| geneid | 6873 |
|---|---|
| ensemblid | ENSG00000064313.13 |
| hgncid | 11536 |
| symbol | TAF2 |
| name | TATA-box binding protein associated factor 2 |
| refseq_nuc | NM_003184.4 |
| refseq_prot | NP_003175.2 |
| ensembl_nuc | ENST00000378164.7 |
| ensembl_prot | ENSP00000367406.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 119730774 |
| end | 119832841 |
| strand | - |
| ver | v1.2 |
| region | chr8:119730774-119832841 |
| region5000 | chr8:119725774-119837841 |
| regionname0 | TAF2_chr8_119730774_119832841 |
| regionname5000 | TAF2_chr8_119725774_119837841 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1199 | 154 | 35 | 31 | 63 | 9 | 16 | 47 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0002 | 1/0 | 1199 | 98 | 14 | 13 | 57 | 3 | 10 | 46 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003 | 0/0 | 1199 | 27 | 18 | 1 | 1 | 0 | 7 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0004 | 0/0 | 1199 | 23 | 17 | 6 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0005 | 0/1 | 1199 | 17 | 6 | 3 | 2 | 2 | 3 | 2 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0006 | 0/0 | 1199 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0007 | 0/0 | 1199 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| 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 | 3600 | 99 | 12 | 21 | 55 | 4 | 7 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0002 | 1/0 | 3600 | 98 | 14 | 13 | 57 | 3 | 10 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0003 | 0/0 | 3600 | 43 | 14 | 8 | 7 | 5 | 9 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0004 | 0/0 | 3600 | 22 | 16 | 6 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0005 | 0/1 | 3600 | 17 | 6 | 3 | 2 | 2 | 3 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0006 | 0/0 | 3600 | 12 | 4 | 1 | 1 | 0 | 6 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0007 | 0/0 | 3600 | 7 | 7 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0008 | 0/0 | 3600 | 6 | 6 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0009 | 0/0 | 3600 | 6 | 5 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0010 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0011 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0012 | 0/0 | 3600 | 2 | 0 | 0 | 0 | 0 | 2 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0013 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0014 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0015 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0016 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0017 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| c0018 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| 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 | 1/0 | 1428 | 264 | 55 | 41 | 120 | 12 | 35 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0002 | 0/0 | 1428 | 24 | 18 | 6 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0003 | 0/1 | 1428 | 23 | 11 | 4 | 2 | 2 | 3 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0004 | 0/0 | 1428 | 3 | 2 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0005 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0006 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0007 | 0/0 | 1428 | 2 | 0 | 2 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0008 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| t0009 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| 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 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| 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 | 3600 | 99 | 12 | 21 | 55 | 4 | 7 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0003 | 0/0 | 3600 | 43 | 14 | 8 | 7 | 5 | 9 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0007 | 0/0 | 3600 | 7 | 7 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0011 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0015 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0016 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0018 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0002c0002 | 1/0 | 3600 | 98 | 14 | 13 | 57 | 3 | 10 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0006 | 0/0 | 3600 | 12 | 4 | 1 | 1 | 0 | 6 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0008 | 0/0 | 3600 | 6 | 6 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0009 | 0/0 | 3600 | 6 | 5 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0010 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0017 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0004c0004 | 0/0 | 3600 | 22 | 16 | 6 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0004c0014 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0005c0005 | 0/1 | 3600 | 17 | 6 | 3 | 2 | 2 | 3 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0006c0012 | 0/0 | 3600 | 2 | 0 | 0 | 0 | 0 | 2 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0007c0013 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5027 | 99 | 12 | 21 | 55 | 4 | 7 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0003t0001 | 0/0 | 5027 | 39 | 11 | 7 | 7 | 5 | 9 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0003t0004 | 0/0 | 5027 | 3 | 2 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0003t0009 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0007t0001 | 0/0 | 5027 | 7 | 7 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0011t0005 | 0/0 | 5027 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0015t0001 | 0/0 | 5027 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0016t0001 | 0/0 | 5027 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0001c0018t0001 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0002c0002t0001 | 1/0 | 5027 | 94 | 14 | 11 | 55 | 3 | 10 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0002c0002t0006 | 0/0 | 5027 | 2 | 0 | 0 | 2 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0002c0002t0007 | 0/0 | 5027 | 2 | 0 | 2 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0006t0001 | 0/0 | 5027 | 7 | 0 | 0 | 1 | 0 | 6 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0006t0003 | 0/0 | 5027 | 5 | 4 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0008t0001 | 0/0 | 5027 | 6 | 6 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0009t0001 | 0/0 | 5027 | 6 | 5 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0010t0002 | 0/0 | 5027 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0003c0017t0003 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0004c0004t0002 | 0/0 | 5027 | 21 | 15 | 6 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0004c0004t0008 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0004c0014t0002 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0005c0005t0003 | 0/1 | 5027 | 17 | 6 | 3 | 2 | 2 | 3 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0006c0012t0001 | 0/0 | 5027 | 2 | 0 | 0 | 0 | 0 | 2 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| a0007c0013t0001 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | copy fasta | chr8 | 119725774 | 119837841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0003t0009g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0007t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0007t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0007t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0007t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0007t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0011t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0011t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0015t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0016t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0001c0018t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0002c0002t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0006t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0008t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0008t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0008t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0008t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0009t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0009t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0009t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0009t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0009t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0010t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0010t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0003c0017t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0004t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0004c0014t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0001 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0005c0005t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0006c0012t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| a0007c0013t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0057 | EUR | GBR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0059 | EUR | GBR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0142 | EUR | GBR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0088 | EUR | FIN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00323 | hp2 | a0005 | c0005 | t0003 | g0286 | EUR | FIN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00639 | hp1 | a0004 | c0004 | t0002 | g0301 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00735 | hp2 | a0005 | c0005 | t0003 | g0001 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00738 | hp1 | a0001 | c0015 | t0001 | g0160 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG00738 | hp2 | a0005 | c0005 | t0003 | g0281 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01070 | hp2 | a0002 | c0002 | t0007 | g0121 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01071 | hp1 | a0002 | c0002 | t0007 | g0099 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01109 | hp2 | a0004 | c0004 | t0002 | g0295 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01167 | hp1 | a0004 | c0004 | t0002 | g0297 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01167 | hp2 | a0003 | c0006 | t0003 | g0273 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0268 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01169 | hp1 | a0004 | c0004 | t0002 | g0298 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0267 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01255 | hp1 | a0004 | c0004 | t0002 | g0296 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01258 | hp2 | a0001 | c0016 | t0001 | g0202 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01261 | hp1 | a0001 | c0003 | t0004 | g0034 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0046 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0036 | EUR | IBS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0042 | EUR | IBS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0069 | EUR | IBS | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0031 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01884 | hp2 | a0001 | c0011 | t0005 | g0008 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01891 | hp2 | a0003 | c0008 | t0001 | g0015 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01975 | hp2 | a0004 | c0004 | t0002 | g0302 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PEL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02027 | hp1 | a0003 | c0006 | t0001 | g0163 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02055 | hp1 | a0003 | c0006 | t0003 | g0272 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02055 | hp2 | a0001 | c0011 | t0005 | g0009 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02145 | hp1 | a0003 | c0009 | t0001 | g0153 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0269 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | CDX | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02155 | hp2 | a0002 | c0002 | t0006 | g0166 | EAS | CDX | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | CDX | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CDX | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02257 | hp1 | a0001 | c0007 | t0001 | g0027 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02257 | hp2 | a0004 | c0004 | t0002 | g0311 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02280 | hp2 | a0003 | c0006 | t0003 | g0274 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0037 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02451 | hp2 | a0004 | c0004 | t0002 | g0307 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02572 | hp1 | a0003 | c0010 | t0002 | g0312 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0054 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02602 | hp2 | a0005 | c0005 | t0003 | g0001 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02630 | hp1 | a0003 | c0008 | t0001 | g0016 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02647 | hp1 | a0003 | c0008 | t0001 | g0011 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02647 | hp2 | a0004 | c0004 | t0002 | g0294 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02698 | hp2 | a0003 | c0006 | t0001 | g0162 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02717 | hp2 | a0004 | c0004 | t0002 | g0293 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02723 | hp1 | a0005 | c0005 | t0003 | g0280 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02735 | hp2 | a0003 | c0006 | t0001 | g0154 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0026 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02818 | hp1 | a0003 | c0008 | t0001 | g0012 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02818 | hp2 | a0001 | c0007 | t0001 | g0029 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0033 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02895 | hp2 | a0003 | c0006 | t0003 | g0275 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0266 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02965 | hp1 | a0005 | c0005 | t0003 | g0290 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02965 | hp2 | a0003 | c0017 | t0003 | g0277 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02970 | hp1 | a0005 | c0005 | t0003 | g0283 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02970 | hp2 | a0004 | c0004 | t0008 | g0271 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02976 | hp2 | a0004 | c0004 | t0002 | g0299 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0047 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03041 | hp1 | a0005 | c0005 | t0003 | g0278 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03041 | hp2 | a0004 | c0004 | t0002 | g0007 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03098 | hp1 | a0005 | c0005 | t0003 | g0291 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03130 | hp1 | a0004 | c0014 | t0002 | g0303 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03130 | hp2 | a0003 | c0009 | t0001 | g0004 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03139 | hp1 | a0003 | c0009 | t0001 | g0158 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03139 | hp2 | a0004 | c0004 | t0002 | g0300 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03195 | hp1 | a0001 | c0007 | t0001 | g0030 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03209 | hp1 | a0003 | c0009 | t0001 | g0004 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03209 | hp2 | a0004 | c0004 | t0002 | g0007 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0064 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03453 | hp2 | a0004 | c0004 | t0002 | g0304 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03486 | hp1 | a0004 | c0004 | t0002 | g0305 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03491 | hp1 | a0006 | c0012 | t0001 | g0005 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03492 | hp2 | a0006 | c0012 | t0001 | g0005 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0107 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03516 | hp2 | a0001 | c0003 | t0004 | g0035 | AFR | ESN | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03540 | hp2 | a0001 | c0003 | t0009 | g0314 | AFR | GWD | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03579 | hp2 | a0001 | c0007 | t0001 | g0028 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03704 | hp1 | a0003 | c0006 | t0001 | g0155 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03710 | hp1 | a0005 | c0005 | t0003 | g0282 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0175 | SAS | PJL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0095 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0061 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0131 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04115 | hp1 | a0005 | c0005 | t0003 | g0284 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0063 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04184 | hp1 | a0003 | c0006 | t0001 | g0159 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0053 | SAS | BEB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0041 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04199 | hp2 | a0003 | c0006 | t0001 | g0161 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04204 | hp1 | a0003 | c0006 | t0001 | g0156 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0032 | SAS | STU | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18522 | hp1 | a0003 | c0008 | t0001 | g0013 | AFR | YRI | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18991 | hp1 | a0001 | c0018 | t0001 | g0182 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18997 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18998 | hp1 | a0005 | c0005 | t0003 | g0288 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19030 | hp1 | a0004 | c0004 | t0002 | g0308 | AFR | LWK | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19030 | hp2 | a0005 | c0005 | t0003 | g0279 | AFR | LWK | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19043 | hp2 | a0004 | c0004 | t0002 | g0310 | AFR | LWK | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19087 | hp1 | a0005 | c0005 | t0003 | g0285 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19088 | hp2 | a0007 | c0013 | t0001 | g0093 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19089 | hp2 | a0002 | c0002 | t0006 | g0167 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20129 | hp1 | a0004 | c0004 | t0002 | g0309 | AFR | ASW | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20129 | hp2 | a0003 | c0008 | t0001 | g0014 | AFR | ASW | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0052 | EUR | TSI | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20805 | hp1 | a0005 | c0005 | t0003 | g0287 | EUR | TSI | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | GIH | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20905 | hp2 | a0003 | c0009 | t0001 | g0164 | SAS | GIH | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG01123 | hp2 | a0005 | c0005 | t0003 | g0289 | AMR | CLM | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02109 | hp2 | a0001 | c0007 | t0001 | g0025 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0120 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02486 | hp2 | a0004 | c0004 | t0002 | g0292 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02559 | hp1 | a0003 | c0010 | t0002 | g0313 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG02559 | hp2 | a0003 | c0009 | t0001 | g0157 | AFR | ACB | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0119 | AFR | MSL | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | USA | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | USA | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0270 | AFR | USA | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | USA | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA21309 | hp1 | a0004 | c0004 | t0002 | g0306 | AFR | LWK | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| NA21309 | hp2 | a0003 | c0006 | t0003 | g0276 | AFR | LWK | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| homoSapiens_chm13v2 | hp1 | a0005 | c0005 | t0003 | g0001 | REF | REF | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0150 | REF | REF | TAF2_chr8_119725774_119837841 | TAF2 | chr8 | 119725774 | 119837841 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:119732109
|
T | C | 3 | a0003a0004a0006 | 52 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(49): Show |
missense_variant | MODERATE | c.3415A>G | p.Thr1139Ala | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 3692/5027 | 3415/3600 | 1139/1199 | chr8 | 119732109 | ||
| chr8:119732159
|
C | T | 1 | a0004 | 23 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(20): Show |
missense_variant | MODERATE | c.3365G>A | p.Ser1122Asn | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 3642/5027 | 3365/3600 | 1122/1199 | chr8 | 119732159 | ||
| chr8:119791397
|
C | G | 5 | a0001a0003a0004others(2): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
missense_variant | MODERATE | c.1340G>C | p.Ser447Thr | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/26 | 1617/5027 | 1340/3600 | 447/1199 | chr8 | 119791397 | ||
| chr8:119793441
|
T | G | 1 | a0006 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1202A>C | p.Lys401Thr | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/26 | 1479/5027 | 1202/3600 | 401/1199 | chr8 | 119793441 | ||
| chr8:119797059
|
A | G | 1 | a0007 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.1022T>C | p.Leu341Ser | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/26 | 1299/5027 | 1022/3600 | 341/1199 | chr8 | 119797059 | ||
| chr8:119832542
|
G | A | 1 | a0005 | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
missense_variant | MODERATE | c.23C>T | p.Pro8Leu | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/26 | 300/5027 | 23/3600 | 8/1199 | chr8 | 119832542 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:119731954
|
C | T | 1 | a0003c0008 | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
synonymous_variant | LOW | c.3570G>A | p.Arg1190Arg | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 3847/5027 | 3570/3600 | 1190/1199 | chr8 | 119731954 | ||
| chr8:119732053
|
C | T | 1 | a0001c0016 | 1 | HG01258.hp2 | synonymous_variant | LOW | c.3471G>A | p.Lys1157Lys | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 3748/5027 | 3471/3600 | 1157/1199 | chr8 | 119732053 | ||
| chr8:119746822
|
A | G | 1 | a0003c0008 | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
synonymous_variant | LOW | c.2991T>C | p.Asn997Asn | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/26 | 3268/5027 | 2991/3600 | 997/1199 | chr8 | 119746822 | ||
| chr8:119756016
|
A | G | 1 | a0001c0011 | 2 | HG01884.hp2 HG02055.hp2 |
synonymous_variant | LOW | c.2868T>C | p.Leu956Leu | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/26 | 3145/5027 | 2868/3600 | 956/1199 | chr8 | 119756016 | ||
| chr8:119762471
|
G | A | 1 | a0004c0014 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.2502C>T | p.Thr834Thr | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/26 | 2779/5027 | 2502/3600 | 834/1199 | chr8 | 119762471 | ||
| chr8:119778064
|
T | C | 15 | a0001c0001a0001c0007a0001c0011others(12): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
synonymous_variant | LOW | c.2319A>G | p.Thr773Thr | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/26 | 2596/5027 | 2319/3600 | 773/1199 | chr8 | 119778064 | ||
| chr8:119781056
|
C | T | 9 | a0001c0015a0003c0006a0003c0009others(6): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
synonymous_variant | LOW | c.2250G>A | p.Gln750Gln | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/26 | 2527/5027 | 2250/3600 | 750/1199 | chr8 | 119781056 | ||
| chr8:119781092
|
T | C | 1 | a0003c0009 | 6 | HG02145.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
synonymous_variant | LOW | c.2214A>G | p.Thr738Thr | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/26 | 2491/5027 | 2214/3600 | 738/1199 | chr8 | 119781092 | ||
| chr8:119783402
|
T | G | 1 | a0001c0007 | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
synonymous_variant | LOW | c.2091A>C | p.Ser697Ser | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/26 | 2368/5027 | 2091/3600 | 697/1199 | chr8 | 119783402 | ||
| chr8:119791414
|
C | T | 4 | a0003c0010a0004c0004a0004c0014others(1): Show | 42 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
synonymous_variant | LOW | c.1323G>A | p.Leu441Leu | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/26 | 1600/5027 | 1323/3600 | 441/1199 | chr8 | 119791414 | ||
| chr8:119801842
|
G | C | 1 | a0003c0017 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.744C>G | p.Ser248Ser | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/26 | 1021/5027 | 744/3600 | 248/1199 | chr8 | 119801842 | ||
| chr8:119806335
|
T | C | 1 | a0001c0018 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.366A>G | p.Gly122Gly | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/26 | 643/5027 | 366/3600 | 122/1199 | chr8 | 119806335 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:119731123
|
G | A | 1 | a0001c0003t0004 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*801C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 801 | chr8 | 119731123 | |||||
| chr8:119731548
|
A | C | 1 | a0001c0003t0004 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 376 | chr8 | 119731548 | |||||
| chr8:119731653
|
C | T | 1 | a0002c0002t0007 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*271G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 271 | chr8 | 119731653 | |||||
| chr8:119731895
|
A | G | 1 | a0002c0002t0006 | 2 | HG02155.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 26/26 | 29 | chr8 | 119731895 | |||||
| chr8:119832606
|
G | C | 4 | a0003c0010t0002a0004c0004t0002a0004c0004t0008others(1): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/26 | chr8 | 119832606 | ||||||
| chr8:119832795
|
G | A | 6 | a0003c0006t0003a0003c0010t0002a0003c0017t0003others(3): Show | 47 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-231C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/26 | 231 | chr8 | 119832795 | |||||
| chr8:119832795
|
G | C | 1 | a0004c0004t0008 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-231C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/26 | 231 | chr8 | 119832795 | |||||
| chr8:119832809
|
C | A | 1 | a0001c0003t0009 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-245G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/26 | 245 | chr8 | 119832809 | |||||
| chr8:119832822
|
A | C | 1 | a0001c0011t0005 | 2 | HG01884.hp2 HG02055.hp2 |
5_prime_UTR_variant | MODIFIER | c.-258T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/26 | 258 | chr8 | 119832822 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:119732314
|
G | C | 1 | a0002c0002t0001g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3338-128C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732314 | ||||||
| chr8:119732341
|
T | G | 29 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(26): Show | 30 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.3338-155A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732341 | ||||||
| chr8:119732405
|
A | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3338-219T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732405 | ||||||
| chr8:119732549
|
A | C | 1 | a0002c0002t0001g0139 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3338-363T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732549 | ||||||
| chr8:119732575
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3338-389C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732575 | ||||||
| chr8:119732671
|
GC | G | 6 | a0002c0002t0001g0022a0002c0002t0001g0080a0002c0002t0001g0109others(3): Show | 6 | HG00423.hp1 NA18943.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338-486delG | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732671 | ||||||
| chr8:119732737
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3338-551C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732737 | ||||||
| chr8:119732814
|
C | T | 1 | a0002c0002t0001g0074 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3338-628G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732814 | ||||||
| chr8:119732905
|
G | A | 29 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(26): Show | 30 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.3338-719C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732905 | ||||||
| chr8:119732981
|
A | G | 13 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.3338-795T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119732981 | ||||||
| chr8:119733042
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3338-856C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733042 | ||||||
| chr8:119733117
|
C | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(86): Show | 90 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3338-931G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733117 | ||||||
| chr8:119733131
|
G | A | 51 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(48): Show | 54 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.3338-945C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733131 | ||||||
| chr8:119733200
|
A | G | 49 | a0003c0006t0001g0154a0003c0006t0001g0155a0003c0006t0001g0156others(46): Show | 52 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.3338-1014T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733200 | ||||||
| chr8:119733203
|
C | G | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3338-1017G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733203 | ||||||
| chr8:119733370
|
TGA | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3338-1186_3338-118 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733370 | ||||||
| chr8:119733397
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3338-1211T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733397 | ||||||
| chr8:119733412
|
C | T | 1 | a0004c0004t0002g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3338-1226G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733412 | ||||||
| chr8:119733423
|
G | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(86): Show | 90 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3338-1237C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733423 | ||||||
| chr8:119733754
|
G | T | 1 | a0001c0011t0005g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3338-1568C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733754 | ||||||
| chr8:119733780
|
G | GC | 28 | a0001c0001t0001g0189a0001c0001t0001g0215a0001c0001t0001g0222others(25): Show | 28 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.3338-1595dupG | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733780 | ||||||
| chr8:119733833
|
C | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3338-1647G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733833 | ||||||
| chr8:119733973
|
A | T | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3338-1787T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119733973 | ||||||
| chr8:119734001
|
T | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0015t0001g0160others(13): Show | 18 | HG00738.hp1 HG01243.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.3338-1815A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734001 | ||||||
| chr8:119734096
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3338-1910G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734096 | ||||||
| chr8:119734102
|
C | G | 1 | a0002c0002t0001g0104 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3338-1916G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734102 | ||||||
| chr8:119734157
|
C | T | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3338-1971G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734157 | ||||||
| chr8:119734158
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3338-1972C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734158 | ||||||
| chr8:119734237
|
T | C | 1 | a0001c0011t0005g0008 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3338-2051A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734237 | ||||||
| chr8:119734351
|
T | A | 6 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0204others(3): Show | 6 | HG02486.hp2 HG03130.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338-2165A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734351 | ||||||
| chr8:119734633
|
C | T | 3 | a0003c0008t0001g0013a0003c0008t0001g0014a0003c0008t0001g0015 | 3 | HG01891.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3338-2447G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734633 | ||||||
| chr8:119734848
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3338-2662T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734848 | ||||||
| chr8:119734964
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3338-2778G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734964 | ||||||
| chr8:119734999
|
T | C | 1 | a0004c0004t0002g0309 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3338-2813A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119734999 | ||||||
| chr8:119735444
|
T | C | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3338-3258A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735444 | ||||||
| chr8:119735507
|
A | G | 1 | a0001c0003t0001g0062 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3338-3321T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735507 | ||||||
| chr8:119735520
|
C | T | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338-3334G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735520 | ||||||
| chr8:119735570
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3338-3384G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735570 | ||||||
| chr8:119735613
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3338-3427G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735613 | ||||||
| chr8:119735662
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3338-3476G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735662 | ||||||
| chr8:119735701
|
C | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3338-3515G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735701 | ||||||
| chr8:119735862
|
G | A | 1 | a0007c0013t0001g0093 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3338-3676C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735862 | ||||||
| chr8:119735968
|
T | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3338-3782A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735968 | ||||||
| chr8:119735978
|
G | C | 2 | a0002c0002t0001g0113a0002c0002t0001g0135 | 2 | HG00597.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.3338-3792C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119735978 | ||||||
| chr8:119736184
|
A | G | 1 | a0002c0002t0001g0087 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3338-3998T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119736184 | ||||||
| chr8:119736214
|
A | G | 151 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(148): Show | 155 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.3338-4028T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119736214 | ||||||
| chr8:119736566
|
T | C | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3338-4380A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119736566 | ||||||
| chr8:119736853
|
T | C | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.3338-4667A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119736853 | ||||||
| chr8:119736926
|
C | T | 243 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(240): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.3338-4740G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119736926 | ||||||
| chr8:119736998
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3338-4812C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119736998 | ||||||
| chr8:119737245
|
T | G | 7 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3338-5059A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737245 | ||||||
| chr8:119737511
|
C | CT | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3337+5022dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737511 | ||||||
| chr8:119737577
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3337+4957A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737577 | ||||||
| chr8:119737612
|
G | A | 1 | a0002c0002t0001g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3337+4922C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737612 | ||||||
| chr8:119737634
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3337+4900C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737634 | ||||||
| chr8:119737799
|
T | C | 1 | a0002c0002t0001g0124 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3337+4735A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737799 | ||||||
| chr8:119737860
|
T | A | 2 | a0002c0002t0001g0103a0002c0002t0001g0147 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3337+4674A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737860 | ||||||
| chr8:119737868
|
GC | G | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.3337+4665delG | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737868 | ||||||
| chr8:119737957
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3337+4577A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737957 | ||||||
| chr8:119737970
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3337+4564C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119737970 | ||||||
| chr8:119738167
|
C | A | 81 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(78): Show | 86 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.3337+4367G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119738167 | ||||||
| chr8:119738183
|
G | A | 158 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(155): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.3337+4351C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119738183 | ||||||
| chr8:119738549
|
A | C | 2 | a0005c0005t0003g0290a0005c0005t0003g0291 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3337+3985T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119738549 | ||||||
| chr8:119738772
|
T | C | 158 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(155): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.3337+3762A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119738772 | ||||||
| chr8:119738896
|
T | TA | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3337+3637dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119738896 | ||||||
| chr8:119738932
|
G | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3337+3602C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119738932 | ||||||
| chr8:119739010
|
GT | G | 7 | a0002c0002t0001g0075a0002c0002t0001g0082a0002c0002t0001g0083others(4): Show | 7 | HG02683.hp2 HG03688.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.3337+3523delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739010 | ||||||
| chr8:119739018
|
T | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3337+3516A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739018 | ||||||
| chr8:119739027
|
TTTA | T | 8 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3337+3504_3337+350 others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739027 | ||||||
| chr8:119739028
|
TTA | T | 26 | a0001c0001t0001g0017a0001c0001t0001g0151a0003c0006t0001g0154others(23): Show | 27 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.3337+3504_3337+350 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739028 | ||||||
| chr8:119739029
|
TA | T | 123 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(120): Show | 126 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.3337+3504delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739029 | ||||||
| chr8:119739030
|
A | T | 1 | a0001c0011t0005g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3337+3504T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739030 | ||||||
| chr8:119739172
|
C | T | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3337+3362G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739172 | ||||||
| chr8:119739244
|
GC | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3337+3289delG | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739244 | ||||||
| chr8:119739295
|
G | T | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3337+3239C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739295 | ||||||
| chr8:119739642
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3337+2892A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739642 | ||||||
| chr8:119739821
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3337+2713T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119739821 | ||||||
| chr8:119740013
|
C | T | 2 | a0001c0011t0005g0008a0001c0011t0005g0009 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3337+2521G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740013 | ||||||
| chr8:119740019
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3337+2515A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740019 | ||||||
| chr8:119740085
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3337+2449C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740085 | ||||||
| chr8:119740184
|
G | C | 3 | a0004c0004t0002g0293a0004c0004t0002g0294a0004c0004t0002g0295 | 3 | HG01109.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3337+2350C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740184 | ||||||
| chr8:119740262
|
C | T | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3337+2272G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740262 | ||||||
| chr8:119740332
|
T | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3337+2202A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740332 | ||||||
| chr8:119740440
|
G | T | 1 | a0002c0002t0001g0074 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3337+2094C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740440 | ||||||
| chr8:119740491
|
T | TA | 101 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(98): Show | 102 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.3337+2042dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740491 | ||||||
| chr8:119740491
|
T | TAA | 26 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0001t0001g0187others(23): Show | 28 | HG00423.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.3337+2041_3337+204 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740491 | ||||||
| chr8:119740491
|
T | TTA | 4 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0028others(1): Show | 4 | HG02109.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3337+2042_3337+204 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740491 | ||||||
| chr8:119740491
|
TA | T | 8 | a0001c0003t0001g0036a0001c0003t0001g0056a0001c0003t0001g0266others(5): Show | 8 | HG00323.hp1 HG01515.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3337+2042delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740491 | ||||||
| chr8:119740573
|
G | A | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3337+1961C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740573 | ||||||
| chr8:119740662
|
C | CA | 43 | a0001c0001t0001g0196a0001c0001t0001g0239a0001c0003t0001g0024others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.3337+1871dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740662 | ||||||
| chr8:119740680
|
GAAAA | G | 7 | a0001c0003t0001g0043a0001c0003t0001g0044a0001c0003t0001g0045others(4): Show | 7 | HG01175.hp2 HG01496.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3337+1850_3337+185 others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740680 | ||||||
| chr8:119740692
|
A | AAAG | 222 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(219): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.3337+1839_3337+184 others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740692 | ||||||
| chr8:119740692
|
AAAG | A | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3337+1839_3337+184 others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740692 | ||||||
| chr8:119740955
|
T | C | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3337+1579A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119740955 | ||||||
| chr8:119741243
|
A | T | 2 | a0001c0007t0001g0025a0001c0007t0001g0028 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3337+1291T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119741243 | ||||||
| chr8:119741458
|
C | T | 33 | a0001c0003t0001g0024a0001c0003t0001g0032a0001c0003t0001g0036others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.3337+1076G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119741458 | ||||||
| chr8:119741650
|
A | T | 1 | a0002c0002t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3337+884T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119741650 | ||||||
| chr8:119741663
|
T | A | 1 | a0005c0005t0003g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3337+871A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119741663 | ||||||
| chr8:119742046
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3337+488A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119742046 | ||||||
| chr8:119742073
|
C | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0199a0001c0001t0001g0212others(1): Show | 4 | HG02523.hp2 NA18950.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.3337+461G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119742073 | ||||||
| chr8:119742337
|
TA | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3337+196delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119742337 | ||||||
| chr8:119742339
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3337+195G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119742339 | ||||||
| chr8:119742405
|
A | G | 58 | a0001c0003t0001g0019a0001c0003t0001g0024a0001c0003t0001g0032others(55): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.3337+129T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 25/25 | chr8 | 119742405 | ||||||
| chr8:119742703
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0221 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3215-47G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119742703 | ||||||
| chr8:119742899
|
T | A | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3215-243A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119742899 | ||||||
| chr8:119743052
|
G | C | 4 | a0004c0004t0002g0296a0004c0004t0002g0297a0004c0004t0002g0298others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.3215-396C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119743052 | ||||||
| chr8:119743079
|
T | A | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3215-423A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119743079 | ||||||
| chr8:119743082
|
A | T | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3215-426T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119743082 | ||||||
| chr8:119743166
|
G | C | 1 | a0002c0002t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3215-510C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119743166 | ||||||
| chr8:119743504
|
A | T | 1 | a0002c0002t0001g0071 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3214+784T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119743504 | ||||||
| chr8:119743775
|
A | C | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3214+513T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119743775 | ||||||
| chr8:119744191
|
G | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3214+97C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 24/25 | chr8 | 119744191 | ||||||
| chr8:119744422
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3109-29A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119744422 | ||||||
| chr8:119744714
|
T | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3109-321A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119744714 | ||||||
| chr8:119744754
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3109-361A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119744754 | ||||||
| chr8:119744768
|
G | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3109-375C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119744768 | ||||||
| chr8:119744780
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3109-387C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119744780 | ||||||
| chr8:119744910
|
C | G | 8 | a0002c0002t0001g0082a0002c0002t0001g0083a0002c0002t0001g0084others(5): Show | 8 | HG02683.hp2 HG03688.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-517G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119744910 | ||||||
| chr8:119745120
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3109-727T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745120 | ||||||
| chr8:119745121
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3109-728A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745121 | ||||||
| chr8:119745331
|
TTATAAA | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3109-944_3109-939d others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745331 | ||||||
| chr8:119745345
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3109-952T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745345 | ||||||
| chr8:119745385
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3109-992A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745385 | ||||||
| chr8:119745424
|
TA | T | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3109-1032delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745424 | ||||||
| chr8:119745426
|
C | T | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3109-1033G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745426 | ||||||
| chr8:119745429
|
C | T | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3109-1036G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745429 | ||||||
| chr8:119745432
|
C | CTATGTAA | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.3109-1040_3109-103 others(11): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745432 | ||||||
| chr8:119745641
|
G | A | 2 | a0001c0007t0001g0030a0001c0007t0001g0031 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3108+1064C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745641 | ||||||
| chr8:119745795
|
A | ATG | 23 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0194others(20): Show | 23 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.3108+908_3108+909d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
A | ATGTG | 13 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0204others(10): Show | 15 | HG00735.hp2 HG02602.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.3108+906_3108+909d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATG | A | 61 | a0001c0001t0001g0017a0001c0001t0001g0176a0001c0001t0001g0177others(58): Show | 62 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.3108+908_3108+909d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTG | A | 43 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0003t0001g0019others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.3108+906_3108+909d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTGTG | A | 4 | a0001c0003t0001g0043a0002c0002t0001g0068a0002c0002t0001g0117others(1): Show | 4 | HG01074.hp2 HG01168.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3108+904_3108+909d others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTGTGT others(1): Show |
A | 21 | a0002c0002t0001g0018a0003c0006t0003g0273a0003c0006t0003g0274others(18): Show | 22 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.3108+902_3108+909d others(10): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTGTGT others(3): Show |
A | 13 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.3108+900_3108+909d others(12): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTGTGT others(5): Show |
A | 5 | a0004c0004t0002g0307a0004c0004t0002g0308a0004c0004t0002g0309others(2): Show | 5 | HG02257.hp2 HG02451.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.3108+898_3108+909d others(14): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTGTGT others(11): Show |
A | 3 | a0001c0001t0001g0207a0001c0003t0001g0041a0003c0009t0001g0158 | 3 | HG02698.hp1 HG03139.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3108+892_3108+909d others(20): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTGTGT others(13): Show |
A | 13 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(10): Show | 15 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.3108+890_3108+909d others(22): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745795
|
ATGTGTGT others(19): Show |
A | 1 | a0002c0002t0001g0106 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3108+884_3108+909d others(28): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745795 | ||||||
| chr8:119745829
|
GTGTGTGT others(6): Show |
G | 1 | a0001c0003t0001g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3108+863_3108+875d others(15): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745829 | ||||||
| chr8:119745838
|
T | A | 3 | a0002c0002t0001g0010a0002c0002t0001g0086a0002c0002t0001g0087 | 3 | NA18985.hp2 NA19002.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3108+867A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119745838 | ||||||
| chr8:119746083
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3108+622T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746083 | ||||||
| chr8:119746243
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | NA18985.hp1 NA18988.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3108+462C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746243 | ||||||
| chr8:119746373
|
C | CA | 34 | a0001c0001t0001g0224a0002c0002t0001g0022a0002c0002t0001g0089others(31): Show | 35 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.3108+331dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746373 | ||||||
| chr8:119746373
|
C | CAA | 6 | a0001c0001t0001g0193a0001c0001t0001g0217a0004c0004t0002g0299others(3): Show | 6 | HG02004.hp1 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3108+330_3108+331d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746373 | ||||||
| chr8:119746373
|
C | CAAA | 67 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(64): Show | 68 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.3108+329_3108+331d others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746373 | ||||||
| chr8:119746373
|
C | CAAAA | 20 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(17): Show | 20 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.3108+328_3108+331d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746373 | ||||||
| chr8:119746373
|
CA | C | 43 | a0001c0003t0001g0024a0001c0003t0001g0032a0001c0003t0001g0036others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.3108+331delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746373 | ||||||
| chr8:119746373
|
CAAA | C | 29 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(26): Show | 31 | HG00738.hp1 HG01167.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.3108+329_3108+331d others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746373 | ||||||
| chr8:119746463
|
C | T | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.3108+242G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746463 | ||||||
| chr8:119746479
|
C | T | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.3108+226G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 23/25 | chr8 | 119746479 | ||||||
| chr8:119747030
|
T | G | 1 | a0003c0006t0001g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2879-96A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747030 | ||||||
| chr8:119747108
|
G | C | 5 | a0004c0004t0002g0007a0004c0004t0002g0299a0004c0004t0002g0300others(2): Show | 6 | HG02970.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2879-174C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747108 | ||||||
| chr8:119747321
|
C | A | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2879-387G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747321 | ||||||
| chr8:119747630
|
T | C | 7 | a0001c0001t0001g0200a0001c0003t0001g0266a0001c0003t0001g0267others(4): Show | 7 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2879-696A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747630 | ||||||
| chr8:119747630
|
T | G | 4 | a0003c0009t0001g0004a0003c0009t0001g0153a0003c0009t0001g0157others(1): Show | 5 | HG02145.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2879-696A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747630 | ||||||
| chr8:119747649
|
G | A | 3 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0001g0126 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2879-715C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747649 | ||||||
| chr8:119747670
|
C | G | 216 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2879-736G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747670 | ||||||
| chr8:119747677
|
C | A | 5 | a0004c0004t0002g0007a0004c0004t0002g0299a0004c0004t0002g0300others(2): Show | 6 | HG02970.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2879-743G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747677 | ||||||
| chr8:119747680
|
G | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2879-746C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747680 | ||||||
| chr8:119747736
|
T | G | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2879-802A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747736 | ||||||
| chr8:119747829
|
G | GA | 5 | a0001c0001t0001g0189a0001c0001t0001g0256a0001c0003t0001g0041others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.2879-896dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747829 | ||||||
| chr8:119747890
|
G | A | 1 | a0002c0002t0001g0075 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2879-956C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747890 | ||||||
| chr8:119747911
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2879-977G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119747911 | ||||||
| chr8:119748024
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2879-1090A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748024 | ||||||
| chr8:119748137
|
A | C | 5 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2879-1203T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748137 | ||||||
| chr8:119748308
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2879-1374C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748308 | ||||||
| chr8:119748375
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2879-1441C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748375 | ||||||
| chr8:119748609
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2879-1675C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748609 | ||||||
| chr8:119748650
|
C | T | 7 | a0001c0003t0001g0043a0001c0003t0001g0044a0001c0003t0001g0045others(4): Show | 7 | HG01175.hp2 HG01496.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2879-1716G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748650 | ||||||
| chr8:119748671
|
T | G | 1 | a0002c0002t0001g0100 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2879-1737A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748671 | ||||||
| chr8:119748917
|
TA | T | 16 | a0001c0015t0001g0160a0002c0002t0001g0088a0002c0002t0001g0137others(13): Show | 18 | HG00323.hp1 HG00738.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.2879-1984delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748917 | ||||||
| chr8:119748929
|
A | AC | 88 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(85): Show | 89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.2879-1996_2879-199 others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119748929 | ||||||
| chr8:119749177
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2879-2243C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119749177 | ||||||
| chr8:119749271
|
C | T | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2879-2337G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119749271 | ||||||
| chr8:119749421
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2879-2487A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119749421 | ||||||
| chr8:119749740
|
G | GA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2879-2807dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119749740 | ||||||
| chr8:119749987
|
T | C | 2 | a0002c0002t0001g0082a0002c0002t0001g0083 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2879-3053A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119749987 | ||||||
| chr8:119749993
|
G | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2879-3059C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119749993 | ||||||
| chr8:119750198
|
G | A | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2879-3264C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750198 | ||||||
| chr8:119750224
|
C | T | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2879-3290G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750224 | ||||||
| chr8:119750335
|
C | T | 2 | a0001c0007t0001g0030a0001c0007t0001g0031 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2879-3401G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750335 | ||||||
| chr8:119750459
|
T | C | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2879-3525A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750459 | ||||||
| chr8:119750663
|
A | G | 1 | a0001c0011t0005g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2879-3729T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750663 | ||||||
| chr8:119750669
|
G | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(85): Show | 89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.2879-3735C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750669 | ||||||
| chr8:119750690
|
G | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2879-3756C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750690 | ||||||
| chr8:119750694
|
CAG | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2879-3762_2879-376 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119750694 | ||||||
| chr8:119751319
|
T | C | 1 | a0001c0007t0001g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2879-4385A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751319 | ||||||
| chr8:119751345
|
G | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2879-4411C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751345 | ||||||
| chr8:119751361
|
C | T | 1 | a0001c0003t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2879-4427G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751361 | ||||||
| chr8:119751491
|
A | G | 6 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0190others(3): Show | 6 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.2878+4515T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751491 | ||||||
| chr8:119751530
|
G | T | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2878+4476C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751530 | ||||||
| chr8:119751596
|
A | G | 1 | a0002c0002t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2878+4410T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751596 | ||||||
| chr8:119751710
|
T | C | 5 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072others(2): Show | 5 | HG01952.hp2 HG03704.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.2878+4296A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751710 | ||||||
| chr8:119751724
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2878+4282T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751724 | ||||||
| chr8:119751875
|
A | G | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2878+4131T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119751875 | ||||||
| chr8:119752170
|
AT | A | 3 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2878+3835delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119752170 | ||||||
| chr8:119752249
|
T | C | 158 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(155): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2878+3757A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119752249 | ||||||
| chr8:119752498
|
T | TC | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2878+3507dupG | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119752498 | ||||||
| chr8:119752518
|
T | C | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.2878+3488A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119752518 | ||||||
| chr8:119752777
|
G | T | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2878+3229C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119752777 | ||||||
| chr8:119753051
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2878+2955G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119753051 | ||||||
| chr8:119753086
|
T | C | 1 | a0002c0002t0001g0089 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2878+2920A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119753086 | ||||||
| chr8:119753325
|
T | A | 3 | a0003c0008t0001g0013a0003c0008t0001g0014a0003c0008t0001g0015 | 3 | HG01891.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2878+2681A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119753325 | ||||||
| chr8:119753360
|
T | C | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2878+2646A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119753360 | ||||||
| chr8:119753584
|
C | G | 1 | a0002c0002t0001g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2878+2422G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119753584 | ||||||
| chr8:119753897
|
T | C | 2 | a0001c0001t0001g0199a0003c0009t0001g0164 | 2 | HG02523.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2878+2109A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119753897 | ||||||
| chr8:119754103
|
T | C | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2878+1903A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754103 | ||||||
| chr8:119754183
|
G | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2878+1823C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754183 | ||||||
| chr8:119754249
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2878+1757A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754249 | ||||||
| chr8:119754275
|
G | T | 1 | a0002c0002t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2878+1731C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754275 | ||||||
| chr8:119754459
|
C | T | 1 | a0003c0009t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2878+1547G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754459 | ||||||
| chr8:119754525
|
A | T | 4 | a0004c0004t0002g0296a0004c0004t0002g0297a0004c0004t0002g0298others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.2878+1481T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754525 | ||||||
| chr8:119754528
|
C | T | 1 | a0002c0002t0001g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2878+1478G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754528 | ||||||
| chr8:119754627
|
A | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2878+1379T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754627 | ||||||
| chr8:119754680
|
CA | C | 11 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2878+1325delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754680 | ||||||
| chr8:119754696
|
T | A | 4 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2878+1310A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754696 | ||||||
| chr8:119754778
|
C | T | 156 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(153): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.2878+1228G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754778 | ||||||
| chr8:119754783
|
T | C | 1 | a0002c0002t0001g0144 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2878+1223A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754783 | ||||||
| chr8:119754944
|
C | T | 2 | a0005c0005t0003g0290a0005c0005t0003g0291 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2878+1062G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754944 | ||||||
| chr8:119754956
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2878+1050T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119754956 | ||||||
| chr8:119755071
|
T | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2878+935A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755071 | ||||||
| chr8:119755145
|
A | G | 1 | a0002c0002t0001g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2878+861T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755145 | ||||||
| chr8:119755256
|
C | T | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2878+750G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755256 | ||||||
| chr8:119755280
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2878+726C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755280 | ||||||
| chr8:119755322
|
C | T | 1 | a0001c0003t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2878+684G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755322 | ||||||
| chr8:119755342
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | NA18985.hp1 NA18988.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2878+664G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755342 | ||||||
| chr8:119755519
|
A | C | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2878+487T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755519 | ||||||
| chr8:119755695
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2878+311G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755695 | ||||||
| chr8:119755725
|
A | G | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2878+281T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 22/25 | chr8 | 119755725 | ||||||
| chr8:119756204
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2769-89A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756204 | ||||||
| chr8:119756206
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2769-91A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756206 | ||||||
| chr8:119756309
|
G | T | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2769-194C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756309 | ||||||
| chr8:119756336
|
T | G | 1 | a0003c0006t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2769-221A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756336 | ||||||
| chr8:119756447
|
C | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2769-332G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756447 | ||||||
| chr8:119756480
|
A | G | 4 | a0002c0002t0001g0021a0002c0002t0001g0096a0002c0002t0001g0097others(1): Show | 4 | HG02165.hp1 NA18989.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-365T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756480 | ||||||
| chr8:119756696
|
G | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2769-581C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756696 | ||||||
| chr8:119756734
|
G | A | 1 | a0003c0008t0001g0013 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2769-619C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756734 | ||||||
| chr8:119756939
|
T | C | 29 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(26): Show | 30 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.2769-824A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756939 | ||||||
| chr8:119756975
|
A | G | 54 | a0001c0003t0001g0019a0001c0003t0001g0024a0001c0003t0001g0032others(51): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2769-860T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119756975 | ||||||
| chr8:119757038
|
G | C | 1 | a0001c0018t0001g0182 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2769-923C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757038 | ||||||
| chr8:119757073
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2769-958T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757073 | ||||||
| chr8:119757079
|
A | T | 2 | a0002c0002t0001g0103a0002c0002t0001g0147 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2769-964T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757079 | ||||||
| chr8:119757221
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2768+852A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757221 | ||||||
| chr8:119757252
|
C | T | 1 | a0004c0004t0002g0293 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2768+821G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757252 | ||||||
| chr8:119757369
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2768+704T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757369 | ||||||
| chr8:119757415
|
G | C | 1 | a0004c0004t0002g0309 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2768+658C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757415 | ||||||
| chr8:119757489
|
T | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2768+584A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757489 | ||||||
| chr8:119757586
|
A | AT | 8 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(5): Show | 8 | HG02717.hp2 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2768+486dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757586 | ||||||
| chr8:119757627
|
C | T | 1 | a0003c0006t0003g0273 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2768+446G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757627 | ||||||
| chr8:119757694
|
G | A | 16 | a0004c0004t0002g0007a0004c0004t0002g0292a0004c0004t0002g0293others(13): Show | 17 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2768+379C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757694 | ||||||
| chr8:119757895
|
C | CA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2768+177dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757895 | ||||||
| chr8:119757984
|
C | T | 1 | a0002c0002t0001g0020 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2768+89G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119757984 | ||||||
| chr8:119758022
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2768+51C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 21/25 | chr8 | 119758022 | ||||||
| chr8:119758207
|
C | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2699-65G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119758207 | ||||||
| chr8:119758303
|
A | G | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2699-161T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119758303 | ||||||
| chr8:119758404
|
C | T | 1 | a0001c0007t0001g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2699-262G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119758404 | ||||||
| chr8:119758480
|
C | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18997.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.2699-338G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119758480 | ||||||
| chr8:119758665
|
A | G | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2699-523T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119758665 | ||||||
| chr8:119758867
|
G | A | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2699-725C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119758867 | ||||||
| chr8:119759123
|
T | C | 1 | a0005c0005t0003g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2699-981A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119759123 | ||||||
| chr8:119759301
|
T | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2699-1159A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119759301 | ||||||
| chr8:119759455
|
G | A | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2698+1144C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119759455 | ||||||
| chr8:119759623
|
G | A | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2698+976C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119759623 | ||||||
| chr8:119759815
|
A | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2698+784T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119759815 | ||||||
| chr8:119759826
|
T | C | 1 | a0002c0002t0001g0089 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2698+773A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119759826 | ||||||
| chr8:119759857
|
G | C | 1 | a0001c0001t0001g0242 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2698+742C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119759857 | ||||||
| chr8:119760029
|
G | GC | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2698+569dupG | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119760029 | ||||||
| chr8:119760058
|
G | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2698+541C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119760058 | ||||||
| chr8:119760087
|
T | A | 4 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0048others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2698+512A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119760087 | ||||||
| chr8:119760189
|
T | C | 13 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2698+410A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119760189 | ||||||
| chr8:119760436
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2698+163A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 20/25 | chr8 | 119760436 | ||||||
| chr8:119760843
|
A | C | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2559-105T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119760843 | ||||||
| chr8:119760884
|
A | T | 158 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(155): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2559-146T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119760884 | ||||||
| chr8:119760949
|
ATTAAT | A | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2559-216_2559-212d others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119760949 | ||||||
| chr8:119761079
|
C | T | 3 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2559-341G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761079 | ||||||
| chr8:119761165
|
T | A | 1 | a0004c0004t0002g0296 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2559-427A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761165 | ||||||
| chr8:119761252
|
T | A | 2 | a0001c0011t0005g0008a0001c0011t0005g0009 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2559-514A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761252 | ||||||
| chr8:119761352
|
G | C | 2 | a0001c0007t0001g0030a0001c0007t0001g0031 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2559-614C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761352 | ||||||
| chr8:119761547
|
A | T | 158 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(155): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2559-809T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761547 | ||||||
| chr8:119761800
|
C | CA | 7 | a0001c0001t0001g0232a0001c0003t0001g0040a0001c0003t0001g0044others(4): Show | 7 | HG01952.hp2 HG02109.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2558+614dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761800 | ||||||
| chr8:119761804
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2558+611T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761804 | ||||||
| chr8:119761905
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2558+510A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 19/25 | chr8 | 119761905 | ||||||
| chr8:119762803
|
T | C | 1 | a0004c0004t0002g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2365-195A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119762803 | ||||||
| chr8:119762903
|
G | A | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2365-295C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119762903 | ||||||
| chr8:119763078
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2365-470T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119763078 | ||||||
| chr8:119763453
|
G | C | 2 | a0001c0011t0005g0008a0001c0011t0005g0009 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2365-845C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119763453 | ||||||
| chr8:119763467
|
C | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-859G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119763467 | ||||||
| chr8:119763481
|
G | A | 1 | a0005c0005t0003g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2365-873C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119763481 | ||||||
| chr8:119763543
|
A | G | 4 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0048others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2365-935T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119763543 | ||||||
| chr8:119763602
|
C | T | 1 | a0001c0003t0009g0314 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2365-994G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119763602 | ||||||
| chr8:119764045
|
C | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2365-1437G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764045 | ||||||
| chr8:119764054
|
C | CAGG | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2365-1447_2365-144 others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764054 | ||||||
| chr8:119764104
|
C | T | 1 | a0001c0003t0004g0034 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2365-1496G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764104 | ||||||
| chr8:119764154
|
T | A | 3 | a0001c0003t0001g0046a0002c0002t0001g0119a0002c0002t0001g0120 | 3 | HG01496.hp1 HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2365-1546A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764154 | ||||||
| chr8:119764270
|
G | A | 29 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(26): Show | 30 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.2365-1662C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764270 | ||||||
| chr8:119764308
|
C | T | 2 | a0001c0001t0001g0243a0001c0016t0001g0202 | 2 | HG01258.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2365-1700G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764308 | ||||||
| chr8:119764319
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2365-1711A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764319 | ||||||
| chr8:119764334
|
T | C | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365-1726A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764334 | ||||||
| chr8:119764355
|
A | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2365-1747T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764355 | ||||||
| chr8:119764446
|
T | G | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2365-1838A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764446 | ||||||
| chr8:119764536
|
T | A | 1 | a0004c0004t0002g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2365-1928A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764536 | ||||||
| chr8:119764757
|
A | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-2149T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764757 | ||||||
| chr8:119764942
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2365-2334A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119764942 | ||||||
| chr8:119765046
|
T | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2365-2438A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765046 | ||||||
| chr8:119765090
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2365-2482T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765090 | ||||||
| chr8:119765097
|
C | T | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2365-2489G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765097 | ||||||
| chr8:119765213
|
C | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0190others(1): Show | 4 | HG00639.hp2 HG01081.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2365-2605G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765213 | ||||||
| chr8:119765484
|
G | C | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2365-2876C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765484 | ||||||
| chr8:119765535
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-2927C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765535 | ||||||
| chr8:119765548
|
A | G | 3 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072 | 3 | HG01952.hp2 NA18612.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.2365-2940T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765548 | ||||||
| chr8:119765562
|
G | T | 2 | a0004c0004t0002g0297a0004c0004t0002g0298 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2365-2954C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765562 | ||||||
| chr8:119765567
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2365-2959C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765567 | ||||||
| chr8:119765667
|
A | C | 3 | a0001c0003t0001g0037a0001c0003t0001g0038a0001c0003t0001g0039 | 3 | HG02451.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2365-3059T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765667 | ||||||
| chr8:119765751
|
T | C | 43 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(40): Show | 46 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2365-3143A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765751 | ||||||
| chr8:119765889
|
C | T | 3 | a0002c0002t0001g0101a0002c0002t0001g0102a0002c0002t0001g0123 | 3 | NA18941.hp1 NA18998.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2365-3281G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765889 | ||||||
| chr8:119765949
|
A | G | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2365-3341T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765949 | ||||||
| chr8:119765992
|
T | C | 1 | a0001c0003t0001g0024 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2365-3384A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119765992 | ||||||
| chr8:119766091
|
A | C | 43 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(40): Show | 46 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2365-3483T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766091 | ||||||
| chr8:119766238
|
G | A | 1 | a0001c0003t0001g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2365-3630C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766238 | ||||||
| chr8:119766356
|
G | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-3748C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766356 | ||||||
| chr8:119766387
|
G | A | 53 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(50): Show | 56 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.2365-3779C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766387 | ||||||
| chr8:119766417
|
C | T | 1 | a0003c0006t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2365-3809G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766417 | ||||||
| chr8:119766477
|
T | C | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2365-3869A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766477 | ||||||
| chr8:119766793
|
C | T | 10 | a0002c0002t0001g0002a0002c0002t0001g0067a0002c0002t0001g0078others(7): Show | 11 | NA18950.hp2 NA18952.hp2 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.2365-4185G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766793 | ||||||
| chr8:119766948
|
A | T | 1 | a0001c0001t0001g0216 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2365-4340T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119766948 | ||||||
| chr8:119767007
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(93): Show | 97 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2365-4399T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767007 | ||||||
| chr8:119767018
|
G | A | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2365-4410C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767018 | ||||||
| chr8:119767185
|
T | C | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.2365-4577A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767185 | ||||||
| chr8:119767222
|
G | T | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365-4614C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767222 | ||||||
| chr8:119767292
|
T | C | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2365-4684A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767292 | ||||||
| chr8:119767377
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-4769C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767377 | ||||||
| chr8:119767551
|
A | G | 216 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2365-4943T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767551 | ||||||
| chr8:119767615
|
G | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2365-5007C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767615 | ||||||
| chr8:119767683
|
C | T | 2 | a0001c0011t0005g0008a0001c0011t0005g0009 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2365-5075G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767683 | ||||||
| chr8:119767855
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2365-5247C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767855 | ||||||
| chr8:119767994
|
G | A | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2365-5386C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119767994 | ||||||
| chr8:119768074
|
G | A | 44 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(41): Show | 47 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2365-5466C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768074 | ||||||
| chr8:119768324
|
C | T | 1 | a0002c0002t0001g0146 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2365-5716G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768324 | ||||||
| chr8:119768325
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2365-5717C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768325 | ||||||
| chr8:119768327
|
C | T | 1 | a0002c0002t0001g0146 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2365-5719G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768327 | ||||||
| chr8:119768414
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2365-5806A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768414 | ||||||
| chr8:119768486
|
AT | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2365-5879delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768486 | ||||||
| chr8:119768541
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2365-5933T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768541 | ||||||
| chr8:119768636
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-6028A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768636 | ||||||
| chr8:119768655
|
G | A | 1 | a0004c0004t0002g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2365-6047C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768655 | ||||||
| chr8:119768792
|
T | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0254 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2365-6184A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768792 | ||||||
| chr8:119768847
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2365-6239C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768847 | ||||||
| chr8:119768852
|
A | T | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365-6244T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119768852 | ||||||
| chr8:119769017
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2365-6409G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769017 | ||||||
| chr8:119769067
|
C | T | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2365-6459G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769067 | ||||||
| chr8:119769401
|
G | A | 2 | a0003c0006t0001g0159a0003c0006t0001g0162 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2365-6793C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769401 | ||||||
| chr8:119769448
|
T | TAATGATT others(13): Show |
9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-6860_2365-684 others(24): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769448 | ||||||
| chr8:119769480
|
T | C | 1 | a0001c0003t0001g0047 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2365-6872A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769480 | ||||||
| chr8:119769550
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2365-6942T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769550 | ||||||
| chr8:119769568
|
A | C | 4 | a0002c0002t0001g0002a0002c0002t0001g0078a0002c0002t0001g0079others(1): Show | 5 | NA18952.hp2 NA18964.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2365-6960T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769568 | ||||||
| chr8:119769599
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2365-6991A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769599 | ||||||
| chr8:119769608
|
T | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-7000A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769608 | ||||||
| chr8:119769615
|
A | G | 1 | a0002c0002t0001g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2365-7007T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769615 | ||||||
| chr8:119769677
|
C | A | 158 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(155): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2365-7069G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769677 | ||||||
| chr8:119769794
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2365-7186A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769794 | ||||||
| chr8:119769828
|
G | A | 12 | a0002c0002t0001g0018a0002c0002t0001g0068a0002c0002t0001g0069others(9): Show | 12 | HG01168.hp2 HG01361.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.2365-7220C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769828 | ||||||
| chr8:119769851
|
G | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2365-7243C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119769851 | ||||||
| chr8:119770061
|
A | AT | 143 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(140): Show | 147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.2365-7454dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770061 | ||||||
| chr8:119770124
|
T | A | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2365-7516A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770124 | ||||||
| chr8:119770623
|
A | G | 53 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(50): Show | 56 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.2364+7396T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770623 | ||||||
| chr8:119770661
|
C | T | 1 | a0002c0002t0001g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2364+7358G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770661 | ||||||
| chr8:119770667
|
C | G | 1 | a0002c0002t0001g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2364+7352G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770667 | ||||||
| chr8:119770796
|
A | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(142): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.2364+7223T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770796 | ||||||
| chr8:119770923
|
T | C | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2364+7096A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770923 | ||||||
| chr8:119770944
|
A | G | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2364+7075T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770944 | ||||||
| chr8:119770951
|
G | A | 1 | a0002c0002t0001g0003 | 2 | NA18999.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2364+7068C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119770951 | ||||||
| chr8:119771049
|
C | T | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.2364+6970G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771049 | ||||||
| chr8:119771280
|
G | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2364+6739C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771280 | ||||||
| chr8:119771342
|
T | C | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2364+6677A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771342 | ||||||
| chr8:119771388
|
A | G | 1 | a0003c0006t0001g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2364+6631T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771388 | ||||||
| chr8:119771447
|
G | GTTGAT | 3 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0016 | 3 | HG02630.hp1 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2364+6571_2364+657 others(9): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771447 | ||||||
| chr8:119771529
|
C | T | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2364+6490G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771529 | ||||||
| chr8:119771709
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+6310A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771709 | ||||||
| chr8:119771820
|
T | C | 1 | a0002c0002t0001g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2364+6199A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771820 | ||||||
| chr8:119771922
|
C | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2364+6097G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119771922 | ||||||
| chr8:119772415
|
A | G | 1 | a0002c0002t0001g0096 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2364+5604T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119772415 | ||||||
| chr8:119772636
|
A | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+5383T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119772636 | ||||||
| chr8:119772672
|
C | A | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2364+5347G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119772672 | ||||||
| chr8:119772674
|
C | A | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2364+5345G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119772674 | ||||||
| chr8:119772855
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2364+5164A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119772855 | ||||||
| chr8:119772873
|
GTTGCAGT others(1227): Show |
G | 4 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG01433.hp2 HG01928.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2364+3912_2364+514 others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119772873 | ||||||
| chr8:119772888
|
G | A | 4 | a0004c0004t0002g0307a0004c0004t0002g0308a0004c0004t0002g0309others(1): Show | 4 | HG02257.hp2 HG02451.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2364+5131C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119772888 | ||||||
| chr8:119773092
|
CA | C | 152 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(149): Show | 156 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.2364+4926delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773092 | ||||||
| chr8:119773276
|
A | G | 1 | a0004c0004t0002g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2364+4743T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773276 | ||||||
| chr8:119773279
|
T | TA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+4739dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773279 | ||||||
| chr8:119773319
|
G | A | 43 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(40): Show | 46 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2364+4700C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773319 | ||||||
| chr8:119773482
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+4537T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773482 | ||||||
| chr8:119773502
|
C | T | 1 | a0004c0004t0002g0302 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2364+4517G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773502 | ||||||
| chr8:119773538
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2364+4481A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773538 | ||||||
| chr8:119773751
|
C | A | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2364+4268G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773751 | ||||||
| chr8:119773790
|
G | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+4229C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773790 | ||||||
| chr8:119773981
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2364+4038G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773981 | ||||||
| chr8:119773987
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2364+4032A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119773987 | ||||||
| chr8:119774000
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2364+4019A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774000 | ||||||
| chr8:119774039
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+3980G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774039 | ||||||
| chr8:119774064
|
G | A | 1 | a0003c0006t0001g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2364+3955C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774064 | ||||||
| chr8:119774131
|
A | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2364+3888T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774131 | ||||||
| chr8:119774170
|
C | CA | 18 | a0001c0003t0001g0267a0001c0003t0001g0268a0001c0015t0001g0160others(15): Show | 20 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2364+3848dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774170 | ||||||
| chr8:119774329
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2364+3690C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774329 | ||||||
| chr8:119774478
|
AT | A | 216 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2364+3540delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774478 | ||||||
| chr8:119774491
|
AT | A | 118 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0001t0001g0213others(115): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2364+3527delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774491 | ||||||
| chr8:119774491
|
ATT | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(86): Show | 90 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2364+3526_2364+352 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774491 | ||||||
| chr8:119774802
|
G | C | 39 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(36): Show | 42 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.2364+3217C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774802 | ||||||
| chr8:119774821
|
T | C | 25 | a0003c0010t0002g0312a0003c0010t0002g0313a0003c0017t0003g0277others(22): Show | 26 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.2364+3198A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774821 | ||||||
| chr8:119774866
|
A | G | 90 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(87): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2364+3153T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774866 | ||||||
| chr8:119774924
|
A | T | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2364+3095T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119774924 | ||||||
| chr8:119775007
|
G | A | 1 | a0001c0003t0001g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2364+3012C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775007 | ||||||
| chr8:119775279
|
C | CA | 82 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0178others(79): Show | 83 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.2364+2739dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775279 | ||||||
| chr8:119775279
|
CA | C | 62 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0001t0001g0169others(59): Show | 65 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.2364+2739delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775279 | ||||||
| chr8:119775371
|
C | A | 2 | a0005c0005t0003g0001a0005c0005t0003g0286 | 4 | HG00323.hp2 HG00735.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.2364+2648G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775371 | ||||||
| chr8:119775567
|
G | A | 1 | a0001c0003t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2364+2452C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775567 | ||||||
| chr8:119775618
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2364+2401C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775618 | ||||||
| chr8:119775652
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2364+2367C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775652 | ||||||
| chr8:119775690
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2364+2329C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775690 | ||||||
| chr8:119775740
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2364+2279A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775740 | ||||||
| chr8:119775815
|
C | T | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.2364+2204G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775815 | ||||||
| chr8:119775847
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2364+2172C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775847 | ||||||
| chr8:119775871
|
T | C | 3 | a0001c0003t0001g0037a0001c0003t0001g0038a0001c0003t0001g0039 | 3 | HG02451.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2364+2148A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119775871 | ||||||
| chr8:119776022
|
T | A | 1 | a0001c0016t0001g0202 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2364+1997A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776022 | ||||||
| chr8:119776024
|
C | CT | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2364+1994dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776024 | ||||||
| chr8:119776089
|
A | C | 1 | a0005c0005t0003g0279 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2364+1930T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776089 | ||||||
| chr8:119776138
|
T | C | 3 | a0002c0002t0001g0089a0002c0002t0001g0091a0002c0002t0001g0145 | 3 | NA18967.hp1 NA18981.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2364+1881A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776138 | ||||||
| chr8:119776346
|
G | A | 3 | a0005c0005t0003g0278a0005c0005t0003g0279a0005c0005t0003g0280 | 3 | HG02723.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2364+1673C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776346 | ||||||
| chr8:119776347
|
C | CT | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2364+1671dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776347 | ||||||
| chr8:119776347
|
CT | C | 108 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0003t0001g0019others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.2364+1671delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776347 | ||||||
| chr8:119776374
|
A | C | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2364+1645T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776374 | ||||||
| chr8:119776410
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2364+1609G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776410 | ||||||
| chr8:119776467
|
G | A | 1 | a0001c0003t0004g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2364+1552C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776467 | ||||||
| chr8:119776483
|
C | T | 1 | a0004c0004t0002g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2364+1536G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776483 | ||||||
| chr8:119776526
|
C | CA | 77 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(74): Show | 82 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.2364+1492dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776526 | ||||||
| chr8:119776545
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2364+1474G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776545 | ||||||
| chr8:119776549
|
C | T | 1 | a0001c0003t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2364+1470G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776549 | ||||||
| chr8:119776638
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0254 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2364+1381C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776638 | ||||||
| chr8:119776644
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+1375C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776644 | ||||||
| chr8:119776778
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+1241A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776778 | ||||||
| chr8:119776846
|
A | G | 12 | a0002c0002t0001g0018a0002c0002t0001g0068a0002c0002t0001g0069others(9): Show | 12 | HG01168.hp2 HG01361.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.2364+1173T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776846 | ||||||
| chr8:119776899
|
T | TG | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2364+1119dupC | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119776899 | ||||||
| chr8:119777034
|
CTTGTCA | C | 10 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0190others(7): Show | 10 | HG00639.hp2 HG01070.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2364+979_2364+984d others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777034 | ||||||
| chr8:119777091
|
G | A | 23 | a0001c0003t0001g0024a0001c0003t0001g0032a0001c0003t0001g0036others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.2364+928C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777091 | ||||||
| chr8:119777172
|
A | C | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2364+847T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777172 | ||||||
| chr8:119777226
|
C | G | 1 | a0006c0012t0001g0005 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2364+793G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777226 | ||||||
| chr8:119777362
|
T | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2364+657A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777362 | ||||||
| chr8:119777500
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+519A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777500 | ||||||
| chr8:119777557
|
CAATTGCT others(12): Show |
C | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2364+443_2364+461d others(21): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777557 | ||||||
| chr8:119777562
|
G | T | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2364+457C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777562 | ||||||
| chr8:119777819
|
A | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+200T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 18/25 | chr8 | 119777819 | ||||||
| chr8:119778138
|
G | GA | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.2254-10dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778138 | ||||||
| chr8:119778161
|
A | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2254-32T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778161 | ||||||
| chr8:119778378
|
T | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2254-249A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778378 | ||||||
| chr8:119778425
|
A | G | 1 | a0001c0003t0001g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2254-296T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778425 | ||||||
| chr8:119778510
|
A | G | 1 | a0004c0004t0002g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2254-381T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778510 | ||||||
| chr8:119778618
|
C | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2254-489G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778618 | ||||||
| chr8:119778772
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2254-643A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778772 | ||||||
| chr8:119778912
|
A | G | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2254-783T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778912 | ||||||
| chr8:119778941
|
T | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2254-812A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778941 | ||||||
| chr8:119778970
|
T | C | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2254-841A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119778970 | ||||||
| chr8:119779186
|
C | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.2254-1057G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779186 | ||||||
| chr8:119779249
|
G | GAC | 73 | a0001c0003t0001g0019a0001c0003t0001g0037a0001c0003t0001g0038others(70): Show | 78 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2254-1122_2254-112 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779249
|
G | GACAC | 34 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(31): Show | 34 | HG00423.hp2 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.2254-1124_2254-112 others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779249
|
G | GACACAC | 86 | a0001c0001t0001g0006a0001c0001t0001g0173a0001c0001t0001g0174others(83): Show | 87 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.2254-1126_2254-112 others(10): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779249
|
G | GACACACA others(1): Show |
9 | a0001c0001t0001g0210a0001c0001t0001g0223a0001c0001t0001g0233others(6): Show | 10 | HG00544.hp1 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2254-1128_2254-112 others(12): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779249
|
G | GACACACA others(3): Show |
6 | a0001c0015t0001g0160a0003c0006t0001g0159a0003c0006t0001g0161others(3): Show | 7 | HG00738.hp1 HG02027.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.2254-1130_2254-112 others(14): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779249
|
G | GACACACA others(5): Show |
4 | a0001c0001t0001g0170a0001c0001t0001g0172a0003c0006t0001g0155others(1): Show | 4 | HG02922.hp1 HG03704.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.2254-1132_2254-112 others(16): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779249
|
GAC | G | 27 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0003t0001g0024others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2254-1122_2254-112 others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779249
|
GACAC | G | 6 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2254-1124_2254-112 others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779249 | ||||||
| chr8:119779362
|
A | T | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2254-1233T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779362 | ||||||
| chr8:119779483
|
T | C | 9 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(6): Show | 10 | HG00738.hp1 HG02027.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.2254-1354A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779483 | ||||||
| chr8:119779593
|
T | A | 1 | a0006c0012t0001g0005 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2253+1460A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779593 | ||||||
| chr8:119779741
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2253+1312G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779741 | ||||||
| chr8:119779915
|
C | G | 1 | a0006c0012t0001g0005 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2253+1138G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779915 | ||||||
| chr8:119779955
|
C | T | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.2253+1098G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779955 | ||||||
| chr8:119779973
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2253+1080A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119779973 | ||||||
| chr8:119780005
|
T | C | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2253+1048A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780005 | ||||||
| chr8:119780032
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2253+1021A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780032 | ||||||
| chr8:119780110
|
T | A | 1 | a0004c0004t0002g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2253+943A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780110 | ||||||
| chr8:119780149
|
C | CATT | 311 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.2253+901_2253+903d others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780149 | ||||||
| chr8:119780279
|
T | C | 1 | a0001c0003t0001g0024 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2253+774A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780279 | ||||||
| chr8:119780302
|
C | T | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.2253+751G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780302 | ||||||
| chr8:119780334
|
C | CA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2253+718dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780334 | ||||||
| chr8:119780534
|
C | G | 6 | a0001c0007t0001g0025a0001c0007t0001g0027a0001c0007t0001g0028others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2253+519G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780534 | ||||||
| chr8:119780577
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG00099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2253+476C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780577 | ||||||
| chr8:119780658
|
G | A | 1 | a0001c0003t0001g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2253+395C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780658 | ||||||
| chr8:119780663
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2253+390G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780663 | ||||||
| chr8:119780731
|
G | C | 217 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2253+322C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780731 | ||||||
| chr8:119780852
|
G | A | 2 | a0003c0006t0001g0159a0003c0006t0001g0162 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2253+201C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780852 | ||||||
| chr8:119780864
|
GGCGGAGC others(9): Show |
G | 1 | a0002c0002t0001g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2253+173_2253+188d others(18): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780864 | ||||||
| chr8:119780872
|
T | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2253+181A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780872 | ||||||
| chr8:119780914
|
G | A | 1 | a0003c0006t0003g0274 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2253+139C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780914 | ||||||
| chr8:119780934
|
C | CA | 15 | a0001c0001t0001g0017a0001c0001t0001g0200a0001c0001t0001g0252others(12): Show | 15 | HG00735.hp1 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2253+118dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780934 | ||||||
| chr8:119780934
|
C | CAA | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2253+117_2253+118d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780934 | ||||||
| chr8:119780934
|
CA | C | 6 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0237others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2253+118delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119780934 | ||||||
| chr8:119781004
|
TAAACTG | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2253+43_2253+48del others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119781004 | ||||||
| chr8:119781028
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2253+25C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 17/25 | chr8 | 119781028 | ||||||
| chr8:119781322
|
T | G | 1 | a0001c0001t0001g0209 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2113-129A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781322 | ||||||
| chr8:119781505
|
C | G | 4 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0048others(1): Show | 4 | HG02280.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2113-312G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781505 | ||||||
| chr8:119781536
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0003t0001g0266others(6): Show | 9 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2113-343G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781536 | ||||||
| chr8:119781589
|
A | C | 1 | a0002c0002t0001g0075 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2113-396T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781589 | ||||||
| chr8:119781627
|
G | T | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2113-434C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781627 | ||||||
| chr8:119781676
|
C | T | 1 | a0005c0005t0003g0279 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2113-483G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781676 | ||||||
| chr8:119781700
|
C | CT | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2113-508dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781700 | ||||||
| chr8:119781734
|
C | T | 1 | a0005c0005t0003g0285 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2113-541G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781734 | ||||||
| chr8:119781779
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2113-586G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781779 | ||||||
| chr8:119781968
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2113-775C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781968 | ||||||
| chr8:119781987
|
C | T | 1 | a0002c0002t0001g0022 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2113-794G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119781987 | ||||||
| chr8:119782107
|
C | T | 1 | a0001c0003t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2113-914G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119782107 | ||||||
| chr8:119782156
|
T | A | 1 | a0001c0003t0001g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2113-963A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119782156 | ||||||
| chr8:119782267
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2113-1074A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119782267 | ||||||
| chr8:119782481
|
T | C | 44 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(41): Show | 47 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.2112+900A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119782481 | ||||||
| chr8:119782879
|
G | A | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.2112+502C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119782879 | ||||||
| chr8:119782959
|
A | G | 2 | a0003c0010t0002g0312a0003c0010t0002g0313 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2112+422T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119782959 | ||||||
| chr8:119783008
|
G | GAC | 20 | a0001c0003t0001g0165a0001c0007t0001g0025a0001c0007t0001g0026others(17): Show | 20 | HG01884.hp1 HG01891.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.2112+371_2112+372d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119783008 | ||||||
| chr8:119783008
|
GAC | G | 64 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(61): Show | 69 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.2112+371_2112+372d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119783008 | ||||||
| chr8:119783008
|
GACAC | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2112+369_2112+372d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119783008 | ||||||
| chr8:119783033
|
A | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2112+348T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119783033 | ||||||
| chr8:119783351
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2112+30A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119783351 | ||||||
| chr8:119783367
|
G | A | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2112+14C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 16/25 | chr8 | 119783367 | ||||||
| chr8:119783830
|
T | A | 1 | a0001c0007t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1860-197A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119783830 | ||||||
| chr8:119784017
|
G | A | 1 | a0004c0004t0002g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1860-384C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119784017 | ||||||
| chr8:119784207
|
A | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1860-574T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119784207 | ||||||
| chr8:119784326
|
G | A | 3 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1860-693C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119784326 | ||||||
| chr8:119784448
|
G | A | 2 | a0001c0007t0001g0030a0001c0007t0001g0031 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1859+753C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119784448 | ||||||
| chr8:119784507
|
A | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1859+694T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119784507 | ||||||
| chr8:119784799
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1859+402T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119784799 | ||||||
| chr8:119784831
|
C | A | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1859+370G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 15/25 | chr8 | 119784831 | ||||||
| chr8:119785358
|
C | T | 3 | a0005c0005t0003g0278a0005c0005t0003g0279a0005c0005t0003g0280 | 3 | HG02723.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1794-92G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119785358 | ||||||
| chr8:119785372
|
C | T | 13 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1794-106G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119785372 | ||||||
| chr8:119785615
|
C | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1794-349G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119785615 | ||||||
| chr8:119785653
|
G | A | 1 | a0001c0003t0001g0047 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1794-387C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119785653 | ||||||
| chr8:119785715
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1794-449T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119785715 | ||||||
| chr8:119785888
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1794-622G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119785888 | ||||||
| chr8:119786062
|
T | C | 2 | a0001c0011t0005g0008a0001c0011t0005g0009 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1794-796A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119786062 | ||||||
| chr8:119786687
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1794-1421G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119786687 | ||||||
| chr8:119786877
|
C | T | 1 | a0002c0002t0001g0118 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1793+1461G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119786877 | ||||||
| chr8:119786888
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1793+1450A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119786888 | ||||||
| chr8:119786923
|
A | C | 1 | a0004c0004t0002g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1793+1415T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119786923 | ||||||
| chr8:119786993
|
G | A | 2 | a0002c0002t0001g0139a0002c0002t0001g0140 | 2 | HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1793+1345C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119786993 | ||||||
| chr8:119787063
|
T | A | 44 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(41): Show | 47 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1793+1275A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787063 | ||||||
| chr8:119787116
|
C | A | 44 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(41): Show | 47 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1793+1222G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787116 | ||||||
| chr8:119787127
|
T | A | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1793+1211A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787127 | ||||||
| chr8:119787154
|
A | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1793+1184T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787154 | ||||||
| chr8:119787215
|
C | A | 1 | a0002c0002t0001g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1793+1123G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787215 | ||||||
| chr8:119787251
|
T | C | 1 | a0002c0002t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1793+1087A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787251 | ||||||
| chr8:119787294
|
A | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1793+1044T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787294 | ||||||
| chr8:119787375
|
A | AAAACAAA others(7): Show |
4 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0001g0116others(1): Show | 4 | HG01891.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793+949_1793+962d others(16): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787375 | ||||||
| chr8:119787485
|
A | G | 1 | a0003c0006t0003g0273 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1793+853T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787485 | ||||||
| chr8:119787550
|
C | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1793+788G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787550 | ||||||
| chr8:119787640
|
G | A | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1793+698C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787640 | ||||||
| chr8:119787780
|
T | C | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1793+558A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787780 | ||||||
| chr8:119787913
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1793+425T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119787913 | ||||||
| chr8:119788049
|
A | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1793+289T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119788049 | ||||||
| chr8:119788056
|
G | A | 100 | a0001c0001t0001g0006a0001c0001t0001g0168a0001c0001t0001g0169others(97): Show | 101 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1793+282C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119788056 | ||||||
| chr8:119788073
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1793+265G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119788073 | ||||||
| chr8:119788094
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1793+244C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 14/25 | chr8 | 119788094 | ||||||
| chr8:119788452
|
T | A | 1 | a0002c0002t0001g0127 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.1684-5A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788452 | ||||||
| chr8:119788452
|
T | TA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1684-6dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788452 | ||||||
| chr8:119788452
|
TA | T | 5 | a0004c0004t0002g0007a0004c0004t0002g0299a0004c0004t0002g0300others(2): Show | 6 | HG02970.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1684-6delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788452 | ||||||
| chr8:119788464
|
G | A | 5 | a0001c0001t0001g0179a0001c0001t0001g0188a0001c0001t0001g0230others(2): Show | 5 | HG02135.hp1 NA18957.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1684-17C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788464 | ||||||
| chr8:119788538
|
T | TAAAATAT others(228): Show |
3 | a0001c0001t0001g0181a0001c0001t0001g0212a0001c0001t0001g0236 | 3 | NA18950.hp1 NA18954.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1684-92_1684-91ins others(235): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788538 | ||||||
| chr8:119788538
|
T | TAAAATAT others(229): Show |
69 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(66): Show | 70 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1684-92_1684-91ins others(236): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788538 | ||||||
| chr8:119788538
|
T | TAAAATAT others(230): Show |
18 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0185others(15): Show | 18 | HG00423.hp2 HG00735.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1684-92_1684-91ins others(237): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788538 | ||||||
| chr8:119788538
|
T | TAAAATAT others(230): Show |
1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1684-92_1684-91ins others(237): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788538 | ||||||
| chr8:119788546
|
TA | T | 3 | a0003c0006t0001g0159a0003c0006t0001g0161a0003c0006t0001g0162 | 3 | HG02698.hp2 HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1684-100delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788546 | ||||||
| chr8:119788618
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1684-171G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 13/25 | chr8 | 119788618 | ||||||
| chr8:119789277
|
A | G | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1568+315T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 12/25 | chr8 | 119789277 | ||||||
| chr8:119789392
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1568+200A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 12/25 | chr8 | 119789392 | ||||||
| chr8:119789401
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1568+191C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 12/25 | chr8 | 119789401 | ||||||
| chr8:119789458
|
T | C | 1 | a0005c0005t0003g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1568+134A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 12/25 | chr8 | 119789458 | ||||||
| chr8:119789565
|
C | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1568+27G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 12/25 | chr8 | 119789565 | ||||||
| chr8:119789778
|
A | G | 1 | a0005c0005t0003g0289 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1414-32T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119789778 | ||||||
| chr8:119789978
|
G | A | 1 | a0004c0004t0002g0305 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1414-232C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119789978 | ||||||
| chr8:119790042
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1414-296C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790042 | ||||||
| chr8:119790238
|
T | A | 1 | a0002c0002t0001g0073 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1414-492A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790238 | ||||||
| chr8:119790412
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1414-666G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790412 | ||||||
| chr8:119790430
|
T | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0188a0001c0001t0001g0242 | 3 | HG02135.hp1 NA18957.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1414-684A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790430 | ||||||
| chr8:119790435
|
C | CA | 10 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1414-690dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790435 | ||||||
| chr8:119790567
|
T | C | 1 | a0001c0003t0001g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1413+757A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790567 | ||||||
| chr8:119790662
|
C | T | 1 | a0003c0006t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1413+662G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790662 | ||||||
| chr8:119790692
|
G | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+632C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790692 | ||||||
| chr8:119790714
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1413+610G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790714 | ||||||
| chr8:119790765
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1413+559A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790765 | ||||||
| chr8:119790801
|
AGTTT | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+519_1413+522d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790801 | ||||||
| chr8:119790802
|
G | GT | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1413+521dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790802 | ||||||
| chr8:119790985
|
T | TG | 98 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1413+338dupC | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 11/25 | chr8 | 119790985 | ||||||
| chr8:119791674
|
A | G | 1 | a0002c0002t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1278-215T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791674 | ||||||
| chr8:119791692
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1278-233A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791692 | ||||||
| chr8:119791757
|
C | G | 1 | a0002c0002t0001g0146 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1278-298G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791757 | ||||||
| chr8:119791782
|
A | T | 2 | a0001c0003t0001g0045a0001c0003t0001g0048 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1278-323T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791782 | ||||||
| chr8:119791815
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1278-356A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791815 | ||||||
| chr8:119791888
|
A | G | 2 | a0002c0002t0001g0094a0002c0002t0001g0130 | 2 | NA18988.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1278-429T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791888 | ||||||
| chr8:119791973
|
G | A | 3 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072 | 3 | HG01952.hp2 NA18612.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1278-514C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791973 | ||||||
| chr8:119791984
|
T | C | 3 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072 | 3 | HG01952.hp2 NA18612.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1278-525A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119791984 | ||||||
| chr8:119792111
|
T | C | 1 | a0002c0002t0001g0089 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1278-652A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792111 | ||||||
| chr8:119792149
|
C | CTT | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1278-692_1278-691d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792149 | ||||||
| chr8:119792152
|
T | TC | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1278-694_1278-693i others(3): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792152 | ||||||
| chr8:119792161
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1278-702A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792161 | ||||||
| chr8:119792186
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1278-727G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792186 | ||||||
| chr8:119792440
|
C | T | 3 | a0004c0004t0002g0293a0004c0004t0002g0294a0004c0004t0002g0295 | 3 | HG01109.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1277+926G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792440 | ||||||
| chr8:119792522
|
A | G | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1277+844T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792522 | ||||||
| chr8:119792526
|
G | A | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+840C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792526 | ||||||
| chr8:119792597
|
G | GT | 6 | a0001c0003t0001g0040a0001c0003t0001g0266a0001c0003t0001g0267others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+768dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792597 | ||||||
| chr8:119792652
|
C | T | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.1277+714G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792652 | ||||||
| chr8:119792701
|
A | G | 1 | a0005c0005t0003g0282 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1277+665T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 10/25 | chr8 | 119792701 | ||||||
| chr8:119793509
|
T | C | 23 | a0001c0003t0001g0024a0001c0003t0001g0032a0001c0003t0001g0036others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1192-58A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119793509 | ||||||
| chr8:119793770
|
T | C | 22 | a0004c0004t0002g0007a0004c0004t0002g0292a0004c0004t0002g0293others(19): Show | 23 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1192-319A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119793770 | ||||||
| chr8:119793785
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1192-334G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119793785 | ||||||
| chr8:119793846
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1192-395G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119793846 | ||||||
| chr8:119793847
|
T | TTAAAATT others(8): Show |
1 | a0002c0002t0001g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1192-397_1192-396i others(17): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119793847 | ||||||
| chr8:119793903
|
G | GA | 20 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0180others(17): Show | 20 | HG00408.hp2 HG01261.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1192-453dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119793903 | ||||||
| chr8:119793928
|
A | G | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.1192-477T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119793928 | ||||||
| chr8:119794080
|
G | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1192-629C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794080 | ||||||
| chr8:119794150
|
C | T | 2 | a0001c0007t0001g0030a0001c0007t0001g0031 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1192-699G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794150 | ||||||
| chr8:119794225
|
G | A | 1 | a0001c0003t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1192-774C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794225 | ||||||
| chr8:119794317
|
G | A | 61 | a0001c0001t0001g0207a0001c0015t0001g0160a0003c0006t0001g0154others(58): Show | 66 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.1192-866C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794317 | ||||||
| chr8:119794353
|
G | A | 1 | a0003c0008t0001g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1192-902C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794353 | ||||||
| chr8:119794390
|
C | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1192-939G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794390 | ||||||
| chr8:119794395
|
C | CA | 62 | a0001c0001t0001g0207a0001c0003t0001g0019a0001c0015t0001g0160others(59): Show | 67 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1192-945dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794395 | ||||||
| chr8:119794513
|
A | C | 2 | a0001c0011t0005g0008a0001c0011t0005g0009 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1191+1019T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794513 | ||||||
| chr8:119794610
|
T | A | 1 | a0001c0003t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1191+922A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794610 | ||||||
| chr8:119794765
|
T | C | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1191+767A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794765 | ||||||
| chr8:119794808
|
C | T | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1191+724G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794808 | ||||||
| chr8:119794908
|
T | A | 2 | a0005c0005t0003g0290a0005c0005t0003g0291 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1191+624A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794908 | ||||||
| chr8:119794918
|
C | T | 2 | a0001c0003t0001g0050a0001c0003t0001g0056 | 2 | NA18997.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1191+614G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794918 | ||||||
| chr8:119794957
|
T | C | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1191+575A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119794957 | ||||||
| chr8:119795028
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1191+504T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119795028 | ||||||
| chr8:119795041
|
T | TA | 32 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035others(29): Show | 36 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1191+490dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119795041 | ||||||
| chr8:119795241
|
A | T | 1 | a0002c0002t0001g0075 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1191+291T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119795241 | ||||||
| chr8:119795267
|
A | G | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1191+265T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119795267 | ||||||
| chr8:119795313
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1191+219G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119795313 | ||||||
| chr8:119795389
|
C | T | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1191+143G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 9/25 | chr8 | 119795389 | ||||||
| chr8:119795782
|
C | T | 1 | a0001c0003t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1092-151G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119795782 | ||||||
| chr8:119795835
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1092-204A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119795835 | ||||||
| chr8:119796034
|
C | T | 13 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1092-403G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796034 | ||||||
| chr8:119796315
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1091+675C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796315 | ||||||
| chr8:119796331
|
C | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1091+659G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796331 | ||||||
| chr8:119796352
|
A | G | 5 | a0004c0004t0002g0007a0004c0004t0002g0299a0004c0004t0002g0300others(2): Show | 6 | HG02970.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+638T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796352 | ||||||
| chr8:119796435
|
A | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1091+555T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796435 | ||||||
| chr8:119796441
|
C | G | 3 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1091+549G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796441 | ||||||
| chr8:119796569
|
T | C | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1091+421A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796569 | ||||||
| chr8:119796587
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1091+403A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796587 | ||||||
| chr8:119796667
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1091+323G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796667 | ||||||
| chr8:119796762
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1091+228G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796762 | ||||||
| chr8:119796957
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1091+33G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 8/25 | chr8 | 119796957 | ||||||
| chr8:119797153
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.978-50A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 7/25 | chr8 | 119797153 | ||||||
| chr8:119797228
|
A | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | NA18985.hp1 NA18988.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.978-125T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 7/25 | chr8 | 119797228 | ||||||
| chr8:119797407
|
C | A | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.977+255G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 7/25 | chr8 | 119797407 | ||||||
| chr8:119797409
|
C | T | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.977+253G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 7/25 | chr8 | 119797409 | ||||||
| chr8:119797465
|
TTTGAG | T | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.977+192_977+196del others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 7/25 | chr8 | 119797465 | ||||||
| chr8:119797870
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-24A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119797870 | ||||||
| chr8:119798053
|
G | A | 2 | a0001c0003t0001g0165a0003c0009t0001g0164 | 2 | NA19003.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.793-207C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119798053 | ||||||
| chr8:119798107
|
C | G | 3 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.793-261G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119798107 | ||||||
| chr8:119798280
|
A | G | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-434T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119798280 | ||||||
| chr8:119798331
|
T | A | 1 | a0002c0002t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.793-485A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119798331 | ||||||
| chr8:119798384
|
T | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(165): Show | 174 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.793-538A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119798384 | ||||||
| chr8:119799071
|
T | C | 5 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-1225A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799071 | ||||||
| chr8:119799151
|
ATTTT | A | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.793-1309_793-1306d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799151 | ||||||
| chr8:119799278
|
G | T | 1 | a0002c0002t0001g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.793-1432C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799278 | ||||||
| chr8:119799293
|
C | T | 1 | a0004c0004t0002g0307 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.793-1447G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799293 | ||||||
| chr8:119799320
|
C | T | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.793-1474G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799320 | ||||||
| chr8:119799321
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-1475C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799321 | ||||||
| chr8:119799335
|
T | C | 6 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG02071.hp2 NA18612.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-1489A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799335 | ||||||
| chr8:119799412
|
T | C | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.793-1566A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799412 | ||||||
| chr8:119799512
|
C | T | 3 | a0005c0005t0003g0278a0005c0005t0003g0279a0005c0005t0003g0280 | 3 | HG02723.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.793-1666G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799512 | ||||||
| chr8:119799560
|
G | A | 4 | a0002c0002t0001g0114a0002c0002t0001g0115a0002c0002t0001g0116others(1): Show | 4 | HG01891.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1714C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799560 | ||||||
| chr8:119799598
|
G | A | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-1752C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799598 | ||||||
| chr8:119799654
|
T | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.793-1808A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799654 | ||||||
| chr8:119799688
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.793-1842T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799688 | ||||||
| chr8:119799702
|
T | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.793-1856A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799702 | ||||||
| chr8:119799712
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.793-1866A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799712 | ||||||
| chr8:119799721
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.793-1875A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799721 | ||||||
| chr8:119799731
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.793-1885A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799731 | ||||||
| chr8:119799820
|
C | T | 44 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(41): Show | 47 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.792+1974G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799820 | ||||||
| chr8:119799979
|
G | A | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+1815C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119799979 | ||||||
| chr8:119800016
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.792+1778A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800016 | ||||||
| chr8:119800037
|
C | T | 12 | a0002c0002t0001g0018a0002c0002t0001g0068a0002c0002t0001g0069others(9): Show | 12 | HG01168.hp2 HG01361.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+1757G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800037 | ||||||
| chr8:119800051
|
G | A | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+1743C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800051 | ||||||
| chr8:119800140
|
T | C | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+1654A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800140 | ||||||
| chr8:119800168
|
T | C | 1 | a0002c0002t0001g0117 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.792+1626A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800168 | ||||||
| chr8:119800232
|
G | A | 44 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(41): Show | 47 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.792+1562C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800232 | ||||||
| chr8:119800283
|
C | T | 1 | a0002c0002t0001g0074 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.792+1511G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800283 | ||||||
| chr8:119800404
|
C | G | 3 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.792+1390G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800404 | ||||||
| chr8:119800415
|
T | G | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792+1379A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800415 | ||||||
| chr8:119800426
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+1368A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800426 | ||||||
| chr8:119800497
|
G | A | 1 | a0002c0002t0001g0118 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.792+1297C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800497 | ||||||
| chr8:119800554
|
G | C | 1 | a0001c0003t0009g0314 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.792+1240C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800554 | ||||||
| chr8:119800669
|
G | A | 1 | a0002c0002t0001g0118 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.792+1125C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800669 | ||||||
| chr8:119800709
|
G | A | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+1085C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800709 | ||||||
| chr8:119800834
|
C | T | 1 | a0005c0005t0003g0281 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.792+960G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800834 | ||||||
| chr8:119800835
|
G | A | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792+959C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800835 | ||||||
| chr8:119800928
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.792+866A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119800928 | ||||||
| chr8:119801187
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.792+607A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801187 | ||||||
| chr8:119801196
|
A | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+598T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801196 | ||||||
| chr8:119801435
|
C | CT | 12 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(9): Show | 12 | HG01884.hp2 HG01981.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+358dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801435 | ||||||
| chr8:119801435
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+359G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801435 | ||||||
| chr8:119801435
|
CT | C | 56 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0003t0001g0019others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.792+358delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801435 | ||||||
| chr8:119801460
|
G | A | 3 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072 | 3 | HG01952.hp2 NA18612.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.792+334C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801460 | ||||||
| chr8:119801530
|
G | A | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+264C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801530 | ||||||
| chr8:119801604
|
A | G | 5 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+190T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801604 | ||||||
| chr8:119801639
|
A | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.792+155T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801639 | ||||||
| chr8:119801713
|
C | A | 1 | a0003c0006t0003g0273 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.792+81G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801713 | ||||||
| chr8:119801780
|
A | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.792+14T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 6/25 | chr8 | 119801780 | ||||||
| chr8:119802070
|
T | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-45A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802070 | ||||||
| chr8:119802267
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-242T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802267 | ||||||
| chr8:119802326
|
T | C | 217 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.561-301A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802326 | ||||||
| chr8:119802353
|
T | C | 3 | a0001c0003t0001g0037a0001c0003t0001g0038a0001c0003t0001g0039 | 3 | HG02451.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.561-328A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802353 | ||||||
| chr8:119802542
|
G | A | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.561-517C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802542 | ||||||
| chr8:119802568
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-543T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802568 | ||||||
| chr8:119802639
|
G | A | 1 | a0005c0005t0003g0278 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.561-614C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802639 | ||||||
| chr8:119802696
|
T | G | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.561-671A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802696 | ||||||
| chr8:119802742
|
G | C | 2 | a0005c0005t0003g0001a0005c0005t0003g0286 | 4 | HG00323.hp2 HG00735.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-717C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802742 | ||||||
| chr8:119802750
|
T | C | 1 | a0004c0004t0002g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.561-725A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802750 | ||||||
| chr8:119802883
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.561-858C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119802883 | ||||||
| chr8:119803144
|
T | C | 1 | a0004c0004t0002g0296 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.560+734A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803144 | ||||||
| chr8:119803164
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.560+714A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803164 | ||||||
| chr8:119803263
|
C | A | 1 | a0001c0003t0001g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.560+615G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803263 | ||||||
| chr8:119803264
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.560+614C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803264 | ||||||
| chr8:119803359
|
C | G | 1 | a0004c0004t0002g0296 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.560+519G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803359 | ||||||
| chr8:119803413
|
G | A | 1 | a0003c0006t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.560+465C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803413 | ||||||
| chr8:119803432
|
T | C | 2 | a0004c0004t0002g0292a0004c0014t0002g0303 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.560+446A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803432 | ||||||
| chr8:119803536
|
T | C | 1 | a0002c0002t0001g0125 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.560+342A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803536 | ||||||
| chr8:119803691
|
G | GA | 64 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0001t0001g0173others(61): Show | 69 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.560+186dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803691 | ||||||
| chr8:119803704
|
G | A | 1 | a0003c0006t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.560+174C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803704 | ||||||
| chr8:119803705
|
A | G | 1 | a0003c0006t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.560+173T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803705 | ||||||
| chr8:119803714
|
T | A | 1 | a0003c0006t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.560+164A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803714 | ||||||
| chr8:119803770
|
A | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.560+108T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 5/25 | chr8 | 119803770 | ||||||
| chr8:119804072
|
A | G | 2 | a0002c0002t0001g0071a0002c0002t0001g0072 | 2 | HG01952.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.419-53T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804072 | ||||||
| chr8:119804265
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.419-246G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804265 | ||||||
| chr8:119804438
|
T | G | 1 | a0002c0002t0001g0089 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.419-419A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804438 | ||||||
| chr8:119804532
|
C | G | 2 | a0001c0011t0005g0008a0001c0011t0005g0009 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.419-513G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804532 | ||||||
| chr8:119804568
|
C | G | 2 | a0005c0005t0003g0285a0005c0005t0003g0288 | 2 | NA18998.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.419-549G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804568 | ||||||
| chr8:119804664
|
A | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-645T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804664 | ||||||
| chr8:119804785
|
A | C | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.419-766T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804785 | ||||||
| chr8:119804845
|
G | A | 2 | a0002c0002t0001g0119a0002c0002t0001g0120 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.419-826C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804845 | ||||||
| chr8:119804874
|
G | A | 1 | a0001c0003t0001g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.419-855C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804874 | ||||||
| chr8:119804940
|
T | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-921A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119804940 | ||||||
| chr8:119805039
|
C | T | 1 | a0002c0002t0001g0144 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.419-1020G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805039 | ||||||
| chr8:119805095
|
A | G | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.419-1076T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805095 | ||||||
| chr8:119805359
|
C | T | 217 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.418+924G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805359 | ||||||
| chr8:119805448
|
G | C | 3 | a0001c0003t0001g0037a0001c0003t0001g0038a0001c0003t0001g0039 | 3 | HG02451.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.418+835C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805448 | ||||||
| chr8:119805630
|
G | A | 13 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.418+653C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805630 | ||||||
| chr8:119805661
|
C | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG00099.hp2 HG01515.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.418+622G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805661 | ||||||
| chr8:119805749
|
C | T | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+534G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805749 | ||||||
| chr8:119805750
|
G | A | 1 | a0004c0004t0002g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.418+533C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805750 | ||||||
| chr8:119805761
|
T | C | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.418+522A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805761 | ||||||
| chr8:119805786
|
G | A | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.418+497C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805786 | ||||||
| chr8:119805909
|
CT | C | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.418+373delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119805909 | ||||||
| chr8:119806047
|
T | C | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.418+236A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119806047 | ||||||
| chr8:119806243
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.418+40C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119806243 | ||||||
| chr8:119806253
|
T | C | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+30A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 4/25 | chr8 | 119806253 | ||||||
| chr8:119806469
|
CT | C | 22 | a0001c0001t0001g0255a0001c0003t0001g0057a0001c0007t0001g0025others(19): Show | 22 | HG00099.hp1 HG01070.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.300-69delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119806469 | ||||||
| chr8:119806469
|
CTT | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(154): Show | 163 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.300-70_300-69delAA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119806469 | ||||||
| chr8:119806475
|
T | C | 53 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(50): Show | 56 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.300-74A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119806475 | ||||||
| chr8:119806522
|
G | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.300-121C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119806522 | ||||||
| chr8:119806828
|
T | C | 1 | a0002c0002t0001g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.300-427A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119806828 | ||||||
| chr8:119807023
|
C | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG03834.hp2 NA18953.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.300-622G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807023 | ||||||
| chr8:119807317
|
C | T | 42 | a0001c0003t0001g0019a0001c0003t0001g0024a0001c0003t0001g0032others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.300-916G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807317 | ||||||
| chr8:119807356
|
C | T | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.300-955G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807356 | ||||||
| chr8:119807436
|
TA | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.300-1036delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807436 | ||||||
| chr8:119807465
|
G | A | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.300-1064C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807465 | ||||||
| chr8:119807475
|
C | T | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.300-1074G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807475 | ||||||
| chr8:119807568
|
G | A | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.300-1167C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807568 | ||||||
| chr8:119807569
|
G | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-1168C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807569 | ||||||
| chr8:119807653
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.300-1252C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807653 | ||||||
| chr8:119807687
|
G | A | 1 | a0002c0002t0001g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.300-1286C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807687 | ||||||
| chr8:119807849
|
G | A | 1 | a0002c0002t0001g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.300-1448C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807849 | ||||||
| chr8:119807959
|
A | T | 1 | a0002c0002t0001g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.300-1558T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807959 | ||||||
| chr8:119807970
|
G | A | 4 | a0001c0003t0001g0032a0001c0003t0001g0057a0001c0003t0001g0059others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.300-1569C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119807970 | ||||||
| chr8:119808100
|
A | G | 1 | a0002c0002t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.300-1699T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808100 | ||||||
| chr8:119808120
|
T | TATTCA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-1724_300-1720d others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808120 | ||||||
| chr8:119808224
|
A | G | 5 | a0004c0004t0002g0007a0004c0004t0002g0299a0004c0004t0002g0300others(2): Show | 6 | HG02970.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-1823T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808224 | ||||||
| chr8:119808273
|
C | T | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.300-1872G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808273 | ||||||
| chr8:119808292
|
C | A | 1 | a0005c0005t0003g0282 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.300-1891G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808292 | ||||||
| chr8:119808337
|
G | C | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.300-1936C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808337 | ||||||
| chr8:119808508
|
C | T | 7 | a0001c0003t0001g0043a0001c0003t0001g0044a0001c0003t0001g0045others(4): Show | 7 | HG01175.hp2 HG01496.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-2107G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808508 | ||||||
| chr8:119808563
|
C | G | 1 | a0001c0007t0001g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.300-2162G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808563 | ||||||
| chr8:119808590
|
G | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.300-2189C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808590 | ||||||
| chr8:119808756
|
T | C | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.300-2355A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808756 | ||||||
| chr8:119808773
|
A | G | 3 | a0001c0003t0001g0037a0001c0003t0001g0038a0001c0003t0001g0039 | 3 | HG02451.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.300-2372T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808773 | ||||||
| chr8:119808919
|
A | G | 1 | a0001c0003t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.300-2518T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119808919 | ||||||
| chr8:119809024
|
C | G | 26 | a0001c0003t0001g0024a0001c0003t0001g0032a0001c0003t0001g0036others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.300-2623G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809024 | ||||||
| chr8:119809024
|
C | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.300-2623G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809024 | ||||||
| chr8:119809292
|
C | T | 7 | a0001c0003t0001g0043a0001c0003t0001g0044a0001c0003t0001g0045others(4): Show | 7 | HG01175.hp2 HG01496.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-2891G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809292 | ||||||
| chr8:119809627
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.300-3226G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809627 | ||||||
| chr8:119809654
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3253A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809654 | ||||||
| chr8:119809697
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.300-3296G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809697 | ||||||
| chr8:119809731
|
C | T | 1 | a0003c0008t0001g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.300-3330G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809731 | ||||||
| chr8:119809857
|
A | C | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.300-3456T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809857 | ||||||
| chr8:119809878
|
G | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.300-3477C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809878 | ||||||
| chr8:119809998
|
T | TA | 55 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.300-3598dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809998 | ||||||
| chr8:119809998
|
T | TAA | 28 | a0001c0003t0001g0056a0001c0007t0001g0029a0001c0011t0005g0009others(25): Show | 29 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.300-3599_300-3598d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809998 | ||||||
| chr8:119809998
|
T | TAAA | 27 | a0001c0003t0001g0040a0001c0018t0001g0182a0003c0006t0003g0272others(24): Show | 29 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.300-3600_300-3598d others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809998 | ||||||
| chr8:119809998
|
T | TAAAA | 86 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(83): Show | 87 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.300-3601_300-3598d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809998 | ||||||
| chr8:119809998
|
T | TAAAAA | 7 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0001t0001g0181others(4): Show | 7 | HG01243.hp1 HG01433.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.300-3602_300-3598d others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119809998 | ||||||
| chr8:119810128
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3727G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119810128 | ||||||
| chr8:119810381
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.300-3980A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119810381 | ||||||
| chr8:119810679
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.300-4278T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119810679 | ||||||
| chr8:119810726
|
T | A | 1 | a0004c0004t0002g0306 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.300-4325A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119810726 | ||||||
| chr8:119810772
|
G | C | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-4371C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119810772 | ||||||
| chr8:119810941
|
G | A | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.300-4540C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119810941 | ||||||
| chr8:119811043
|
TATA | T | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-4645_300-4643d others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811043 | ||||||
| chr8:119811134
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.300-4733A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811134 | ||||||
| chr8:119811250
|
AAT | A | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.300-4851_300-4850d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811250 | ||||||
| chr8:119811307
|
A | AT | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-4907dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811307 | ||||||
| chr8:119811360
|
A | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.300-4959T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811360 | ||||||
| chr8:119811369
|
A | AGAAGTAA others(9): Show |
9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-4984_300-4969d others(18): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811369 | ||||||
| chr8:119811425
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.300-5024G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811425 | ||||||
| chr8:119811520
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-5119T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811520 | ||||||
| chr8:119811544
|
C | T | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.300-5143G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811544 | ||||||
| chr8:119811622
|
C | T | 1 | a0002c0002t0006g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.300-5221G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811622 | ||||||
| chr8:119811805
|
C | CA | 65 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0193others(62): Show | 68 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.300-5405dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811805 | ||||||
| chr8:119811805
|
CA | C | 13 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(10): Show | 13 | HG00408.hp1 HG01496.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.300-5405delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811805 | ||||||
| chr8:119811820
|
A | T | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.300-5419T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811820 | ||||||
| chr8:119811992
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-5591G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119811992 | ||||||
| chr8:119812117
|
T | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.300-5716A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812117 | ||||||
| chr8:119812298
|
C | A | 5 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-5897G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812298 | ||||||
| chr8:119812316
|
T | A | 1 | a0003c0009t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.300-5915A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812316 | ||||||
| chr8:119812325
|
A | AT | 22 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(19): Show | 24 | HG00738.hp1 HG01884.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.300-5925dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812325 | ||||||
| chr8:119812325
|
AT | A | 18 | a0002c0002t0001g0126a0002c0002t0001g0129a0004c0004t0002g0305others(15): Show | 20 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.300-5925delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812325 | ||||||
| chr8:119812357
|
T | C | 4 | a0002c0002t0001g0020a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 4 | HG02523.hp1 NA18991.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.300-5956A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812357 | ||||||
| chr8:119812693
|
T | C | 1 | a0003c0008t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.300-6292A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812693 | ||||||
| chr8:119812701
|
G | A | 1 | a0002c0002t0001g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.300-6300C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812701 | ||||||
| chr8:119812718
|
G | GGT | 34 | a0001c0003t0001g0019a0001c0003t0001g0024a0001c0003t0001g0032others(31): Show | 34 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.300-6319_300-6318d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
G | GGTGT | 9 | a0001c0003t0001g0065a0002c0002t0001g0018a0002c0002t0001g0068others(6): Show | 9 | HG01168.hp2 HG01361.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.300-6321_300-6318d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
G | GGTGTGTG others(3): Show |
1 | a0002c0002t0001g0071 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.300-6327_300-6318d others(12): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
G | GGTGTGTG others(5): Show |
1 | a0002c0002t0001g0070 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.300-6329_300-6318d others(14): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
GGT | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0003t0001g0040others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.300-6319_300-6318d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
GGTGT | G | 17 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0207others(14): Show | 17 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.300-6321_300-6318d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
GGTGTGT | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(85): Show | 89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.300-6323_300-6318d others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.300-6325_300-6318d others(10): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812718
|
GGTGTGTG others(3): Show |
G | 16 | a0001c0001t0001g0243a0001c0015t0001g0160a0003c0006t0001g0154others(13): Show | 18 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.300-6327_300-6318d others(12): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812718 | ||||||
| chr8:119812739
|
GTGTGTGT others(7): Show |
G | 1 | a0004c0004t0002g0007 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.300-6352_300-6339d others(16): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812739 | ||||||
| chr8:119812743
|
GTGTGTGT others(3): Show |
G | 23 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0292others(20): Show | 23 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.300-6352_300-6343d others(12): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812743 | ||||||
| chr8:119812745
|
GTGTGTGT others(1): Show |
G | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-6352_300-6345d others(10): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812745 | ||||||
| chr8:119812749
|
GTGTA | G | 13 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(10): Show | 15 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.300-6352_300-6349d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812749 | ||||||
| chr8:119812791
|
TAC | T | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.300-6392_300-6391d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812791 | ||||||
| chr8:119812811
|
C | CA | 313 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(310): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.300-6411_300-6410i others(3): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812811 | ||||||
| chr8:119812818
|
T | C | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.300-6417A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812818 | ||||||
| chr8:119812824
|
C | CA | 313 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(310): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.300-6424_300-6423i others(3): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812824 | ||||||
| chr8:119812874
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.299+6472A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812874 | ||||||
| chr8:119812985
|
A | C | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.299+6361T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119812985 | ||||||
| chr8:119813237
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.299+6109T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813237 | ||||||
| chr8:119813383
|
C | A | 13 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+5963G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813383 | ||||||
| chr8:119813400
|
T | A | 6 | a0001c0003t0001g0040a0001c0003t0001g0266a0001c0003t0001g0267others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+5946A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813400 | ||||||
| chr8:119813509
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.299+5837A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813509 | ||||||
| chr8:119813592
|
AG | A | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.299+5753delC | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813592 | ||||||
| chr8:119813675
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+5671A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813675 | ||||||
| chr8:119813749
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.299+5597T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813749 | ||||||
| chr8:119813825
|
TATA | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.299+5518_299+5520d others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813825 | ||||||
| chr8:119813894
|
C | A | 1 | a0002c0002t0001g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299+5452G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813894 | ||||||
| chr8:119813894
|
C | T | 1 | a0002c0002t0001g0086 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.299+5452G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119813894 | ||||||
| chr8:119814050
|
A | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.299+5296T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814050 | ||||||
| chr8:119814163
|
G | A | 1 | a0002c0002t0001g0089 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.299+5183C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814163 | ||||||
| chr8:119814282
|
A | T | 1 | a0001c0003t0001g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.299+5064T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814282 | ||||||
| chr8:119814484
|
G | A | 1 | a0002c0002t0001g0146 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.299+4862C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814484 | ||||||
| chr8:119814502
|
T | C | 2 | a0003c0010t0002g0312a0003c0010t0002g0313 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.299+4844A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814502 | ||||||
| chr8:119814628
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+4718A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814628 | ||||||
| chr8:119814695
|
C | G | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.299+4651G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814695 | ||||||
| chr8:119814737
|
C | CA | 59 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0001t0001g0168others(56): Show | 62 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.299+4608dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814737 | ||||||
| chr8:119814737
|
C | CAA | 18 | a0001c0001t0001g0174a0002c0002t0001g0140a0003c0006t0001g0154others(15): Show | 20 | HG01109.hp2 HG01928.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.299+4607_299+4608d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814737 | ||||||
| chr8:119814737
|
CA | C | 105 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(102): Show | 106 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.299+4608delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814737 | ||||||
| chr8:119814737
|
CAA | C | 26 | a0001c0003t0001g0019a0001c0003t0001g0036a0001c0003t0001g0037others(23): Show | 26 | HG00099.hp1 HG01175.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.299+4607_299+4608d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814737 | ||||||
| chr8:119814765
|
C | T | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.299+4581G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814765 | ||||||
| chr8:119814790
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.299+4556A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814790 | ||||||
| chr8:119814906
|
C | CT | 3 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | NA18985.hp1 NA18988.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.299+4439dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814906 | ||||||
| chr8:119814939
|
C | T | 1 | a0001c0016t0001g0202 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.299+4407G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814939 | ||||||
| chr8:119814979
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+4367G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119814979 | ||||||
| chr8:119815130
|
A | T | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.299+4216T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815130 | ||||||
| chr8:119815132
|
A | C | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.299+4214T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815132 | ||||||
| chr8:119815133
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.299+4213A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815133 | ||||||
| chr8:119815137
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.299+4209G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815137 | ||||||
| chr8:119815138
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.299+4208G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815138 | ||||||
| chr8:119815140
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.299+4206C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815140 | ||||||
| chr8:119815146
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.299+4200C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815146 | ||||||
| chr8:119815151
|
G | A | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.299+4195C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815151 | ||||||
| chr8:119815237
|
G | A | 1 | a0001c0003t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299+4109C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815237 | ||||||
| chr8:119815261
|
G | A | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.299+4085C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815261 | ||||||
| chr8:119815269
|
G | A | 2 | a0002c0002t0001g0139a0002c0002t0001g0140 | 2 | HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.299+4077C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815269 | ||||||
| chr8:119815279
|
C | CT | 11 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(8): Show | 11 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.299+4066dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815279 | ||||||
| chr8:119815391
|
C | G | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.299+3955G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815391 | ||||||
| chr8:119815420
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.299+3926C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815420 | ||||||
| chr8:119815505
|
A | G | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.299+3841T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815505 | ||||||
| chr8:119815743
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+3603T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815743 | ||||||
| chr8:119815879
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.299+3467G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815879 | ||||||
| chr8:119815918
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+3428A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119815918 | ||||||
| chr8:119816050
|
C | CT | 29 | a0001c0001t0001g0265a0001c0003t0001g0032a0001c0003t0001g0037others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.299+3295dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816050 | ||||||
| chr8:119816074
|
G | A | 5 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.299+3272C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816074 | ||||||
| chr8:119816137
|
G | A | 1 | a0002c0002t0001g0135 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.299+3209C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816137 | ||||||
| chr8:119816184
|
G | A | 36 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(33): Show | 39 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.299+3162C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816184 | ||||||
| chr8:119816244
|
A | C | 1 | a0002c0002t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.299+3102T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816244 | ||||||
| chr8:119816304
|
G | A | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.299+3042C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816304 | ||||||
| chr8:119816346
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.299+3000G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816346 | ||||||
| chr8:119816502
|
C | T | 1 | a0001c0003t0001g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.299+2844G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816502 | ||||||
| chr8:119816540
|
T | C | 1 | a0002c0002t0001g0073 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.299+2806A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816540 | ||||||
| chr8:119816759
|
G | A | 3 | a0005c0005t0003g0278a0005c0005t0003g0279a0005c0005t0003g0280 | 3 | HG02723.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.299+2587C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816759 | ||||||
| chr8:119816813
|
C | T | 2 | a0005c0005t0003g0290a0005c0005t0003g0291 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.299+2533G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816813 | ||||||
| chr8:119816916
|
C | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.299+2430G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119816916 | ||||||
| chr8:119817080
|
CATTTACT others(4): Show |
C | 43 | a0001c0003t0001g0019a0001c0003t0001g0024a0001c0003t0001g0032others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.299+2255_299+2265d others(13): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817080 | ||||||
| chr8:119817287
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.299+2059C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817287 | ||||||
| chr8:119817327
|
G | C | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+2019C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817327 | ||||||
| chr8:119817413
|
G | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | NA18981.hp1 NA19000.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.299+1933C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817413 | ||||||
| chr8:119817425
|
C | T | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.299+1921G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817425 | ||||||
| chr8:119817478
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.299+1868G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817478 | ||||||
| chr8:119817479
|
G | A | 1 | a0003c0009t0001g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.299+1867C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817479 | ||||||
| chr8:119817498
|
A | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.299+1848T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817498 | ||||||
| chr8:119817519
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.299+1827G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817519 | ||||||
| chr8:119817565
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299+1781C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817565 | ||||||
| chr8:119817706
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.299+1640G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817706 | ||||||
| chr8:119817948
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.299+1398A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119817948 | ||||||
| chr8:119818122
|
C | T | 2 | a0002c0002t0006g0166a0002c0002t0006g0167 | 2 | HG02155.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.299+1224G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818122 | ||||||
| chr8:119818169
|
G | A | 1 | a0003c0006t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.299+1177C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818169 | ||||||
| chr8:119818299
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+1047C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818299 | ||||||
| chr8:119818350
|
C | A | 1 | a0002c0002t0001g0146 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.299+996G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818350 | ||||||
| chr8:119818730
|
GTCCACAC others(3): Show |
G | 6 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(3): Show | 6 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+606_299+615del others(10): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818730 | ||||||
| chr8:119818730
|
GTCCACAC others(5): Show |
G | 39 | a0003c0010t0002g0312a0003c0010t0002g0313a0003c0017t0003g0277others(36): Show | 42 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.299+604_299+615del others(12): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818730 | ||||||
| chr8:119818730
|
GTCCACAC others(7): Show |
G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+602_299+615del others(14): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818730 | ||||||
| chr8:119818730
|
GTCCACAC others(11): Show |
G | 1 | a0003c0006t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299+598_299+615del others(18): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818730 | ||||||
| chr8:119818730
|
GTCCACAC others(13): Show |
G | 13 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(10): Show | 15 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.299+596_299+615del others(20): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818730 | ||||||
| chr8:119818732
|
C | CCA | 22 | a0001c0003t0001g0041a0001c0003t0004g0033a0001c0003t0004g0034others(19): Show | 22 | HG01106.hp2 HG01261.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.299+612_299+613dup others(2): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818732 | ||||||
| chr8:119818732
|
C | CCACA | 22 | a0001c0003t0001g0024a0001c0003t0001g0037a0001c0003t0001g0038others(19): Show | 22 | HG00140.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.299+610_299+613dup others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818732 | ||||||
| chr8:119818732
|
C | CCACACA | 18 | a0001c0003t0001g0032a0001c0003t0001g0036a0001c0003t0001g0050others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.299+608_299+613dup others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818732 | ||||||
| chr8:119818732
|
C | CCACACAC others(1): Show |
3 | a0001c0003t0001g0062a0001c0003t0001g0063a0001c0003t0001g0065 | 3 | HG02135.hp2 HG02155.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.299+606_299+613dup others(8): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818732 | ||||||
| chr8:119818732
|
CCA | C | 4 | a0001c0001t0001g0251a0001c0003t0001g0040a0002c0002t0001g0088others(1): Show | 4 | HG00323.hp1 HG02109.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+612_299+613del others(2): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818732 | ||||||
| chr8:119818732
|
CCACA | C | 86 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(83): Show | 87 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.299+610_299+613del others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818732 | ||||||
| chr8:119818732
|
CCACACA | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0192a0001c0001t0001g0197others(2): Show | 5 | HG03225.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+608_299+613del others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818732 | ||||||
| chr8:119818742
|
A | C | 6 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(3): Show | 6 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+604T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818742 | ||||||
| chr8:119818744
|
A | C | 39 | a0003c0010t0002g0312a0003c0010t0002g0313a0003c0017t0003g0277others(36): Show | 42 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.299+602T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818744 | ||||||
| chr8:119818746
|
A | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+600T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818746 | ||||||
| chr8:119818750
|
A | C | 1 | a0003c0006t0001g0156 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299+596T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818750 | ||||||
| chr8:119818752
|
A | C | 13 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(10): Show | 15 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.299+594T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818752 | ||||||
| chr8:119818767
|
C | G | 2 | a0002c0002t0001g0086a0003c0006t0003g0273 | 2 | HG01167.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.299+579G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818767 | ||||||
| chr8:119818813
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.299+533T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818813 | ||||||
| chr8:119818986
|
C | A | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.299+360G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119818986 | ||||||
| chr8:119819226
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+120A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 3/25 | chr8 | 119819226 | ||||||
| chr8:119819601
|
C | G | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.139-95G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119819601 | ||||||
| chr8:119819603
|
G | C | 1 | a0002c0002t0001g0144 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.139-97C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119819603 | ||||||
| chr8:119819616
|
T | A | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.139-110A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119819616 | ||||||
| chr8:119819616
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.139-110A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119819616 | ||||||
| chr8:119819869
|
G | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.139-363C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119819869 | ||||||
| chr8:119820200
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-694G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119820200 | ||||||
| chr8:119820220
|
T | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-714A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119820220 | ||||||
| chr8:119820384
|
G | A | 1 | a0001c0003t0004g0035 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-878C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119820384 | ||||||
| chr8:119820410
|
G | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-904C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119820410 | ||||||
| chr8:119820547
|
CAGATA | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0195others(2): Show | 5 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-1046_139-1042d others(7): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119820547 | ||||||
| chr8:119820650
|
C | T | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-1144G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119820650 | ||||||
| chr8:119820805
|
T | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-1299A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119820805 | ||||||
| chr8:119821030
|
G | GA | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.139-1525dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821030 | ||||||
| chr8:119821033
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-1527C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821033 | ||||||
| chr8:119821188
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.139-1682G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821188 | ||||||
| chr8:119821266
|
T | C | 7 | a0005c0005t0003g0001a0005c0005t0003g0283a0005c0005t0003g0284others(4): Show | 9 | HG00323.hp2 HG00735.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-1760A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821266 | ||||||
| chr8:119821348
|
A | G | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-1842T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821348 | ||||||
| chr8:119821350
|
C | G | 1 | a0002c0002t0001g0085 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.139-1844G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821350 | ||||||
| chr8:119821425
|
A | G | 1 | a0002c0002t0001g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.139-1919T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821425 | ||||||
| chr8:119821440
|
G | C | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139-1934C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821440 | ||||||
| chr8:119821524
|
G | C | 1 | a0001c0001t0001g0253 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.139-2018C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821524 | ||||||
| chr8:119821857
|
C | G | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-2351G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821857 | ||||||
| chr8:119821929
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.139-2423C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821929 | ||||||
| chr8:119821933
|
G | A | 1 | a0001c0003t0001g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.139-2427C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821933 | ||||||
| chr8:119821993
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.139-2487G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119821993 | ||||||
| chr8:119822117
|
C | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.139-2611G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822117 | ||||||
| chr8:119822149
|
T | C | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.139-2643A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822149 | ||||||
| chr8:119822159
|
T | C | 45 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(42): Show | 48 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.139-2653A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822159 | ||||||
| chr8:119822316
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-2810C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822316 | ||||||
| chr8:119822317
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.139-2811C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822317 | ||||||
| chr8:119822368
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.139-2862T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822368 | ||||||
| chr8:119822431
|
C | T | 3 | a0001c0003t0001g0037a0001c0003t0001g0038a0001c0003t0001g0039 | 3 | HG02451.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.139-2925G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822431 | ||||||
| chr8:119822591
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.139-3085G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822591 | ||||||
| chr8:119822636
|
A | G | 2 | a0003c0010t0002g0312a0003c0010t0002g0313 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.139-3130T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822636 | ||||||
| chr8:119822731
|
G | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-3225C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119822731 | ||||||
| chr8:119823203
|
C | T | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.139-3697G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823203 | ||||||
| chr8:119823292
|
C | T | 3 | a0002c0002t0001g0082a0002c0002t0001g0083a0002c0002t0001g0084 | 3 | HG03688.hp1 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.139-3786G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823292 | ||||||
| chr8:119823309
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.139-3803G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823309 | ||||||
| chr8:119823323
|
G | A | 1 | a0002c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.139-3817C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823323 | ||||||
| chr8:119823459
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-3953T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823459 | ||||||
| chr8:119823492
|
G | GCCAC | 44 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(41): Show | 47 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.139-3990_139-3987d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823492 | ||||||
| chr8:119823601
|
T | G | 1 | a0001c0003t0001g0270 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.139-4095A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823601 | ||||||
| chr8:119823780
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.139-4274G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823780 | ||||||
| chr8:119823895
|
T | C | 1 | a0003c0017t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.139-4389A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823895 | ||||||
| chr8:119823940
|
G | T | 4 | a0003c0009t0001g0004a0003c0009t0001g0153a0003c0009t0001g0157others(1): Show | 5 | HG02145.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-4434C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119823940 | ||||||
| chr8:119824152
|
C | T | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.139-4646G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824152 | ||||||
| chr8:119824171
|
C | G | 1 | a0005c0005t0003g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139-4665G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824171 | ||||||
| chr8:119824185
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-4679G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824185 | ||||||
| chr8:119824186
|
A | C | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-4680T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824186 | ||||||
| chr8:119824247
|
A | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.139-4741T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824247 | ||||||
| chr8:119824302
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.139-4796G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824302 | ||||||
| chr8:119824306
|
T | C | 3 | a0004c0004t0002g0293a0004c0004t0002g0294a0004c0004t0002g0295 | 3 | HG01109.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.139-4800A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824306 | ||||||
| chr8:119824405
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.139-4899C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824405 | ||||||
| chr8:119824423
|
C | T | 14 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(11): Show | 14 | HG00099.hp2 HG01106.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-4917G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824423 | ||||||
| chr8:119824424
|
G | A | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-4918C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824424 | ||||||
| chr8:119824428
|
C | CAA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-4924_139-4923d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824428 | ||||||
| chr8:119824428
|
CA | C | 158 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(155): Show | 164 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.139-4923delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824428 | ||||||
| chr8:119824496
|
T | C | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.139-4990A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824496 | ||||||
| chr8:119824601
|
C | T | 1 | a0002c0002t0001g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.139-5095G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824601 | ||||||
| chr8:119824649
|
C | T | 1 | a0003c0008t0001g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.139-5143G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824649 | ||||||
| chr8:119824652
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.139-5146G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824652 | ||||||
| chr8:119824653
|
G | A | 8 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-5147C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824653 | ||||||
| chr8:119824794
|
A | C | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.139-5288T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824794 | ||||||
| chr8:119824795
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.139-5289C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824795 | ||||||
| chr8:119824862
|
G | A | 7 | a0005c0005t0003g0001a0005c0005t0003g0283a0005c0005t0003g0284others(4): Show | 9 | HG00323.hp2 HG00735.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-5356C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824862 | ||||||
| chr8:119824873
|
C | T | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.139-5367G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824873 | ||||||
| chr8:119824990
|
T | C | 1 | a0001c0003t0001g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.139-5484A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119824990 | ||||||
| chr8:119825083
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0190others(1): Show | 4 | HG00639.hp2 HG01081.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-5577G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825083 | ||||||
| chr8:119825103
|
C | T | 3 | a0005c0005t0003g0278a0005c0005t0003g0279a0005c0005t0003g0280 | 3 | HG02723.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.139-5597G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825103 | ||||||
| chr8:119825158
|
C | A | 5 | a0004c0004t0002g0307a0004c0004t0002g0308a0004c0004t0002g0309others(2): Show | 5 | HG02257.hp2 HG02451.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-5652G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825158 | ||||||
| chr8:119825513
|
T | C | 1 | a0004c0004t0002g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.139-6007A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825513 | ||||||
| chr8:119825525
|
A | G | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-6019T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825525 | ||||||
| chr8:119825626
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+6051C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825626 | ||||||
| chr8:119825630
|
A | G | 13 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.138+6047T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825630 | ||||||
| chr8:119825675
|
G | GT | 8 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(5): Show | 8 | HG02055.hp1 HG02523.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+6001dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825675 | ||||||
| chr8:119825679
|
T | G | 1 | a0002c0002t0006g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.138+5998A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825679 | ||||||
| chr8:119825711
|
A | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(171): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.138+5966T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825711 | ||||||
| chr8:119825851
|
A | AT | 114 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0003t0001g0019others(111): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.138+5825dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825851 | ||||||
| chr8:119825851
|
A | ATT | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0178others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+5824_138+5825d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825851 | ||||||
| chr8:119825851
|
A | ATTTT | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+5822_138+5825d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825851 | ||||||
| chr8:119825939
|
G | A | 4 | a0002c0002t0001g0073a0002c0002t0001g0074a0002c0002t0001g0075others(1): Show | 4 | HG03017.hp1 HG03491.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+5738C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825939 | ||||||
| chr8:119825948
|
T | G | 1 | a0001c0003t0001g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.138+5729A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825948 | ||||||
| chr8:119825972
|
G | A | 1 | a0005c0005t0003g0289 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.138+5705C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119825972 | ||||||
| chr8:119826019
|
G | T | 1 | a0002c0002t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.138+5658C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826019 | ||||||
| chr8:119826053
|
T | C | 1 | a0002c0002t0001g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.138+5624A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826053 | ||||||
| chr8:119826106
|
C | T | 5 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+5571G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826106 | ||||||
| chr8:119826111
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+5566G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826111 | ||||||
| chr8:119826153
|
C | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+5524G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826153 | ||||||
| chr8:119826154
|
T | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+5523A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826154 | ||||||
| chr8:119826261
|
TA | T | 12 | a0002c0002t0001g0018a0002c0002t0001g0068a0002c0002t0001g0069others(9): Show | 12 | HG01168.hp2 HG01361.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+5415delT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826261 | ||||||
| chr8:119826262
|
A | T | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.138+5415T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826262 | ||||||
| chr8:119826278
|
GAAAC | G | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+5395_138+5398d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826278 | ||||||
| chr8:119826386
|
T | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+5291A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826386 | ||||||
| chr8:119826452
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.138+5225T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826452 | ||||||
| chr8:119826595
|
C | CT | 17 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0015t0001g0160others(14): Show | 19 | HG00738.hp1 HG01243.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.138+5081dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826595 | ||||||
| chr8:119826606
|
T | C | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+5071A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826606 | ||||||
| chr8:119826651
|
T | C | 2 | a0005c0005t0003g0290a0005c0005t0003g0291 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.138+5026A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826651 | ||||||
| chr8:119826653
|
C | T | 3 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0035 | 3 | HG01261.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138+5024G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826653 | ||||||
| chr8:119826665
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+5012C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826665 | ||||||
| chr8:119826785
|
G | A | 1 | a0002c0002t0001g0003 | 2 | NA18999.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.138+4892C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826785 | ||||||
| chr8:119826861
|
T | C | 5 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 5 | HG00099.hp2 HG01106.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+4816A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826861 | ||||||
| chr8:119826899
|
G | A | 68 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(65): Show | 73 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.138+4778C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119826899 | ||||||
| chr8:119827022
|
C | T | 3 | a0004c0004t0002g0293a0004c0004t0002g0294a0004c0004t0002g0295 | 3 | HG01109.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.138+4655G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827022 | ||||||
| chr8:119827323
|
A | C | 1 | a0002c0002t0001g0067 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.138+4354T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827323 | ||||||
| chr8:119827349
|
A | G | 5 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+4328T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827349 | ||||||
| chr8:119827404
|
T | G | 1 | a0001c0001t0001g0262 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.138+4273A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827404 | ||||||
| chr8:119827495
|
TAC | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+4180_138+4181d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827495 | ||||||
| chr8:119827577
|
G | A | 2 | a0003c0010t0002g0312a0003c0010t0002g0313 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.138+4100C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827577 | ||||||
| chr8:119827624
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.138+4053G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827624 | ||||||
| chr8:119827635
|
T | C | 1 | a0001c0003t0001g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138+4042A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827635 | ||||||
| chr8:119827734
|
AT | A | 59 | a0001c0003t0001g0019a0001c0003t0001g0036a0001c0003t0001g0037others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.138+3942delA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827734 | ||||||
| chr8:119827734
|
ATT | A | 42 | a0001c0001t0001g0017a0001c0001t0001g0151a0001c0003t0001g0024others(39): Show | 45 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.138+3941_138+3942d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827734 | ||||||
| chr8:119827734
|
ATTT | A | 28 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(25): Show | 30 | HG00738.hp1 HG01884.hp2 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.138+3940_138+3942d others(5): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827734 | ||||||
| chr8:119827734
|
ATTTT | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(84): Show | 88 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.138+3939_138+3942d others(6): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827734 | ||||||
| chr8:119827943
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.138+3734G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119827943 | ||||||
| chr8:119828127
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.138+3550G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828127 | ||||||
| chr8:119828151
|
C | T | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.138+3526G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828151 | ||||||
| chr8:119828267
|
G | C | 1 | a0001c0003t0001g0019 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.138+3410C>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828267 | ||||||
| chr8:119828422
|
T | C | 1 | a0002c0002t0001g0146 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.138+3255A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828422 | ||||||
| chr8:119828456
|
A | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(158): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.138+3221T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828456 | ||||||
| chr8:119828482
|
C | G | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.138+3195G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828482 | ||||||
| chr8:119828590
|
A | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+3087T>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828590 | ||||||
| chr8:119828795
|
C | A | 59 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(56): Show | 64 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.138+2882G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828795 | ||||||
| chr8:119828956
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.138+2721C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119828956 | ||||||
| chr8:119829010
|
C | G | 1 | a0002c0002t0001g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138+2667G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829010 | ||||||
| chr8:119829011
|
T | A | 1 | a0002c0002t0001g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138+2666A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829011 | ||||||
| chr8:119829012
|
T | G | 1 | a0002c0002t0001g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138+2665A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829012 | ||||||
| chr8:119829051
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+2626C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829051 | ||||||
| chr8:119829060
|
C | T | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.138+2617G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829060 | ||||||
| chr8:119829083
|
C | T | 217 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.138+2594G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829083 | ||||||
| chr8:119829162
|
C | T | 7 | a0001c0007t0001g0025a0001c0007t0001g0026a0001c0007t0001g0027others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+2515G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829162 | ||||||
| chr8:119829169
|
C | T | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.138+2508G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829169 | ||||||
| chr8:119829186
|
A | G | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+2491T>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829186 | ||||||
| chr8:119829291
|
C | T | 311 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.138+2386G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829291 | ||||||
| chr8:119829493
|
C | G | 313 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0151others(310): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.138+2184G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829493 | ||||||
| chr8:119829530
|
T | A | 1 | a0001c0003t0001g0024 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.138+2147A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829530 | ||||||
| chr8:119829737
|
G | A | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+1940C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829737 | ||||||
| chr8:119829860
|
G | GT | 10 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0180others(7): Show | 10 | HG00423.hp1 HG01243.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+1816dupA | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829860 | ||||||
| chr8:119829860
|
GTT | G | 13 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(10): Show | 15 | HG00738.hp1 HG02027.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+1815_138+1816d others(4): Show |
TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829860 | ||||||
| chr8:119829862
|
T | G | 3 | a0003c0008t0001g0013a0003c0008t0001g0014a0003c0008t0001g0015 | 3 | HG01891.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.138+1815A>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829862 | ||||||
| chr8:119829944
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.138+1733G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829944 | ||||||
| chr8:119829969
|
G | A | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+1708C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119829969 | ||||||
| chr8:119830001
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.138+1676G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119830001 | ||||||
| chr8:119830370
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.138+1307C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119830370 | ||||||
| chr8:119830719
|
A | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0151 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.138+958T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119830719 | ||||||
| chr8:119830904
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+773C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119830904 | ||||||
| chr8:119831241
|
T | A | 14 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(11): Show | 16 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+436A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831241 | ||||||
| chr8:119831283
|
G | A | 1 | a0003c0008t0001g0016 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138+394C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831283 | ||||||
| chr8:119831348
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+329A>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831348 | ||||||
| chr8:119831426
|
T | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+251A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831426 | ||||||
| chr8:119831451
|
T | C | 1 | a0002c0002t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138+226A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831451 | ||||||
| chr8:119831466
|
G | GA | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+210dupT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831466 | ||||||
| chr8:119831535
|
T | C | 58 | a0001c0015t0001g0160a0003c0006t0001g0154a0003c0006t0001g0155others(55): Show | 63 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.138+142A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831535 | ||||||
| chr8:119831539
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+138C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 2/25 | chr8 | 119831539 | ||||||
| chr8:119831876
|
T | C | 1 | a0001c0003t0001g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.84-145A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119831876 | ||||||
| chr8:119831928
|
C | T | 6 | a0003c0008t0001g0011a0003c0008t0001g0012a0003c0008t0001g0013others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.84-197G>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119831928 | ||||||
| chr8:119831948
|
C | G | 1 | a0002c0002t0001g0010 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.84-217G>C | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119831948 | ||||||
| chr8:119832066
|
G | A | 24 | a0003c0010t0002g0312a0003c0010t0002g0313a0004c0004t0002g0007others(21): Show | 25 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.84-335C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832066 | ||||||
| chr8:119832089
|
G | A | 2 | a0002c0002t0006g0166a0002c0002t0006g0167 | 2 | HG02155.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.84-358C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832089 | ||||||
| chr8:119832138
|
G | A | 15 | a0005c0005t0003g0001a0005c0005t0003g0278a0005c0005t0003g0279others(12): Show | 17 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+344C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832138 | ||||||
| chr8:119832171
|
T | TAA | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+309_83+310dupTT | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832171 | ||||||
| chr8:119832184
|
A | C | 5 | a0003c0006t0003g0272a0003c0006t0003g0273a0003c0006t0003g0274others(2): Show | 5 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+298T>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832184 | ||||||
| chr8:119832227
|
C | A | 1 | a0002c0002t0001g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.83+255G>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832227 | ||||||
| chr8:119832293
|
G | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA18974.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.83+189C>A | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832293 | ||||||
| chr8:119832349
|
T | C | 2 | a0005c0005t0003g0290a0005c0005t0003g0291 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+133A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832349 | ||||||
| chr8:119832350
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0177others(88): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.83+132A>G | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832350 | ||||||
| chr8:119832362
|
G | A | 5 | a0001c0003t0001g0266a0001c0003t0001g0267a0001c0003t0001g0268others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+120C>T | TAF2 | ENSG00000064313.13 | transcript | ENST00000378164.7 | protein_coding | 1/25 | chr8 | 119832362 |