Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 157769 |
|---|---|
| ensemblid | ENSG00000176853.16 |
| hgncid | 26306 |
| symbol | FAM91A1 |
| name | family with sequence similarity 91 member A1 |
| refseq_nuc | NM_144963.4 |
| refseq_prot | NP_659400.3 |
| ensembl_nuc | ENST00000334705.12 |
| ensembl_prot | ENSP00000335082.7 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 123768439 |
| end | 123815452 |
| strand | + |
| ver | v1.2 |
| region | chr8:123768439-123815452 |
| region5000 | chr8:123763439-123820452 |
| regionname0 | FAM91A1_chr8_123768439_123815452 |
| regionname5000 | FAM91A1_chr8_123763439_123820452 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 838 | 331 | 83 | 54 | 143 | 10 | 40 | 107 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0002 | 0/0 | 838 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0003 | 0/0 | 838 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0004 | 0/0 | 838 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0005 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0006 | 1/0 | 838 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0007 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0008 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2517 | 281 | 55 | 49 | 131 | 10 | 35 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0002 | 0/0 | 2517 | 32 | 17 | 4 | 11 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0003 | 0/0 | 2517 | 4 | 4 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0004 | 0/0 | 2517 | 3 | 0 | 1 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0005 | 0/0 | 2517 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0006 | 0/0 | 2517 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0007 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0008 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0009 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0010 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0011 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0012 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0013 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0014 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0015 | 1/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0016 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0017 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0018 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0019 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| c0020 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3013 | 144 | 7 | 26 | 80 | 7 | 23 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0002 | 0/0 | 3013 | 81 | 27 | 9 | 37 | 2 | 6 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0003 | 1/0 | 3013 | 59 | 23 | 15 | 8 | 1 | 11 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0004 | 0/0 | 3013 | 12 | 0 | 0 | 11 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0005 | 0/0 | 3013 | 8 | 7 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0006 | 0/0 | 3013 | 4 | 4 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0007 | 0/0 | 3012 | 3 | 2 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0008 | 0/0 | 3013 | 3 | 3 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0009 | 0/0 | 3013 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0010 | 0/0 | 3012 | 2 | 1 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0011 | 0/0 | 3013 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0012 | 0/0 | 3013 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0013 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0014 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0015 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0016 | 0/0 | 3013 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0017 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0018 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0019 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0020 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0021 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0022 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0023 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0024 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0025 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0026 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0027 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| t0028 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 23 | 1 | 2 | 18 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0002 | 0/0 | 17 | 0 | 4 | 7 | 1 | 5 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0003 | 0/0 | 15 | 0 | 6 | 8 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0004 | 0/0 | 9 | 0 | 2 | 4 | 1 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0005 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0008 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2517 | 281 | 55 | 49 | 131 | 10 | 35 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0002 | 0/0 | 2517 | 32 | 17 | 4 | 11 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0003 | 0/0 | 2517 | 4 | 4 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0004 | 0/0 | 2517 | 3 | 0 | 1 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0005 | 0/0 | 2517 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0006 | 0/0 | 2517 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0007 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0009 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0010 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0012 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0014 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0018 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0020 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0002c0008 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0003c0017 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0004c0019 | 0/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0005c0011 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0006c0015 | 1/0 | 2517 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0007c0016 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0008c0013 | 0/0 | 2517 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5529 | 139 | 6 | 25 | 80 | 7 | 20 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0002 | 0/0 | 5529 | 66 | 15 | 8 | 35 | 2 | 6 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0003 | 0/0 | 5529 | 39 | 9 | 13 | 8 | 1 | 8 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0005 | 0/0 | 5529 | 8 | 7 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0006 | 0/0 | 5529 | 4 | 4 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0007 | 0/0 | 5528 | 3 | 2 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0008 | 0/0 | 5529 | 3 | 3 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0009 | 0/0 | 5529 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0010 | 0/0 | 5528 | 2 | 1 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0011 | 0/0 | 5529 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0012 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0013 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0014 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0015 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0016 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0018 | 0/0 | 5528 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0022 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0023 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0024 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0025 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0026 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0001t0027 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0002t0002 | 0/0 | 5529 | 8 | 7 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0002t0003 | 0/0 | 5529 | 11 | 9 | 2 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0002t0004 | 0/0 | 5529 | 11 | 0 | 0 | 11 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0002t0017 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0002t0028 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0003t0002 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0003t0003 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0003t0020 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0004t0001 | 0/0 | 5529 | 3 | 0 | 1 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0005t0003 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0006t0003 | 0/0 | 5529 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0007t0019 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0009t0002 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0010t0002 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0012t0001 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0014t0002 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0018t0002 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0001c0020t0021 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0002c0008t0002 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0003c0017t0004 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0004c0019t0003 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0005c0011t0003 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0006c0015t0003 | 1/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0007c0016t0003 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| a0008c0013t0001 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | copy fasta | chr8 | 123763439 | 123820452 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 3 | 7 | 1 | 5 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 6 | 7 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 2 | 4 | 1 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0001 | 0/0 | 17 | 0 | 2 | 14 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0008 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0010g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0012g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0016g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0018g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0022g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0023g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0024g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0025g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0026g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0001t0027g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0017g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0002t0028g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0003t0020g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0004t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0005t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0005t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0006t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0006t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0007t0019g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0009t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0010t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0012t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0014t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0018t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0001c0020t0021g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0002c0008t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0003c0017t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0004c0019t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0005c0011t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0006c0015t0003g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0007c0016t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| a0008c0013t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00673 | hp1 | a0001 | c0001 | t0015 | g0131 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01070 | hp2 | a0001 | c0001 | t0018 | g0108 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0083 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01261 | hp2 | a0001 | c0002 | t0028 | g0061 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0047 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0007 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0204 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02040 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02055 | hp1 | a0001 | c0018 | t0002 | g0053 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0034 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02083 | hp2 | a0001 | c0001 | t0014 | g0130 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0209 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0206 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02258 | hp1 | a0008 | c0013 | t0001 | g0162 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0074 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0208 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0198 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02572 | hp1 | a0001 | c0009 | t0002 | g0192 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02615 | hp1 | a0001 | c0020 | t0021 | g0207 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02683 | hp2 | a0001 | c0006 | t0003 | g0014 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0036 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02738 | hp1 | a0001 | c0006 | t0003 | g0203 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0048 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02896 | hp2 | a0001 | c0001 | t0024 | g0052 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0049 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02922 | hp2 | a0001 | c0001 | t0023 | g0096 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0007 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03041 | hp1 | a0001 | c0003 | t0020 | g0196 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03130 | hp1 | a0001 | c0003 | t0003 | g0205 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0068 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0041 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03239 | hp2 | a0001 | c0004 | t0001 | g0151 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0007 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03453 | hp2 | a0001 | c0010 | t0002 | g0111 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03516 | hp2 | a0001 | c0005 | t0003 | g0112 | AFR | ESN | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03540 | hp2 | a0001 | c0001 | t0022 | g0194 | AFR | GWD | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03704 | hp1 | a0001 | c0012 | t0001 | g0136 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03710 | hp2 | a0004 | c0019 | t0003 | g0014 | SAS | PJL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03927 | hp2 | a0001 | c0001 | t0016 | g0165 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03942 | hp2 | a0003 | c0017 | t0004 | g0062 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | STU | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | STU | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18522 | hp1 | a0001 | c0001 | t0025 | g0195 | AFR | YRI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | YRI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | YRI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18941 | hp1 | a0001 | c0002 | t0004 | g0064 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18947 | hp1 | a0002 | c0008 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0117 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18950 | hp1 | a0001 | c0002 | t0004 | g0066 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18962 | hp2 | a0001 | c0001 | t0010 | g0037 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18965 | hp2 | a0001 | c0001 | t0009 | g0158 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18971 | hp2 | a0001 | c0001 | t0027 | g0102 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18975 | hp1 | a0001 | c0002 | t0004 | g0067 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0059 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18984 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18986 | hp2 | a0001 | c0001 | t0011 | g0120 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19005 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19006 | hp2 | a0001 | c0002 | t0004 | g0065 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19043 | hp1 | a0001 | c0002 | t0017 | g0072 | AFR | LWK | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0183 | AFR | LWK | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19060 | hp1 | a0001 | c0014 | t0002 | g0024 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19060 | hp2 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19070 | hp1 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | YRI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ASW | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ASW | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | GIH | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0046 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02486 | hp2 | a0001 | c0005 | t0003 | g0051 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02559 | hp1 | a0005 | c0011 | t0003 | g0070 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ACB | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03471 | hp1 | a0001 | c0007 | t0019 | g0197 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG03471 | hp2 | a0001 | c0001 | t0026 | g0101 | AFR | MSL | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | USA | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | USA | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| NA21309 | hp2 | a0007 | c0016 | t0003 | g0191 | AFR | LWK | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0127 | REF | REF | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| homoSapiens_grch38 | hp1 | a0006 | c0015 | t0003 | g0213 | REF | REF | FAM91A1_chr8_123763439_123820452 | FAM91A1 | chr8 | 123763439 | 123820452 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123779998
|
C | A | 1 | a0002 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.563C>A | p.Pro188His | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 7/24 | 827/5529 | 563/2517 | 188/838 | chr8 | 123779998 | ||
| chr8:123799623
|
C | T | 1 | a0003 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1664C>T | p.Thr555Ile | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 17/24 | 1928/5529 | 1664/2517 | 555/838 | chr8 | 123799623 | ||
| chr8:123799773
|
G | A | 1 | a0004 | 1 | HG03710.hp2 | missense_variant&splice_region_variant | MODERATE | c.1697G>A | p.Ser566Asn | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/24 | 1961/5529 | 1697/2517 | 566/838 | chr8 | 123799773 | ||
| chr8:123805274
|
G | A | 1 | a0005 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1817G>A | p.Gly606Asp | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 19/24 | 2081/5529 | 1817/2517 | 606/838 | chr8 | 123805274 | ||
| chr8:123808335
|
T | C | 1 | a0008 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.2096T>C | p.Ile699Thr | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 21/24 | 2360/5529 | 2096/2517 | 699/838 | chr8 | 123808335 | ||
| chr8:123808349
|
A | G | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2110A>G | p.Ile704Val | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 21/24 | 2374/5529 | 2110/2517 | 704/838 | chr8 | 123808349 | ||
| chr8:123812586
|
G | A | 7 | a0001a0002a0003others(4): Show | 337 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(334): Show |
missense_variant | MODERATE | c.2399G>A | p.Cys800Tyr | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2663/5529 | 2399/2517 | 800/838 | chr8 | 123812586 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123775169
|
A | G | 1 | a0001c0020 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.180A>G | p.Glu60Glu | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/24 | 444/5529 | 180/2517 | 60/838 | chr8 | 123775169 | ||
| chr8:123778700
|
A | T | 2 | a0001c0006a0004c0019 | 3 | HG02683.hp2 HG02738.hp1 HG03710.hp2 |
synonymous_variant | LOW | c.477A>T | p.Ile159Ile | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/24 | 741/5529 | 477/2517 | 159/838 | chr8 | 123778700 | ||
| chr8:123778736
|
G | A | 1 | a0001c0007 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.513G>A | p.Val171Val | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/24 | 777/5529 | 513/2517 | 171/838 | chr8 | 123778736 | ||
| chr8:123784477
|
T | A | 1 | a0001c0009 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.711T>A | p.Pro237Pro | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 9/24 | 975/5529 | 711/2517 | 237/838 | chr8 | 123784477 | ||
| chr8:123786543
|
A | G | 1 | a0001c0004 | 3 | HG01433.hp2 HG02735.hp2 HG03239.hp2 |
synonymous_variant | LOW | c.1011A>G | p.Glu337Glu | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/24 | 1275/5529 | 1011/2517 | 337/838 | chr8 | 123786543 | ||
| chr8:123787678
|
T | C | 1 | a0001c0010 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1206T>C | p.His402His | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/24 | 1470/5529 | 1206/2517 | 402/838 | chr8 | 123787678 | ||
| chr8:123789714
|
G | A | 1 | a0001c0003 | 4 | HG01891.hp2 HG02257.hp1 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.1380G>A | p.Ala460Ala | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/24 | 1644/5529 | 1380/2517 | 460/838 | chr8 | 123789714 | ||
| chr8:123789738
|
C | T | 1 | a0001c0018 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1404C>T | p.Pro468Pro | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/24 | 1668/5529 | 1404/2517 | 468/838 | chr8 | 123789738 | ||
| chr8:123799882
|
T | C | 1 | a0001c0005 | 2 | HG02486.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1806T>C | p.Ile602Ile | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/24 | 2070/5529 | 1806/2517 | 602/838 | chr8 | 123799882 | ||
| chr8:123806207
|
C | G | 4 | a0001c0002a0001c0003a0001c0018others(1): Show | 38 | HG01243.hp1 HG01243.hp2 HG01261.hp2 others(35): Show |
synonymous_variant | LOW | c.2010C>G | p.Leu670Leu | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/24 | 2274/5529 | 2010/2517 | 670/838 | chr8 | 123806207 | ||
| chr8:123808285
|
G | A | 1 | a0001c0012 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2046G>A | p.Leu682Leu | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 21/24 | 2310/5529 | 2046/2517 | 682/838 | chr8 | 123808285 | ||
| chr8:123812599
|
T | C | 1 | a0001c0014 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.2412T>C | p.Gly804Gly | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2676/5529 | 2412/2517 | 804/838 | chr8 | 123812599 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123768498
|
C | T | 3 | a0001c0002t0004a0001c0002t0028a0003c0017t0004 | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-205C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/24 | 205 | chr8 | 123768498 | |||||
| chr8:123768581
|
C | T | 3 | a0001c0002t0004a0001c0002t0028a0003c0017t0004 | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-122C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/24 | 122 | chr8 | 123768581 | |||||
| chr8:123768584
|
C | A | 11 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(8): Show | 154 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-119C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/24 | chr8 | 123768584 | ||||||
| chr8:123768618
|
C | T | 3 | a0001c0002t0004a0001c0002t0028a0003c0017t0004 | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-85C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/24 | 85 | chr8 | 123768618 | |||||
| chr8:123768633
|
G | T | 1 | a0001c0001t0016 | 1 | HG03927.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/24 | chr8 | 123768633 | ||||||
| chr8:123812926
|
C | T | 1 | a0001c0001t0027 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 222 | chr8 | 123812926 | |||||
| chr8:123813000
|
A | C | 2 | a0001c0001t0005a0001c0001t0026 | 9 | HG01109.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*296A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 296 | chr8 | 123813000 | |||||
| chr8:123813013
|
G | T | 1 | a0001c0001t0008 | 3 | HG02723.hp2 HG03209.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*309G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 309 | chr8 | 123813013 | |||||
| chr8:123813034
|
A | G | 2 | a0001c0001t0024a0001c0001t0025 | 2 | HG02896.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 330 | chr8 | 123813034 | |||||
| chr8:123813650
|
G | A | 1 | a0001c0001t0009 | 2 | HG02040.hp2 NA18965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*946G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 946 | chr8 | 123813650 | |||||
| chr8:123813846
|
G | C | 1 | a0001c0001t0024 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1142G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1142 | chr8 | 123813846 | |||||
| chr8:123814262
|
A | G | 2 | a0001c0001t0014a0001c0001t0015 | 2 | HG00673.hp1 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1558A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1558 | chr8 | 123814262 | |||||
| chr8:123814289
|
C | A | 1 | a0001c0002t0017 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1585C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1585 | chr8 | 123814289 | |||||
| chr8:123814343
|
AT | A | 3 | a0001c0001t0007a0001c0001t0010a0001c0001t0018 | 6 | HG01070.hp2 HG01934.hp1 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1651delT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1651 | INFO_REALIGN_3_PRIME | chr8 | 123814343 | ||||
| chr8:123814413
|
T | G | 1 | a0001c0001t0013 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1709 | chr8 | 123814413 | |||||
| chr8:123814421
|
A | G | 1 | a0001c0001t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1717A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1717 | chr8 | 123814421 | |||||
| chr8:123814551
|
T | C | 2 | a0001c0002t0004a0003c0017t0004 | 12 | HG03942.hp2 NA18941.hp1 NA18950.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1847T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1847 | chr8 | 123814551 | |||||
| chr8:123814564
|
G | T | 23 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(20): Show | 120 | HG00408.hp2 HG00558.hp1 HG00741.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1860G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1860 | chr8 | 123814564 | |||||
| chr8:123814638
|
C | G | 1 | a0001c0001t0022 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1934C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1934 | chr8 | 123814638 | |||||
| chr8:123814693
|
C | T | 1 | a0001c0001t0015 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1989C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 1989 | chr8 | 123814693 | |||||
| chr8:123814717
|
G | A | 1 | a0001c0007t0019 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2013G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2013 | chr8 | 123814717 | |||||
| chr8:123814796
|
A | T | 1 | a0001c0020t0021 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2092A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2092 | chr8 | 123814796 | |||||
| chr8:123814809
|
T | C | 3 | a0001c0002t0004a0001c0002t0028a0003c0017t0004 | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2105T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2105 | chr8 | 123814809 | |||||
| chr8:123814833
|
A | G | 1 | a0001c0001t0016 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2129A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2129 | chr8 | 123814833 | |||||
| chr8:123814913
|
C | A | 1 | a0001c0020t0021 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2209C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2209 | chr8 | 123814913 | |||||
| chr8:123815082
|
C | T | 2 | a0001c0001t0012a0001c0007t0019 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2378C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2378 | chr8 | 123815082 | |||||
| chr8:123815282
|
A | G | 1 | a0001c0002t0017 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2578A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2578 | chr8 | 123815282 | |||||
| chr8:123815357
|
T | C | 1 | a0001c0001t0006 | 4 | HG02451.hp2 HG02559.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2653T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2653 | chr8 | 123815357 | |||||
| chr8:123815446
|
A | T | 1 | a0001c0003t0020 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2742A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 24/24 | 2742 | chr8 | 123815446 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123768851
|
G | A | 10 | a0001c0001t0024g0052a0001c0002t0002g0021a0001c0002t0002g0044others(7): Show | 11 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+77G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123768851 | ||||||
| chr8:123769113
|
G | A | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.72+339G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769113 | ||||||
| chr8:123769121
|
T | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 329 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.72+347T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769121 | ||||||
| chr8:123769124
|
A | T | 2 | a0001c0002t0003g0208a0001c0002t0003g0209 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.72+350A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769124 | ||||||
| chr8:123769222
|
T | G | 36 | a0001c0001t0003g0012a0001c0001t0003g0054a0001c0001t0003g0055others(33): Show | 46 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.72+448T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769222 | ||||||
| chr8:123769257
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.72+483A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769257 | ||||||
| chr8:123769298
|
G | GT | 40 | a0001c0001t0003g0012a0001c0001t0003g0054a0001c0001t0003g0055others(37): Show | 50 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.72+524_72+525insT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769298 | ||||||
| chr8:123769350
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.72+576G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769350 | ||||||
| chr8:123769508
|
A | G | 1 | a0001c0006t0003g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.72+734A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769508 | ||||||
| chr8:123769685
|
C | A | 5 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0006g0056others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+911C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769685 | ||||||
| chr8:123769714
|
A | AAGAT | 36 | a0001c0001t0003g0012a0001c0001t0003g0054a0001c0001t0003g0055others(33): Show | 46 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.72+943_72+944insTA others(2): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr8 | 123769714 | |||||
| chr8:123769830
|
C | T | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.72+1056C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769830 | ||||||
| chr8:123769853
|
C | T | 1 | a0001c0001t0024g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.72+1079C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769853 | ||||||
| chr8:123769901
|
G | C | 36 | a0001c0001t0003g0012a0001c0001t0003g0054a0001c0001t0003g0055others(33): Show | 46 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.72+1127G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769901 | ||||||
| chr8:123769933
|
A | C | 4 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG03490.hp2 HG03834.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+1159A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123769933 | ||||||
| chr8:123769986
|
C | CCTT | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 221 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.72+1214_72+1215ins others(3): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr8 | 123769986 | |||||
| chr8:123770099
|
C | T | 3 | a0001c0001t0002g0113a0001c0001t0024g0052a0001c0005t0003g0051 | 3 | HG00408.hp2 HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.72+1325C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123770099 | ||||||
| chr8:123770100
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 156 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.72+1326G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123770100 | ||||||
| chr8:123770100
|
G | GCGC | 3 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075 | 3 | HG02258.hp2 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.72+1328_72+1330dup others(3): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr8 | 123770100 | |||||
| chr8:123770202
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.72+1428C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123770202 | ||||||
| chr8:123770398
|
A | G | 2 | a0001c0001t0024g0052a0001c0005t0003g0051 | 2 | HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.72+1624A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123770398 | ||||||
| chr8:123770601
|
T | A | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.72+1827T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123770601 | ||||||
| chr8:123771004
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.72+2230C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771004 | ||||||
| chr8:123771114
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.72+2340C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771114 | ||||||
| chr8:123771230
|
G | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(81): Show | 126 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.72+2456G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771230 | ||||||
| chr8:123771340
|
T | G | 1 | a0001c0001t0001g0032 | 2 | HG02155.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.72+2566T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771340 | ||||||
| chr8:123771375
|
T | C | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.72+2601T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771375 | ||||||
| chr8:123771458
|
C | G | 1 | a0001c0001t0006g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.73-2622C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771458 | ||||||
| chr8:123771738
|
C | G | 111 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(108): Show | 158 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(155): Show |
intron_variant | MODIFIER | c.73-2342C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771738 | ||||||
| chr8:123771822
|
C | T | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.73-2258C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771822 | ||||||
| chr8:123771869
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.73-2211G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123771869 | ||||||
| chr8:123772192
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG02155.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.73-1888C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123772192 | ||||||
| chr8:123772485
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.73-1595A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123772485 | ||||||
| chr8:123772648
|
A | G | 4 | a0001c0001t0024g0052a0001c0001t0025g0195a0001c0005t0003g0051others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-1432A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123772648 | ||||||
| chr8:123772754
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73-1326A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123772754 | ||||||
| chr8:123772775
|
C | T | 1 | a0001c0001t0022g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.73-1305C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123772775 | ||||||
| chr8:123772820
|
A | G | 1 | a0001c0002t0004g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.73-1260A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123772820 | ||||||
| chr8:123773067
|
C | T | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.73-1013C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773067 | ||||||
| chr8:123773079
|
C | T | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.73-1001C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773079 | ||||||
| chr8:123773082
|
A | G | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.73-998A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773082 | ||||||
| chr8:123773221
|
A | G | 3 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075 | 3 | HG02258.hp2 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.73-859A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773221 | ||||||
| chr8:123773235
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.73-845C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773235 | ||||||
| chr8:123773405
|
C | A | 123 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(120): Show | 173 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(170): Show |
intron_variant | MODIFIER | c.73-675C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773405 | ||||||
| chr8:123773440
|
G | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(78): Show | 123 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(120): Show |
intron_variant | MODIFIER | c.73-640G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773440 | ||||||
| chr8:123773468
|
A | G | 10 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(7): Show | 11 | HG01099.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-612A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773468 | ||||||
| chr8:123773516
|
C | T | 1 | a0001c0001t0003g0031 | 2 | HG04204.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.73-564C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773516 | ||||||
| chr8:123773587
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.73-493G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773587 | ||||||
| chr8:123773649
|
A | G | 1 | a0001c0010t0002g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-431A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773649 | ||||||
| chr8:123773679
|
T | C | 1 | a0001c0003t0020g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.73-401T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773679 | ||||||
| chr8:123773712
|
A | G | 4 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG03490.hp2 HG03834.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-368A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773712 | ||||||
| chr8:123773800
|
T | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG01074.hp2 HG03831.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-280T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 1/23 | chr8 | 123773800 | ||||||
| chr8:123774248
|
A | T | 1 | a0001c0009t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.157+84A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 2/23 | chr8 | 123774248 | ||||||
| chr8:123774468
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.157+304A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 2/23 | chr8 | 123774468 | ||||||
| chr8:123774723
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.158-424T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 2/23 | chr8 | 123774723 | ||||||
| chr8:123774759
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.158-388A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 2/23 | chr8 | 123774759 | ||||||
| chr8:123774852
|
T | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(28): Show | 51 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.158-295T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 2/23 | chr8 | 123774852 | ||||||
| chr8:123774882
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.158-265G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 2/23 | chr8 | 123774882 | ||||||
| chr8:123775070
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.158-77G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 2/23 | chr8 | 123775070 | ||||||
| chr8:123775652
|
G | T | 63 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(60): Show | 102 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.309+354G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123775652 | ||||||
| chr8:123775849
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.309+551T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123775849 | ||||||
| chr8:123776100
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.309+802T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776100 | ||||||
| chr8:123776113
|
A | G | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.309+815A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776113 | ||||||
| chr8:123776262
|
T | C | 102 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(99): Show | 148 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.309+964T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776262 | ||||||
| chr8:123776263
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.309+965G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776263 | ||||||
| chr8:123776295
|
G | A | 10 | a0001c0002t0002g0021a0001c0002t0002g0044a0001c0002t0002g0045others(7): Show | 11 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.310-970G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776295 | ||||||
| chr8:123776441
|
A | G | 3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0003g0030 | 4 | HG02735.hp1 HG03927.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-824A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776441 | ||||||
| chr8:123776495
|
A | C | 1 | a0001c0001t0001g0035 | 2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.310-770A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776495 | ||||||
| chr8:123776529
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.310-736C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776529 | ||||||
| chr8:123776574
|
G | C | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-691G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776574 | ||||||
| chr8:123776625
|
G | T | 2 | a0001c0002t0003g0048a0001c0002t0003g0049 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.310-640G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776625 | ||||||
| chr8:123776669
|
A | G | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.310-596A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776669 | ||||||
| chr8:123776779
|
T | A | 1 | a0001c0001t0012g0041 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.310-486T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776779 | ||||||
| chr8:123776847
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.310-418C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123776847 | ||||||
| chr8:123777143
|
A | G | 7 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0012g0041others(4): Show | 8 | HG02615.hp2 HG03139.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-122A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123777143 | ||||||
| chr8:123777177
|
G | A | 64 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(61): Show | 105 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.310-88G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123777177 | ||||||
| chr8:123777180
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.310-85A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 3/23 | chr8 | 123777180 | ||||||
| chr8:123777507
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.367+185G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 4/23 | chr8 | 123777507 | ||||||
| chr8:123777808
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.368-217A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 4/23 | chr8 | 123777808 | ||||||
| chr8:123777927
|
G | A | 4 | a0001c0001t0003g0014a0001c0006t0003g0014a0001c0006t0003g0203others(1): Show | 4 | HG02683.hp2 HG02738.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-98G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 4/23 | chr8 | 123777927 | ||||||
| chr8:123777934
|
A | T | 8 | a0001c0002t0002g0021a0001c0002t0002g0044a0001c0002t0002g0045others(5): Show | 9 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.368-91A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 4/23 | chr8 | 123777934 | ||||||
| chr8:123777942
|
G | A | 2 | a0001c0001t0006g0056a0001c0001t0006g0057 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.368-83G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 4/23 | chr8 | 123777942 | ||||||
| chr8:123778122
|
T | C | 1 | a0001c0001t0003g0115 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.435+30T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 5/23 | chr8 | 123778122 | ||||||
| chr8:123778170
|
G | A | 1 | a0001c0001t0001g0127 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.435+78G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 5/23 | chr8 | 123778170 | ||||||
| chr8:123778306
|
A | G | 1 | a0001c0001t0013g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+214A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 5/23 | chr8 | 123778306 | ||||||
| chr8:123778320
|
A | C | 1 | a0001c0001t0002g0109 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.435+228A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 5/23 | chr8 | 123778320 | ||||||
| chr8:123778406
|
T | C | 15 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(12): Show | 19 | HG01099.hp2 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.436-253T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 5/23 | chr8 | 123778406 | ||||||
| chr8:123778476
|
AAC | A | 8 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075others(5): Show | 11 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-181_436-180del others(2): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr8 | 123778476 | |||||
| chr8:123778488
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.436-171A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 5/23 | chr8 | 123778488 | ||||||
| chr8:123778819
|
A | T | 2 | a0001c0002t0003g0208a0001c0002t0003g0209 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.549+47A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123778819 | ||||||
| chr8:123778931
|
G | A | 2 | a0001c0002t0003g0208a0001c0002t0003g0209 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.549+159G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123778931 | ||||||
| chr8:123779022
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.549+250T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779022 | ||||||
| chr8:123779089
|
G | A | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.549+317G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779089 | ||||||
| chr8:123779111
|
T | C | 3 | a0001c0001t0002g0189a0001c0001t0002g0190a0007c0016t0003g0191 | 3 | HG03195.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.549+339T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779111 | ||||||
| chr8:123779197
|
A | T | 2 | a0001c0002t0003g0208a0001c0002t0003g0209 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.549+425A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779197 | ||||||
| chr8:123779466
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.550-519G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779466 | ||||||
| chr8:123779534
|
G | A | 1 | a0001c0001t0003g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.550-451G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779534 | ||||||
| chr8:123779647
|
A | T | 4 | a0001c0002t0003g0046a0001c0002t0003g0047a0001c0002t0003g0048others(1): Show | 4 | HG01433.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-338A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779647 | ||||||
| chr8:123779778
|
C | G | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.550-207C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779778 | ||||||
| chr8:123779826
|
C | A | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-159C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 6/23 | chr8 | 123779826 | ||||||
| chr8:123780317
|
G | A | 23 | a0001c0002t0002g0021a0001c0002t0002g0044a0001c0002t0002g0045others(20): Show | 27 | HG01243.hp2 HG01261.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.641-163G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 7/23 | chr8 | 123780317 | ||||||
| chr8:123780346
|
T | C | 1 | a0001c0003t0020g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.641-134T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 7/23 | chr8 | 123780346 | ||||||
| chr8:123780659
|
G | A | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.703+117G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123780659 | ||||||
| chr8:123780803
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(59): Show | 99 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.703+261T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123780803 | ||||||
| chr8:123780903
|
C | T | 1 | a0001c0001t0006g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+361C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123780903 | ||||||
| chr8:123781089
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+547A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781089 | ||||||
| chr8:123781141
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0186 | 2 | HG02135.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.703+599A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781141 | ||||||
| chr8:123781474
|
A | AT | 20 | a0001c0001t0001g0124a0001c0001t0001g0137a0001c0001t0001g0138others(17): Show | 23 | HG01261.hp2 HG02135.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.703+953dupT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr8 | 123781474 | |||||
| chr8:123781474
|
AT | A | 95 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0129others(92): Show | 139 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(136): Show |
intron_variant | MODIFIER | c.703+953delT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr8 | 123781474 | |||||
| chr8:123781500
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.703+958C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781500 | ||||||
| chr8:123781504
|
T | G | 98 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(95): Show | 144 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(141): Show |
intron_variant | MODIFIER | c.703+962T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781504 | ||||||
| chr8:123781516
|
C | T | 73 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(70): Show | 114 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.703+974C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781516 | ||||||
| chr8:123781667
|
T | C | 1 | a0001c0002t0004g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.703+1125T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781667 | ||||||
| chr8:123781724
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.703+1182A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781724 | ||||||
| chr8:123781732
|
G | A | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.703+1190G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781732 | ||||||
| chr8:123781736
|
C | T | 1 | a0001c0009t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.703+1194C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781736 | ||||||
| chr8:123781930
|
G | A | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.703+1388G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781930 | ||||||
| chr8:123781999
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(61): Show | 105 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.703+1457C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123781999 | ||||||
| chr8:123782046
|
A | G | 1 | a0001c0001t0002g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.703+1504A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782046 | ||||||
| chr8:123782113
|
A | G | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.703+1571A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782113 | ||||||
| chr8:123782169
|
G | A | 2 | a0001c0002t0003g0007a0001c0002t0003g0068 | 5 | HG01243.hp1 HG01891.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+1627G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782169 | ||||||
| chr8:123782190
|
G | T | 11 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(8): Show | 14 | HG01261.hp2 HG02055.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.703+1648G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782190 | ||||||
| chr8:123782200
|
A | G | 1 | a0001c0003t0020g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.703+1658A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782200 | ||||||
| chr8:123782266
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.703+1724A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782266 | ||||||
| chr8:123782312
|
T | G | 7 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0012g0041others(4): Show | 8 | HG02615.hp2 HG03139.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+1770T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782312 | ||||||
| chr8:123782409
|
C | T | 8 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075others(5): Show | 11 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.703+1867C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782409 | ||||||
| chr8:123782499
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.703+1957G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782499 | ||||||
| chr8:123782609
|
G | A | 123 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(120): Show | 173 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(170): Show |
intron_variant | MODIFIER | c.704-1861G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782609 | ||||||
| chr8:123782618
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.704-1852A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782618 | ||||||
| chr8:123782643
|
T | G | 1 | a0001c0002t0004g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.704-1827T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782643 | ||||||
| chr8:123782652
|
A | G | 1 | a0001c0002t0004g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.704-1818A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782652 | ||||||
| chr8:123782755
|
A | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0186 | 4 | HG00408.hp1 HG02135.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1715A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782755 | ||||||
| chr8:123782894
|
G | A | 2 | a0001c0002t0003g0208a0001c0002t0003g0209 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.704-1576G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782894 | ||||||
| chr8:123782909
|
C | G | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.704-1561C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782909 | ||||||
| chr8:123782946
|
A | G | 92 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(89): Show | 135 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(132): Show |
intron_variant | MODIFIER | c.704-1524A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123782946 | ||||||
| chr8:123783037
|
G | A | 1 | a0008c0013t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-1433G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783037 | ||||||
| chr8:123783045
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.704-1425A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783045 | ||||||
| chr8:123783112
|
G | A | 2 | a0001c0002t0028g0061a0003c0017t0004g0062 | 2 | HG01261.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.704-1358G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783112 | ||||||
| chr8:123783296
|
A | G | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-1174A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783296 | ||||||
| chr8:123783297
|
C | G | 3 | a0001c0003t0002g0204a0001c0003t0002g0206a0001c0003t0003g0205 | 3 | HG01891.hp2 HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.704-1173C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783297 | ||||||
| chr8:123783353
|
ATAAT | A | 64 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(61): Show | 105 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.704-1112_704-1109d others(6): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr8 | 123783353 | |||||
| chr8:123783373
|
C | T | 123 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(120): Show | 173 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(170): Show |
intron_variant | MODIFIER | c.704-1097C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783373 | ||||||
| chr8:123783621
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.704-849G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783621 | ||||||
| chr8:123783687
|
G | A | 76 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(73): Show | 117 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(114): Show |
intron_variant | MODIFIER | c.704-783G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783687 | ||||||
| chr8:123783722
|
A | G | 5 | a0001c0001t0002g0042a0001c0001t0002g0211a0001c0001t0003g0042others(2): Show | 5 | HG02922.hp1 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-748A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783722 | ||||||
| chr8:123783923
|
C | T | 1 | a0001c0001t0009g0158 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.704-547C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783923 | ||||||
| chr8:123783938
|
A | C | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.704-532A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783938 | ||||||
| chr8:123783966
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.704-504A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123783966 | ||||||
| chr8:123784060
|
C | A | 1 | a0001c0001t0001g0033 | 2 | HG00438.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.704-410C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123784060 | ||||||
| chr8:123784238
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.704-232T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123784238 | ||||||
| chr8:123784333
|
A | G | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.704-137A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 8/23 | chr8 | 123784333 | ||||||
| chr8:123784686
|
G | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0143a0001c0001t0001g0163others(3): Show | 8 | HG00140.hp2 HG00735.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.810+110G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 9/23 | chr8 | 123784686 | ||||||
| chr8:123784709
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.810+133A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 9/23 | chr8 | 123784709 | ||||||
| chr8:123784720
|
C | A | 3 | a0001c0001t0006g0056a0001c0001t0006g0057a0001c0001t0006g0058 | 3 | HG02559.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.810+144C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 9/23 | chr8 | 123784720 | ||||||
| chr8:123784809
|
G | A | 5 | a0001c0001t0001g0146a0001c0001t0024g0052a0001c0001t0025g0195others(2): Show | 5 | HG02040.hp1 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.810+233G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 9/23 | chr8 | 123784809 | ||||||
| chr8:123784853
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.811-228G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 9/23 | chr8 | 123784853 | ||||||
| chr8:123784895
|
A | G | 123 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(120): Show | 173 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(170): Show |
intron_variant | MODIFIER | c.811-186A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 9/23 | chr8 | 123784895 | ||||||
| chr8:123785199
|
A | G | 4 | a0001c0001t0024g0052a0001c0001t0025g0195a0001c0005t0003g0051others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+80A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 10/23 | chr8 | 123785199 | ||||||
| chr8:123785487
|
A | G | 1 | a0001c0001t0006g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.850-142A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 10/23 | chr8 | 123785487 | ||||||
| chr8:123785600
|
G | C | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-29G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 10/23 | chr8 | 123785600 | ||||||
| chr8:123785920
|
C | T | 1 | a0003c0017t0004g0062 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.962+179C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 11/23 | chr8 | 123785920 | ||||||
| chr8:123786036
|
G | C | 123 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(120): Show | 173 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(170): Show |
intron_variant | MODIFIER | c.962+295G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 11/23 | chr8 | 123786036 | ||||||
| chr8:123786669
|
A | G | 1 | a0001c0001t0022g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1078+59A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/23 | chr8 | 123786669 | ||||||
| chr8:123786718
|
C | T | 11 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(8): Show | 14 | HG01261.hp2 HG02055.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.1078+108C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/23 | chr8 | 123786718 | ||||||
| chr8:123787069
|
G | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0211a0001c0001t0003g0042others(2): Show | 5 | HG02922.hp1 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-192G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/23 | chr8 | 123787069 | ||||||
| chr8:123787140
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1079-121G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/23 | chr8 | 123787140 | ||||||
| chr8:123787166
|
G | T | 3 | a0001c0002t0003g0208a0001c0002t0003g0209a0001c0002t0017g0072 | 3 | HG02145.hp1 HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1079-95G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/23 | chr8 | 123787166 | ||||||
| chr8:123787217
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1079-44G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/23 | chr8 | 123787217 | ||||||
| chr8:123787240
|
T | G | 1 | a0001c0001t0001g0032 | 2 | HG02155.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1079-21T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 12/23 | chr8 | 123787240 | ||||||
| chr8:123787383
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0161 | 2 | HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1191+10A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 13/23 | chr8 | 123787383 | ||||||
| chr8:123787756
|
T | C | 3 | a0001c0001t0001g0166a0001c0001t0003g0012a0008c0013t0001g0162 | 5 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1278+6T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123787756 | ||||||
| chr8:123787884
|
A | T | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1278+134A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123787884 | ||||||
| chr8:123788033
|
G | T | 121 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(118): Show | 171 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(168): Show |
intron_variant | MODIFIER | c.1278+283G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123788033 | ||||||
| chr8:123788068
|
A | G | 1 | a0001c0002t0004g0066 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1278+318A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123788068 | ||||||
| chr8:123788248
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0144a0001c0001t0001g0167others(1): Show | 5 | HG00597.hp1 NA18612.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278+498G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123788248 | ||||||
| chr8:123788401
|
T | G | 1 | a0001c0001t0002g0079 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1278+651T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123788401 | ||||||
| chr8:123788476
|
T | TA | 8 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075others(5): Show | 11 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1278+736dupA | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr8 | 123788476 | |||||
| chr8:123788798
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1279-815A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123788798 | ||||||
| chr8:123789425
|
A | G | 24 | a0001c0001t0006g0056a0001c0001t0006g0057a0001c0001t0006g0058others(21): Show | 28 | HG01243.hp1 HG01243.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.1279-188A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123789425 | ||||||
| chr8:123789439
|
A | G | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1279-174A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 14/23 | chr8 | 123789439 | ||||||
| chr8:123789784
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1411+39T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123789784 | ||||||
| chr8:123790174
|
G | T | 5 | a0001c0001t0002g0010a0001c0001t0002g0082a0001c0001t0002g0103others(2): Show | 8 | NA18939.hp2 NA18948.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.1411+429G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123790174 | ||||||
| chr8:123790251
|
A | T | 1 | a0001c0005t0003g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1411+506A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123790251 | ||||||
| chr8:123790349
|
C | T | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1411+604C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123790349 | ||||||
| chr8:123790563
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1411+818A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123790563 | ||||||
| chr8:123790754
|
A | C | 4 | a0001c0002t0003g0046a0001c0002t0003g0047a0001c0002t0003g0048others(1): Show | 4 | HG01433.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+1009A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123790754 | ||||||
| chr8:123790767
|
T | G | 1 | a0001c0001t0003g0078 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1411+1022T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123790767 | ||||||
| chr8:123790990
|
G | A | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411+1245G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123790990 | ||||||
| chr8:123791001
|
G | T | 1 | a0001c0001t0022g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1411+1256G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791001 | ||||||
| chr8:123791065
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1411+1320T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791065 | ||||||
| chr8:123791293
|
A | AT | 79 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0179others(76): Show | 122 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.1411+1559dupT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr8 | 123791293 | |||||
| chr8:123791416
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0114a0001c0001t0001g0175others(3): Show | 9 | HG02132.hp1 NA18940.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1411+1671A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791416 | ||||||
| chr8:123791439
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1411+1694G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791439 | ||||||
| chr8:123791457
|
A | T | 75 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(72): Show | 116 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.1411+1712A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791457 | ||||||
| chr8:123791464
|
C | G | 1 | a0001c0001t0003g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1411+1719C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791464 | ||||||
| chr8:123791567
|
G | A | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1411+1822G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791567 | ||||||
| chr8:123791722
|
A | G | 93 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(90): Show | 138 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.1411+1977A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791722 | ||||||
| chr8:123791747
|
C | T | 1 | a0001c0001t0027g0102 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1411+2002C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791747 | ||||||
| chr8:123791896
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1411+2151C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791896 | ||||||
| chr8:123791950
|
G | A | 125 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(122): Show | 175 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.1411+2205G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123791950 | ||||||
| chr8:123792003
|
C | T | 1 | a0001c0002t0002g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1411+2258C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792003 | ||||||
| chr8:123792067
|
C | CGGGAGGC others(25): Show |
1 | a0001c0003t0020g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1411+2335_1411+236 others(36): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr8 | 123792067 | |||||
| chr8:123792216
|
G | T | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1411+2471G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792216 | ||||||
| chr8:123792283
|
A | G | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1411+2538A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792283 | ||||||
| chr8:123792393
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1411+2648A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792393 | ||||||
| chr8:123792429
|
C | T | 121 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(118): Show | 171 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.1411+2684C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792429 | ||||||
| chr8:123792762
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(57): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1411+3017T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792762 | ||||||
| chr8:123792864
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1411+3119A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792864 | ||||||
| chr8:123792994
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1411+3249C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123792994 | ||||||
| chr8:123793059
|
T | G | 2 | a0001c0001t0002g0024a0001c0014t0002g0024 | 2 | NA18970.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1411+3314T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793059 | ||||||
| chr8:123793110
|
T | C | 1 | a0001c0001t0005g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1411+3365T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793110 | ||||||
| chr8:123793157
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1411+3412C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793157 | ||||||
| chr8:123793354
|
C | T | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1411+3609C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793354 | ||||||
| chr8:123793401
|
G | T | 101 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(98): Show | 147 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(144): Show |
intron_variant | MODIFIER | c.1411+3656G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793401 | ||||||
| chr8:123793491
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+3746C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793491 | ||||||
| chr8:123793493
|
A | G | 1 | a0001c0001t0013g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1411+3748A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793493 | ||||||
| chr8:123793522
|
C | T | 1 | a0001c0001t0026g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1411+3777C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793522 | ||||||
| chr8:123793547
|
C | T | 4 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG03490.hp2 HG03834.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+3802C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793547 | ||||||
| chr8:123793666
|
A | T | 1 | a0001c0002t0002g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1411+3921A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793666 | ||||||
| chr8:123793674
|
T | G | 1 | a0001c0001t0002g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1411+3929T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793674 | ||||||
| chr8:123793807
|
T | C | 1 | a0001c0001t0002g0029 | 2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1411+4062T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793807 | ||||||
| chr8:123793844
|
A | C | 66 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(63): Show | 107 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1411+4099A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123793844 | ||||||
| chr8:123794375
|
T | C | 28 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(25): Show | 33 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1412-3715T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794375 | ||||||
| chr8:123794411
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1412-3679A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794411 | ||||||
| chr8:123794490
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1412-3600C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794490 | ||||||
| chr8:123794735
|
A | G | 1 | a0001c0001t0001g0039 | 2 | NA18942.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1412-3355A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794735 | ||||||
| chr8:123794852
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0185 | 2 | HG02647.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1412-3238G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794852 | ||||||
| chr8:123794871
|
A | G | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1412-3219A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794871 | ||||||
| chr8:123794970
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1412-3120T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794970 | ||||||
| chr8:123794974
|
G | A | 4 | a0001c0001t0024g0052a0001c0001t0025g0195a0001c0005t0003g0051others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-3116G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123794974 | ||||||
| chr8:123795243
|
A | G | 3 | a0001c0001t0006g0056a0001c0001t0006g0057a0001c0001t0006g0058 | 3 | HG02559.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1412-2847A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795243 | ||||||
| chr8:123795364
|
G | C | 5 | a0001c0001t0002g0042a0001c0001t0002g0211a0001c0001t0003g0042others(2): Show | 5 | HG02922.hp1 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-2726G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795364 | ||||||
| chr8:123795384
|
G | A | 1 | a0001c0001t0002g0029 | 2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1412-2706G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795384 | ||||||
| chr8:123795389
|
C | G | 1 | a0001c0001t0002g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-2701C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795389 | ||||||
| chr8:123795569
|
C | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(66): Show | 110 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.1412-2521C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795569 | ||||||
| chr8:123795662
|
C | T | 1 | a0007c0016t0003g0191 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1412-2428C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795662 | ||||||
| chr8:123795664
|
G | A | 4 | a0001c0001t0024g0052a0001c0001t0025g0195a0001c0005t0003g0051others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-2426G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795664 | ||||||
| chr8:123795668
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(79): Show | 124 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(121): Show |
intron_variant | MODIFIER | c.1412-2422G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795668 | ||||||
| chr8:123795735
|
G | C | 82 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(79): Show | 124 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(121): Show |
intron_variant | MODIFIER | c.1412-2355G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123795735 | ||||||
| chr8:123796003
|
A | C | 8 | a0001c0002t0002g0021a0001c0002t0002g0044a0001c0002t0002g0045others(5): Show | 9 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-2087A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796003 | ||||||
| chr8:123796004
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1412-2086G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796004 | ||||||
| chr8:123796090
|
G | T | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1412-2000G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796090 | ||||||
| chr8:123796165
|
CAG | C | 4 | a0001c0001t0024g0052a0001c0001t0025g0195a0001c0005t0003g0051others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-1924_1412-192 others(6): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796165 | ||||||
| chr8:123796166
|
A | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0020others(28): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1412-1924A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796166 | ||||||
| chr8:123796204
|
T | C | 2 | a0001c0002t0003g0007a0001c0002t0003g0068 | 5 | HG01243.hp1 HG01891.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-1886T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796204 | ||||||
| chr8:123796461
|
CT | C | 117 | a0001c0001t0001g0036a0001c0001t0001g0119a0001c0001t0001g0129others(114): Show | 167 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(164): Show |
intron_variant | MODIFIER | c.1412-1612delT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr8 | 123796461 | |||||
| chr8:123796546
|
G | A | 1 | a0001c0009t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1412-1544G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796546 | ||||||
| chr8:123796602
|
G | T | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1412-1488G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796602 | ||||||
| chr8:123796679
|
G | A | 12 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075others(9): Show | 15 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1412-1411G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796679 | ||||||
| chr8:123796697
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1412-1393T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796697 | ||||||
| chr8:123796732
|
C | G | 1 | a0001c0001t0002g0027 | 2 | NA18966.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1412-1358C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796732 | ||||||
| chr8:123796886
|
A | G | 1 | a0001c0003t0002g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1412-1204A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123796886 | ||||||
| chr8:123797038
|
C | A | 2 | a0001c0001t0014g0130a0001c0001t0015g0131 | 2 | HG00673.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1412-1052C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797038 | ||||||
| chr8:123797087
|
T | C | 4 | a0001c0002t0003g0046a0001c0002t0003g0047a0001c0002t0003g0048others(1): Show | 4 | HG01433.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-1003T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797087 | ||||||
| chr8:123797349
|
C | T | 1 | a0001c0001t0022g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1412-741C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797349 | ||||||
| chr8:123797454
|
T | A | 1 | a0001c0010t0002g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1412-636T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797454 | ||||||
| chr8:123797497
|
G | A | 1 | a0001c0005t0003g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-593G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797497 | ||||||
| chr8:123797700
|
G | A | 1 | a0001c0003t0020g0196 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1412-390G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797700 | ||||||
| chr8:123797722
|
T | C | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1412-368T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797722 | ||||||
| chr8:123797743
|
A | G | 4 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0010t0002g0111others(1): Show | 4 | HG03195.hp1 HG03453.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-347A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797743 | ||||||
| chr8:123797785
|
T | C | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1412-305T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797785 | ||||||
| chr8:123797852
|
C | T | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1412-238C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797852 | ||||||
| chr8:123797949
|
A | G | 1 | a0001c0001t0022g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1412-141A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123797949 | ||||||
| chr8:123798025
|
T | C | 1 | a0001c0001t0006g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1412-65T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123798025 | ||||||
| chr8:123798080
|
C | G | 4 | a0001c0001t0024g0052a0001c0001t0025g0195a0001c0005t0003g0051others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-10C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 15/23 | chr8 | 123798080 | ||||||
| chr8:123798592
|
G | C | 1 | a0001c0010t0002g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1560+354G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123798592 | ||||||
| chr8:123798712
|
A | G | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1560+474A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123798712 | ||||||
| chr8:123798787
|
T | G | 1 | a0001c0009t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1560+549T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123798787 | ||||||
| chr8:123798793
|
G | C | 1 | a0001c0001t0022g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1560+555G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123798793 | ||||||
| chr8:123798851
|
A | G | 6 | a0001c0001t0002g0026a0001c0001t0002g0097a0001c0001t0008g0026others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1560+613A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123798851 | ||||||
| chr8:123799012
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1561-508A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123799012 | ||||||
| chr8:123799044
|
G | A | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1561-476G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123799044 | ||||||
| chr8:123799109
|
G | A | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1561-411G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123799109 | ||||||
| chr8:123799229
|
G | C | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1561-291G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123799229 | ||||||
| chr8:123799249
|
C | G | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1561-271C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 16/23 | chr8 | 123799249 | ||||||
| chr8:123799739
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1696-33A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 17/23 | chr8 | 123799739 | ||||||
| chr8:123800018
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1809+133T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800018 | ||||||
| chr8:123800035
|
C | T | 4 | a0001c0001t0024g0052a0001c0001t0025g0195a0001c0005t0003g0051others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1809+150C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800035 | ||||||
| chr8:123800118
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1809+233C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800118 | ||||||
| chr8:123800119
|
G | A | 8 | a0001c0002t0002g0021a0001c0002t0002g0044a0001c0002t0002g0045others(5): Show | 9 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1809+234G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800119 | ||||||
| chr8:123800136
|
T | G | 1 | a0001c0002t0028g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1809+251T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800136 | ||||||
| chr8:123800236
|
C | T | 1 | a0001c0003t0003g0205 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1809+351C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800236 | ||||||
| chr8:123800264
|
G | GTA | 12 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(9): Show | 15 | HG01261.hp2 HG03041.hp1 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1809+394_1809+395d others(4): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123800264 | |||||
| chr8:123800264
|
GTA | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(74): Show | 119 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(116): Show |
intron_variant | MODIFIER | c.1809+394_1809+395d others(4): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123800264 | |||||
| chr8:123800406
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1809+521C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800406 | ||||||
| chr8:123800491
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1809+606G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800491 | ||||||
| chr8:123800534
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1809+649A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800534 | ||||||
| chr8:123800638
|
T | C | 2 | a0001c0001t0002g0189a0001c0009t0002g0192 | 2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1809+753T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800638 | ||||||
| chr8:123800674
|
C | T | 2 | a0001c0001t0006g0198a0001c0001t0008g0098 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1809+789C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800674 | ||||||
| chr8:123800693
|
T | C | 82 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(79): Show | 124 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(121): Show |
intron_variant | MODIFIER | c.1809+808T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800693 | ||||||
| chr8:123800732
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1809+847A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800732 | ||||||
| chr8:123800766
|
A | G | 1 | a0001c0018t0002g0053 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1809+881A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800766 | ||||||
| chr8:123800783
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1809+898G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123800783 | ||||||
| chr8:123801052
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1809+1167A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801052 | ||||||
| chr8:123801356
|
A | G | 2 | a0001c0002t0003g0208a0001c0002t0003g0209 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1809+1471A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801356 | ||||||
| chr8:123801490
|
G | A | 3 | a0001c0003t0002g0204a0001c0003t0002g0206a0001c0003t0003g0205 | 3 | HG01891.hp2 HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1809+1605G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801490 | ||||||
| chr8:123801517
|
A | G | 3 | a0001c0003t0002g0204a0001c0003t0002g0206a0001c0003t0003g0205 | 3 | HG01891.hp2 HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1809+1632A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801517 | ||||||
| chr8:123801525
|
C | T | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1809+1640C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801525 | ||||||
| chr8:123801611
|
A | C | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809+1726A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801611 | ||||||
| chr8:123801682
|
C | A | 1 | a0001c0001t0003g0087 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1809+1797C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801682 | ||||||
| chr8:123801800
|
A | AT | 76 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(73): Show | 117 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.1809+1928dupT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123801800 | |||||
| chr8:123801841
|
T | C | 1 | a0001c0010t0002g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1809+1956T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801841 | ||||||
| chr8:123801902
|
A | G | 2 | a0001c0001t0012g0041a0001c0007t0019g0197 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1809+2017A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123801902 | ||||||
| chr8:123802032
|
G | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0143a0001c0001t0001g0164others(2): Show | 7 | HG00735.hp2 HG01168.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1809+2147G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123802032 | ||||||
| chr8:123802048
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1809+2163C>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123802048 | ||||||
| chr8:123802206
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1809+2321G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123802206 | ||||||
| chr8:123802241
|
C | T | 75 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(72): Show | 116 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.1809+2356C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123802241 | ||||||
| chr8:123802425
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1809+2540A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123802425 | ||||||
| chr8:123802848
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1810-2419C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123802848 | ||||||
| chr8:123803122
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1810-2145A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803122 | ||||||
| chr8:123803152
|
A | T | 1 | a0001c0009t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1810-2115A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803152 | ||||||
| chr8:123803237
|
G | GT | 4 | a0001c0001t0001g0166a0001c0001t0003g0012a0001c0001t0003g0078others(1): Show | 6 | HG00673.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1810-2016dupT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123803237 | |||||
| chr8:123803237
|
GT | G | 98 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(95): Show | 141 | HG00544.hp1 HG00558.hp1 HG00733.hp2 others(138): Show |
intron_variant | MODIFIER | c.1810-2016delT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123803237 | |||||
| chr8:123803310
|
T | C | 5 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0022g0194others(2): Show | 5 | HG03195.hp1 HG03453.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810-1957T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803310 | ||||||
| chr8:123803365
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0132a0001c0001t0001g0137 | 5 | NA18960.hp2 NA18979.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1810-1902G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803365 | ||||||
| chr8:123803450
|
A | G | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1810-1817A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803450 | ||||||
| chr8:123803460
|
G | A | 8 | a0001c0002t0002g0021a0001c0002t0002g0044a0001c0002t0002g0045others(5): Show | 9 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1810-1807G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803460 | ||||||
| chr8:123803467
|
T | G | 1 | a0001c0002t0028g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1810-1800T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803467 | ||||||
| chr8:123803495
|
G | A | 4 | a0001c0002t0003g0046a0001c0002t0003g0047a0001c0002t0003g0048others(1): Show | 4 | HG01433.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1810-1772G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803495 | ||||||
| chr8:123803913
|
G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0150a0001c0001t0010g0037 | 3 | HG02132.hp2 NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1810-1354G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123803913 | ||||||
| chr8:123804140
|
T | G | 4 | a0001c0001t0006g0056a0001c0001t0006g0057a0001c0001t0006g0058others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1810-1127T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804140 | ||||||
| chr8:123804487
|
T | TC | 4 | a0001c0001t0001g0133a0001c0002t0002g0044a0001c0007t0019g0197others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1810-780_1810-779i others(3): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804487 | ||||||
| chr8:123804488
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 333 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.1810-779T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804488 | ||||||
| chr8:123804490
|
T | A | 4 | a0001c0001t0001g0133a0001c0002t0002g0044a0001c0007t0019g0197others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1810-777T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804490 | ||||||
| chr8:123804490
|
TA | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 142 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1810-746delA | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123804490 | |||||
| chr8:123804490
|
TAA | T | 22 | a0001c0001t0001g0132a0001c0001t0001g0172a0001c0001t0001g0173others(19): Show | 26 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1810-747_1810-746d others(4): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123804490 | |||||
| chr8:123804490
|
TAAA | T | 19 | a0001c0001t0002g0008a0001c0001t0002g0028a0001c0001t0002g0084others(16): Show | 25 | HG01071.hp2 HG01261.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1810-748_1810-746d others(5): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123804490 | |||||
| chr8:123804490
|
TAAAA | T | 53 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(50): Show | 91 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.1810-749_1810-746d others(6): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123804490 | |||||
| chr8:123804490
|
TAAAAA | T | 7 | a0001c0001t0002g0092a0001c0001t0002g0094a0001c0001t0002g0104others(4): Show | 7 | HG02895.hp1 HG02922.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1810-750_1810-746d others(7): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123804490 | |||||
| chr8:123804490
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0007g0022 | 2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1810-759_1810-746d others(16): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr8 | 123804490 | |||||
| chr8:123804622
|
A | G | 118 | a0001c0001t0001g0119a0001c0001t0002g0001a0001c0001t0002g0008others(115): Show | 168 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(165): Show |
intron_variant | MODIFIER | c.1810-645A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804622 | ||||||
| chr8:123804742
|
A | C | 37 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(34): Show | 45 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1810-525A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804742 | ||||||
| chr8:123804756
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1810-511A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804756 | ||||||
| chr8:123804791
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1810-476G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804791 | ||||||
| chr8:123804819
|
A | G | 1 | a0001c0001t0008g0095 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1810-448A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804819 | ||||||
| chr8:123804834
|
G | A | 1 | a0001c0002t0003g0208 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1810-433G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804834 | ||||||
| chr8:123804905
|
G | A | 37 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(34): Show | 45 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1810-362G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123804905 | ||||||
| chr8:123805141
|
G | T | 10 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(7): Show | 11 | HG01099.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1810-126G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 18/23 | chr8 | 123805141 | ||||||
| chr8:123805365
|
CT | C | 83 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(80): Show | 127 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.1882+40delT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr8 | 123805365 | |||||
| chr8:123805685
|
T | A | 11 | a0001c0002t0002g0021a0001c0002t0002g0044a0001c0002t0002g0045others(8): Show | 12 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1882+346T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 19/23 | chr8 | 123805685 | ||||||
| chr8:123805795
|
A | G | 2 | a0001c0001t0005g0016a0001c0001t0005g0083 | 4 | HG01109.hp1 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883-285A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 19/23 | chr8 | 123805795 | ||||||
| chr8:123805942
|
A | G | 76 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(73): Show | 118 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(115): Show |
intron_variant | MODIFIER | c.1883-138A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 19/23 | chr8 | 123805942 | ||||||
| chr8:123806029
|
C | T | 3 | a0001c0001t0006g0056a0001c0001t0006g0057a0001c0001t0006g0058 | 3 | HG02559.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1883-51C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 19/23 | chr8 | 123806029 | ||||||
| chr8:123806316
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032+87T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123806316 | ||||||
| chr8:123806391
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2032+162C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123806391 | ||||||
| chr8:123806510
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2032+281G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123806510 | ||||||
| chr8:123806541
|
A | G | 1 | a0001c0009t0002g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2032+312A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123806541 | ||||||
| chr8:123806879
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2032+650A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123806879 | ||||||
| chr8:123806901
|
CT | C | 43 | a0001c0001t0001g0119a0001c0001t0001g0143a0001c0001t0001g0184others(40): Show | 51 | HG00735.hp2 HG01099.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.2032+685delT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr8 | 123806901 | |||||
| chr8:123806931
|
T | G | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.2032+702T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123806931 | ||||||
| chr8:123807016
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2032+787T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123807016 | ||||||
| chr8:123807194
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2032+965T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123807194 | ||||||
| chr8:123807217
|
C | A | 1 | a0001c0007t0019g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2032+988C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123807217 | ||||||
| chr8:123807456
|
C | T | 1 | a0001c0010t0002g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033-816C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123807456 | ||||||
| chr8:123807480
|
C | CA | 70 | a0001c0001t0001g0152a0001c0001t0001g0155a0001c0001t0001g0160others(67): Show | 111 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(108): Show |
intron_variant | MODIFIER | c.2033-770dupA | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr8 | 123807480 | |||||
| chr8:123807480
|
C | CAA | 7 | a0001c0001t0002g0024a0001c0001t0002g0030a0001c0001t0003g0030others(4): Show | 7 | HG01109.hp1 HG01346.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2033-771_2033-770d others(4): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr8 | 123807480 | |||||
| chr8:123807480
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2033-777_2033-770d others(10): Show |
FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr8 | 123807480 | |||||
| chr8:123807518
|
A | G | 4 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0010t0002g0111others(1): Show | 4 | HG03195.hp1 HG03453.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2033-754A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123807518 | ||||||
| chr8:123807548
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2033-724G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123807548 | ||||||
| chr8:123807989
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2033-283A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123807989 | ||||||
| chr8:123808073
|
G | A | 1 | a0001c0001t0022g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2033-199G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123808073 | ||||||
| chr8:123808171
|
C | T | 36 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(33): Show | 44 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.2033-101C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123808171 | ||||||
| chr8:123808190
|
C | A | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2033-82C>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 20/23 | chr8 | 123808190 | ||||||
| chr8:123808470
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2137+94T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 21/23 | chr8 | 123808470 | ||||||
| chr8:123808675
|
C | T | 3 | a0001c0001t0006g0056a0001c0001t0006g0057a0001c0001t0006g0058 | 3 | HG02559.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2138-218C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 21/23 | chr8 | 123808675 | ||||||
| chr8:123809107
|
G | T | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2261+91G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809107 | ||||||
| chr8:123809250
|
A | C | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2261+234A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809250 | ||||||
| chr8:123809296
|
G | C | 41 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(38): Show | 49 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.2261+280G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809296 | ||||||
| chr8:123809330
|
A | G | 5 | a0001c0001t0002g0042a0001c0001t0002g0211a0001c0001t0003g0042others(2): Show | 5 | HG02922.hp1 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2261+314A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809330 | ||||||
| chr8:123809473
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(79): Show | 124 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(121): Show |
intron_variant | MODIFIER | c.2261+457G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809473 | ||||||
| chr8:123809644
|
A | G | 81 | a0001c0001t0001g0179a0001c0001t0002g0001a0001c0001t0002g0008others(78): Show | 123 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(120): Show |
intron_variant | MODIFIER | c.2261+628A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809644 | ||||||
| chr8:123809657
|
A | G | 1 | a0001c0010t0002g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2262-625A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809657 | ||||||
| chr8:123809693
|
A | C | 1 | a0001c0001t0015g0131 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2262-589A>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809693 | ||||||
| chr8:123809904
|
T | A | 65 | a0001c0001t0001g0179a0001c0001t0002g0001a0001c0001t0002g0008others(62): Show | 106 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.2262-378T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123809904 | ||||||
| chr8:123810042
|
T | C | 1 | a0001c0001t0016g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2262-240T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123810042 | ||||||
| chr8:123810058
|
C | T | 1 | a0001c0001t0016g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2262-224C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123810058 | ||||||
| chr8:123810059
|
G | A | 1 | a0001c0001t0002g0025 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2262-223G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123810059 | ||||||
| chr8:123810090
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2262-192G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123810090 | ||||||
| chr8:123810106
|
T | A | 1 | a0001c0001t0001g0200 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2262-176T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123810106 | ||||||
| chr8:123810264
|
C | T | 1 | a0001c0020t0021g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2262-18C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | chr8 | 123810264 | ||||||
| chr8:123810267
|
C | CTT | 7 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075others(4): Show | 10 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.2262-5_2262-4dupTT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr8 | 123810267 | |||||
| chr8:123810373
|
A | G | 1 | a0001c0002t0002g0075 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2331+22A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123810373 | ||||||
| chr8:123810467
|
T | A | 1 | a0001c0001t0024g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2331+116T>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123810467 | ||||||
| chr8:123810590
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0003g0069a0001c0001t0003g0071others(2): Show | 6 | HG01099.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2331+239G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123810590 | ||||||
| chr8:123810712
|
G | C | 1 | a0001c0001t0003g0012 | 3 | HG01168.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2331+361G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123810712 | ||||||
| chr8:123810729
|
C | T | 119 | a0001c0001t0001g0119a0001c0001t0001g0179a0001c0001t0002g0001others(116): Show | 169 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(166): Show |
intron_variant | MODIFIER | c.2331+378C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123810729 | ||||||
| chr8:123811024
|
A | G | 1 | a0001c0001t0006g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2331+673A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811024 | ||||||
| chr8:123811153
|
G | C | 1 | a0001c0001t0003g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2331+802G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811153 | ||||||
| chr8:123811283
|
G | A | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2331+932G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811283 | ||||||
| chr8:123811352
|
A | G | 10 | a0001c0002t0004g0006a0001c0002t0004g0059a0001c0002t0004g0060others(7): Show | 13 | HG01261.hp2 HG03942.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.2331+1001A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811352 | ||||||
| chr8:123811387
|
T | G | 1 | a0001c0002t0003g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2331+1036T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811387 | ||||||
| chr8:123811533
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2332-986G>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811533 | ||||||
| chr8:123811537
|
A | G | 5 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0091others(2): Show | 7 | HG01169.hp1 HG01175.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.2332-982A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811537 | ||||||
| chr8:123811694
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2332-825A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811694 | ||||||
| chr8:123811780
|
G | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18960.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2332-739G>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811780 | ||||||
| chr8:123811851
|
T | C | 1 | a0001c0001t0003g0193 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2332-668T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811851 | ||||||
| chr8:123811862
|
T | G | 1 | a0001c0002t0017g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2332-657T>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811862 | ||||||
| chr8:123811946
|
A | T | 1 | a0001c0001t0002g0013 | 3 | HG02647.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2332-573A>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123811946 | ||||||
| chr8:123812142
|
G | A | 1 | a0001c0001t0006g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2332-377G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123812142 | ||||||
| chr8:123812182
|
G | GT | 78 | a0001c0001t0001g0126a0001c0001t0001g0179a0001c0001t0001g0199others(75): Show | 120 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(117): Show |
intron_variant | MODIFIER | c.2332-322dupT | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr8 | 123812182 | |||||
| chr8:123812341
|
C | T | 77 | a0001c0001t0001g0179a0001c0001t0002g0001a0001c0001t0002g0008others(74): Show | 115 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(112): Show |
intron_variant | MODIFIER | c.2332-178C>T | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123812341 | ||||||
| chr8:123812390
|
G | A | 8 | a0001c0002t0002g0073a0001c0002t0002g0074a0001c0002t0002g0075others(5): Show | 11 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2332-129G>A | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123812390 | ||||||
| chr8:123812434
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2332-85A>G | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123812434 | ||||||
| chr8:123812491
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2332-28T>C | FAM91A1 | ENSG00000176853.16 | transcript | ENST00000334705.12 | protein_coding | 23/23 | chr8 | 123812491 |