 | a0001c0003t0001g0162a0001c0003t0001g0163 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0001t0001g0022a0001c0001t0001g0206a0001c0001t0001g0212others(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 | a0001c0003t0001g0018 | 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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | a0001c0006t0001g0239 | 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 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | 94 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(91): 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 | a0001c0003t0001g0127 | 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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0019t0001g0025a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | 9 | a0002c0004t0001g0003a0002c0004t0001g0009a0002c0004t0001g0010others(6): 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 | 61 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(58): 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | a0001c0001t0001g0207 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | 94 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(91): 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 | a0001c0029t0001g0114 | 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 | a0001c0002t0001g0249a0001c0002t0001g0252 | 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 | a0001c0019t0001g0025 | 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 | 118 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(115): 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 | a0001c0003t0001g0126 | 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 | a0001c0002t0001g0105 | 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | a0002c0004t0001g0104 | 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 | a0001c0003t0001g0125a0001c0003t0001g0126 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0208 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0030 | 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 | 33 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(30): 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | a0002c0010t0001g0170a0002c0010t0001g0171a0002c0010t0001g0172others(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 | a0001c0006t0001g0239 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0003t0001g0019 | 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 | 192 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(189): 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 | a0001c0002t0001g0249 | 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 | a0001c0003t0001g0164 | 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 | a0001c0029t0001g0114 | 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 | a0001c0006t0001g0024a0001c0006t0001g0240a0001c0006t0001g0241others(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 | a0001c0002t0001g0097 | 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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0188others(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 | a0001c0019t0001g0025 | 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 | a0002c0004t0001g0250 | 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 | a0001c0002t0001g0248a0001c0002t0001g0249a0002c0027t0001g0253 | 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 | a0001c0002t0001g0251a0001c0002t0001g0252 | 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 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0006t0001g0024others(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 | a0001c0002t0001g0061a0001c0002t0001g0101a0001c0002t0001g0102others(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 |
59 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(56): 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 |
17 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0006t0001g0239others(14): 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 | a0001c0007t0001g0039a0002c0005t0001g0052a0002c0005t0001g0053others(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 | a0001c0029t0001g0114 | 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 | a0001c0001t0001g0028a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0001c0003t0001g0124 | 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 | 94 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(91): 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 | a0001c0006t0001g0024a0001c0006t0001g0240a0001c0006t0001g0241others(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 | a0001c0003t0001g0118 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0001c0002t0001g0095 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0001c0003t0001g0034a0001c0003t0001g0123 | 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 | a0001c0001t0001g0176 | 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 | 33 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(30): 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 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(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 | a0001c0019t0001g0025 | 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 | a0002c0009t0001g0219 | 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 | 94 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(91): 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | 27 | a0001c0007t0001g0036a0001c0007t0001g0039a0001c0007t0001g0047others(24): 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 | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(16): 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 | a0001c0003t0001g0122 | 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 | a0001c0002t0003g0035 | 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 | a0002c0023t0001g0247 | 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 | a0009c0018t0001g0121 | 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 | a0002c0005t0001g0167a0002c0005t0001g0174 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0002t0001g0249 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0029t0001g0114 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0002c0009t0001g0219 | 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 | 55 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(52): 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 | a0001c0003t0001g0034 | 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 | 110 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(107): 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 | a0002c0023t0001g0247 | 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 | a0001c0001t0001g0175 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0006t0001g0239 | 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(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 | a0001c0019t0001g0025 | 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 | a0001c0002t0001g0096 | 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 | a0001c0019t0001g0025 | 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 | a0001c0002t0001g0097a0001c0002t0001g0098 | 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 | 108 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(105): 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 | a0002c0004t0001g0104 | 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 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0001t0001g0023a0001c0001t0001g0237 | 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 | a0001c0019t0001g0025 | 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 | a0001c0006t0001g0239 | 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 | a0001c0029t0001g0114a0004c0013t0001g0099a0004c0013t0001g0100 | 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 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(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 | 75 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(72): 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 | a0001c0002t0001g0108a0001c0002t0001g0109a0002c0009t0001g0238 | 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 | a0001c0003t0001g0166 | 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 | a0001c0007t0001g0036a0001c0007t0001g0039a0002c0005t0001g0037others(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 | 192 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0020others(189): 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 | a0003c0011t0001g0110a0003c0011t0001g0111a0003c0011t0001g0112others(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 | a0001c0029t0001g0114 | 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 | a0001c0003t0001g0117 | 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 | a0001c0002t0003g0035 | 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 | a0001c0002t0001g0115a0001c0002t0001g0116 | 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 | a0001c0019t0001g0025 | 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 | 107 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0011others(104): 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 | a0001c0006t0001g0024a0001c0006t0001g0239a0001c0006t0001g0240others(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 | a0001c0003t0001g0034 | 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 | a0002c0027t0001g0253 | 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 | a0001c0003t0001g0032a0001c0003t0001g0033 | 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 | a0001c0002t0001g0248a0001c0002t0001g0249a0001c0002t0001g0251others(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 | a0001c0001t0001g0030a0001c0001t0001g0031 | 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 | a0001c0001t0001g0028a0003c0008t0001g0026a0003c0008t0001g0027 | 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 | a0001c0019t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-6-44C>A | ABCB4 | ENSG00000005471.19 | transcript | ENST00000649586.2 | protein_coding | 1/27 | chr7 | 87475515 |