Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 129685 |
|---|---|
| ensemblid | ENSG00000137413.17 |
| hgncid | 17300 |
| symbol | TAF8 |
| name | TATA-box binding protein associated factor 8 |
| refseq_nuc | NM_138572.3 |
| refseq_prot | NP_612639.2 |
| ensembl_nuc | ENST00000372977.8 |
| ensembl_prot | ENSP00000362068.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 42050524 |
| end | 42083272 |
| strand | + |
| ver | v1.2 |
| region | chr6:42050524-42083272 |
| region5000 | chr6:42045524-42088272 |
| regionname0 | TAF8_chr6_42050524_42083272 |
| regionname5000 | TAF8_chr6_42045524_42088272 |
| 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 | 1/1 | 310 | 454 | 96 | 80 | 214 | 18 | 44 | 166 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| 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 | 0/0 | 933 | 332 | 35 | 62 | 190 | 13 | 32 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| c0002 | 1/1 | 933 | 119 | 59 | 18 | 23 | 5 | 12 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| c0003 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| c0004 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| c0005 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| 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 | 0/0 | 5742 | 118 | 2 | 32 | 60 | 10 | 14 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0002 | 0/0 | 5751 | 43 | 0 | 13 | 27 | 0 | 3 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0003 | 0/0 | 5752 | 41 | 1 | 1 | 36 | 0 | 3 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0004 | 0/0 | 5745 | 35 | 5 | 11 | 11 | 4 | 4 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0005 | 0/0 | 5751 | 23 | 4 | 1 | 18 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0006 | 0/0 | 5751 | 19 | 3 | 6 | 3 | 2 | 5 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0007 | 0/0 | 5750 | 12 | 12 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0008 | 0/0 | 5742 | 10 | 1 | 3 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0009 | 0/0 | 5751 | 9 | 0 | 0 | 8 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0010 | 0/1 | 5748 | 8 | 3 | 1 | 1 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0011 | 0/0 | 5750 | 7 | 6 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0012 | 0/0 | 5751 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0013 | 0/0 | 5743 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0014 | 0/0 | 5746 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0015 | 0/0 | 5745 | 6 | 0 | 0 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0016 | 0/0 | 5742 | 5 | 5 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0017 | 0/0 | 5744 | 5 | 0 | 0 | 4 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0018 | 0/0 | 5744 | 5 | 0 | 0 | 5 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0019 | 0/0 | 5743 | 4 | 4 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0020 | 0/0 | 5736 | 4 | 0 | 0 | 4 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0021 | 0/0 | 5751 | 4 | 3 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0022 | 0/0 | 5741 | 3 | 0 | 0 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0023 | 0/0 | 5750 | 3 | 3 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0024 | 0/0 | 5752 | 3 | 3 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0025 | 0/0 | 5742 | 3 | 0 | 2 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0026 | 0/0 | 5744 | 3 | 0 | 1 | 0 | 1 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0027 | 0/0 | 5742 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0028 | 0/0 | 5744 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0029 | 0/0 | 5742 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0030 | 0/0 | 5744 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0031 | 0/0 | 5746 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0032 | 0/0 | 5743 | 2 | 0 | 1 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0033 | 0/0 | 5748 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0034 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0035 | 0/0 | 5752 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0036 | 0/0 | 5752 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0037 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0038 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0039 | 0/0 | 5752 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0040 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0041 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0042 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0043 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0044 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0045 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0046 | 0/0 | 5742 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0047 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0048 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0049 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0050 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0051 | 0/0 | 5751 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0052 | 0/0 | 5746 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0053 | 0/0 | 5747 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0054 | 0/0 | 5750 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0055 | 0/0 | 5742 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0056 | 0/0 | 5736 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0057 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0058 | 0/0 | 5742 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0059 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0060 | 0/0 | 5742 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0061 | 0/0 | 5752 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0062 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0063 | 0/0 | 5794 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0064 | 0/0 | 5747 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0065 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0066 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0067 | 0/0 | 5747 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0068 | 0/0 | 5741 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0069 | 0/0 | 5749 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0070 | 1/0 | 5746 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0071 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0072 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0073 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0074 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0075 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0076 | 0/0 | 5745 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0077 | 0/0 | 5746 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0078 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0079 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0080 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0081 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| t0082 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| 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 | 14 | 0 | 4 | 7 | 2 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0002 | 0/0 | 9 | 0 | 5 | 0 | 0 | 4 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0003 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0005 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0006 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0013 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0015 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0016 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0343 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| 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 | 0/0 | 933 | 332 | 35 | 62 | 190 | 13 | 32 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002 | 1/1 | 933 | 119 | 59 | 18 | 23 | 5 | 12 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0003 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0004 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0005 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6674 | 118 | 2 | 32 | 60 | 10 | 14 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0002 | 0/0 | 6683 | 43 | 0 | 13 | 27 | 0 | 3 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0003 | 0/0 | 6684 | 41 | 1 | 1 | 36 | 0 | 3 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0005 | 0/0 | 6683 | 23 | 4 | 1 | 18 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0006 | 0/0 | 6683 | 19 | 3 | 6 | 3 | 2 | 5 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0008 | 0/0 | 6674 | 10 | 1 | 3 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0009 | 0/0 | 6683 | 9 | 0 | 0 | 8 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0011 | 0/0 | 6682 | 7 | 6 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0012 | 0/0 | 6683 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0017 | 0/0 | 6676 | 5 | 0 | 0 | 4 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0018 | 0/0 | 6676 | 5 | 0 | 0 | 5 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0020 | 0/0 | 6668 | 4 | 0 | 0 | 4 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0022 | 0/0 | 6673 | 3 | 0 | 0 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0023 | 0/0 | 6682 | 3 | 3 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0024 | 0/0 | 6684 | 3 | 3 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0025 | 0/0 | 6674 | 3 | 0 | 2 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0029 | 0/0 | 6674 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0034 | 0/0 | 6683 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0035 | 0/0 | 6684 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0036 | 0/0 | 6684 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0037 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0038 | 0/0 | 6683 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0039 | 0/0 | 6684 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0046 | 0/0 | 6674 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0047 | 0/0 | 6673 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0048 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0049 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0050 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0051 | 0/0 | 6683 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0053 | 0/0 | 6679 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0054 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0055 | 0/0 | 6674 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0056 | 0/0 | 6668 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0058 | 0/0 | 6674 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0059 | 0/0 | 6680 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0060 | 0/0 | 6674 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0061 | 0/0 | 6684 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0062 | 0/0 | 6683 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0063 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0064 | 0/0 | 6679 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0065 | 0/0 | 6683 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0066 | 0/0 | 6683 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0067 | 0/0 | 6679 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0068 | 0/0 | 6673 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0001t0082 | 0/0 | 6680 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0004 | 0/0 | 6677 | 35 | 5 | 11 | 11 | 4 | 4 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0007 | 0/0 | 6682 | 12 | 12 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0010 | 0/1 | 6680 | 8 | 3 | 1 | 1 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0013 | 0/0 | 6675 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0014 | 0/0 | 6678 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0015 | 0/0 | 6677 | 6 | 0 | 0 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0016 | 0/0 | 6674 | 5 | 5 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0019 | 0/0 | 6675 | 4 | 4 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0021 | 0/0 | 6683 | 4 | 3 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0026 | 0/0 | 6676 | 3 | 0 | 1 | 0 | 1 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0027 | 0/0 | 6674 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0028 | 0/0 | 6676 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0030 | 0/0 | 6676 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0031 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0032 | 0/0 | 6675 | 2 | 0 | 1 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0033 | 0/0 | 6680 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0040 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0041 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0042 | 0/0 | 6682 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0043 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0044 | 0/0 | 6677 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0045 | 0/0 | 6677 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0069 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0070 | 1/0 | 6678 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0071 | 0/0 | 6680 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0072 | 0/0 | 6682 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0073 | 0/0 | 6677 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0074 | 0/0 | 6677 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0075 | 0/0 | 6676 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0076 | 0/0 | 6677 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0077 | 0/0 | 6678 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0078 | 0/0 | 6677 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0079 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0080 | 0/0 | 6680 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0002t0081 | 0/0 | 6680 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0003t0052 | 0/0 | 6678 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0004t0057 | 0/0 | 6674 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| a0001c0005t0031 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | copy fasta | chr6 | 42045524 | 42088272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 3 | 2 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0015 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0008g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0008g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0011g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0011g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0012g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0012g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0012g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0012g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0012g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0017g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0017g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0017g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0018g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0018g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0020g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0020g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0020g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0022g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0022g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0022g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0023g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0023g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0023g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0024g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0024g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0024g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0025g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0025g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0025g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0029g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0034g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0035g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0036g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0037g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0038g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0039g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0046g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0047g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0048g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0049g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0050g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0051g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0053g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0054g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0055g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0056g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0058g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0059g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0060g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0061g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0062g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0063g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0064g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0065g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0066g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0067g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0068g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0001t0082g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0013g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0014g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0015g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0015g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0015g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0015g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0015g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0016g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0016g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0019g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0019g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0019g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0021g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0021g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0021g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0026g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0026g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0026g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0027g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0027g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0028g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0028g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0030g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0030g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0031g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0032g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0032g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0033g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0033g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0040g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0041g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0042g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0043g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0044g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0045g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0069g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0070g0343 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0071g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0072g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0073g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0074g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0075g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0076g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0077g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0078g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0079g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0080g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0002t0081g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0003t0052g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0004t0057g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| a0001c0005t0031g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0004 | g0037 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0101 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0019 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0242 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00280 | hp2 | a0001 | c0002 | t0026 | g0301 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0070 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0075 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00408 | hp2 | a0001 | c0002 | t0078 | g0286 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0309 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0322 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00438 | hp2 | a0001 | c0001 | t0018 | g0009 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00544 | hp2 | a0001 | c0001 | t0018 | g0009 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00597 | hp1 | a0001 | c0001 | t0056 | g0297 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00621 | hp1 | a0001 | c0001 | t0009 | g0190 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0168 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0030 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00733 | hp1 | a0001 | c0001 | t0025 | g0001 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00741 | hp1 | a0001 | c0002 | t0032 | g0170 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG00741 | hp2 | a0001 | c0002 | t0021 | g0151 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01081 | hp2 | a0001 | c0001 | t0061 | g0156 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0073 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0058 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01169 | hp1 | a0001 | c0002 | t0010 | g0175 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0078 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0183 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01175 | hp2 | a0001 | c0002 | t0080 | g0268 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0025 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0065 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0267 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01243 | hp2 | a0001 | c0002 | t0076 | g0300 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0150 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0173 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01361 | hp1 | a0001 | c0002 | t0004 | g0019 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01361 | hp2 | a0001 | c0001 | t0025 | g0014 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0307 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01891 | hp1 | a0001 | c0002 | t0027 | g0236 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0311 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01928 | hp1 | a0001 | c0001 | t0058 | g0006 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0025 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01934 | hp2 | a0001 | c0002 | t0033 | g0265 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0196 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0018 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0191 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0287 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01978 | hp2 | a0001 | c0002 | t0004 | g0289 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01981 | hp1 | a0001 | c0001 | t0068 | g0171 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02055 | hp2 | a0001 | c0004 | t0057 | g0182 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02056 | hp2 | a0001 | c0001 | t0009 | g0127 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0080 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02145 | hp1 | a0001 | c0001 | t0023 | g0333 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02145 | hp2 | a0001 | c0002 | t0073 | g0187 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02155 | hp2 | a0001 | c0002 | t0004 | g0313 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02165 | hp2 | a0001 | c0001 | t0017 | g0009 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02257 | hp2 | a0001 | c0002 | t0042 | g0164 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0154 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02258 | hp2 | a0001 | c0002 | t0021 | g0129 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0279 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02280 | hp1 | a0001 | c0002 | t0007 | g0261 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02280 | hp2 | a0001 | c0001 | t0038 | g0298 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0278 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02451 | hp1 | a0001 | c0002 | t0030 | g0136 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02451 | hp2 | a0001 | c0002 | t0081 | g0238 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02572 | hp1 | a0001 | c0001 | t0023 | g0332 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02572 | hp2 | a0001 | c0001 | t0062 | g0159 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02602 | hp1 | a0001 | c0002 | t0026 | g0181 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0323 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02615 | hp2 | a0001 | c0002 | t0079 | g0253 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02622 | hp1 | a0001 | c0002 | t0043 | g0340 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02622 | hp2 | a0001 | c0002 | t0010 | g0147 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02630 | hp1 | a0001 | c0002 | t0072 | g0338 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02630 | hp2 | a0001 | c0001 | t0082 | g0272 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02647 | hp1 | a0001 | c0002 | t0013 | g0255 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0293 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0157 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02717 | hp2 | a0001 | c0002 | t0013 | g0148 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02723 | hp1 | a0001 | c0002 | t0033 | g0264 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0345 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0139 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02738 | hp1 | a0001 | c0001 | t0066 | g0282 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02809 | hp2 | a0001 | c0002 | t0019 | g0260 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02886 | hp1 | a0001 | c0001 | t0064 | g0188 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0339 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02895 | hp1 | a0001 | c0002 | t0007 | g0273 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02895 | hp2 | a0001 | c0002 | t0013 | g0248 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02896 | hp1 | a0001 | c0002 | t0010 | g0149 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02896 | hp2 | a0001 | c0002 | t0007 | g0033 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02922 | hp1 | a0001 | c0003 | t0052 | g0269 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0230 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02965 | hp1 | a0001 | c0002 | t0071 | g0344 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02965 | hp2 | a0001 | c0002 | t0007 | g0155 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02970 | hp1 | a0001 | c0002 | t0007 | g0085 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0296 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02976 | hp1 | a0001 | c0002 | t0014 | g0010 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02976 | hp2 | a0001 | c0002 | t0016 | g0130 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0037 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03041 | hp2 | a0001 | c0002 | t0014 | g0010 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03098 | hp2 | a0001 | c0002 | t0013 | g0145 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03130 | hp1 | a0001 | c0002 | t0030 | g0346 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03130 | hp2 | a0001 | c0002 | t0014 | g0010 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03139 | hp1 | a0001 | c0002 | t0019 | g0161 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03139 | hp2 | a0001 | c0002 | t0027 | g0233 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0237 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0033 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0229 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03209 | hp2 | a0001 | c0001 | t0067 | g0341 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0334 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03225 | hp2 | a0001 | c0002 | t0016 | g0160 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03239 | hp1 | a0001 | c0002 | t0010 | g0176 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03239 | hp2 | a0001 | c0002 | t0074 | g0114 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03453 | hp1 | a0001 | c0002 | t0007 | g0259 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0337 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03486 | hp1 | a0001 | c0002 | t0016 | g0275 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03490 | hp1 | a0001 | c0002 | t0075 | g0206 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03490 | hp2 | a0001 | c0001 | t0029 | g0002 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03491 | hp1 | a0001 | c0002 | t0032 | g0169 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03492 | hp2 | a0001 | c0001 | t0029 | g0002 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03516 | hp1 | a0001 | c0002 | t0010 | g0266 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03540 | hp1 | a0001 | c0002 | t0016 | g0274 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0263 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03579 | hp1 | a0001 | c0002 | t0041 | g0232 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03579 | hp2 | a0001 | c0002 | t0016 | g0158 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03654 | hp1 | a0001 | c0001 | t0035 | g0280 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0319 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03688 | hp2 | a0001 | c0002 | t0044 | g0252 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03710 | hp1 | a0001 | c0002 | t0004 | g0285 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0036 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03831 | hp1 | a0001 | c0002 | t0010 | g0122 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0284 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03942 | hp1 | a0001 | c0001 | t0053 | g0087 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04115 | hp2 | a0001 | c0002 | t0077 | g0207 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0202 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04228 | hp1 | a0001 | c0001 | t0017 | g0283 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18522 | hp1 | a0001 | c0002 | t0019 | g0162 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18522 | hp2 | a0001 | c0002 | t0069 | g0239 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18747 | hp1 | a0001 | c0001 | t0018 | g0005 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0310 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0235 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18941 | hp1 | a0001 | c0001 | t0022 | g0270 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18944 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18945 | hp1 | a0001 | c0002 | t0015 | g0056 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18952 | hp2 | a0001 | c0001 | t0020 | g0051 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18956 | hp2 | a0001 | c0001 | t0009 | g0027 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18957 | hp1 | a0001 | c0001 | t0022 | g0016 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18957 | hp2 | a0001 | c0001 | t0022 | g0121 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18959 | hp2 | a0001 | c0002 | t0015 | g0195 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18961 | hp1 | a0001 | c0001 | t0037 | g0290 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18961 | hp2 | a0001 | c0001 | t0063 | g0247 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0251 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0204 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18963 | hp2 | a0001 | c0001 | t0054 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0089 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18966 | hp2 | a0001 | c0002 | t0015 | g0257 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18967 | hp1 | a0001 | c0001 | t0017 | g0112 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18969 | hp1 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18969 | hp2 | a0001 | c0001 | t0020 | g0034 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18973 | hp2 | a0001 | c0002 | t0015 | g0241 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18981 | hp2 | a0001 | c0001 | t0034 | g0043 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18985 | hp2 | a0001 | c0002 | t0015 | g0243 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18986 | hp2 | a0001 | c0001 | t0050 | g0312 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18988 | hp1 | a0001 | c0002 | t0045 | g0028 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0321 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18989 | hp1 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18990 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18991 | hp1 | a0001 | c0002 | t0004 | g0325 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18992 | hp2 | a0001 | c0001 | t0060 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18993 | hp1 | a0001 | c0001 | t0009 | g0246 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18994 | hp2 | a0001 | c0002 | t0010 | g0185 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18998 | hp1 | a0001 | c0001 | t0049 | g0117 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19000 | hp2 | a0001 | c0002 | t0031 | g0291 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19004 | hp1 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19006 | hp2 | a0001 | c0001 | t0055 | g0055 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19007 | hp1 | a0001 | c0002 | t0004 | g0299 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19009 | hp2 | a0001 | c0002 | t0004 | g0326 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19012 | hp1 | a0001 | c0002 | t0004 | g0209 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19030 | hp1 | a0001 | c0002 | t0021 | g0023 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0133 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19043 | hp1 | a0001 | c0001 | t0024 | g0314 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19043 | hp2 | a0001 | c0002 | t0013 | g0146 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19056 | hp1 | a0001 | c0005 | t0031 | g0118 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19056 | hp2 | a0001 | c0001 | t0048 | g0178 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19057 | hp2 | a0001 | c0002 | t0028 | g0258 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19058 | hp1 | a0001 | c0002 | t0028 | g0063 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19060 | hp1 | a0001 | c0001 | t0020 | g0053 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19062 | hp2 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19063 | hp1 | a0001 | c0001 | t0036 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19066 | hp1 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19067 | hp1 | a0001 | c0001 | t0018 | g0009 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19068 | hp1 | a0001 | c0001 | t0020 | g0034 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19070 | hp1 | a0001 | c0002 | t0015 | g0028 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19072 | hp2 | a0001 | c0001 | t0047 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19076 | hp1 | a0001 | c0001 | t0008 | g0331 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19077 | hp2 | a0001 | c0001 | t0059 | g0107 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19080 | hp2 | a0001 | c0001 | t0051 | g0048 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19086 | hp1 | a0001 | c0001 | t0046 | g0224 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19086 | hp2 | a0001 | c0001 | t0009 | g0027 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0254 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19090 | hp2 | a0001 | c0001 | t0039 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19240 | hp1 | a0001 | c0002 | t0014 | g0010 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA19240 | hp2 | a0001 | c0001 | t0023 | g0131 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ASW | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0240 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20905 | hp2 | a0001 | c0001 | t0025 | g0005 | SAS | GIH | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01123 | hp1 | a0001 | c0002 | t0026 | g0302 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02109 | hp1 | a0001 | c0002 | t0014 | g0010 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02109 | hp2 | a0001 | c0002 | t0040 | g0231 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0030 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02486 | hp2 | a0001 | c0002 | t0007 | g0180 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02559 | hp1 | a0001 | c0002 | t0021 | g0023 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG02559 | hp2 | a0001 | c0002 | t0013 | g0342 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0336 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG03471 | hp2 | a0001 | c0002 | t0007 | g0134 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG06807 | hp1 | a0001 | c0002 | t0014 | g0163 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| HG06807 | hp2 | a0001 | c0002 | t0019 | g0234 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0201 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0276 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA21309 | hp1 | a0001 | c0001 | t0065 | g0152 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| NA21309 | hp2 | a0001 | c0002 | t0007 | g0347 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0010 | g0174 | REF | REF | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0070 | g0343 | REF | REF | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:42050559
|
C | T | 1 | a0001c0005 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.18C>T | p.Ala6Ala | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/9 | 36/6678 | 18/933 | 6/310 | chr6 | 42050559 | ||
| chr6:42050574
|
T | G | 1 | a0001c0003 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.33T>G | p.Gly11Gly | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/9 | 51/6678 | 33/933 | 11/310 | chr6 | 42050574 | ||
| chr6:42057513
|
G | A | 1 | a0001c0004 | 1 | HG02055.hp2 | splice_region_variant&synonymous_variant | LOW | c.489G>A | p.Pro163Pro | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/9 | 507/6678 | 489/933 | 163/310 | chr6 | 42057513 | ||
| chr6:42077207
|
G | A | 3 | a0001c0001a0001c0003a0001c0004 | 334 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(331): Show |
synonymous_variant | LOW | c.888G>A | p.Arg296Arg | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/9 | 906/6678 | 888/933 | 296/310 | chr6 | 42077207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:42077626
|
G | A | 9 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(6): Show | 72 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*81G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 81 | chr6 | 42077626 | |||||
| chr6:42077633
|
C | T | 1 | a0001c0001t0082 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 88 | chr6 | 42077633 | |||||
| chr6:42077758
|
T | A | 9 | a0001c0002t0013a0001c0002t0014a0001c0002t0016others(6): Show | 27 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*213T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 213 | chr6 | 42077758 | |||||
| chr6:42077792
|
A | G | 1 | a0001c0002t0043 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 247 | chr6 | 42077792 | |||||
| chr6:42077951
|
TC | T | 1 | a0001c0001t0011 | 7 | HG00642.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*407delC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 407 | chr6 | 42077951 | |||||
| chr6:42078233
|
G | C | 1 | a0001c0002t0044 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*688G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 688 | chr6 | 42078233 | |||||
| chr6:42078304
|
G | A | 4 | a0001c0002t0015a0001c0002t0028a0001c0002t0044others(1): Show | 10 | HG03688.hp2 NA18945.hp1 NA18959.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*759G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 759 | chr6 | 42078304 | |||||
| chr6:42078337
|
A | T | 5 | a0001c0002t0010a0001c0002t0026a0001c0002t0033others(2): Show | 15 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*792A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 792 | chr6 | 42078337 | |||||
| chr6:42078341
|
G | A | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | 363 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*796G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 796 | chr6 | 42078341 | |||||
| chr6:42078347
|
CTG | C | 5 | a0001c0002t0010a0001c0002t0026a0001c0002t0033others(2): Show | 15 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*804_*805delGT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 804 | INFO_REALIGN_3_PRIME | chr6 | 42078347 | ||||
| chr6:42078512
|
C | T | 2 | a0001c0002t0032a0001c0002t0079 | 3 | HG00741.hp1 HG02615.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*967C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 967 | chr6 | 42078512 | |||||
| chr6:42078622
|
C | G | 2 | a0001c0001t0025a0001c0001t0068 | 4 | HG00733.hp1 HG01361.hp2 HG01981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1077C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1077 | chr6 | 42078622 | |||||
| chr6:42078631
|
G | C | 2 | a0001c0002t0019a0001c0002t0040 | 5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1086G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1086 | chr6 | 42078631 | |||||
| chr6:42078787
|
A | G | 1 | a0001c0002t0078 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1242A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1242 | chr6 | 42078787 | |||||
| chr6:42078845
|
C | T | 1 | a0001c0001t0008 | 10 | HG01943.hp2 HG01952.hp2 HG02148.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1300C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1300 | chr6 | 42078845 | |||||
| chr6:42078860
|
G | A | 1 | a0001c0002t0027 | 2 | HG01891.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1315G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1315 | chr6 | 42078860 | |||||
| chr6:42078919
|
C | T | 13 | a0001c0001t0018a0001c0002t0004a0001c0002t0015others(10): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1374C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1374 | chr6 | 42078919 | |||||
| chr6:42078949
|
C | T | 11 | a0001c0001t0005a0001c0001t0011a0001c0001t0023others(8): Show | 43 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1404C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1404 | chr6 | 42078949 | |||||
| chr6:42078950
|
C | T | 11 | a0001c0001t0005a0001c0001t0011a0001c0001t0023others(8): Show | 43 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1405C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1405 | chr6 | 42078950 | |||||
| chr6:42078978
|
C | T | 12 | a0001c0002t0004a0001c0002t0015a0001c0002t0028others(9): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1433C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1433 | chr6 | 42078978 | |||||
| chr6:42078979
|
G | A | 1 | a0001c0002t0041 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1434G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1434 | chr6 | 42078979 | |||||
| chr6:42079009
|
C | T | 1 | a0001c0002t0072 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1464C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1464 | chr6 | 42079009 | |||||
| chr6:42079110
|
A | G | 1 | a0001c0002t0041 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1565A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1565 | chr6 | 42079110 | |||||
| chr6:42079279
|
G | A | 1 | a0001c0001t0061 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1734G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1734 | chr6 | 42079279 | |||||
| chr6:42079433
|
T | G | 1 | a0001c0001t0046 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1888 | chr6 | 42079433 | |||||
| chr6:42079568
|
C | A | 1 | a0001c0002t0074 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2023C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2023 | chr6 | 42079568 | |||||
| chr6:42079656
|
G | A | 1 | a0001c0001t0047 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2111 | chr6 | 42079656 | |||||
| chr6:42079684
|
G | T | 2 | a0001c0002t0019a0001c0002t0040 | 5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2139G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2139 | chr6 | 42079684 | |||||
| chr6:42079697
|
C | T | 1 | a0001c0002t0073 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2152C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2152 | chr6 | 42079697 | |||||
| chr6:42079715
|
A | AT | 20 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(17): Show | 163 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*2188dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2189 | INFO_REALIGN_3_PRIME | chr6 | 42079715 | ||||
| chr6:42079715
|
AT | A | 12 | a0001c0001t0023a0001c0001t0034a0001c0001t0048others(9): Show | 25 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2188delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2188 | INFO_REALIGN_3_PRIME | chr6 | 42079715 | ||||
| chr6:42079741
|
A | G | 8 | a0001c0002t0013a0001c0002t0016a0001c0002t0019others(5): Show | 22 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2196A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2196 | chr6 | 42079741 | |||||
| chr6:42079743
|
G | A | 1 | a0001c0001t0061 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2198 | chr6 | 42079743 | |||||
| chr6:42079834
|
G | A | 8 | a0001c0002t0013a0001c0002t0016a0001c0002t0019others(5): Show | 22 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2289G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2289 | chr6 | 42079834 | |||||
| chr6:42079852
|
C | T | 1 | a0001c0001t0060 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2307C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2307 | chr6 | 42079852 | |||||
| chr6:42079904
|
G | A | 1 | a0001c0002t0013 | 6 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2359G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2359 | chr6 | 42079904 | |||||
| chr6:42079995
|
T | TA | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(17): Show | 202 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*2463dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2464 | INFO_REALIGN_3_PRIME | chr6 | 42079995 | ||||
| chr6:42079995
|
TA | T | 25 | a0001c0001t0050a0001c0001t0054a0001c0002t0004others(22): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2463delA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2463 | INFO_REALIGN_3_PRIME | chr6 | 42079995 | ||||
| chr6:42080009
|
T | A | 1 | a0001c0001t0055 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2464 | chr6 | 42080009 | |||||
| chr6:42080075
|
C | T | 1 | a0001c0002t0021 | 4 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2530C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2530 | chr6 | 42080075 | |||||
| chr6:42080095
|
A | G | 1 | a0001c0001t0082 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2550 | chr6 | 42080095 | |||||
| chr6:42080129
|
A | G | 1 | a0001c0001t0067 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2584A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2584 | chr6 | 42080129 | |||||
| chr6:42080131
|
C | T | 2 | a0001c0002t0013a0001c0002t0041 | 7 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2586C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2586 | chr6 | 42080131 | |||||
| chr6:42080177
|
C | T | 1 | a0001c0002t0033 | 2 | HG01934.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2632C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2632 | chr6 | 42080177 | |||||
| chr6:42080256
|
G | T | 16 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(13): Show | 158 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*2711G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2711 | chr6 | 42080256 | |||||
| chr6:42080308
|
A | C | 2 | a0001c0002t0016a0001c0002t0027 | 7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2763A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2763 | chr6 | 42080308 | |||||
| chr6:42080372
|
T | C | 1 | a0001c0002t0041 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2827 | chr6 | 42080372 | |||||
| chr6:42080373
|
C | CT | 3 | a0001c0002t0021a0001c0002t0031a0001c0005t0031 | 6 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2844dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2845 | INFO_REALIGN_3_PRIME | chr6 | 42080373 | ||||
| chr6:42080376
|
T | TTC | 2 | a0001c0002t0013a0001c0002t0041 | 7 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2832_*2833insCT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2833 | INFO_REALIGN_3_PRIME | chr6 | 42080376 | ||||
| chr6:42080377
|
T | TC | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | 353 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*2832_*2833insC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2833 | chr6 | 42080377 | |||||
| chr6:42080378
|
T | C | 2 | a0001c0001t0037a0001c0001t0047 | 2 | NA18961.hp1 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2833T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2833 | chr6 | 42080378 | |||||
| chr6:42080418
|
G | A | 1 | a0001c0001t0051 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2873G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2873 | chr6 | 42080418 | |||||
| chr6:42080596
|
G | A | 1 | a0001c0002t0076 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3051G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3051 | chr6 | 42080596 | |||||
| chr6:42080638
|
T | C | 1 | a0001c0001t0062 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3093T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3093 | chr6 | 42080638 | |||||
| chr6:42080844
|
C | T | 1 | a0001c0002t0081 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3299C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3299 | chr6 | 42080844 | |||||
| chr6:42080923
|
A | G | 1 | a0001c0001t0066 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3378A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3378 | chr6 | 42080923 | |||||
| chr6:42080952
|
A | G | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(33): Show | 195 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*3407A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3407 | chr6 | 42080952 | |||||
| chr6:42081006
|
A | G | 1 | a0001c0001t0067 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3461A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3461 | chr6 | 42081006 | |||||
| chr6:42081048
|
TAGAG | T | 2 | a0001c0002t0032a0001c0002t0079 | 3 | HG00741.hp1 HG02615.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3506_*3509delAGAG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3506 | INFO_REALIGN_3_PRIME | chr6 | 42081048 | ||||
| chr6:42081054
|
G | GCAAAATA others(36): Show |
1 | a0001c0001t0063 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3511_*3553dupAAAA others(39): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3554 | INFO_REALIGN_3_PRIME | chr6 | 42081054 | ||||
| chr6:42081105
|
G | A | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 361 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*3560G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3560 | chr6 | 42081105 | |||||
| chr6:42081138
|
C | G | 1 | a0001c0002t0021 | 4 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3593C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3593 | chr6 | 42081138 | |||||
| chr6:42081170
|
A | AGT | 5 | a0001c0002t0014a0001c0002t0032a0001c0002t0071others(2): Show | 11 | HG00741.hp1 HG02109.hp1 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3645_*3646dupTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3647 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | ||||
| chr6:42081170
|
A | AGTGT | 10 | a0001c0001t0082a0001c0002t0007a0001c0002t0010others(7): Show | 32 | HG00741.hp2 HG01169.hp1 HG01175.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3643_*3646dupTGTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3647 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | ||||
| chr6:42081170
|
AGT | A | 2 | a0001c0001t0017a0001c0001t0018 | 10 | HG00438.hp2 HG00544.hp2 HG02165.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3645_*3646delTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3645 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | ||||
| chr6:42081170
|
AGTGT | A | 12 | a0001c0001t0001a0001c0001t0008a0001c0001t0022others(9): Show | 143 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3643_*3646delTGTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3643 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | ||||
| chr6:42081170
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0020a0001c0001t0056 | 5 | HG00597.hp1 NA18952.hp2 NA18969.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3637_*3646delTGTG others(6): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3637 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | ||||
| chr6:42081190
|
T | TGTGC | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(22): Show | 170 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*3646_*3647insTGCG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3647 | INFO_REALIGN_3_PRIME | chr6 | 42081190 | ||||
| chr6:42081204
|
T | C | 11 | a0001c0001t0005a0001c0001t0011a0001c0001t0023others(8): Show | 43 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3659T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3659 | chr6 | 42081204 | |||||
| chr6:42081220
|
G | A | 1 | a0001c0002t0080 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3675G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3675 | chr6 | 42081220 | |||||
| chr6:42081221
|
C | T | 1 | a0001c0001t0036 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3676C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3676 | chr6 | 42081221 | |||||
| chr6:42081270
|
G | A | 2 | a0001c0002t0016a0001c0002t0027 | 7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3725G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3725 | chr6 | 42081270 | |||||
| chr6:42081325
|
TACC | T | 27 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(24): Show | 188 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*3792_*3794delCAC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3792 | INFO_REALIGN_3_PRIME | chr6 | 42081325 | ||||
| chr6:42081332
|
A | T | 1 | a0001c0001t0058 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3787A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3787 | chr6 | 42081332 | |||||
| chr6:42081395
|
G | A | 1 | a0001c0001t0035 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3850G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3850 | chr6 | 42081395 | |||||
| chr6:42081445
|
C | T | 26 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(23): Show | 186 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*3900C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3900 | chr6 | 42081445 | |||||
| chr6:42081446
|
G | A | 1 | a0001c0001t0065 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3901G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3901 | chr6 | 42081446 | |||||
| chr6:42081454
|
C | T | 1 | a0001c0002t0043 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3909C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3909 | chr6 | 42081454 | |||||
| chr6:42081470
|
G | A | 1 | a0001c0001t0056 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3925G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3925 | chr6 | 42081470 | |||||
| chr6:42081525
|
C | T | 2 | a0001c0002t0016a0001c0002t0027 | 7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3980C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3980 | chr6 | 42081525 | |||||
| chr6:42081725
|
T | C | 12 | a0001c0001t0048a0001c0002t0007a0001c0002t0010others(9): Show | 36 | HG00280.hp2 HG00741.hp2 HG01123.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4180T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4180 | chr6 | 42081725 | |||||
| chr6:42081738
|
C | T | 1 | a0001c0001t0012 | 6 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4193C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4193 | chr6 | 42081738 | |||||
| chr6:42081797
|
C | T | 19 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(16): Show | 166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4252C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4252 | chr6 | 42081797 | |||||
| chr6:42081860
|
T | G | 19 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(16): Show | 166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4315T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4315 | chr6 | 42081860 | |||||
| chr6:42081868
|
C | T | 1 | a0001c0002t0079 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4323C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4323 | chr6 | 42081868 | |||||
| chr6:42081869
|
G | A | 2 | a0001c0002t0019a0001c0002t0040 | 5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4324G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4324 | chr6 | 42081869 | |||||
| chr6:42082007
|
T | C | 1 | a0001c0002t0043 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4462T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4462 | chr6 | 42082007 | |||||
| chr6:42082045
|
A | G | 1 | a0001c0001t0029 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4500A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4500 | chr6 | 42082045 | |||||
| chr6:42082126
|
C | T | 1 | a0001c0004t0057 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4581C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4581 | chr6 | 42082126 | |||||
| chr6:42082162
|
G | C | 26 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(23): Show | 186 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*4617G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4617 | chr6 | 42082162 | |||||
| chr6:42082428
|
T | C | 1 | a0001c0002t0019 | 4 | HG02809.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4883T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4883 | chr6 | 42082428 | |||||
| chr6:42082432
|
G | A | 19 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(16): Show | 166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4887G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4887 | chr6 | 42082432 | |||||
| chr6:42082478
|
A | G | 3 | a0001c0002t0019a0001c0002t0040a0001c0002t0043 | 6 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4933A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4933 | chr6 | 42082478 | |||||
| chr6:42082485
|
T | C | 2 | a0001c0002t0016a0001c0002t0027 | 7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4940T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4940 | chr6 | 42082485 | |||||
| chr6:42082621
|
G | C | 8 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(5): Show | 71 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*5076G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5076 | chr6 | 42082621 | |||||
| chr6:42082632
|
C | A | 1 | a0001c0001t0009 | 9 | HG00323.hp1 HG00621.hp1 HG02056.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5087C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5087 | chr6 | 42082632 | |||||
| chr6:42082682
|
T | C | 1 | a0001c0001t0061 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5137T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5137 | chr6 | 42082682 | |||||
| chr6:42082692
|
G | T | 1 | a0001c0004t0057 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5147G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5147 | chr6 | 42082692 | |||||
| chr6:42082882
|
A | G | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | 360 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(357): Show |
3_prime_UTR_variant | MODIFIER | c.*5337A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5337 | chr6 | 42082882 | |||||
| chr6:42082967
|
T | C | 1 | a0001c0002t0041 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5422T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5422 | chr6 | 42082967 | |||||
| chr6:42083085
|
C | T | 8 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(5): Show | 71 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*5540C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5540 | chr6 | 42083085 | |||||
| chr6:42083188
|
A | C | 1 | a0001c0002t0043 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5643A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5643 | chr6 | 42083188 | |||||
| chr6:42083259
|
T | C | 19 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(16): Show | 166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*5714T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5714 | chr6 | 42083259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:42050611
|
G | T | 1 | a0001c0001t0001g0348 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.45+25G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050611 | ||||||
| chr6:42050683
|
C | G | 1 | a0001c0002t0007g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+97C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050683 | ||||||
| chr6:42050794
|
C | T | 3 | a0001c0001t0012g0345a0001c0002t0030g0346a0001c0002t0071g0344 | 3 | HG02723.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.45+208C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050794 | ||||||
| chr6:42050902
|
T | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0042others(49): Show | 66 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+316T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050902 | ||||||
| chr6:42050915
|
T | G | 1 | a0001c0002t0007g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.45+329T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050915 | ||||||
| chr6:42051140
|
T | C | 355 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(352): Show | 443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
intron_variant | MODIFIER | c.46-217T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42051140 | ||||||
| chr6:42051145
|
G | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.46-212G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42051145 | ||||||
| chr6:42051168
|
T | G | 1 | a0001c0001t0009g0040 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.46-189T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42051168 | ||||||
| chr6:42051625
|
G | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0288a0001c0001t0017g0283others(10): Show | 14 | HG00408.hp2 HG01975.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+112G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051625 | ||||||
| chr6:42051790
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0042others(49): Show | 66 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.202+277G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051790 | ||||||
| chr6:42051834
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.202+321C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051834 | ||||||
| chr6:42051884
|
T | G | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.202+371T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051884 | ||||||
| chr6:42052144
|
G | GCTCACTT others(11): Show |
1 | a0001c0001t0001g0128 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+631_202+632ins others(18): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052144 | ||||||
| chr6:42052146
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+633G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052146 | ||||||
| chr6:42052147
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+634A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052147 | ||||||
| chr6:42052148
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+635G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052148 | ||||||
| chr6:42052153
|
A | G | 1 | a0001c0001t0003g0277 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202+640A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052153 | ||||||
| chr6:42052317
|
G | GC | 24 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0132others(21): Show | 27 | HG00099.hp2 HG00408.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.202+815dupC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42052317 | |||||
| chr6:42052317
|
GC | G | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(131): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.202+815delC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42052317 | |||||
| chr6:42052318
|
C | CG | 5 | a0001c0001t0011g0276a0001c0001t0082g0272a0001c0002t0007g0273others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.202+805_202+806ins others(1): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052318 | ||||||
| chr6:42052328
|
C | CTT | 9 | a0001c0001t0012g0230a0001c0002t0004g0235a0001c0002t0004g0237others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+825_202+826dup others(2): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42052328 | |||||
| chr6:42052558
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0005g0292 | 3 | HG00558.hp1 NA18978.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.202+1045G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052558 | ||||||
| chr6:42052725
|
T | G | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1212T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052725 | ||||||
| chr6:42052727
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1214G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052727 | ||||||
| chr6:42052738
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1225G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052738 | ||||||
| chr6:42052802
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1289G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052802 | ||||||
| chr6:42052806
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1293G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052806 | ||||||
| chr6:42052814
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0137others(58): Show | 80 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.202+1301C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052814 | ||||||
| chr6:42052829
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1316G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052829 | ||||||
| chr6:42052856
|
G | A | 1 | a0001c0002t0007g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+1343G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052856 | ||||||
| chr6:42052864
|
T | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1351T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052864 | ||||||
| chr6:42052865
|
A | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1352A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052865 | ||||||
| chr6:42052873
|
C | G | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1360C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052873 | ||||||
| chr6:42052878
|
G | C | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1365G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052878 | ||||||
| chr6:42052879
|
G | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1366G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052879 | ||||||
| chr6:42052883
|
A | G | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1370A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052883 | ||||||
| chr6:42052884
|
T | G | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1371T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052884 | ||||||
| chr6:42052885
|
T | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1372T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052885 | ||||||
| chr6:42052965
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.202+1452G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052965 | ||||||
| chr6:42053067
|
C | T | 1 | a0001c0001t0001g0335 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.202+1554C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053067 | ||||||
| chr6:42053138
|
G | T | 1 | a0001c0001t0064g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.202+1625G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053138 | ||||||
| chr6:42053328
|
C | T | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.202+1815C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053328 | ||||||
| chr6:42053437
|
C | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(114): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.202+1924C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053437 | ||||||
| chr6:42053444
|
A | G | 14 | a0001c0001t0011g0276a0001c0001t0082g0272a0001c0002t0004g0235others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+1931A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053444 | ||||||
| chr6:42053565
|
CA | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(143): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.203-1953delA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42053565 | |||||
| chr6:42053565
|
CAA | C | 49 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(46): Show | 64 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-1954_203-1953d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42053565 | |||||
| chr6:42053565
|
CAAAAAAA others(7): Show |
C | 8 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(5): Show | 8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.203-1956_203-1943d others(16): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42053565 | |||||
| chr6:42053583
|
A | G | 1 | a0001c0001t0002g0022 | 2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.203-1948A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053583 | ||||||
| chr6:42053618
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0137others(56): Show | 78 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.203-1913C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053618 | ||||||
| chr6:42053638
|
C | G | 1 | a0001c0002t0007g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.203-1893C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053638 | ||||||
| chr6:42053773
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.203-1758G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053773 | ||||||
| chr6:42053801
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0137others(59): Show | 81 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.203-1730A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053801 | ||||||
| chr6:42053959
|
G | C | 1 | a0001c0002t0007g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203-1572G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053959 | ||||||
| chr6:42054154
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(221): Show | 279 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.203-1377T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054154 | ||||||
| chr6:42054175
|
C | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1356C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054175 | ||||||
| chr6:42054176
|
A | C | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1355A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054176 | ||||||
| chr6:42054178
|
A | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1353A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054178 | ||||||
| chr6:42054180
|
A | C | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1351A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054180 | ||||||
| chr6:42054181
|
G | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1350G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054181 | ||||||
| chr6:42054192
|
AAAACTCC others(7): Show |
A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1334_203-1321d others(16): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42054192 | |||||
| chr6:42054210
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG00609.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.203-1321C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054210 | ||||||
| chr6:42054214
|
T | C | 364 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(361): Show | 452 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(449): Show |
intron_variant | MODIFIER | c.203-1317T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054214 | ||||||
| chr6:42054218
|
C | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1313C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054218 | ||||||
| chr6:42054219
|
T | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1312T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054219 | ||||||
| chr6:42054233
|
T | C | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1298T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054233 | ||||||
| chr6:42054238
|
C | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1293C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054238 | ||||||
| chr6:42054243
|
C | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1288C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054243 | ||||||
| chr6:42054250
|
A | C | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1281A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054250 | ||||||
| chr6:42054265
|
C | G | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1266C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054265 | ||||||
| chr6:42054266
|
A | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1265A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054266 | ||||||
| chr6:42054273
|
A | G | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1258A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054273 | ||||||
| chr6:42054274
|
G | C | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1257G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054274 | ||||||
| chr6:42054388
|
G | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1143G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054388 | ||||||
| chr6:42054390
|
A | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1141A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054390 | ||||||
| chr6:42054391
|
C | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1140C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054391 | ||||||
| chr6:42054493
|
C | T | 6 | a0001c0001t0005g0336a0001c0001t0012g0337a0001c0001t0012g0339others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-1038C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054493 | ||||||
| chr6:42054549
|
G | A | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-982G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054549 | ||||||
| chr6:42054680
|
CTCACTGC others(1): Show |
C | 6 | a0001c0001t0005g0150a0001c0002t0010g0147a0001c0002t0010g0149others(3): Show | 6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-850_203-843del others(8): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054680 | ||||||
| chr6:42054692
|
A | T | 6 | a0001c0001t0005g0150a0001c0002t0010g0147a0001c0002t0010g0149others(3): Show | 6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-839A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054692 | ||||||
| chr6:42054696
|
C | G | 6 | a0001c0001t0005g0150a0001c0002t0010g0147a0001c0002t0010g0149others(3): Show | 6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-835C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054696 | ||||||
| chr6:42054697
|
C | CTTGA | 6 | a0001c0001t0005g0150a0001c0002t0010g0147a0001c0002t0010g0149others(3): Show | 6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-834_203-833ins others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054697 | ||||||
| chr6:42054739
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.203-792G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054739 | ||||||
| chr6:42054806
|
A | G | 8 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(5): Show | 8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.203-725A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054806 | ||||||
| chr6:42054825
|
T | C | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-706T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054825 | ||||||
| chr6:42054904
|
C | T | 2 | a0001c0001t0049g0117a0001c0005t0031g0118 | 2 | NA18998.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.203-627C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054904 | ||||||
| chr6:42054931
|
C | CT | 9 | a0001c0001t0001g0083a0001c0001t0012g0157a0001c0001t0061g0156others(6): Show | 9 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.203-585dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42054931 | |||||
| chr6:42054931
|
CT | C | 52 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(49): Show | 68 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.203-585delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42054931 | |||||
| chr6:42055077
|
C | T | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-454C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055077 | ||||||
| chr6:42055128
|
T | C | 10 | a0001c0001t0012g0230a0001c0002t0004g0235a0001c0002t0004g0237others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-403T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055128 | ||||||
| chr6:42055207
|
C | T | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-324C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055207 | ||||||
| chr6:42055215
|
C | T | 1 | a0001c0001t0005g0334 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.203-316C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055215 | ||||||
| chr6:42055361
|
G | A | 355 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(352): Show | 443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
intron_variant | MODIFIER | c.203-170G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055361 | ||||||
| chr6:42055373
|
G | A | 10 | a0001c0001t0012g0230a0001c0002t0004g0235a0001c0002t0004g0237others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-158G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055373 | ||||||
| chr6:42055783
|
A | G | 78 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 95 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.301+154A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 3/8 | chr6 | 42055783 | ||||||
| chr6:42055880
|
A | ATAC | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.302-63_302-61dupCT others(1): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 42055880 | |||||
| chr6:42056071
|
AAGTAATT others(4): Show |
A | 1 | a0001c0002t0004g0289 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.364+59_364+69delGT others(9): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 42056071 | |||||
| chr6:42056239
|
T | A | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+225T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056239 | ||||||
| chr6:42056401
|
A | G | 12 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0002g0007others(9): Show | 18 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.364+387A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056401 | ||||||
| chr6:42056491
|
C | T | 1 | a0001c0002t0004g0262 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.364+477C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056491 | ||||||
| chr6:42056547
|
G | A | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.364+533G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056547 | ||||||
| chr6:42056552
|
GAGT | G | 7 | a0001c0001t0011g0276a0001c0001t0082g0272a0001c0002t0007g0273others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.364+540_364+542del others(3): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 42056552 | |||||
| chr6:42056558
|
C | T | 2 | a0001c0001t0023g0332a0001c0001t0023g0333 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.364+544C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056558 | ||||||
| chr6:42056633
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.364+619C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056633 | ||||||
| chr6:42056688
|
C | T | 1 | a0001c0003t0052g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.364+674C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056688 | ||||||
| chr6:42056754
|
C | T | 1 | a0001c0001t0064g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.365-635C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056754 | ||||||
| chr6:42056858
|
G | A | 3 | a0001c0001t0012g0345a0001c0002t0030g0346a0001c0002t0071g0344 | 3 | HG02723.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.365-531G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056858 | ||||||
| chr6:42056867
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(284): Show | 358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.365-522G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056867 | ||||||
| chr6:42056896
|
G | A | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.365-493G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056896 | ||||||
| chr6:42056902
|
G | A | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-487G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056902 | ||||||
| chr6:42057051
|
G | A | 1 | a0001c0001t0005g0334 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.365-338G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057051 | ||||||
| chr6:42057123
|
G | A | 1 | a0001c0002t0007g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.365-266G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057123 | ||||||
| chr6:42057305
|
G | C | 1 | a0001c0001t0003g0119 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.365-84G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057305 | ||||||
| chr6:42057320
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(138): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.365-69G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057320 | ||||||
| chr6:42057537
|
G | A | 1 | a0001c0002t0021g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.489+24G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057537 | ||||||
| chr6:42057580
|
G | A | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.489+67G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057580 | ||||||
| chr6:42057664
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(141): Show | 184 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.489+151A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057664 | ||||||
| chr6:42057772
|
T | G | 2 | a0001c0001t0001g0084a0001c0001t0003g0047 | 2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.489+259T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057772 | ||||||
| chr6:42057776
|
G | GA | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(282): Show | 356 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.489+273dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42057776 | |||||
| chr6:42057807
|
A | C | 64 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(61): Show | 80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.489+294A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057807 | ||||||
| chr6:42057855
|
G | A | 3 | a0001c0001t0011g0029a0001c0001t0011g0030a0001c0001t0011g0263 | 5 | HG00642.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+342G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057855 | ||||||
| chr6:42057967
|
T | C | 8 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(5): Show | 8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.489+454T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057967 | ||||||
| chr6:42058147
|
G | T | 7 | a0001c0001t0011g0276a0001c0001t0082g0272a0001c0002t0007g0273others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+634G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058147 | ||||||
| chr6:42058254
|
C | T | 1 | a0001c0002t0019g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.489+741C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058254 | ||||||
| chr6:42058255
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(284): Show | 358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.489+742A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058255 | ||||||
| chr6:42058306
|
G | T | 12 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0002g0007others(9): Show | 18 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+793G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058306 | ||||||
| chr6:42058389
|
T | G | 2 | a0001c0001t0002g0041a0001c0001t0051g0048 | 2 | HG02135.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.489+876T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058389 | ||||||
| chr6:42058452
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0132others(56): Show | 72 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.489+939G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058452 | ||||||
| chr6:42058467
|
T | C | 1 | a0001c0002t0014g0010 | 5 | HG02109.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+954T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058467 | ||||||
| chr6:42058544
|
TC | T | 3 | a0001c0001t0005g0165a0001c0001t0006g0024a0001c0002t0073g0187 | 4 | HG02145.hp2 HG02257.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+1033delC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42058544 | |||||
| chr6:42058748
|
C | G | 1 | a0001c0002t0074g0114 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.489+1235C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058748 | ||||||
| chr6:42058764
|
C | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(152): Show | 187 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.489+1251C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058764 | ||||||
| chr6:42058978
|
T | A | 1 | a0001c0002t0013g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.489+1465T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058978 | ||||||
| chr6:42059043
|
G | C | 4 | a0001c0001t0061g0156a0001c0002t0007g0154a0001c0002t0007g0155others(1): Show | 4 | HG01081.hp2 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1530G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059043 | ||||||
| chr6:42059341
|
C | T | 5 | a0001c0001t0006g0267a0001c0002t0010g0266a0001c0002t0033g0264others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+1828C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059341 | ||||||
| chr6:42059361
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.489+1848C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059361 | ||||||
| chr6:42059386
|
A | G | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+1873A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059386 | ||||||
| chr6:42059390
|
A | C | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.489+1877A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059390 | ||||||
| chr6:42059391
|
A | G | 2 | a0001c0001t0006g0024a0001c0002t0073g0187 | 3 | HG02145.hp2 HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.489+1878A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059391 | ||||||
| chr6:42059632
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0219 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.489+2119A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059632 | ||||||
| chr6:42059983
|
G | A | 1 | a0001c0001t0022g0270 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.489+2470G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059983 | ||||||
| chr6:42059992
|
G | A | 2 | a0001c0002t0032g0169a0001c0002t0032g0170 | 2 | HG00741.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.489+2479G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059992 | ||||||
| chr6:42060162
|
A | G | 1 | a0001c0002t0019g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.489+2649A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060162 | ||||||
| chr6:42060177
|
A | C | 2 | a0001c0001t0002g0012a0001c0001t0005g0113 | 4 | NA18951.hp2 NA18975.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2664A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060177 | ||||||
| chr6:42060200
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(227): Show | 285 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.489+2687A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060200 | ||||||
| chr6:42060307
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.489+2794T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060307 | ||||||
| chr6:42060492
|
G | A | 38 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(35): Show | 48 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.489+2979G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060492 | ||||||
| chr6:42060834
|
T | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0052others(9): Show | 12 | HG00673.hp2 NA18945.hp1 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+3321T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060834 | ||||||
| chr6:42061020
|
G | A | 1 | a0001c0001t0068g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.489+3507G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061020 | ||||||
| chr6:42061025
|
A | T | 8 | a0001c0001t0005g0336a0001c0001t0012g0337a0001c0001t0012g0339others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3512A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061025 | ||||||
| chr6:42061058
|
A | G | 1 | a0001c0002t0007g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489+3545A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061058 | ||||||
| chr6:42061385
|
T | C | 3 | a0001c0001t0012g0345a0001c0002t0030g0346a0001c0002t0071g0344 | 3 | HG02723.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.489+3872T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061385 | ||||||
| chr6:42061502
|
C | T | 1 | a0001c0001t0011g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.489+3989C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061502 | ||||||
| chr6:42061533
|
C | A | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.489+4020C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061533 | ||||||
| chr6:42061724
|
A | T | 6 | a0001c0001t0002g0111a0001c0001t0003g0086a0001c0001t0003g0110others(3): Show | 9 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+4211A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061724 | ||||||
| chr6:42061734
|
A | G | 1 | a0001c0001t0064g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.489+4221A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061734 | ||||||
| chr6:42061791
|
C | T | 5 | a0001c0001t0006g0267a0001c0002t0010g0266a0001c0002t0033g0264others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+4278C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061791 | ||||||
| chr6:42061843
|
AGTTTGTC others(11): Show |
A | 11 | a0001c0001t0005g0336a0001c0001t0012g0337a0001c0001t0012g0339others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+4335_489+4352d others(20): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42061843 | |||||
| chr6:42061904
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0132others(62): Show | 86 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.489+4391A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061904 | ||||||
| chr6:42061950
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(284): Show | 358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.490-4362G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061950 | ||||||
| chr6:42062084
|
G | GA | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-4224dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062084 | |||||
| chr6:42062128
|
A | G | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-4184A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062128 | ||||||
| chr6:42062167
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(133): Show | 167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.490-4145C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062167 | ||||||
| chr6:42062168
|
G | A | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-4144G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062168 | ||||||
| chr6:42062529
|
C | CT | 49 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0018others(46): Show | 60 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.490-3759dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | |||||
| chr6:42062529
|
C | CTT | 91 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0026others(88): Show | 116 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(113): Show |
intron_variant | MODIFIER | c.490-3760_490-3759d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | |||||
| chr6:42062529
|
C | CTTT | 63 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0046others(60): Show | 77 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.490-3761_490-3759d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | |||||
| chr6:42062529
|
C | CTTTT | 6 | a0001c0001t0001g0042a0001c0001t0001g0082a0001c0001t0003g0079others(3): Show | 6 | HG00544.hp1 HG00621.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-3762_490-3759d others(6): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | |||||
| chr6:42062529
|
CT | C | 57 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(54): Show | 73 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.490-3759delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | |||||
| chr6:42062730
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(284): Show | 358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.490-3582T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062730 | ||||||
| chr6:42062731
|
G | A | 1 | a0001c0002t0007g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.490-3581G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062731 | ||||||
| chr6:42062742
|
A | G | 9 | a0001c0001t0001g0126a0001c0001t0012g0157a0001c0001t0061g0156others(6): Show | 9 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-3570A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062742 | ||||||
| chr6:42062846
|
ATCTTTAA others(5): Show |
A | 1 | a0001c0001t0001g0227 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.490-3462_490-3451d others(14): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062846 | |||||
| chr6:42062907
|
G | T | 38 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(35): Show | 48 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-3405G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062907 | ||||||
| chr6:42063003
|
C | G | 1 | a0001c0001t0002g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.490-3309C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063003 | ||||||
| chr6:42063108
|
G | C | 1 | a0001c0001t0002g0193 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.490-3204G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063108 | ||||||
| chr6:42063122
|
C | T | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-3190C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063122 | ||||||
| chr6:42063140
|
C | G | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-3172C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063140 | ||||||
| chr6:42063287
|
C | A | 1 | a0001c0001t0053g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-3025C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063287 | ||||||
| chr6:42063360
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(284): Show | 358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.490-2952G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063360 | ||||||
| chr6:42063509
|
T | C | 2 | a0001c0001t0012g0296a0001c0002t0007g0033 | 3 | HG02896.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.490-2803T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063509 | ||||||
| chr6:42064219
|
C | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | NA19010.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.490-2093C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064219 | ||||||
| chr6:42064251
|
T | G | 1 | a0001c0001t0034g0043 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.490-2061T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064251 | ||||||
| chr6:42064255
|
G | GT | 56 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0042others(53): Show | 70 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.490-2050dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064255 | |||||
| chr6:42064255
|
G | T | 1 | a0001c0001t0034g0043 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.490-2057G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064255 | ||||||
| chr6:42064322
|
G | A | 8 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(5): Show | 8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-1990G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064322 | ||||||
| chr6:42064362
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.490-1950C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064362 | ||||||
| chr6:42064378
|
C | A | 7 | a0001c0002t0004g0235a0001c0002t0004g0237a0001c0002t0019g0162others(4): Show | 7 | HG01891.hp1 HG03139.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-1934C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064378 | ||||||
| chr6:42064443
|
C | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.490-1869C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064443 | ||||||
| chr6:42064634
|
C | T | 1 | a0001c0001t0024g0314 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-1678C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064634 | ||||||
| chr6:42064754
|
G | A | 1 | a0001c0002t0007g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-1558G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064754 | ||||||
| chr6:42064830
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | NA19010.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.490-1482G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064830 | ||||||
| chr6:42064872
|
G | C | 2 | a0001c0001t0001g0194a0001c0002t0015g0195 | 2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.490-1440G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064872 | ||||||
| chr6:42064881
|
CGGGGGGC others(3): Show |
C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(269): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.490-1429_490-1420d others(12): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064881 | |||||
| chr6:42064894
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(269): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.490-1418T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064894 | ||||||
| chr6:42064895
|
TG | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(269): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.490-1416delG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064895 | ||||||
| chr6:42064898
|
AGTGAG | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(269): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.490-1413_490-1409d others(7): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064898 | ||||||
| chr6:42064913
|
C | T | 1 | a0001c0002t0004g0313 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.490-1399C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064913 | ||||||
| chr6:42064914
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0132others(55): Show | 71 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.490-1398G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064914 | ||||||
| chr6:42064914
|
G | T | 2 | a0001c0002t0004g0058a0001c0002t0004g0078 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.490-1398G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064914 | ||||||
| chr6:42064956
|
C | CA | 58 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0026others(55): Show | 78 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.490-1334dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | |||||
| chr6:42064956
|
C | CAAA | 7 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(4): Show | 7 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-1336_490-1334d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | |||||
| chr6:42064956
|
CA | C | 71 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0090others(68): Show | 87 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.490-1334delA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | |||||
| chr6:42064956
|
CAA | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0106others(62): Show | 80 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.490-1335_490-1334d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | |||||
| chr6:42065071
|
C | G | 1 | a0001c0001t0002g0115 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.490-1241C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065071 | ||||||
| chr6:42065170
|
A | G | 1 | a0001c0001t0005g0057 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.490-1142A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065170 | ||||||
| chr6:42065241
|
G | T | 2 | a0001c0002t0007g0347a0001c0002t0014g0010 | 6 | HG02109.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-1071G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065241 | ||||||
| chr6:42065311
|
A | T | 3 | a0001c0001t0005g0165a0001c0001t0006g0024a0001c0002t0073g0187 | 4 | HG02145.hp2 HG02257.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-1001A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065311 | ||||||
| chr6:42065331
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(126): Show | 169 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.490-981G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065331 | ||||||
| chr6:42065442
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0132others(55): Show | 71 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.490-870A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065442 | ||||||
| chr6:42065538
|
A | G | 2 | a0001c0001t0012g0230a0001c0002t0040g0231 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.490-774A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065538 | ||||||
| chr6:42065697
|
C | T | 1 | a0001c0001t0003g0045 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.490-615C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065697 | ||||||
| chr6:42065702
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(140): Show | 175 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.490-610C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065702 | ||||||
| chr6:42065898
|
T | A | 4 | a0001c0001t0001g0074a0001c0002t0004g0058a0001c0002t0004g0075others(1): Show | 4 | HG00323.hp2 HG01123.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-414T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065898 | ||||||
| chr6:42065938
|
C | T | 2 | a0001c0001t0001g0194a0001c0002t0015g0195 | 2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.490-374C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065938 | ||||||
| chr6:42066060
|
C | T | 1 | a0001c0002t0026g0181 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.490-252C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42066060 | ||||||
| chr6:42066149
|
C | G | 1 | a0001c0001t0005g0329 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.490-163C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42066149 | ||||||
| chr6:42066308
|
G | A | 1 | a0001c0002t0028g0063 | 1 | NA19058.hp1 | splice_region_variant&intron_variant | LOW | c.490-4G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42066308 | ||||||
| chr6:42066670
|
C | G | 1 | a0001c0002t0019g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.637+211C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066670 | ||||||
| chr6:42066671
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(269): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.637+212T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066671 | ||||||
| chr6:42066795
|
C | T | 2 | a0001c0002t0007g0347a0001c0002t0014g0010 | 6 | HG02109.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+336C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066795 | ||||||
| chr6:42066917
|
C | T | 6 | a0001c0001t0005g0150a0001c0002t0010g0147a0001c0002t0010g0149others(3): Show | 6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+458C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066917 | ||||||
| chr6:42066934
|
C | T | 12 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0002g0007others(9): Show | 18 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.637+475C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066934 | ||||||
| chr6:42066947
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(211): Show | 269 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.637+488C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066947 | ||||||
| chr6:42067312
|
G | A | 8 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(5): Show | 8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+853G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067312 | ||||||
| chr6:42067326
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.637+867C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067326 | ||||||
| chr6:42067370
|
C | T | 1 | a0001c0001t0011g0276 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.637+911C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067370 | ||||||
| chr6:42067499
|
G | C | 6 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(3): Show | 6 | HG01081.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-966G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067499 | ||||||
| chr6:42067521
|
A | G | 1 | a0001c0001t0006g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.638-944A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067521 | ||||||
| chr6:42067856
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.638-609C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067856 | ||||||
| chr6:42068189
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(269): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.638-276T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068189 | ||||||
| chr6:42068322
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.638-143G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068322 | ||||||
| chr6:42068331
|
T | C | 6 | a0001c0001t0023g0131a0001c0001t0065g0152a0001c0002t0016g0130others(3): Show | 7 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-134T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068331 | ||||||
| chr6:42068461
|
C | T | 1 | a0001c0001t0005g0327 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.638-4C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068461 | ||||||
| chr6:42068657
|
A | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(277): Show | 351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.780+50A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068657 | ||||||
| chr6:42068706
|
C | T | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+99C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068706 | ||||||
| chr6:42068767
|
A | G | 7 | a0001c0001t0011g0276a0001c0001t0082g0272a0001c0002t0007g0273others(4): Show | 7 | HG02257.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+160A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068767 | ||||||
| chr6:42068909
|
G | A | 3 | a0001c0002t0004g0279a0001c0002t0004g0287a0001c0002t0004g0289 | 3 | HG01975.hp2 HG01978.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.780+302G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068909 | ||||||
| chr6:42069011
|
A | G | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+404A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069011 | ||||||
| chr6:42069062
|
CCT | C | 8 | a0001c0001t0012g0157a0001c0001t0061g0156a0001c0001t0062g0159others(5): Show | 8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+456_780+457del others(2): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069062 | ||||||
| chr6:42069084
|
T | C | 1 | a0001c0001t0005g0334 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+477T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069084 | ||||||
| chr6:42069112
|
G | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0132others(61): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.780+505G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069112 | ||||||
| chr6:42069352
|
A | G | 1 | a0001c0001t0038g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.780+745A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069352 | ||||||
| chr6:42069360
|
T | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(152): Show | 195 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.780+753T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069360 | ||||||
| chr6:42069369
|
G | A | 1 | a0001c0002t0004g0299 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.780+762G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069369 | ||||||
| chr6:42069429
|
C | T | 58 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(55): Show | 76 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.780+822C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069429 | ||||||
| chr6:42069439
|
G | C | 1 | a0001c0001t0023g0333 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.780+832G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069439 | ||||||
| chr6:42069604
|
T | C | 12 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0002g0111others(9): Show | 15 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.780+997T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069604 | ||||||
| chr6:42069610
|
T | C | 50 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(47): Show | 66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.780+1003T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069610 | ||||||
| chr6:42069725
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.780+1118G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069725 | ||||||
| chr6:42069890
|
C | G | 58 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(55): Show | 76 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.780+1283C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069890 | ||||||
| chr6:42069944
|
A | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0220 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.780+1337A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069944 | ||||||
| chr6:42069977
|
C | T | 1 | a0001c0001t0064g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.780+1370C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069977 | ||||||
| chr6:42069982
|
A | G | 2 | a0001c0001t0068g0171a0001c0002t0007g0229 | 2 | HG01981.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.780+1375A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069982 | ||||||
| chr6:42070214
|
C | T | 5 | a0001c0001t0006g0267a0001c0002t0010g0266a0001c0002t0033g0264others(2): Show | 5 | HG01175.hp2 HG01243.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1607C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070214 | ||||||
| chr6:42070293
|
C | T | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.780+1686C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070293 | ||||||
| chr6:42070332
|
C | CA | 144 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(141): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.780+1735dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42070332 | |||||
| chr6:42070340
|
A | C | 49 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0094others(46): Show | 65 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.780+1733A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070340 | ||||||
| chr6:42070392
|
C | T | 1 | a0001c0001t0005g0198 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.780+1785C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070392 | ||||||
| chr6:42070407
|
G | T | 8 | a0001c0001t0006g0267a0001c0001t0011g0029a0001c0001t0011g0030others(5): Show | 10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+1800G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070407 | ||||||
| chr6:42070433
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.780+1826C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070433 | ||||||
| chr6:42070447
|
G | A | 1 | a0001c0001t0003g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.780+1840G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070447 | ||||||
| chr6:42070690
|
A | G | 12 | a0001c0001t0012g0157a0001c0001t0012g0230a0001c0001t0012g0345others(9): Show | 12 | HG01081.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+2083A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070690 | ||||||
| chr6:42070711
|
C | T | 66 | a0001c0001t0001g0032a0001c0001t0001g0091a0001c0001t0001g0099others(63): Show | 83 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.780+2104C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070711 | ||||||
| chr6:42070964
|
T | G | 2 | a0001c0002t0021g0023a0001c0002t0021g0129 | 3 | HG02258.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.780+2357T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070964 | ||||||
| chr6:42070983
|
C | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0083others(72): Show | 89 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.780+2376C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070983 | ||||||
| chr6:42071029
|
C | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0077others(9): Show | 16 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.780+2422C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071029 | ||||||
| chr6:42071127
|
T | C | 10 | a0001c0001t0006g0024a0001c0001t0012g0337a0001c0001t0012g0345others(7): Show | 11 | HG02257.hp1 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+2520T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071127 | ||||||
| chr6:42071187
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(253): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.780+2580G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071187 | ||||||
| chr6:42071230
|
T | C | 1 | a0001c0002t0043g0340 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.780+2623T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071230 | ||||||
| chr6:42071249
|
G | A | 1 | a0001c0002t0033g0264 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+2642G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071249 | ||||||
| chr6:42071311
|
C | CT | 26 | a0001c0001t0002g0062a0001c0001t0002g0095a0001c0001t0002g0153others(23): Show | 27 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+2737dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
C | CTT | 10 | a0001c0001t0005g0292a0001c0001t0005g0322a0001c0001t0009g0027others(7): Show | 11 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+2736_780+2737d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
C | CTTTT | 8 | a0001c0001t0005g0150a0001c0001t0066g0282a0001c0002t0010g0149others(5): Show | 8 | HG01255.hp1 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+2734_780+2737d others(6): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
CT | C | 32 | a0001c0001t0001g0295a0001c0001t0001g0308a0001c0001t0003g0004others(29): Show | 44 | HG00673.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.780+2737delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
CTT | C | 15 | a0001c0001t0001g0303a0001c0001t0002g0142a0001c0001t0003g0049others(12): Show | 15 | HG01123.hp1 HG01175.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.780+2736_780+2737d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
CTTT | C | 31 | a0001c0001t0001g0103a0001c0001t0002g0066a0001c0001t0002g0088others(28): Show | 32 | HG00280.hp2 HG00733.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.780+2735_780+2737d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0083a0001c0001t0001g0324a0001c0001t0003g0192others(2): Show | 5 | HG02735.hp1 NA18949.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+2724_780+2737d others(16): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
CTTTTTTT others(8): Show |
C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(140): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.780+2723_780+2737d others(17): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0213a0001c0001t0006g0319 | 2 | HG03669.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.780+2722_780+2737d others(18): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071311
|
CTTTTTTT others(13): Show |
C | 6 | a0001c0001t0001g0032a0001c0001t0001g0064a0001c0001t0001g0222others(3): Show | 15 | HG00558.hp1 HG00735.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.780+2718_780+2737d others(22): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | |||||
| chr6:42071342
|
T | G | 1 | a0001c0003t0052g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.780+2735T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071342 | ||||||
| chr6:42071344
|
T | A | 26 | a0001c0001t0001g0032a0001c0001t0001g0064a0001c0001t0001g0103others(23): Show | 35 | HG00558.hp1 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.780+2737T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071344 | ||||||
| chr6:42071359
|
T | A | 2 | a0001c0002t0021g0023a0001c0002t0021g0129 | 3 | HG02258.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.780+2752T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071359 | ||||||
| chr6:42071394
|
T | C | 47 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0003g0004others(44): Show | 55 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.780+2787T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071394 | ||||||
| chr6:42071412
|
G | A | 1 | a0001c0002t0079g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.780+2805G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071412 | ||||||
| chr6:42071475
|
A | G | 13 | a0001c0001t0002g0007a0001c0001t0002g0022a0001c0001t0002g0041others(10): Show | 19 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+2868A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071475 | ||||||
| chr6:42071487
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.780+2880G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071487 | ||||||
| chr6:42071488
|
G | T | 2 | a0001c0001t0006g0024a0001c0002t0004g0037 | 4 | HG00099.hp1 HG02257.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+2881G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071488 | ||||||
| chr6:42071515
|
G | A | 17 | a0001c0001t0012g0157a0001c0001t0038g0298a0001c0001t0056g0297others(14): Show | 17 | HG00280.hp2 HG00597.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.780+2908G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071515 | ||||||
| chr6:42071526
|
G | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 385 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(382): Show |
intron_variant | MODIFIER | c.780+2919G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071526 | ||||||
| chr6:42071537
|
G | A | 3 | a0001c0002t0032g0169a0001c0002t0032g0170a0001c0002t0079g0253 | 3 | HG00741.hp1 HG02615.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.780+2930G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071537 | ||||||
| chr6:42071626
|
G | A | 4 | a0001c0001t0024g0307a0001c0001t0024g0314a0001c0001t0061g0156others(1): Show | 4 | HG01081.hp2 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+3019G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071626 | ||||||
| chr6:42071639
|
T | C | 3 | a0001c0002t0030g0136a0001c0002t0030g0346a0001c0002t0041g0232 | 3 | HG02451.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.780+3032T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071639 | ||||||
| chr6:42071749
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 223 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.780+3142T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071749 | ||||||
| chr6:42071762
|
A | G | 3 | a0001c0001t0012g0230a0001c0001t0012g0337a0001c0001t0012g0345 | 3 | HG02723.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.780+3155A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071762 | ||||||
| chr6:42071774
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.780+3167G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071774 | ||||||
| chr6:42071801
|
C | A | 2 | a0001c0001t0024g0307a0001c0001t0024g0314 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.780+3194C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071801 | ||||||
| chr6:42071804
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(100): Show | 146 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.780+3197G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071804 | ||||||
| chr6:42071813
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 152 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.780+3206C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071813 | ||||||
| chr6:42071834
|
A | G | 38 | a0001c0001t0001g0179a0001c0001t0005g0035a0001c0001t0005g0057others(35): Show | 41 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.780+3227A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071834 | ||||||
| chr6:42071928
|
C | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(303): Show | 390 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(387): Show |
intron_variant | MODIFIER | c.780+3321C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071928 | ||||||
| chr6:42072060
|
G | A | 1 | a0001c0001t0067g0341 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+3453G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072060 | ||||||
| chr6:42072077
|
C | T | 4 | a0001c0001t0024g0307a0001c0001t0024g0314a0001c0001t0061g0156others(1): Show | 4 | HG01081.hp2 HG01884.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3470C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072077 | ||||||
| chr6:42072139
|
G | A | 1 | a0001c0001t0005g0249 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.780+3532G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072139 | ||||||
| chr6:42072145
|
C | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(308): Show | 395 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(392): Show |
intron_variant | MODIFIER | c.780+3538C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072145 | ||||||
| chr6:42072222
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.780+3615A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072222 | ||||||
| chr6:42072288
|
A | G | 91 | a0001c0001t0001g0103a0001c0001t0001g0179a0001c0001t0002g0003others(88): Show | 111 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.780+3681A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072288 | ||||||
| chr6:42072404
|
CCCTGT | C | 4 | a0001c0002t0007g0180a0001c0002t0007g0259a0001c0002t0007g0261others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3798_780+3802d others(7): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072404 | ||||||
| chr6:42072492
|
T | G | 1 | a0001c0001t0008g0331 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.780+3885T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072492 | ||||||
| chr6:42072553
|
C | T | 44 | a0001c0001t0001g0103a0001c0001t0002g0003a0001c0001t0002g0007others(41): Show | 61 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.780+3946C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072553 | ||||||
| chr6:42072583
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(110): Show | 157 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.780+3976G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072583 | ||||||
| chr6:42072587
|
C | T | 1 | a0001c0002t0004g0310 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.780+3980C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072587 | ||||||
| chr6:42072648
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.780+4041C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072648 | ||||||
| chr6:42072729
|
G | GT | 11 | a0001c0001t0005g0035a0001c0001t0005g0177a0001c0001t0009g0254others(8): Show | 12 | HG01169.hp1 HG02109.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.780+4133dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42072729 | |||||
| chr6:42072783
|
C | T | 5 | a0001c0002t0019g0161a0001c0002t0019g0162a0001c0002t0019g0234others(2): Show | 5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+4176C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072783 | ||||||
| chr6:42072848
|
C | G | 6 | a0001c0001t0002g0098a0001c0001t0012g0157a0001c0002t0007g0134others(3): Show | 6 | HG00733.hp2 HG02717.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+4241C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072848 | ||||||
| chr6:42072851
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.780+4244C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072851 | ||||||
| chr6:42072856
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.781-4244A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072856 | ||||||
| chr6:42072863
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.781-4237C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072863 | ||||||
| chr6:42072868
|
G | A | 46 | a0001c0001t0001g0103a0001c0001t0002g0003a0001c0001t0002g0007others(43): Show | 63 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.781-4232G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072868 | ||||||
| chr6:42072880
|
G | T | 3 | a0001c0002t0014g0010a0001c0002t0014g0163a0001c0003t0052g0269 | 7 | HG02109.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-4220G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072880 | ||||||
| chr6:42072884
|
G | C | 1 | a0001c0001t0008g0331 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.781-4216G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072884 | ||||||
| chr6:42072891
|
T | G | 1 | a0001c0002t0004g0284 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.781-4209T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072891 | ||||||
| chr6:42072953
|
G | A | 45 | a0001c0001t0001g0103a0001c0001t0002g0003a0001c0001t0002g0007others(42): Show | 62 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.781-4147G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072953 | ||||||
| chr6:42072978
|
C | T | 4 | a0001c0001t0024g0307a0001c0001t0024g0314a0001c0001t0061g0156others(1): Show | 4 | HG01081.hp2 HG01884.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-4122C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072978 | ||||||
| chr6:42073002
|
C | G | 83 | a0001c0001t0001g0103a0001c0001t0001g0179a0001c0001t0002g0003others(80): Show | 103 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.781-4098C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073002 | ||||||
| chr6:42073214
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.781-3886C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073214 | ||||||
| chr6:42073214
|
C | T | 1 | a0001c0001t0024g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.781-3886C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073214 | ||||||
| chr6:42073333
|
G | A | 1 | a0001c0002t0004g0299 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.781-3767G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073333 | ||||||
| chr6:42073437
|
G | A | 1 | a0001c0001t0022g0270 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.781-3663G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073437 | ||||||
| chr6:42073488
|
G | T | 1 | a0001c0002t0007g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781-3612G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073488 | ||||||
| chr6:42073536
|
G | A | 1 | a0001c0003t0052g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781-3564G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073536 | ||||||
| chr6:42073708
|
G | A | 17 | a0001c0001t0005g0336a0001c0001t0012g0157a0001c0001t0012g0230others(14): Show | 17 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.781-3392G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073708 | ||||||
| chr6:42073778
|
G | C | 1 | a0001c0002t0043g0340 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.781-3322G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073778 | ||||||
| chr6:42073800
|
G | A | 2 | a0001c0002t0030g0136a0001c0002t0030g0346 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.781-3300G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073800 | ||||||
| chr6:42073803
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(226): Show | 293 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.781-3297C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073803 | ||||||
| chr6:42073862
|
G | C | 1 | a0001c0002t0073g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.781-3238G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073862 | ||||||
| chr6:42074097
|
G | C | 1 | a0001c0001t0038g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781-3003G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074097 | ||||||
| chr6:42074205
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0320 | 2 | HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.781-2895G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074205 | ||||||
| chr6:42074225
|
G | A | 4 | a0001c0001t0012g0230a0001c0001t0012g0337a0001c0001t0012g0345others(1): Show | 4 | HG02145.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2875G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074225 | ||||||
| chr6:42074297
|
C | T | 13 | a0001c0001t0048g0178a0001c0002t0010g0174a0001c0002t0010g0175others(10): Show | 13 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.781-2803C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074297 | ||||||
| chr6:42074827
|
C | T | 3 | a0001c0002t0007g0134a0001c0002t0007g0347a0001c0002t0069g0239 | 3 | HG03471.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.781-2273C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074827 | ||||||
| chr6:42074838
|
CT | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.781-2244delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42074838 | |||||
| chr6:42074838
|
CTT | C | 56 | a0001c0001t0001g0294a0001c0001t0005g0336a0001c0001t0012g0157others(53): Show | 58 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.781-2245_781-2244d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42074838 | |||||
| chr6:42074838
|
CTTT | C | 45 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0012others(42): Show | 62 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.781-2246_781-2244d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42074838 | |||||
| chr6:42075074
|
T | C | 2 | a0001c0002t0007g0033a0001c0002t0007g0273 | 3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.781-2026T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075074 | ||||||
| chr6:42075148
|
A | G | 12 | a0001c0002t0010g0147a0001c0002t0010g0149a0001c0002t0010g0174others(9): Show | 12 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-1952A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075148 | ||||||
| chr6:42075182
|
A | G | 1 | a0001c0002t0010g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.781-1918A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075182 | ||||||
| chr6:42075262
|
G | A | 1 | a0001c0002t0016g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.781-1838G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075262 | ||||||
| chr6:42075327
|
G | A | 6 | a0001c0002t0016g0130a0001c0002t0016g0274a0001c0002t0016g0275others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-1773G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075327 | ||||||
| chr6:42075395
|
A | G | 5 | a0001c0001t0005g0035a0001c0001t0005g0177a0001c0001t0005g0305others(2): Show | 6 | NA18954.hp2 NA18961.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1705A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075395 | ||||||
| chr6:42075419
|
C | T | 1 | a0001c0002t0004g0289 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.781-1681C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075419 | ||||||
| chr6:42075526
|
G | A | 33 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0062others(30): Show | 44 | HG00323.hp1 HG00621.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.781-1574G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075526 | ||||||
| chr6:42075656
|
GACTTCTT others(12): Show |
G | 1 | a0001c0003t0052g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781-1432_781-1414d others(21): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42075656 | |||||
| chr6:42075664
|
C | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0012others(79): Show | 101 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.781-1436C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075664 | ||||||
| chr6:42075706
|
C | T | 1 | a0001c0002t0004g0299 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.781-1394C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075706 | ||||||
| chr6:42075772
|
A | T | 32 | a0001c0001t0048g0178a0001c0002t0007g0033a0001c0002t0007g0085others(29): Show | 34 | HG00280.hp2 HG00741.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.781-1328A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075772 | ||||||
| chr6:42075858
|
T | C | 1 | a0001c0001t0005g0104 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.781-1242T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075858 | ||||||
| chr6:42076001
|
AGAT | A | 7 | a0001c0001t0005g0336a0001c0001t0012g0157a0001c0001t0012g0230others(4): Show | 7 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-1098_781-1096d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076001 | ||||||
| chr6:42076036
|
C | T | 1 | a0001c0002t0015g0243 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.781-1064C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076036 | ||||||
| chr6:42076037
|
G | A | 2 | a0001c0001t0003g0045a0001c0001t0003g0093 | 2 | HG02083.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.781-1063G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076037 | ||||||
| chr6:42076206
|
C | CA | 9 | a0001c0001t0012g0345a0001c0002t0016g0130a0001c0002t0016g0158others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-882dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42076206 | |||||
| chr6:42076279
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0219 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.781-821G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076279 | ||||||
| chr6:42076306
|
C | T | 1 | a0001c0001t0008g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.781-794C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076306 | ||||||
| chr6:42076375
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0208a0001c0001t0082g0272 | 3 | HG02630.hp2 HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.781-725C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076375 | ||||||
| chr6:42076399
|
G | A | 1 | a0001c0003t0052g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781-701G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076399 | ||||||
| chr6:42076451
|
A | G | 3 | a0001c0001t0023g0131a0001c0001t0023g0332a0001c0001t0023g0333 | 3 | HG02145.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.781-649A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076451 | ||||||
| chr6:42076466
|
A | C | 60 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0021others(57): Show | 74 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.781-634A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076466 | ||||||
| chr6:42076493
|
G | C | 2 | a0001c0001t0005g0249a0001c0001t0064g0188 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.781-607G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076493 | ||||||
| chr6:42076535
|
C | T | 47 | a0001c0001t0005g0035a0001c0001t0005g0057a0001c0001t0005g0071others(44): Show | 50 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.781-565C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076535 | ||||||
| chr6:42076681
|
G | T | 1 | a0001c0001t0055g0055 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.781-419G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076681 | ||||||
| chr6:42076682
|
C | G | 1 | a0001c0001t0055g0055 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.781-418C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076682 | ||||||
| chr6:42076683
|
G | C | 1 | a0001c0001t0055g0055 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.781-417G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076683 | ||||||
| chr6:42076793
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.781-307G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076793 | ||||||
| chr6:42076867
|
T | C | 8 | a0001c0002t0016g0130a0001c0002t0016g0158a0001c0002t0016g0160others(5): Show | 8 | HG01891.hp1 HG02257.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-233T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076867 | ||||||
| chr6:42076877
|
G | A | 6 | a0001c0001t0012g0157a0001c0001t0012g0230a0001c0001t0012g0296others(3): Show | 6 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-223G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076877 | ||||||
| chr6:42076880
|
G | A | 6 | a0001c0001t0012g0157a0001c0001t0012g0230a0001c0001t0012g0296others(3): Show | 6 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-220G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076880 | ||||||
| chr6:42076915
|
T | C | 2 | a0001c0002t0004g0281a0001c0002t0078g0286 | 2 | HG00408.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.781-185T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076915 | ||||||
| chr6:42076917
|
C | G | 44 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0012others(41): Show | 61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.781-183C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076917 | ||||||
| chr6:42077009
|
A | G | 1 | a0001c0002t0007g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.781-91A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42077009 | ||||||
| chr6:42077087
|
C | T | 5 | a0001c0002t0019g0161a0001c0002t0019g0162a0001c0002t0019g0234others(2): Show | 5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-13C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42077087 | ||||||
| chr6:42077288
|
G | A | 35 | a0001c0002t0007g0033a0001c0002t0007g0085a0001c0002t0007g0134others(32): Show | 37 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.920+49G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077288 | ||||||
| chr6:42077292
|
T | C | 1 | a0001c0002t0007g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.920+53T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077292 | ||||||
| chr6:42077325
|
G | T | 1 | a0001c0002t0013g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.920+86G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077325 | ||||||
| chr6:42077348
|
C | T | 12 | a0001c0002t0010g0147a0001c0002t0010g0149a0001c0002t0010g0174others(9): Show | 12 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.920+109C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077348 | ||||||
| chr6:42077367
|
T | C | 1 | a0001c0001t0001g0324 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.920+128T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077367 | ||||||
| chr6:42077368
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.920+129C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077368 | ||||||
| chr6:42077433
|
A | G | 36 | a0001c0001t0048g0178a0001c0002t0007g0033a0001c0002t0007g0085others(33): Show | 38 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.921-100A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077433 | ||||||
| chr6:42077496
|
C | T | 1 | a0001c0001t0008g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.921-37C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077496 |