Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23457 |
| ensemblid | ENSG00000150967.19 |
| hgncid | 50 |
| symbol | ABCB9 |
| name | ATP binding cassette subfamily B member 9 |
| refseq_nuc | NM_019625.4 |
| refseq_prot | NP_062571.1 |
| ensembl_nuc | ENST00000280560.13 |
| ensembl_prot | ENSP00000280560.8 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 122928992 |
| end | 122966463 |
| strand | - |
| ver | v1.2 |
| region | chr12:122928992-122966463 |
| region5000 | chr12:122923992-122971463 |
| regionname0 | ABCB9_chr12_122928992_122966463 |
| regionname5000 | ABCB9_chr12_122923992_122971463 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 766 | 257 | 78 | 54 | 84 | 6 | 33 | 52 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0002 | 0/0 | 766 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0003 | 0/0 | 766 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0004 | 0/0 | 766 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0005 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0006 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0007 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0008 | 0/0 | 766 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| a0009 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | MRLWK others(761): Show |
chr12 | 122923992 | 122971463 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2298 | 252 | 74 | 54 | 84 | 6 | 32 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0001c0003 | 0/0 | 2298 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0001c0010 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0001c0012 | 0/0 | 2298 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0001c0013 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0002c0002 | 0/0 | 2298 | 6 | 0 | 0 | 6 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0003c0005 | 0/0 | 2298 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0004c0004 | 0/0 | 2298 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0005c0008 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0006c0009 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0007c0006 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0008c0007 | 0/0 | 2298 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 | ||
| a0009c0011 | 0/0 | 2298 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | ATGCG others(2293): Show |
chr12 | 122923992 | 122971463 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3484 | 152 | 22 | 47 | 52 | 6 | 23 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0002 | 0/0 | 3484 | 51 | 8 | 3 | 32 | 0 | 8 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0003 | 0/0 | 3484 | 23 | 20 | 3 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0004 | 0/0 | 3484 | 14 | 14 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0005 | 0/0 | 3484 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0006 | 0/0 | 3484 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0007 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0008 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0009 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0010 | 0/0 | 3484 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0001t0011 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0003t0002 | 0/0 | 3484 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0010t0002 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0012t0001 | 0/0 | 3484 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0001c0013t0003 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0002c0002t0002 | 0/0 | 3484 | 6 | 0 | 0 | 6 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0003c0005t0001 | 0/0 | 3484 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0004c0004t0001 | 0/0 | 3484 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0005c0008t0003 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0006c0009t0001 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0007c0006t0001 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0008c0007t0001 | 0/0 | 3484 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| a0009c0011t0002 | 0/0 | 3484 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | AGTCT others(3479): Show |
chr12 | 122923992 | 122971463 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 8 | 7 | 0 | 3 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0002 | 0/0 | 11 | 1 | 4 | 3 | 1 | 2 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0003t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0010t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0012t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0001c0013t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0003c0005t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0003c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0004c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0005c0008t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0006c0009t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0007c0006t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0008c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| a0009c0011t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01168 | hp2 | a0003 | c0005 | t0001 | g0176 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01169 | hp2 | a0003 | c0005 | t0001 | g0158 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0221 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0093 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02615 | hp2 | a0005 | c0008 | t0003 | g0072 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0014 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0062 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0014 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0107 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03209 | hp2 | a0006 | c0009 | t0001 | g0048 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0100 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03486 | hp2 | a0007 | c0006 | t0001 | g0035 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03516 | hp1 | a0001 | c0010 | t0002 | g0188 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03942 | hp1 | a0008 | c0007 | t0001 | g0142 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG04228 | hp1 | a0001 | c0012 | t0001 | g0179 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18957 | hp1 | a0004 | c0004 | t0001 | g0139 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19056 | hp2 | a0004 | c0004 | t0001 | g0155 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA19240 | hp2 | a0009 | c0011 | t0002 | g0095 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ASW | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | ASW | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02109 | hp1 | a0001 | c0013 | t0003 | g0118 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | USA | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0068 | REF | REF | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0036 | REF | REF | ABCB9_chr12_122923992_122971463 | ABCB9 | chr12 | 122923992 | 122971463 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122930092 | G | A | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.2120C>T | p.Ala707Val | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 2384/3484 | 2120/2301 | 707/766 | chr12 | 122930092 | |||
| chr12:122940823 | T | A | 1 | a0009 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1553A>T | p.His518Leu | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 8/12 | 1817/3484 | 1553/2301 | 518/766 | chr12 | 122940823 | |||
| chr12:122946050 | T | G | 1 | a0004 | 2 | NA18957.hp1 NA19056.hp2 |
missense_variant | MODERATE | c.1226A>C | p.Tyr409Ser | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/12 | 1490/3484 | 1226/2301 | 409/766 | chr12 | 122946050 | |||
| chr12:122946140 | C | T | 1 | a0005 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1136G>A | p.Arg379Gln | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/12 | 1400/3484 | 1136/2301 | 379/766 | chr12 | 122946140 | |||
| chr12:122950536 | G | A | 1 | a0003 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.631C>T | p.Arg211Cys | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 3/12 | 895/3484 | 631/2301 | 211/766 | chr12 | 122950536 | |||
| chr12:122950563 | C | T | 1 | a0008 | 1 | HG03942.hp1 | missense_variant&splice_region_variant | MODERATE | c.604G>A | p.Glu202Lys | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 3/12 | 868/3484 | 604/2301 | 202/766 | chr12 | 122950563 | |||
| chr12:122959752 | C | T | 1 | a0007 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.484G>A | p.Gly162Ser | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/12 | 748/3484 | 484/2301 | 162/766 | chr12 | 122959752 | |||
| chr12:122959875 | C | T | 1 | a0002 | 6 | NA18966.hp1 NA18981.hp1 NA18989.hp1 others(3): Show |
missense_variant | MODERATE | c.361G>A | p.Val121Met | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/12 | 625/3484 | 361/2301 | 121/766 | chr12 | 122959875 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122929917 | C | T | 1 | a0001c0003 | 2 | HG02717.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.2295G>A | p.Lys765Lys | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 2559/3484 | 2295/2301 | 765/766 | chr12 | 122929917 | |||
| chr12:122935369 | G | A | 1 | a0001c0010 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1806C>T | p.Tyr602Tyr | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/12 | 2070/3484 | 1806/2301 | 602/766 | chr12 | 122935369 | |||
| chr12:122959972 | G | A | 1 | a0001c0012 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.264C>T | p.Leu88Leu | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/12 | 528/3484 | 264/2301 | 88/766 | chr12 | 122959972 | |||
| chr12:122960179 | G | A | 1 | a0001c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.57C>T | p.Cys19Cys | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/12 | 321/3484 | 57/2301 | 19/766 | chr12 | 122960179 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122929193 | G | A | 1 | a0001c0001t0011 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*718C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 718 | chr12 | 122929193 | ||||||
| chr12:122929218 | C | T | 1 | a0001c0001t0010 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 693 | chr12 | 122929218 | ||||||
| chr12:122929231 | C | A | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(2): Show |
31 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*680G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 680 | chr12 | 122929231 | ||||||
| chr12:122929782 | A | G | 2 | a0001c0001t0007 a0001c0001t0009 |
2 | HG02572.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*129T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 129 | chr12 | 122929782 | ||||||
| chr12:122929802 | T | C | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
111 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*109A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 109 | chr12 | 122929802 | ||||||
| chr12:122929854 | C | T | 1 | a0001c0001t0008 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 12/12 | 57 | chr12 | 122929854 | ||||||
| chr12:122966311 | C | G | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-112G>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/12 | 6076 | chr12 | 122966311 | ||||||
| chr12:122966320 | G | A | 1 | a0001c0001t0006 | 2 | HG01175.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-121C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/12 | 6085 | chr12 | 122966320 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122930412 | C | CT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0162 others(3): Show |
6 | HG02056.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2041-242dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122930412 | |||||||
| chr12:122930412 | CT | C | 15 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0041 others(12): Show |
15 | HG01069.hp1 HG01243.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.2041-242delA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122930412 | |||||||
| chr12:122930412 | CTT | C | 16 | a0001c0001t0001g0001 a0001c0001t0004g0003 a0001c0001t0004g0009 others(13): Show |
19 | HG01884.hp1 HG02040.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2041-243_2041-242d others(4): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122930412 | |||||||
| chr12:122930766 | CTT | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0038 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2041-597_2041-596d others(4): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122930766 | |||||||
| chr12:122930784 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2041-613G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122930784 | |||||||
| chr12:122930979 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2041-808C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122930979 | |||||||
| chr12:122931189 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2040+1003C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931189 | |||||||
| chr12:122931234 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2040+958G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931234 | |||||||
| chr12:122931321 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2040+871T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931321 | |||||||
| chr12:122931324 | C | CT | 28 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0046 others(25): Show |
29 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.2040+867dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931324 | |||||||
| chr12:122931324 | CT | C | 22 | a0001c0001t0002g0111 a0001c0001t0003g0012 a0001c0001t0003g0013 others(19): Show |
24 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2040+867delA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931324 | |||||||
| chr12:122931450 | G | A | 13 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0080 others(10): Show |
15 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2040+742C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931450 | |||||||
| chr12:122931801 | A | G | 98 | a0001c0001t0001g0086 a0001c0001t0001g0200 a0001c0001t0001g0205 others(95): Show |
113 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.2040+391T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931801 | |||||||
| chr12:122931981 | C | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2040+211G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122931981 | |||||||
| chr12:122932100 | G | A | 5 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2040+92C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122932100 | |||||||
| chr12:122932121 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2040+71C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122932121 | |||||||
| chr12:122932185 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02922.hp2 | splice_region_variant&intron_variant | LOW | c.2040+7C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 11/11 | chr12 | 122932185 | |||||||
| chr12:122933006 | T | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0112 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1904-678A>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933006 | |||||||
| chr12:122933284 | T | C | 1 | a0001c0001t0006g0221 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1904-956A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933284 | |||||||
| chr12:122933411 | G | A | 13 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(10): Show |
18 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1904-1083C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933411 | |||||||
| chr12:122933508 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1904-1180G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933508 | |||||||
| chr12:122933535 | C | T | 4 | a0001c0001t0003g0097 a0001c0001t0003g0113 a0001c0001t0003g0119 others(1): Show |
4 | HG02451.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1904-1207G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933535 | |||||||
| chr12:122933543 | G | A | 2 | a0001c0001t0003g0104 a0001c0001t0003g0112 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1904-1215C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933543 | |||||||
| chr12:122933684 | G | A | 41 | a0001c0001t0001g0086 a0001c0001t0001g0200 a0001c0001t0002g0006 others(38): Show |
48 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1904-1356C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933684 | |||||||
| chr12:122933692 | T | C | 1 | a0001c0001t0004g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1904-1364A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122933692 | |||||||
| chr12:122934027 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1903+1245A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122934027 | |||||||
| chr12:122934109 | G | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0170 a0003c0005t0001g0158 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1903+1163C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122934109 | |||||||
| chr12:122934226 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1903+1046G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122934226 | |||||||
| chr12:122934309 | A | C | 4 | a0001c0001t0005g0010 a0001c0001t0005g0024 a0001c0001t0005g0030 others(1): Show |
5 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1903+963T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122934309 | |||||||
| chr12:122934640 | C | CA | 50 | a0001c0001t0001g0067 a0001c0001t0001g0076 a0001c0001t0001g0086 others(47): Show |
58 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1903+631dupT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122934640 | |||||||
| chr12:122934776 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1903+496A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122934776 | |||||||
| chr12:122935119 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1903+153G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122935119 | |||||||
| chr12:122935182 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1903+90T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 10/11 | chr12 | 122935182 | |||||||
| chr12:122935496 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1744-65G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122935496 | |||||||
| chr12:122935567 | T | C | 7 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(4): Show |
11 | HG01884.hp1 HG02055.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1744-136A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122935567 | |||||||
| chr12:122936022 | A | G | 1 | a0001c0001t0004g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1744-591T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122936022 | |||||||
| chr12:122936104 | ATTAG | A | 3 | a0001c0001t0003g0085 a0001c0001t0003g0109 a0001c0001t0003g0117 |
3 | HG01109.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1744-677_1744-674d others(6): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122936104 | |||||||
| chr12:122936370 | G | A | 8 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(5): Show |
12 | HG01884.hp1 HG02055.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1744-939C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122936370 | |||||||
| chr12:122936679 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1744-1248G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122936679 | |||||||
| chr12:122936957 | A | AGGAGGCT others(5): Show |
1 | a0001c0001t0002g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1744-1538_1744-152 others(16): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122936957 | |||||||
| chr12:122937091 | C | T | 5 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1744-1660G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937091 | |||||||
| chr12:122937129 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1744-1698C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937129 | |||||||
| chr12:122937307 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1744-1876G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937307 | |||||||
| chr12:122937337 | C | T | 1 | a0001c0001t0003g0120 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1744-1906G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937337 | |||||||
| chr12:122937355 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0134 others(1): Show |
5 | HG01081.hp1 HG02145.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-1924A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937355 | |||||||
| chr12:122937433 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1744-2002C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937433 | |||||||
| chr12:122937565 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1744-2134G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937565 | |||||||
| chr12:122937740 | T | A | 1 | a0001c0001t0003g0013 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1744-2309A>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122937740 | |||||||
| chr12:122938194 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1743+1917G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122938194 | |||||||
| chr12:122938263 | G | A | 1 | a0001c0001t0004g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1743+1848C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122938263 | |||||||
| chr12:122938343 | G | C | 7 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(4): Show |
11 | HG01884.hp1 HG02055.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1743+1768C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122938343 | |||||||
| chr12:122938603 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1743+1508A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122938603 | |||||||
| chr12:122938777 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1743+1334C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122938777 | |||||||
| chr12:122938822 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1743+1289A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122938822 | |||||||
| chr12:122938893 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1743+1218C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122938893 | |||||||
| chr12:122939040 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1743+1071G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122939040 | |||||||
| chr12:122939524 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(62): Show |
84 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1743+587T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122939524 | |||||||
| chr12:122939678 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1743+433A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122939678 | |||||||
| chr12:122939691 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1743+420G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122939691 | |||||||
| chr12:122939785 | G | A | 1 | a0001c0001t0004g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1743+326C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122939785 | |||||||
| chr12:122939825 | T | A | 1 | a0001c0001t0003g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1743+286A>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122939825 | |||||||
| chr12:122939982 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1743+129C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122939982 | |||||||
| chr12:122940033 | C | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1743+78G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 9/11 | chr12 | 122940033 | |||||||
| chr12:122940296 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1570-12T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 8/11 | chr12 | 122940296 | |||||||
| chr12:122940395 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1570-111A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 8/11 | chr12 | 122940395 | |||||||
| chr12:122941028 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
82 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1381-33G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122941028 | |||||||
| chr12:122941310 | C | CT | 35 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0086 others(32): Show |
37 | HG00735.hp1 HG01099.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1381-316dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122941310 | |||||||
| chr12:122941310 | CT | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0081 others(2): Show |
5 | HG00558.hp2 HG01070.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.1381-316delA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122941310 | |||||||
| chr12:122941410 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02280.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1381-415C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122941410 | |||||||
| chr12:122941412 | G | A | 2 | a0001c0001t0002g0190 a0001c0003t0002g0014 |
3 | HG02717.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1381-417C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122941412 | |||||||
| chr12:122941471 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1381-476C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122941471 | |||||||
| chr12:122942252 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1381-1257A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942252 | |||||||
| chr12:122942326 | A | G | 98 | a0001c0001t0001g0086 a0001c0001t0001g0200 a0001c0001t0001g0205 others(95): Show |
113 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1381-1331T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942326 | |||||||
| chr12:122942407 | G | A | 1 | a0002c0002t0002g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1381-1412C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942407 | |||||||
| chr12:122942410 | C | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1415G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942410 | |||||||
| chr12:122942413 | C | T | 4 | a0001c0001t0005g0010 a0001c0001t0005g0024 a0001c0001t0005g0030 others(1): Show |
5 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-1418G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942413 | |||||||
| chr12:122942417 | A | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1422T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942417 | |||||||
| chr12:122942419 | T | C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1424A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942419 | |||||||
| chr12:122942421 | CTACTGAA others(24): Show |
C | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1457_1381-142 others(35): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942421 | |||||||
| chr12:122942544 | G | A | 2 | a0001c0001t0002g0091 a0001c0010t0002g0188 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1381-1549C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942544 | |||||||
| chr12:122942560 | G | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1565C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942560 | |||||||
| chr12:122942595 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1381-1600C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942595 | |||||||
| chr12:122942605 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1381-1610G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942605 | |||||||
| chr12:122942618 | C | CA | 20 | a0001c0001t0001g0077 a0001c0001t0001g0143 a0001c0001t0001g0154 others(17): Show |
20 | HG00642.hp2 HG00741.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1381-1624dupT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122942618 | |||||||
| chr12:122943026 | A | G | 25 | a0001c0001t0002g0111 a0001c0001t0003g0012 a0001c0001t0003g0013 others(22): Show |
27 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1380+1365T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943026 | |||||||
| chr12:122943193 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1380+1198C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943193 | |||||||
| chr12:122943373 | C | T | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1380+1018G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943373 | |||||||
| chr12:122943404 | C | T | 34 | a0001c0001t0001g0200 a0001c0001t0002g0006 a0001c0001t0002g0007 others(31): Show |
41 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1380+987G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943404 | |||||||
| chr12:122943426 | G | A | 21 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0099 others(18): Show |
26 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1380+965C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943426 | |||||||
| chr12:122943569 | T | C | 2 | a0001c0001t0002g0190 a0001c0003t0002g0014 |
3 | HG02717.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1380+822A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943569 | |||||||
| chr12:122943577 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1380+814G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943577 | |||||||
| chr12:122943837 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1380+554C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943837 | |||||||
| chr12:122943922 | C | T | 4 | a0001c0001t0002g0083 a0001c0001t0002g0099 a0001c0001t0002g0101 others(1): Show |
4 | HG02132.hp2 HG02738.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380+469G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943922 | |||||||
| chr12:122943942 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1380+449C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122943942 | |||||||
| chr12:122944149 | G | A | 2 | a0001c0001t0002g0091 a0001c0010t0002g0188 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1380+242C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122944149 | |||||||
| chr12:122944188 | CAAAGTTC others(15): Show |
C | 1 | a0002c0002t0002g0194 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1380+181_1380+202d others(24): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 7/11 | chr12 | 122944188 | |||||||
| chr12:122945121 | C | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG00741.hp1 HG01175.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1252-602G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945121 | |||||||
| chr12:122945150 | T | C | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1252-631A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945150 | |||||||
| chr12:122945431 | G | C | 7 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(4): Show |
7 | HG00558.hp1 HG02056.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251+594C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945431 | |||||||
| chr12:122945535 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00140.hp1 HG01109.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251+490G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945535 | |||||||
| chr12:122945605 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0054 others(1): Show |
6 | HG00741.hp2 HG01074.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+420G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945605 | |||||||
| chr12:122945877 | C | CA | 35 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0055 others(32): Show |
38 | HG01099.hp1 HG01106.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.1251+147dupT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945877 | |||||||
| chr12:122945877 | CA | C | 28 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0001t0001g0070 others(25): Show |
33 | HG01069.hp1 HG01081.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.1251+147delT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945877 | |||||||
| chr12:122945901 | A | C | 2 | a0001c0001t0001g0049 a0006c0009t0001g0048 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1251+124T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945901 | |||||||
| chr12:122945930 | A | G | 1 | a0001c0001t0003g0013 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251+95T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945930 | |||||||
| chr12:122946358 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1054-136G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122946358 | |||||||
| chr12:122946481 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1054-259C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122946481 | |||||||
| chr12:122946600 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1054-378G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122946600 | |||||||
| chr12:122946653 | A | G | 2 | a0001c0001t0002g0091 a0001c0010t0002g0188 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1054-431T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122946653 | |||||||
| chr12:122946749 | G | A | 1 | a0001c0001t0004g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1054-527C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122946749 | |||||||
| chr12:122946978 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0064 a0001c0001t0002g0058 |
3 | HG02280.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1054-756C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122946978 | |||||||
| chr12:122947224 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1054-1002G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947224 | |||||||
| chr12:122947334 | G | A | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1054-1112C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947334 | |||||||
| chr12:122947454 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1053+1170A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947454 | |||||||
| chr12:122947486 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1053+1138G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947486 | |||||||
| chr12:122947716 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1053+908C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947716 | |||||||
| chr12:122947742 | TGATGGCA others(15): Show |
T | 98 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0143 others(95): Show |
113 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1053+860_1053+881d others(24): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947742 | |||||||
| chr12:122947835 | C | A | 1 | a0001c0001t0004g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1053+789G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947835 | |||||||
| chr12:122947894 | A | G | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1053+730T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122947894 | |||||||
| chr12:122948110 | T | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02280.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1053+514A>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122948110 | |||||||
| chr12:122948119 | G | T | 1 | a0001c0001t0002g0135 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1053+505C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122948119 | |||||||
| chr12:122948220 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0003g0109 a0001c0001t0003g0117 |
3 | HG01109.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1053+404C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122948220 | |||||||
| chr12:122948522 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1053+102G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122948522 | |||||||
| chr12:122948955 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.848-126C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 4/11 | chr12 | 122948955 | |||||||
| chr12:122949083 | C | A | 2 | a0001c0001t0002g0059 a0001c0001t0003g0115 |
2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.848-254G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 4/11 | chr12 | 122949083 | |||||||
| chr12:122949102 | C | T | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.848-273G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 4/11 | chr12 | 122949102 | |||||||
| chr12:122949669 | CAGG | C | 3 | a0001c0001t0003g0085 a0001c0001t0003g0109 a0001c0001t0003g0117 |
3 | HG01109.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.847+116_847+118del others(3): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 4/11 | chr12 | 122949669 | |||||||
| chr12:122949977 | G | A | 6 | a0001c0001t0001g0086 a0001c0001t0002g0121 a0001c0001t0002g0122 others(3): Show |
6 | HG01175.hp1 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.717-59C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 3/11 | chr12 | 122949977 | |||||||
| chr12:122950170 | C | T | 2 | a0001c0001t0002g0190 a0001c0003t0002g0014 |
3 | HG02717.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.717-252G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 3/11 | chr12 | 122950170 | |||||||
| chr12:122950269 | G | A | 1 | a0001c0001t0002g0007 | 3 | HG00621.hp2 HG02523.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.716+182C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 3/11 | chr12 | 122950269 | |||||||
| chr12:122950420 | C | T | 5 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.716+31G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 3/11 | chr12 | 122950420 | |||||||
| chr12:122950701 | G | A | 23 | a0001c0001t0002g0111 a0001c0001t0003g0012 a0001c0001t0003g0013 others(20): Show |
25 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.602-136C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122950701 | |||||||
| chr12:122950821 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.602-256G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122950821 | |||||||
| chr12:122950893 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.602-328C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122950893 | |||||||
| chr12:122951008 | A | AT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(87): Show |
112 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.602-444dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951008 | |||||||
| chr12:122951008 | A | ATT | 17 | a0001c0001t0001g0141 a0001c0001t0001g0166 a0001c0001t0001g0184 others(14): Show |
22 | HG00621.hp1 HG01123.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.602-445_602-444dup others(2): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951008 | |||||||
| chr12:122951163 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.602-598A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951163 | |||||||
| chr12:122951192 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.602-627A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951192 | |||||||
| chr12:122951240 | C | CT | 40 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0087 others(37): Show |
48 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.602-676dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951240 | |||||||
| chr12:122951240 | CT | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0079 a0001c0001t0001g0160 others(4): Show |
7 | HG01168.hp2 HG02109.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.602-676delA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951240 | |||||||
| chr12:122951348 | C | T | 1 | a0004c0004t0001g0139 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.602-783G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951348 | |||||||
| chr12:122951518 | C | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.602-953G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951518 | |||||||
| chr12:122951587 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.602-1022C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122951587 | |||||||
| chr12:122952115 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.602-1550G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122952115 | |||||||
| chr12:122952582 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.602-2017G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122952582 | |||||||
| chr12:122952647 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.602-2082G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122952647 | |||||||
| chr12:122952842 | C | A | 1 | a0001c0001t0002g0211 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.602-2277G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122952842 | |||||||
| chr12:122952970 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.602-2405G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122952970 | |||||||
| chr12:122953035 | C | T | 6 | a0001c0001t0001g0086 a0001c0001t0002g0121 a0001c0001t0002g0122 others(3): Show |
6 | HG01175.hp1 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-2470G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122953035 | |||||||
| chr12:122953181 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02165.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.602-2616A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122953181 | |||||||
| chr12:122953277 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.602-2712T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122953277 | |||||||
| chr12:122953754 | T | C | 4 | a0001c0001t0003g0012 a0001c0001t0003g0080 a0001c0001t0003g0103 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-3189A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122953754 | |||||||
| chr12:122953800 | G | A | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.602-3235C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122953800 | |||||||
| chr12:122953971 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.602-3406C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122953971 | |||||||
| chr12:122954171 | C | CA | 25 | a0001c0001t0001g0032 a0001c0001t0001g0164 a0001c0001t0002g0082 others(22): Show |
30 | HG00558.hp1 HG00642.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.602-3607dupT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954171 | |||||||
| chr12:122954311 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.602-3746G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954311 | |||||||
| chr12:122954353 | C | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0165 |
2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.602-3788G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954353 | |||||||
| chr12:122954370 | A | G | 28 | a0001c0001t0001g0086 a0001c0001t0002g0082 a0001c0001t0002g0083 others(25): Show |
33 | HG00558.hp1 HG01175.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.602-3805T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954370 | |||||||
| chr12:122954452 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0102 |
2 | NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.602-3887G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954452 | |||||||
| chr12:122954456 | C | A | 15 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0020 others(12): Show |
20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.602-3891G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954456 | |||||||
| chr12:122954690 | A | G | 50 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0092 others(47): Show |
57 | HG00558.hp1 HG01109.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.602-4125T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954690 | |||||||
| chr12:122954830 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.602-4265A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122954830 | |||||||
| chr12:122955119 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+4516A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955119 | |||||||
| chr12:122955244 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.601+4391C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955244 | |||||||
| chr12:122955264 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.601+4371G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955264 | |||||||
| chr12:122955707 | G | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG01099.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+3928C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955707 | |||||||
| chr12:122955710 | T | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0112 |
2 | HG01099.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.601+3925A>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955710 | |||||||
| chr12:122955715 | G | GT | 19 | a0001c0001t0001g0200 a0001c0001t0002g0102 a0001c0001t0002g0193 others(16): Show |
24 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+3919dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955715 | |||||||
| chr12:122955868 | T | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0061 others(2): Show |
7 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+3767A>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955868 | |||||||
| chr12:122955951 | A | T | 1 | a0001c0001t0002g0199 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.601+3684T>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122955951 | |||||||
| chr12:122956065 | A | G | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+3570T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122956065 | |||||||
| chr12:122956624 | A | G | 97 | a0001c0001t0001g0086 a0001c0001t0001g0200 a0001c0001t0001g0205 others(94): Show |
112 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.601+3011T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122956624 | |||||||
| chr12:122956811 | T | C | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+2824A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122956811 | |||||||
| chr12:122956899 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.601+2736G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122956899 | |||||||
| chr12:122956989 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.601+2646G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122956989 | |||||||
| chr12:122957009 | A | C | 1 | a0001c0001t0001g0134 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.601+2626T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957009 | |||||||
| chr12:122957039 | AT | A | 24 | a0001c0001t0001g0063 a0001c0001t0001g0168 a0001c0001t0002g0082 others(21): Show |
29 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+2595delA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957039 | |||||||
| chr12:122957128 | G | A | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+2507C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957128 | |||||||
| chr12:122957463 | T | C | 5 | a0001c0001t0003g0097 a0001c0001t0003g0113 a0001c0001t0003g0114 others(2): Show |
5 | HG02451.hp2 HG02615.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+2172A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957463 | |||||||
| chr12:122957600 | T | C | 1 | a0001c0001t0003g0114 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.601+2035A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957600 | |||||||
| chr12:122957664 | C | CT | 8 | a0001c0001t0001g0038 a0001c0001t0001g0064 a0001c0001t0001g0132 others(5): Show |
9 | HG02647.hp1 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+1970dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957664 | |||||||
| chr12:122957699 | G | GT | 6 | a0001c0001t0001g0037 a0001c0001t0001g0064 a0001c0001t0001g0132 others(3): Show |
6 | HG00735.hp2 HG02056.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+1935dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957699 | |||||||
| chr12:122957778 | C | CACTCTGA others(20): Show |
1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.601+1830_601+1856d others(29): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957778 | |||||||
| chr12:122957925 | C | T | 22 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(19): Show |
27 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+1710G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122957925 | |||||||
| chr12:122958169 | C | CA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
200 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.601+1465dupT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122958169 | |||||||
| chr12:122958169 | C | CAA | 49 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0064 others(46): Show |
58 | HG00558.hp1 HG00642.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.601+1464_601+1465d others(4): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122958169 | |||||||
| chr12:122958169 | C | CAAA | 8 | a0001c0001t0002g0083 a0001c0001t0002g0102 a0001c0001t0004g0020 others(5): Show |
8 | HG01175.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+1463_601+1465d others(5): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122958169 | |||||||
| chr12:122958276 | A | G | 7 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0098 others(4): Show |
7 | HG00558.hp1 HG02056.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+1359T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122958276 | |||||||
| chr12:122958658 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.601+977C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122958658 | |||||||
| chr12:122959369 | C | CAATA | 2 | a0001c0001t0001g0090 a0001c0001t0001g0177 |
2 | HG00438.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.601+262_601+265dup others(4): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122959369 | |||||||
| chr12:122959541 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.601+94C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 2/11 | chr12 | 122959541 | |||||||
| chr12:122960760 | C | CA | 41 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(38): Show |
48 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-87-439dupT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122960760 | |||||||
| chr12:122960814 | G | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-87-492C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122960814 | |||||||
| chr12:122960885 | GCAAACAA others(1): Show |
G | 34 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0210 others(31): Show |
41 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.-87-571_-87-564del others(8): Show |
ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122960885 | |||||||
| chr12:122961074 | T | A | 1 | a0001c0001t0002g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-87-752A>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961074 | |||||||
| chr12:122961081 | T | A | 1 | a0001c0001t0002g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-87-759A>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961081 | |||||||
| chr12:122961122 | G | C | 1 | a0001c0001t0003g0120 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-87-800C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961122 | |||||||
| chr12:122961132 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-87-810C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961132 | |||||||
| chr12:122961138 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-87-816C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961138 | |||||||
| chr12:122961145 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-87-823C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961145 | |||||||
| chr12:122961230 | C | A | 1 | a0001c0003t0002g0014 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-87-908G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961230 | |||||||
| chr12:122961249 | G | A | 6 | a0001c0001t0001g0086 a0001c0001t0002g0121 a0001c0001t0002g0122 others(3): Show |
6 | HG01175.hp1 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-87-927C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961249 | |||||||
| chr12:122961345 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-87-1023A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961345 | |||||||
| chr12:122961394 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-87-1072A>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961394 | |||||||
| chr12:122961549 | G | A | 5 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87-1227C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961549 | |||||||
| chr12:122961625 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-87-1303G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961625 | |||||||
| chr12:122961804 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-87-1482A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122961804 | |||||||
| chr12:122962300 | A | T | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-87-1978T>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122962300 | |||||||
| chr12:122962487 | A | G | 2 | a0002c0002t0002g0194 a0002c0002t0002g0195 |
2 | NA18966.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-87-2165T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122962487 | |||||||
| chr12:122962676 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-87-2354C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122962676 | |||||||
| chr12:122962758 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-87-2436C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122962758 | |||||||
| chr12:122962968 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-87-2646T>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122962968 | |||||||
| chr12:122963170 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-87-2848G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122963170 | |||||||
| chr12:122963177 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-87-2855T>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122963177 | |||||||
| chr12:122963179 | C | A | 1 | a0001c0001t0001g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-87-2857G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122963179 | |||||||
| chr12:122963381 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
97 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-88+2906A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122963381 | |||||||
| chr12:122963636 | C | G | 2 | a0001c0001t0002g0091 a0001c0010t0002g0188 |
2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-88+2651G>C | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122963636 | |||||||
| chr12:122964170 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-88+2117C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122964170 | |||||||
| chr12:122964558 | G | A | 5 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+1729C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122964558 | |||||||
| chr12:122964602 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0004g0020 a0001c0001t0004g0021 |
4 | HG02055.hp1 HG03195.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88+1685G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122964602 | |||||||
| chr12:122964640 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-88+1647C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122964640 | |||||||
| chr12:122964829 | A | C | 1 | a0001c0001t0002g0193 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-88+1458T>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122964829 | |||||||
| chr12:122964885 | T | C | 36 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0210 others(33): Show |
43 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.-88+1402A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122964885 | |||||||
| chr12:122965317 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-88+970G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965317 | |||||||
| chr12:122965419 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-88+868A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965419 | |||||||
| chr12:122965511 | T | C | 16 | a0001c0001t0002g0190 a0001c0001t0004g0003 a0001c0001t0004g0009 others(13): Show |
21 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.-88+776A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965511 | |||||||
| chr12:122965575 | T | C | 1 | a0005c0008t0003g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-88+712A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965575 | |||||||
| chr12:122965594 | C | T | 5 | a0001c0001t0002g0092 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+693G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965594 | |||||||
| chr12:122965597 | G | T | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-88+690C>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965597 | |||||||
| chr12:122965729 | C | CT | 13 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0086 others(10): Show |
13 | HG00438.hp1 HG00558.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.-88+557dupA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965729 | |||||||
| chr12:122965729 | CT | C | 33 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0210 others(30): Show |
40 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-88+557delA | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122965729 | |||||||
| chr12:122966029 | T | C | 5 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG02129.hp1 NA18948.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-88+258A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122966029 | |||||||
| chr12:122966042 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-88+245C>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122966042 | |||||||
| chr12:122966056 | TA | T | 3 | a0001c0001t0001g0081 a0001c0001t0003g0012 a0001c0001t0003g0080 |
4 | HG01243.hp1 HG01891.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88+230delT | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122966056 | |||||||
| chr12:122966218 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(166): Show |
205 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.-88+69C>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 1/11 | chr12 | 122966218 |