Search by Gene
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 766 | 257 | 78 | 54 | 84 | 6 | 33 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0002 | 0/0 | 766 | 6 | 0 | 0 | 6 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0003 | 0/0 | 766 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0004 | 0/0 | 766 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0005 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0006 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0007 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0008 | 0/0 | 766 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0009 | 0/0 | 766 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2301 | 252 | 74 | 54 | 84 | 6 | 32 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0002 | 0/0 | 2301 | 6 | 0 | 0 | 6 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0003 | 0/0 | 2301 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0004 | 0/0 | 2301 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0005 | 0/0 | 2301 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0006 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0007 | 0/0 | 2301 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0008 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0009 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0010 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0011 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0012 | 0/0 | 2301 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| c0013 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1184 | 160 | 24 | 49 | 54 | 6 | 25 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0002 | 0/0 | 1184 | 61 | 12 | 3 | 38 | 0 | 8 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0003 | 0/0 | 1184 | 25 | 22 | 3 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0004 | 0/0 | 1184 | 14 | 14 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0005 | 0/0 | 1184 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0006 | 0/0 | 1184 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0007 | 0/0 | 1184 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0008 | 0/0 | 1184 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0009 | 0/0 | 1184 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0010 | 0/0 | 1184 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| t0011 | 0/0 | 1184 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 17 | 0 | 8 | 6 | 0 | 3 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0002 | 0/0 | 11 | 1 | 4 | 3 | 1 | 2 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 252 | 74 | 54 | 84 | 6 | 32 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0013 | a0001 | c0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0003c0005 | a0003 | c0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0004c0004 | a0004 | c0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0005c0008 | a0005 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0006c0009 | a0006 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0007c0011 | a0007 | c0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0008c0007 | a0008 | c0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0009c0006 | a0009 | c0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 152 | 22 | 47 | 52 | 6 | 23 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 51 | 8 | 3 | 32 | 0 | 8 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 23 | 20 | 3 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 14 | 14 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0003t0002 | a0001 | c0003 | t0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0010t0002 | a0001 | c0010 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0012t0001 | a0001 | c0012 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0001c0013t0003 | a0001 | c0013 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0003c0005t0001 | a0003 | c0005 | t0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0004c0004t0001 | a0004 | c0004 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0005c0008t0003 | a0005 | c0008 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0006c0009t0001 | a0006 | c0009 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0007c0011t0002 | a0007 | c0011 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0008c0007t0001 | a0008 | c0007 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| a0009c0006t0001 | a0009 | c0006 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 17 | 0 | 8 | 6 | 0 | 3 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 11 | 1 | 4 | 3 | 1 | 2 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0005 | a0001 | c0001 | t0002 | g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0006 | a0001 | c0001 | t0002 | g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0057 | a0001 | c0001 | t0002 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0084 | a0001 | c0001 | t0002 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0093 | a0001 | c0001 | t0002 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0101 | a0001 | c0001 | t0002 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0104 | a0001 | c0001 | t0002 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0122 | a0001 | c0001 | t0002 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0136 | a0001 | c0001 | t0002 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0171 | a0001 | c0001 | t0002 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0195 | a0001 | c0001 | t0002 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0196 | a0001 | c0001 | t0002 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0204 | a0001 | c0001 | t0002 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0207 | a0001 | c0001 | t0002 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0208 | a0001 | c0001 | t0002 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0209 | a0001 | c0001 | t0002 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0210 | a0001 | c0001 | t0002 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0212 | a0001 | c0001 | t0002 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0213 | a0001 | c0001 | t0002 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0214 | a0001 | c0001 | t0002 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0215 | a0001 | c0001 | t0002 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0217 | a0001 | c0001 | t0002 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0218 | a0001 | c0001 | t0002 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0220 | a0001 | c0001 | t0002 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0221 | a0001 | c0001 | t0002 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0222 | a0001 | c0001 | t0002 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0223 | a0001 | c0001 | t0002 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0224 | a0001 | c0001 | t0002 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0002g0225 | a0001 | c0001 | t0002 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0011 | a0001 | c0001 | t0003 | g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0080 | a0001 | c0001 | t0003 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0081 | a0001 | c0001 | t0003 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0082 | a0001 | c0001 | t0003 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0086 | a0001 | c0001 | t0003 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0087 | a0001 | c0001 | t0003 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0099 | a0001 | c0001 | t0003 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0105 | a0001 | c0001 | t0003 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0106 | a0001 | c0001 | t0003 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0107 | a0001 | c0001 | t0003 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0108 | a0001 | c0001 | t0003 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0110 | a0001 | c0001 | t0003 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0111 | a0001 | c0001 | t0003 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0112 | a0001 | c0001 | t0003 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0113 | a0001 | c0001 | t0003 | g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0114 | a0001 | c0001 | t0003 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0115 | a0001 | c0001 | t0003 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0116 | a0001 | c0001 | t0003 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0117 | a0001 | c0001 | t0003 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0119 | a0001 | c0001 | t0003 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0121 | a0001 | c0001 | t0003 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0003g0191 | a0001 | c0001 | t0003 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0007 | a0001 | c0001 | t0004 | g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0009 | a0001 | c0001 | t0004 | g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0010 | a0001 | c0001 | t0004 | g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0018 | a0001 | c0001 | t0004 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0019 | a0001 | c0001 | t0004 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0020 | a0001 | c0001 | t0004 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0023 | a0001 | c0001 | t0004 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0024 | a0001 | c0001 | t0004 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0025 | a0001 | c0001 | t0004 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0026 | a0001 | c0001 | t0004 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0004g0027 | a0001 | c0001 | t0004 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0005g0008 | a0001 | c0001 | t0005 | g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0005g0022 | a0001 | c0001 | t0005 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0005g0028 | a0001 | c0001 | t0005 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0005g0029 | a0001 | c0001 | t0005 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0006g0226 | a0001 | c0001 | t0006 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0006g0227 | a0001 | c0001 | t0006 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0007g0021 | a0001 | c0001 | t0007 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0008g0062 | a0001 | c0001 | t0008 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0009g0095 | a0001 | c0001 | t0009 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0010g0102 | a0001 | c0001 | t0010 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0001t0011g0109 | a0001 | c0001 | t0011 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0003t0002g0012 | a0001 | c0003 | t0002 | g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0010t0002g0193 | a0001 | c0010 | t0002 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0012t0001g0183 | a0001 | c0012 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0001c0013t0003g0118 | a0001 | c0013 | t0003 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0002c0002t0002g0194 | a0002 | c0002 | t0002 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0002c0002t0002g0199 | a0002 | c0002 | t0002 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0002c0002t0002g0200 | a0002 | c0002 | t0002 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0002c0002t0002g0201 | a0002 | c0002 | t0002 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0002c0002t0002g0202 | a0002 | c0002 | t0002 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0002c0002t0002g0203 | a0002 | c0002 | t0002 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0003c0005t0001g0160 | a0003 | c0005 | t0001 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0003c0005t0001g0180 | a0003 | c0005 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0004c0004t0001g0140 | a0004 | c0004 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0004c0004t0001g0157 | a0004 | c0004 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0005c0008t0003g0072 | a0005 | c0008 | t0003 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0006c0009t0001g0046 | a0006 | c0009 | t0001 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0007c0011t0002g0097 | a0007 | c0011 | t0002 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0008c0007t0001g0143 | a0008 | c0007 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| a0009c0006t0001g0033 | a0009 | c0006 | t0001 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB9_chr12_122923992_122971463 | ABCB9 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01168 | hp2 | a0003 | c0005 | t0001 | g0180 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01169 | hp2 | a0003 | c0005 | t0001 | g0160 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0095 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02615 | hp2 | a0005 | c0008 | t0003 | g0072 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0062 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0109 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03209 | hp2 | a0006 | c0009 | t0001 | g0046 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0102 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03486 | hp2 | a0009 | c0006 | t0001 | g0033 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03516 | hp1 | a0001 | c0010 | t0002 | g0193 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03942 | hp1 | a0008 | c0007 | t0001 | g0143 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG04228 | hp1 | a0001 | c0012 | t0001 | g0183 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | STU | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18957 | hp1 | a0004 | c0004 | t0001 | g0140 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19056 | hp2 | a0004 | c0004 | t0001 | g0157 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA19240 | hp2 | a0007 | c0011 | t0002 | g0097 | AFR | YRI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ASW | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | ASW | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02109 | hp1 | a0001 | c0013 | t0003 | g0118 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | USA | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | LWK | ABCB9_chr12_122923992_122971463 | ABCB9 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | ABCB9_chr12_122923992_122971463 | ABCB9 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0034 | REF | REF | ABCB9_chr12_122923992_122971463 | ABCB9 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0007 | 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 | a0009 | 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 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(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 | a0001c0001t0007a0001c0001t0009 | 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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(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 | a0001c0001t0004a0001c0001t0005a0001c0001t0007 | 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 |
| chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122930412
|
C | CT | 6 | a0001c0001t0001g0051a0001c0001t0001g0164a0001c0001t0001g0173others(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 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0149a0001c0001t0004g0007a0001c0001t0004g0010others(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 | 9 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0051others(6): 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 | a0001c0001t0002g0195 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0004g0020 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(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 | 23 | a0001c0001t0002g0120a0001c0001t0003g0011a0001c0001t0003g0080others(20): 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 | 14 | a0001c0001t0003g0011a0001c0001t0003g0080a0001c0001t0003g0081others(11): 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 | 101 | a0001c0001t0001g0088a0001c0001t0001g0205a0001c0001t0001g0211others(98): 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0098others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0002g0195 | 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 | a0001c0001t0003g0106a0001c0001t0003g0113 | 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 | a0001c0001t0006g0227 | 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 | 14 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(11): 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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 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 | a0001c0001t0003g0099a0001c0001t0003g0114a0001c0001t0003g0119others(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 | a0001c0001t0003g0106a0001c0001t0003g0113 | 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 | 42 | a0001c0001t0001g0088a0001c0001t0001g0205a0001c0001t0002g0005others(39): 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 | a0001c0001t0004g0023 | 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 | a0001c0001t0003g0191 | 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 | a0001c0001t0001g0148a0001c0001t0001g0172a0003c0005t0001g0160others(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 | a0001c0001t0002g0094 | 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 | a0001c0001t0005g0008a0001c0001t0005g0022a0001c0001t0005g0028others(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 | 51 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0088others(48): 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0151 | 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 | 8 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(5): 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 | a0001c0001t0004g0023 | 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 | a0001c0001t0003g0087a0001c0001t0003g0111a0001c0001t0003g0117 | 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 | 9 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(6): 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 | a0001c0001t0002g0209 | 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 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0098others(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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0003g0121 | 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 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0135others(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 | a0001c0001t0002g0197 | 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 | a0001c0001t0003g0107 | 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 | a0001c0001t0003g0011 | 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 | a0001c0001t0004g0024 | 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 | 8 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(5): 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | a0001c0001t0001g0142 | 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0158 | 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 | 67 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0066others(64): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0004g0024 | 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 | a0001c0001t0003g0111 | 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0003g0111 | 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 | 65 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0043others(62): 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 | 36 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0088others(33): 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 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0083others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 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 | a0001c0001t0002g0195a0001c0003t0002g0012 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0190 | 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 | 101 | a0001c0001t0001g0088a0001c0001t0001g0205a0001c0001t0001g0211others(98): 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 | a0002c0002t0002g0202 | 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | a0001c0001t0005g0008a0001c0001t0005g0022a0001c0001t0005g0028others(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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | a0001c0001t0002g0093a0001c0010t0002g0193 | 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | a0001c0001t0001g0039a0001c0001t0001g0040 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0077a0001c0001t0001g0144a0001c0001t0001g0156others(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 | 26 | a0001c0001t0002g0120a0001c0001t0003g0011a0001c0001t0003g0080others(23): 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 | a0001c0001t0002g0212 | 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | 35 | a0001c0001t0001g0205a0001c0001t0002g0005a0001c0001t0002g0006others(32): 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 | 22 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0101others(19): 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 | a0001c0001t0002g0195a0001c0003t0002g0012 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0003g0086 | 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 | a0001c0001t0002g0085a0001c0001t0002g0101a0001c0001t0002g0103others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0002g0093a0001c0010t0002g0193 | 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 | a0002c0002t0002g0199 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(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 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(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 | 5 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0054others(2): Show | 7 | HG00741.hp2 HG01074.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251+420G>A | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 6/11 | chr12 | 122945605 | ||||||
| chr12:122945877
|
C | CA | 36 | a0001c0001t0001g0036a0001c0001t0001g0054a0001c0001t0001g0055others(33): 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 | 29 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070others(26): 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 | a0001c0001t0001g0047a0006c0009t0001g0046 | 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 | a0001c0001t0003g0011 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0002g0195 | 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 | a0001c0001t0002g0093a0001c0010t0002g0193 | 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 | a0001c0001t0004g0018 | 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 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0002g0057 | 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 | a0001c0001t0001g0091 | 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0158 | 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 | 101 | a0001c0001t0001g0069a0001c0001t0001g0088a0001c0001t0001g0144others(98): 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 | a0001c0001t0004g0020 | 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040 | 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0003g0087a0001c0001t0003g0111a0001c0001t0003g0117 | 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 | a0001c0001t0001g0041 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1053+102G>T | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122948522 | ||||||
| chr12:122948590
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 271 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(268): Show |
intron_variant | MODIFIER | c.1053+34A>G | ABCB9 | ENSG00000150967.19 | transcript | ENST00000280560.13 | protein_coding | 5/11 | chr12 | 122948590 | ||||||
| chr12:122948955
|
G | C | 1 | a0001c0001t0001g0159 | 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 | a0001c0001t0002g0059a0001c0001t0003g0191 | 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | a0001c0001t0003g0087a0001c0001t0003g0111a0001c0001t0003g0117 | 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 | a0001c0001t0001g0088a0001c0001t0002g0122a0001c0001t0002g0123others(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 | a0001c0001t0002g0195a0001c0003t0002g0012 | 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 | a0001c0001t0002g0005 | 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 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0098others(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 | 24 | a0001c0001t0002g0120a0001c0001t0003g0011a0001c0001t0003g0080others(21): 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 | a0001c0001t0001g0129 | 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 | 92 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(89): 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 | 18 | a0001c0001t0001g0142a0001c0001t0001g0168a0001c0001t0001g0188others(15): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0003g0191 | 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 | 41 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0001g0089others(38): 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 | a0001c0001t0001g0040a0001c0001t0001g0079a0001c0001t0001g0162others(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 | a0004c0004t0001g0140 | 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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0002g0217 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0088a0001c0001t0002g0122a0001c0001t0002g0123others(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 | a0001c0001t0001g0164a0001c0001t0001g0165 | 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 | a0001c0001t0001g0041 | 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 | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | a0001c0001t0002g0218 | 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 | 26 | a0001c0001t0001g0030a0001c0001t0001g0166a0001c0001t0002g0084others(23): 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 | a0001c0001t0003g0191 | 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 | a0001c0001t0001g0130a0001c0001t0001g0167 | 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 | 29 | a0001c0001t0001g0088a0001c0001t0002g0084a0001c0001t0002g0085others(26): 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 | a0001c0001t0002g0101a0001c0001t0002g0104 | 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 | 16 | a0001c0001t0004g0007a0001c0001t0004g0009a0001c0001t0004g0010others(13): 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 | 52 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0094others(49): 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0002g0206 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(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 | a0001c0001t0003g0106a0001c0001t0003g0113 | 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 | 20 | a0001c0001t0001g0205a0001c0001t0002g0104a0001c0001t0002g0198others(17): 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 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0061others(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 | a0001c0001t0002g0204 | 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | 100 | a0001c0001t0001g0088a0001c0001t0001g0205a0001c0001t0001g0211others(97): 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0135 | 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 | 25 | a0001c0001t0001g0063a0001c0001t0001g0170a0001c0001t0002g0084others(22): 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | a0001c0001t0003g0099a0001c0001t0003g0114a0001c0001t0003g0115others(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 | a0001c0001t0003g0115 | 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 | a0001c0001t0001g0036a0001c0001t0001g0064a0001c0001t0001g0133others(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 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0133others(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 | a0001c0001t0001g0089 | 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 | 23 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(20): 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 | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): 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 | 52 | a0001c0001t0001g0031a0001c0001t0001g0064a0001c0001t0001g0065others(49): Show | 59 | HG00558.hp1 HG00642.hp1 HG00738.hp1 others(56): 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 | a0001c0001t0002g0085a0001c0001t0002g0104a0001c0001t0004g0018others(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 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0100others(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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0092a0001c0001t0001g0181 | 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 | a0001c0001t0001g0182 | 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 | 42 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(39): 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 | a0001c0001t0001g0078a0001c0001t0001g0079 | 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 | 35 | a0001c0001t0001g0205a0001c0001t0001g0211a0001c0001t0001g0216others(32): 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0002g0224 | 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 | a0001c0001t0003g0121 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0187 | 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 | a0001c0003t0002g0012 | 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 | a0001c0001t0001g0088a0001c0001t0002g0122a0001c0001t0002g0123others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0098others(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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0089 | 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 | a0002c0002t0002g0199a0002c0002t0002g0200 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 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 | 78 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(75): 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 | a0001c0001t0002g0093a0001c0010t0002g0193 | 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 | a0001c0001t0003g0191 | 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 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0098others(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 | a0001c0001t0004g0007a0001c0001t0004g0018a0001c0001t0004g0019 | 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 | a0001c0001t0002g0192 | 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 | a0001c0001t0002g0198 | 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 | 37 | a0001c0001t0001g0205a0001c0001t0001g0211a0001c0001t0001g0216others(34): 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 | a0001c0001t0003g0099 | 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 | 17 | a0001c0001t0002g0195a0001c0001t0004g0007a0001c0001t0004g0009others(14): 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 | a0001c0001t0002g0094a0001c0001t0002g0096a0001c0001t0002g0098others(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 | a0001c0001t0002g0196a0001c0001t0002g0197 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0088others(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 | 34 | a0001c0001t0001g0205a0001c0001t0001g0211a0001c0001t0001g0216others(31): 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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0078a0001c0001t0001g0079 | 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 | 4 | a0001c0001t0001g0083a0001c0001t0003g0080a0001c0001t0003g0081others(1): Show | 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 | 174 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(171): 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 |