Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6872 |
|---|---|
| ensemblid | ENSG00000147133.17 |
| hgncid | 11535 |
| symbol | TAF1 |
| name | TATA-box binding protein associated factor 1 |
| refseq_nuc | NM_004606.5 |
| refseq_prot | NP_004597.3 |
| ensembl_nuc | ENST00000423759.6 |
| ensembl_prot | ENSP00000406549.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 71366357 |
| end | 71466005 |
| strand | + |
| ver | v1.2 |
| region | chrX:71366357-71466005 |
| region5000 | chrX:71361357-71471005 |
| regionname0 | TAF1_chrX_71366357_71466005 |
| regionname5000 | TAF1_chrX_71361357_71471005 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1873 | 180 | 58 | 26 | 71 | 5 | 18 | 52 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0002 | 0/0 | 1873 | 13 | 0 | 11 | 0 | 0 | 2 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0003 | 0/0 | 1873 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0004 | 0/0 | 459 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0005 | 0/0 | 1775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0006 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| 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 | 1/1 | 5622 | 161 | 41 | 24 | 71 | 5 | 18 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0002 | 0/0 | 5622 | 17 | 16 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0003 | 0/0 | 5622 | 13 | 0 | 11 | 0 | 0 | 2 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0004 | 0/0 | 5622 | 4 | 4 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0005 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0006 | 0/0 | 5619 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0007 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0008 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| c0009 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| 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 | 1/1 | 1978 | 176 | 56 | 29 | 68 | 3 | 18 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0002 | 0/0 | 1978 | 6 | 4 | 2 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0003 | 0/0 | 1978 | 4 | 0 | 4 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0004 | 0/0 | 1978 | 4 | 0 | 2 | 0 | 0 | 2 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0005 | 0/0 | 1977 | 4 | 0 | 0 | 2 | 2 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0006 | 0/0 | 1979 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0007 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0008 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0009 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| t0010 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| 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 | 1/1 | 5622 | 161 | 41 | 24 | 71 | 5 | 18 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0002 | 0/0 | 5622 | 17 | 16 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0005 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0008 | 0/0 | 5622 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0002c0003 | 0/0 | 5622 | 13 | 0 | 11 | 0 | 0 | 2 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0003c0004 | 0/0 | 5622 | 4 | 4 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0004c0009 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0005c0006 | 0/0 | 5619 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0006c0007 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7599 | 137 | 35 | 16 | 65 | 3 | 16 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0002 | 0/0 | 7599 | 6 | 4 | 2 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0003 | 0/0 | 7599 | 4 | 0 | 4 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0004 | 0/0 | 7599 | 4 | 0 | 2 | 0 | 0 | 2 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0005 | 0/0 | 7598 | 4 | 0 | 0 | 2 | 2 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0006 | 0/0 | 7600 | 2 | 0 | 0 | 2 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0007 | 0/0 | 7599 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0008 | 0/0 | 7599 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0009 | 0/0 | 7599 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0001t0010 | 0/0 | 7599 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0002t0001 | 0/0 | 7599 | 17 | 16 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0005t0001 | 0/0 | 7599 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0001c0008t0001 | 0/0 | 7599 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0002c0003t0001 | 0/0 | 7599 | 13 | 0 | 11 | 0 | 0 | 2 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0003c0004t0001 | 0/0 | 7599 | 4 | 4 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0004c0009t0001 | 0/0 | 7600 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0005c0006t0001 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| a0006c0007t0001 | 0/0 | 7599 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | copy fasta | chrX | 71361357 | 71471005 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0001t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0001c0008t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0003c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0003c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0003c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0003c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0004c0009t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0005c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| a0006c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0199 | EUR | GBR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01071 | hp1 | a0001 | c0008 | t0001 | g0034 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0052 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0055 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01257 | hp2 | a0002 | c0003 | t0001 | g0049 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0053 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0054 | AMR | CLM | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0070 | EUR | IBS | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0051 | AMR | PEL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0050 | AMR | PEL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0059 | AMR | PEL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0056 | AMR | PEL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0058 | AMR | PEL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0082 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0151 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0057 | AMR | PEL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0194 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02809 | hp1 | a0003 | c0004 | t0001 | g0193 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0135 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02976 | hp1 | a0003 | c0004 | t0001 | g0195 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | ESN | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0166 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | STU | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | BEB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0100 | SAS | STU | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18944 | hp1 | a0006 | c0007 | t0001 | g0112 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18988 | hp1 | a0005 | c0006 | t0001 | g0011 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0186 | AFR | LWK | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | LWK | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19076 | hp1 | a0004 | c0009 | t0001 | g0142 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | YRI | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0191 | AFR | ACB | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0036 | REF | REF | TAF1_chrX_71361357_71471005 | TAF1 | chrX | 71361357 | 71471005 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71377696
|
C | G | 1 | a0002 | 13 | HG01109.hp1 HG01169.hp2 HG01257.hp2 others(10): Show |
missense_variant | MODERATE | c.808C>G | p.Leu270Val | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 6/38 | 826/7599 | 808/5622 | 270/1873 | chrX | 71377696 | ||
| chrX:71377781
|
C | G | 1 | a0003 | 4 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.893C>G | p.Ala298Gly | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 6/38 | 911/7599 | 893/5622 | 298/1873 | chrX | 71377781 | ||
| chrX:71378368
|
TC | T | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1070delC | p.Pro357fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 7/38 | 1088/7599 | 1070/5622 | 357/1873 | INFO_REALIGN_3_PRIME | chrX | 71378368 | |
| chrX:71378402
|
C | CA | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1104dupA | p.Leu369fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 7/38 | 1123/7599 | 1105/5622 | 369/1873 | INFO_REALIGN_3_PRIME | chrX | 71378402 | |
| chrX:71379001
|
A | AG | 1 | a0004 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1332dupG | p.Asn445fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/38 | 1351/7599 | 1333/5622 | 445/1873 | INFO_REALIGN_3_PRIME | chrX | 71379001 | |
| chrX:71393346
|
A | G | 1 | a0006 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.3097A>G | p.Met1033Val | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 21/38 | 3115/7599 | 3097/5622 | 1033/1873 | chrX | 71393346 | ||
| chrX:71460645
|
TG | T | 1 | a0005 | 1 | NA18988.hp1 | frameshift_variant | HIGH | c.5243delG | p.Gly1748fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/38 | 5261/7599 | 5243/5622 | 1748/1873 | INFO_REALIGN_3_PRIME | chrX | 71460645 | |
| chrX:71460662
|
TG | T | 1 | a0005 | 1 | NA18988.hp1 | frameshift_variant | HIGH | c.5261delG | p.Gly1754fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/38 | 5279/7599 | 5261/5622 | 1754/1873 | INFO_REALIGN_3_PRIME | chrX | 71460662 | |
| chrX:71460765
|
TG | T | 1 | a0005 | 1 | NA18988.hp1 | frameshift_variant | HIGH | c.5365delG | p.Glu1789fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/38 | 5383/7599 | 5365/5622 | 1789/1873 | INFO_REALIGN_3_PRIME | chrX | 71460765 | |
| chrX:71460782
|
G | GT | 1 | a0005 | 1 | NA18988.hp1 | frameshift_variant | HIGH | c.5381dupT | p.Leu1794fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/38 | 5400/7599 | 5382/5622 | 1794/1873 | INFO_REALIGN_3_PRIME | chrX | 71460782 | |
| chrX:71463944
|
TG | T | 1 | a0005 | 1 | NA18988.hp1 | frameshift_variant | HIGH | c.5523delG | p.Pro1842fs | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 5541/7599 | 5523/5622 | 1841/1873 | INFO_REALIGN_3_PRIME | chrX | 71463944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71375282
|
T | C | 3 | a0001c0002a0001c0005a0003c0004 | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
synonymous_variant | LOW | c.468T>C | p.Thr156Thr | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/38 | 486/7599 | 468/5622 | 156/1873 | chrX | 71375282 | ||
| chrX:71381855
|
C | G | 1 | a0001c0008 | 1 | HG01071.hp1 | synonymous_variant | LOW | c.1473C>G | p.Ala491Ala | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 9/38 | 1491/7599 | 1473/5622 | 491/1873 | chrX | 71381855 | ||
| chrX:71406641
|
G | A | 1 | a0001c0005 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.4002G>A | p.Ala1334Ala | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/38 | 4020/7599 | 4002/5622 | 1334/1873 | chrX | 71406641 | ||
| chrX:71407627
|
G | A | 3 | a0001c0002a0001c0005a0003c0004 | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
synonymous_variant | LOW | c.4161G>A | p.Ser1387Ser | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 27/38 | 4179/7599 | 4161/5622 | 1387/1873 | chrX | 71407627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71464178
|
T | G | 1 | a0001c0001t0007 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 132 | chrX | 71464178 | |||||
| chrX:71464684
|
C | T | 1 | a0001c0001t0010 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*638C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 638 | chrX | 71464684 | |||||
| chrX:71464705
|
C | CA | 1 | a0001c0001t0006 | 2 | HG02129.hp1 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*672dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 673 | INFO_REALIGN_3_PRIME | chrX | 71464705 | ||||
| chrX:71464705
|
CA | C | 1 | a0001c0001t0005 | 4 | HG00140.hp1 HG01515.hp1 NA19062.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*672delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 672 | INFO_REALIGN_3_PRIME | chrX | 71464705 | ||||
| chrX:71464927
|
A | G | 1 | a0001c0001t0004 | 4 | HG01069.hp1 HG01071.hp2 HG03688.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*881A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 881 | chrX | 71464927 | |||||
| chrX:71465102
|
C | T | 1 | a0001c0001t0009 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 1056 | chrX | 71465102 | |||||
| chrX:71465388
|
T | C | 1 | a0001c0001t0008 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1342T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 1342 | chrX | 71465388 | |||||
| chrX:71465535
|
T | C | 1 | a0001c0001t0003 | 4 | HG01256.hp1 HG01261.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1489T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 1489 | chrX | 71465535 | |||||
| chrX:71465758
|
G | A | 1 | a0001c0001t0002 | 6 | HG00738.hp1 HG01081.hp1 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1712G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 38/38 | 1712 | chrX | 71465758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71366582
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.120+88C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 1/37 | chrX | 71366582 | ||||||
| chrX:71366629
|
C | T | 1 | a0001c0001t0005g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.120+135C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 1/37 | chrX | 71366629 | ||||||
| chrX:71366631
|
T | TG | 1 | a0001c0001t0001g0001 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.120+140dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chrX | 71366631 | |||||
| chrX:71366883
|
A | G | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+389A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 1/37 | chrX | 71366883 | ||||||
| chrX:71367063
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121-436T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 1/37 | chrX | 71367063 | ||||||
| chrX:71367264
|
G | GTAT | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-234_121-232dup others(3): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chrX | 71367264 | |||||
| chrX:71367693
|
C | T | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.235+80C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 2/37 | chrX | 71367693 | ||||||
| chrX:71367817
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.235+204C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 2/37 | chrX | 71367817 | ||||||
| chrX:71367832
|
G | T | 2 | a0001c0002t0001g0197a0001c0002t0001g0198 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.235+219G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 2/37 | chrX | 71367832 | ||||||
| chrX:71367914
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.236-140G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 2/37 | chrX | 71367914 | ||||||
| chrX:71367937
|
C | T | 5 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(2): Show | 5 | HG00438.hp1 NA18952.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-117C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 2/37 | chrX | 71367937 | ||||||
| chrX:71368572
|
C | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.352+402C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71368572 | ||||||
| chrX:71368608
|
G | A | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+438G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71368608 | ||||||
| chrX:71368640
|
T | C | 8 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(5): Show | 8 | HG01255.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.352+470T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71368640 | ||||||
| chrX:71368810
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.352+640G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71368810 | ||||||
| chrX:71368814
|
C | CA | 15 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG00735.hp2 HG01243.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.352+661dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71368814 | |||||
| chrX:71368849
|
G | GT | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0162others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.352+694dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71368849 | |||||
| chrX:71368849
|
GT | G | 1 | a0001c0001t0001g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.352+694delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71368849 | |||||
| chrX:71368871
|
C | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18955.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.352+701C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71368871 | ||||||
| chrX:71369041
|
A | G | 23 | a0001c0001t0001g0159a0001c0002t0001g0177a0001c0002t0001g0178others(20): Show | 23 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.352+871A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369041 | ||||||
| chrX:71369042
|
G | A | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+872G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369042 | ||||||
| chrX:71369217
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0162 | 2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.352+1047G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369217 | ||||||
| chrX:71369467
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.352+1297T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369467 | ||||||
| chrX:71369539
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.352+1369T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369539 | ||||||
| chrX:71369546
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.352+1376G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369546 | ||||||
| chrX:71369605
|
C | CT | 6 | a0001c0001t0001g0158a0001c0001t0006g0016a0001c0002t0001g0192others(3): Show | 6 | HG02280.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+1453dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71369605 | |||||
| chrX:71369605
|
CT | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0160others(2): Show | 5 | HG01074.hp1 HG01099.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+1453delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71369605 | |||||
| chrX:71369670
|
A | G | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+1500A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369670 | ||||||
| chrX:71369750
|
C | T | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+1580C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369750 | ||||||
| chrX:71369770
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0017 | 2 | HG00735.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.352+1600T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369770 | ||||||
| chrX:71369798
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.352+1628A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71369798 | ||||||
| chrX:71370422
|
C | CTGCAACT others(26): Show |
1 | a0001c0002t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352+2269_352+2270i others(35): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71370422 | |||||
| chrX:71370440
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.352+2270G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71370440 | ||||||
| chrX:71370844
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.352+2674C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71370844 | ||||||
| chrX:71371052
|
C | G | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.352+2882C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71371052 | ||||||
| chrX:71371417
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG00735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.352+3247G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71371417 | ||||||
| chrX:71371481
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0162 | 2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.352+3311T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71371481 | ||||||
| chrX:71372169
|
C | T | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.353-2998C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71372169 | ||||||
| chrX:71372229
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | NA18906.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.353-2938C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71372229 | ||||||
| chrX:71372413
|
CAA | C | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.353-2753_353-2752d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71372413 | ||||||
| chrX:71372432
|
C | CAAAAAA | 1 | a0001c0001t0001g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.353-2714_353-2709d others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71372432 | |||||
| chrX:71372432
|
CA | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 155 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.353-2709delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71372432 | |||||
| chrX:71372432
|
CAA | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0147a0001c0001t0001g0148others(12): Show | 15 | HG01192.hp1 HG01255.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.353-2710_353-2709d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71372432 | |||||
| chrX:71372531
|
C | CA | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | NA18950.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.353-2635dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71372531 | |||||
| chrX:71372639
|
C | CA | 15 | a0001c0001t0001g0043a0001c0001t0002g0042a0001c0002t0001g0177others(12): Show | 15 | HG00738.hp1 HG01255.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.353-2515dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71372639 | |||||
| chrX:71372639
|
C | CAA | 1 | a0001c0002t0001g0182 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.353-2516_353-2515d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71372639 | |||||
| chrX:71372639
|
CA | C | 1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.353-2515delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71372639 | |||||
| chrX:71372682
|
T | C | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.353-2485T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71372682 | ||||||
| chrX:71372892
|
A | T | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.353-2275A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71372892 | ||||||
| chrX:71372893
|
G | C | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.353-2274G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71372893 | ||||||
| chrX:71372897
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.353-2270C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71372897 | ||||||
| chrX:71373056
|
C | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.353-2111C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71373056 | ||||||
| chrX:71373167
|
C | CT | 11 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(8): Show | 11 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.353-1982dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71373167 | |||||
| chrX:71373167
|
CT | C | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.353-1982delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71373167 | |||||
| chrX:71373492
|
A | G | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.353-1675A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71373492 | ||||||
| chrX:71373746
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.353-1421T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71373746 | ||||||
| chrX:71374001
|
A | G | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.353-1166A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71374001 | ||||||
| chrX:71374103
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.353-1064T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71374103 | ||||||
| chrX:71374163
|
A | C | 1 | a0003c0004t0001g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.353-1004A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71374163 | ||||||
| chrX:71374355
|
G | A | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.353-812G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71374355 | ||||||
| chrX:71374504
|
TCA | T | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.353-659_353-658del others(2): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71374504 | |||||
| chrX:71374523
|
C | G | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.353-644C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71374523 | ||||||
| chrX:71374945
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.353-222C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | chrX | 71374945 | ||||||
| chrX:71375075
|
C | CA | 2 | a0001c0001t0001g0028a0001c0002t0001g0183 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.353-76dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71375075 | |||||
| chrX:71375075
|
CA | C | 2 | a0001c0001t0001g0152a0004c0009t0001g0142 | 2 | HG03041.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.353-76delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chrX | 71375075 | |||||
| chrX:71375551
|
T | TA | 1 | a0001c0001t0001g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.472+277dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chrX | 71375551 | |||||
| chrX:71375556
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.472+270A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | chrX | 71375556 | ||||||
| chrX:71375575
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.472+289C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | chrX | 71375575 | ||||||
| chrX:71376027
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.472+741A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | chrX | 71376027 | ||||||
| chrX:71376534
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.473-416G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | chrX | 71376534 | ||||||
| chrX:71376666
|
C | CA | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.473-271dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chrX | 71376666 | |||||
| chrX:71376666
|
CA | C | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.473-271delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chrX | 71376666 | |||||
| chrX:71376795
|
A | C | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.473-155A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | chrX | 71376795 | ||||||
| chrX:71376812
|
A | G | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-138A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | chrX | 71376812 | ||||||
| chrX:71376903
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0165 | 2 | HG00438.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.473-47A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 4/37 | chrX | 71376903 | ||||||
| chrX:71377277
|
T | C | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+86T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 5/37 | chrX | 71377277 | ||||||
| chrX:71377575
|
T | C | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-28T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 5/37 | chrX | 71377575 | ||||||
| chrX:71377980
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.933+159C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 6/37 | chrX | 71377980 | ||||||
| chrX:71378171
|
C | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0150a0001c0001t0001g0152others(1): Show | 4 | HG02258.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-64C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 6/37 | chrX | 71378171 | ||||||
| chrX:71378668
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1153-156G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 7/37 | chrX | 71378668 | ||||||
| chrX:71378671
|
TGG | T | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1153-151_1153-150d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 7/37 | INFO_REALIGN_3_PRIME | chrX | 71378671 | |||||
| chrX:71378689
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1153-135C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 7/37 | chrX | 71378689 | ||||||
| chrX:71379105
|
A | AT | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(23): Show | 26 | HG00609.hp1 HG01192.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1360+97dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
A | ATT | 1 | a0001c0001t0001g0136 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1360+96_1360+97dup others(2): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
A | ATTTTTTT others(1): Show |
2 | a0001c0002t0001g0188a0001c0002t0001g0190 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+90_1360+97dup others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
A | ATTTTTTT others(2): Show |
2 | a0001c0002t0001g0187a0001c0005t0001g0186 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1360+89_1360+97dup others(9): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
A | ATTTTTTT others(3): Show |
4 | a0001c0002t0001g0182a0001c0002t0001g0184a0001c0002t0001g0189others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+88_1360+97dup others(10): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
A | ATTTTTTT others(4): Show |
4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0185others(1): Show | 4 | HG02055.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+87_1360+97dup others(11): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
A | ATTTTTTT others(5): Show |
9 | a0001c0002t0001g0177a0001c0002t0001g0180a0001c0002t0001g0181others(6): Show | 9 | HG01255.hp1 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1360+86_1360+97dup others(12): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0159a0003c0004t0001g0195 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1360+85_1360+97dup others(13): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
AT | A | 9 | a0001c0001t0001g0047a0001c0001t0001g0152a0001c0001t0001g0160others(6): Show | 9 | HG01069.hp1 HG01071.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1360+97delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379105
|
ATT | A | 1 | a0001c0001t0001g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1360+96_1360+97del others(2): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379105 | |||||
| chrX:71379145
|
C | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+114C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71379145 | ||||||
| chrX:71379410
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1360+379C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71379410 | ||||||
| chrX:71379596
|
CT | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1360+585delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379596 | |||||
| chrX:71379596
|
CTT | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0159others(11): Show | 14 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1360+584_1360+585d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71379596 | |||||
| chrX:71379622
|
G | A | 23 | a0001c0001t0001g0159a0001c0002t0001g0177a0001c0002t0001g0178others(20): Show | 23 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1360+591G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71379622 | ||||||
| chrX:71379651
|
G | A | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+620G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71379651 | ||||||
| chrX:71379706
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1360+675G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71379706 | ||||||
| chrX:71379938
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18955.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1360+907T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71379938 | ||||||
| chrX:71380008
|
G | GT | 1 | a0001c0001t0001g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1360+988dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | INFO_REALIGN_3_PRIME | chrX | 71380008 | |||||
| chrX:71380134
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+1103G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71380134 | ||||||
| chrX:71380243
|
A | G | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+1212A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71380243 | ||||||
| chrX:71380590
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1361-1153A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71380590 | ||||||
| chrX:71380729
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-1014C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71380729 | ||||||
| chrX:71380811
|
CT | C | 1 | a0001c0001t0001g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1361-931delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71380811 | ||||||
| chrX:71380941
|
T | C | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1361-802T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71380941 | ||||||
| chrX:71380945
|
T | C | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1361-798T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71380945 | ||||||
| chrX:71381095
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1361-648G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71381095 | ||||||
| chrX:71381488
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1361-255C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 8/37 | chrX | 71381488 | ||||||
| chrX:71381962
|
C | T | 1 | a0001c0002t0001g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1537+43C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 9/37 | chrX | 71381962 | ||||||
| chrX:71382396
|
T | TG | 1 | a0001c0001t0001g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1538-131dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chrX | 71382396 | |||||
| chrX:71382402
|
G | C | 11 | a0002c0003t0001g0049a0002c0003t0001g0050a0002c0003t0001g0051others(8): Show | 11 | HG01109.hp1 HG01169.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1538-134G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 9/37 | chrX | 71382402 | ||||||
| chrX:71382923
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1773+55G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 11/37 | chrX | 71382923 | ||||||
| chrX:71383353
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1947+189G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 12/37 | chrX | 71383353 | ||||||
| chrX:71383476
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1947+312C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 12/37 | chrX | 71383476 | ||||||
| chrX:71383744
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1948-218A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 12/37 | chrX | 71383744 | ||||||
| chrX:71383823
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1948-139C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 12/37 | chrX | 71383823 | ||||||
| chrX:71383864
|
TA | T | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1948-94delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 12/37 | INFO_REALIGN_3_PRIME | chrX | 71383864 | |||||
| chrX:71383940
|
G | C | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1948-22G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 12/37 | chrX | 71383940 | ||||||
| chrX:71384191
|
T | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0060others(15): Show | 18 | HG00735.hp2 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2121+56T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 13/37 | chrX | 71384191 | ||||||
| chrX:71384268
|
A | G | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2121+133A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 13/37 | chrX | 71384268 | ||||||
| chrX:71384414
|
C | CT | 2 | a0001c0001t0001g0008a0001c0001t0001g0101 | 2 | HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2121+294dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chrX | 71384414 | |||||
| chrX:71384909
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18950.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2122-36T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 13/37 | chrX | 71384909 | ||||||
| chrX:71385473
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2226+424G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71385473 | ||||||
| chrX:71385483
|
T | C | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2226+434T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71385483 | ||||||
| chrX:71385550
|
A | C | 1 | a0001c0002t0001g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2226+501A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71385550 | ||||||
| chrX:71385927
|
C | T | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2226+878C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71385927 | ||||||
| chrX:71386161
|
C | CA | 4 | a0001c0001t0001g0157a0001c0002t0001g0188a0001c0002t0001g0189others(1): Show | 4 | HG02615.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2227-1084dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chrX | 71386161 | |||||
| chrX:71386161
|
C | CAA | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2227-1085_2227-108 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chrX | 71386161 | |||||
| chrX:71386358
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0159others(22): Show | 25 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.2227-903G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71386358 | ||||||
| chrX:71386605
|
T | C | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2227-656T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71386605 | ||||||
| chrX:71386783
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2227-478A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71386783 | ||||||
| chrX:71386892
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2227-369T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 14/37 | chrX | 71386892 | ||||||
| chrX:71387719
|
A | AG | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2427+260dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 15/37 | INFO_REALIGN_3_PRIME | chrX | 71387719 | |||||
| chrX:71387865
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2428-372G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 15/37 | chrX | 71387865 | ||||||
| chrX:71387933
|
C | CA | 1 | a0001c0001t0001g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2428-288dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 15/37 | INFO_REALIGN_3_PRIME | chrX | 71387933 | |||||
| chrX:71387933
|
CA | C | 4 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198others(1): Show | 4 | HG01943.hp1 HG02055.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2428-288delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 15/37 | INFO_REALIGN_3_PRIME | chrX | 71387933 | |||||
| chrX:71388227
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2428-10T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 15/37 | chrX | 71388227 | ||||||
| chrX:71388913
|
G | GT | 2 | a0001c0001t0001g0157a0001c0002t0001g0197 | 2 | HG03130.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2700+56dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 17/37 | INFO_REALIGN_3_PRIME | chrX | 71388913 | |||||
| chrX:71389094
|
A | G | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2700+226A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 17/37 | chrX | 71389094 | ||||||
| chrX:71389253
|
G | T | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2701-332G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 17/37 | chrX | 71389253 | ||||||
| chrX:71389485
|
A | G | 1 | a0003c0004t0001g0191 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2701-100A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 17/37 | chrX | 71389485 | ||||||
| chrX:71389518
|
T | TA | 1 | a0001c0001t0001g0035 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2701-57dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 17/37 | INFO_REALIGN_3_PRIME | chrX | 71389518 | |||||
| chrX:71389697
|
T | G | 1 | a0002c0003t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2781+32T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71389697 | ||||||
| chrX:71389715
|
C | T | 13 | a0002c0003t0001g0049a0002c0003t0001g0050a0002c0003t0001g0051others(10): Show | 13 | HG01109.hp1 HG01169.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2781+50C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71389715 | ||||||
| chrX:71389935
|
A | G | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2781+270A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71389935 | ||||||
| chrX:71390721
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2781+1056C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71390721 | ||||||
| chrX:71390753
|
TG | T | 1 | a0001c0001t0001g0160 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2781+1091delG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71390753 | |||||
| chrX:71390995
|
C | CA | 1 | a0001c0002t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2781+1342dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71390995 | |||||
| chrX:71391024
|
A | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0171a0001c0001t0005g0122 | 3 | NA18994.hp1 NA19062.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2781+1359A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391024 | ||||||
| chrX:71391047
|
AT | A | 1 | a0001c0001t0001g0160 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2781+1386delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391047 | |||||
| chrX:71391073
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(36): Show | 39 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.2781+1408C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391073 | ||||||
| chrX:71391349
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2782-1220G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391349 | ||||||
| chrX:71391397
|
T | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 69 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.2782-1172T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391397 | ||||||
| chrX:71391412
|
A | G | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2782-1157A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391412 | ||||||
| chrX:71391481
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2782-1088C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391481 | ||||||
| chrX:71391518
|
TA | T | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2782-1045delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391518 | |||||
| chrX:71391605
|
A | ATT | 1 | a0001c0001t0001g0160 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2782-961_2782-960d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391605 | |||||
| chrX:71391629
|
C | CT | 9 | a0001c0001t0002g0015a0001c0002t0001g0192a0001c0002t0001g0196others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2782-923dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391629 | |||||
| chrX:71391629
|
CT | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0150others(2): Show | 5 | HG01515.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2782-923delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391629 | |||||
| chrX:71391793
|
A | AT | 1 | a0001c0001t0001g0160 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2782-771dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391793 | |||||
| chrX:71391802
|
C | CT | 1 | a0001c0001t0001g0160 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2782-763dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391802 | |||||
| chrX:71391812
|
A | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01884.hp2 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2782-757A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391812 | ||||||
| chrX:71391824
|
AC | A | 1 | a0001c0001t0001g0160 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2782-743delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chrX | 71391824 | |||||
| chrX:71391874
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2782-695G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391874 | ||||||
| chrX:71391933
|
A | G | 1 | a0001c0001t0010g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2782-636A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71391933 | ||||||
| chrX:71392456
|
A | C | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2782-113A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 18/37 | chrX | 71392456 | ||||||
| chrX:71393084
|
G | T | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3051+90G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | chrX | 71393084 | ||||||
| chrX:71393221
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3052-80G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | chrX | 71393221 | ||||||
| chrX:71393222
|
A | AAT | 2 | a0001c0002t0001g0179a0001c0002t0001g0187 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3052-79_3052-78ins others(2): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | chrX | 71393222 | ||||||
| chrX:71393222
|
A | AATTGTG | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3052-79_3052-78ins others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | chrX | 71393222 | ||||||
| chrX:71393223
|
T | A | 4 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0180others(1): Show | 4 | HG01255.hp1 HG02145.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3052-78T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | chrX | 71393223 | ||||||
| chrX:71393224
|
T | G | 3 | a0001c0002t0001g0179a0001c0002t0001g0187a0001c0005t0001g0186 | 3 | HG02622.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3052-77T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | chrX | 71393224 | ||||||
| chrX:71393224
|
T | TGTG | 1 | a0001c0001t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3052-77_3052-76ins others(3): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | chrX | 71393224 | ||||||
| chrX:71393224
|
T | TTG | 46 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.3052-37_3052-36dup others(2): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393224
|
T | TTGTG | 8 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(5): Show | 8 | HG02523.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3052-39_3052-36dup others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393224
|
T | TTGTGTG | 4 | a0001c0001t0001g0095a0001c0001t0005g0109a0001c0002t0001g0196others(1): Show | 4 | HG03130.hp1 HG03490.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3052-41_3052-36dup others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393224
|
T | TTGTGTGT others(1): Show |
1 | a0001c0002t0001g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3052-43_3052-36dup others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393224
|
TTG | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0104a0001c0001t0001g0131others(17): Show | 20 | HG01257.hp1 HG01496.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.3052-37_3052-36del others(2): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393224
|
TTGTG | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0043others(8): Show | 11 | HG03579.hp1 NA18950.hp2 NA18970.hp1 others(8): Show |
intron_variant | MODIFIER | c.3052-39_3052-36del others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393224
|
TTGTGTG | T | 2 | a0001c0001t0001g0071a0001c0002t0001g0182 | 2 | HG02818.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.3052-41_3052-36del others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393224
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3052-47_3052-36del others(12): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chrX | 71393224 | |||||
| chrX:71393719
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3227+243T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 21/37 | chrX | 71393719 | ||||||
| chrX:71394008
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3228-59C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 21/37 | chrX | 71394008 | ||||||
| chrX:71394616
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3406+371A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | chrX | 71394616 | ||||||
| chrX:71395085
|
A | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3406+840A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | chrX | 71395085 | ||||||
| chrX:71395178
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3406+933G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | chrX | 71395178 | ||||||
| chrX:71396059
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3407-1194G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | chrX | 71396059 | ||||||
| chrX:71396127
|
C | G | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3407-1126C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | chrX | 71396127 | ||||||
| chrX:71396148
|
C | CA | 2 | a0001c0001t0001g0118a0001c0001t0001g0141 | 2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3407-1091dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71396148 | |||||
| chrX:71396148
|
CA | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0157 | 2 | HG01074.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.3407-1091delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71396148 | |||||
| chrX:71396295
|
C | CT | 2 | a0001c0001t0001g0104a0001c0001t0001g0157 | 2 | NA18965.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3407-941dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71396295 | |||||
| chrX:71396295
|
CT | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0159others(22): Show | 25 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.3407-941delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71396295 | |||||
| chrX:71396984
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3407-269C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | chrX | 71396984 | ||||||
| chrX:71397028
|
C | CA | 25 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 25 | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.3407-201dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71397028 | |||||
| chrX:71397028
|
C | CAA | 2 | a0001c0001t0001g0046a0001c0002t0001g0196 | 2 | HG00621.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3407-202_3407-201d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71397028 | |||||
| chrX:71397028
|
CA | C | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3407-201delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71397028 | |||||
| chrX:71397028
|
CAAAAAAA others(1): Show |
C | 4 | a0003c0004t0001g0191a0003c0004t0001g0193a0003c0004t0001g0194others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3407-208_3407-201d others(10): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chrX | 71397028 | |||||
| chrX:71397082
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3407-171G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 22/37 | chrX | 71397082 | ||||||
| chrX:71397511
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3620+45T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 23/37 | chrX | 71397511 | ||||||
| chrX:71397593
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 198 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.3620+127A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 23/37 | chrX | 71397593 | ||||||
| chrX:71397808
|
GGGA | G | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3620+344_3620+346d others(5): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chrX | 71397808 | |||||
| chrX:71398164
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3621-408C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 23/37 | chrX | 71398164 | ||||||
| chrX:71398344
|
G | GA | 2 | a0001c0001t0001g0073a0001c0001t0001g0149 | 2 | HG01192.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.3621-213dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chrX | 71398344 | |||||
| chrX:71398344
|
GAAAA | G | 1 | a0001c0001t0001g0063 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3621-216_3621-213d others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chrX | 71398344 | |||||
| chrX:71398823
|
TG | T | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3786+89delG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71398823 | |||||
| chrX:71398910
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3786+173G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71398910 | ||||||
| chrX:71399087
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18950.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3786+350G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399087 | ||||||
| chrX:71399130
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0063 | 3 | HG00735.hp2 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3786+393G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399130 | ||||||
| chrX:71399253
|
C | CT | 19 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0076others(16): Show | 19 | HG01192.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3786+537dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71399253 | |||||
| chrX:71399253
|
C | CTT | 1 | a0001c0001t0003g0023 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3786+536_3786+537d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71399253 | |||||
| chrX:71399253
|
CT | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0102a0001c0001t0001g0133others(8): Show | 11 | HG01257.hp1 HG01257.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.3786+537delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71399253 | |||||
| chrX:71399287
|
C | T | 2 | a0002c0003t0001g0100a0002c0003t0001g0166 | 2 | HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3786+550C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399287 | ||||||
| chrX:71399567
|
C | CT | 2 | a0001c0002t0001g0196a0001c0002t0001g0198 | 2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3786+852dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71399567 | |||||
| chrX:71399567
|
CT | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 158 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.3786+852delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71399567 | |||||
| chrX:71399567
|
CTT | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0156 | 2 | HG02015.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.3786+851_3786+852d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71399567 | |||||
| chrX:71399567
|
CTTTTTTT others(1): Show |
C | 1 | a0001c0002t0001g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3786+845_3786+852d others(10): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71399567 | |||||
| chrX:71399603
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3786+866A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399603 | ||||||
| chrX:71399719
|
G | A | 1 | a0002c0003t0001g0050 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3786+982G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399719 | ||||||
| chrX:71399744
|
T | G | 1 | a0001c0002t0001g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3786+1007T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399744 | ||||||
| chrX:71399930
|
C | T | 11 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(8): Show | 11 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3786+1193C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399930 | ||||||
| chrX:71399978
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3786+1241C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71399978 | ||||||
| chrX:71400080
|
G | GT | 1 | a0001c0001t0001g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3786+1352dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chrX | 71400080 | |||||
| chrX:71400086
|
T | G | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3786+1349T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71400086 | ||||||
| chrX:71400294
|
T | C | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3787-1234T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71400294 | ||||||
| chrX:71400369
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0106others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.3787-1159G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71400369 | ||||||
| chrX:71400399
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3787-1129G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71400399 | ||||||
| chrX:71400693
|
T | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3787-835T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71400693 | ||||||
| chrX:71400777
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3787-751A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71400777 | ||||||
| chrX:71401266
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3787-262T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 24/37 | chrX | 71401266 | ||||||
| chrX:71401791
|
TTA | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0171a0001c0001t0005g0122 | 3 | NA18994.hp1 NA19062.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.3998+56_3998+57del others(2): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71401791 | |||||
| chrX:71402001
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0092a0001c0001t0001g0093others(8): Show | 11 | HG00609.hp1 HG01256.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.3998+262A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71402001 | ||||||
| chrX:71402128
|
G | GT | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3998+397dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71402128 | |||||
| chrX:71402155
|
G | GT | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3998+420dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71402155 | |||||
| chrX:71402232
|
C | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3998+493C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71402232 | ||||||
| chrX:71402448
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3998+709A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71402448 | ||||||
| chrX:71403070
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3998+1331C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403070 | ||||||
| chrX:71403087
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3998+1348G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403087 | ||||||
| chrX:71403184
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3998+1445A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403184 | ||||||
| chrX:71403376
|
A | G | 1 | a0001c0001t0001g0012 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3998+1637A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403376 | ||||||
| chrX:71403573
|
A | G | 1 | a0001c0002t0001g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3998+1834A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403573 | ||||||
| chrX:71403589
|
A | G | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3998+1850A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403589 | ||||||
| chrX:71403638
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0002g0065 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3998+1899T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403638 | ||||||
| chrX:71403766
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3998+2027T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71403766 | ||||||
| chrX:71403911
|
CT | C | 2 | a0001c0001t0001g0078a0001c0002t0001g0192 | 2 | HG00280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3998+2186delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71403911 | |||||
| chrX:71404026
|
T | G | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3998+2287T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71404026 | ||||||
| chrX:71404180
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3998+2441G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71404180 | ||||||
| chrX:71404425
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0150a0001c0001t0001g0152 | 3 | HG02965.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3999-2213C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71404425 | ||||||
| chrX:71404775
|
AAAT | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.3999-1862_3999-186 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71404775 | ||||||
| chrX:71404899
|
G | GT | 1 | a0001c0001t0001g0091 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3999-1736dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71404899 | |||||
| chrX:71404945
|
T | G | 1 | a0001c0001t0005g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3999-1693T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71404945 | ||||||
| chrX:71404951
|
C | CT | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(17): Show | 20 | HG01243.hp1 HG01358.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3999-1664dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71404951 | |||||
| chrX:71404951
|
C | CTT | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3999-1665_3999-166 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71404951 | |||||
| chrX:71404951
|
CT | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0080others(5): Show | 8 | HG00280.hp1 HG01192.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3999-1664delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71404951 | |||||
| chrX:71404951
|
CTT | C | 1 | a0001c0001t0001g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3999-1665_3999-166 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71404951 | |||||
| chrX:71405210
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3999-1428C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71405210 | ||||||
| chrX:71405255
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3999-1383G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71405255 | ||||||
| chrX:71405412
|
G | A | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3999-1226G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71405412 | ||||||
| chrX:71405413
|
C | A | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3999-1225C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71405413 | ||||||
| chrX:71405675
|
A | G | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3999-963A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71405675 | ||||||
| chrX:71405684
|
A | G | 1 | a0001c0002t0001g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3999-954A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71405684 | ||||||
| chrX:71405863
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0027 | 2 | HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3999-775A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71405863 | ||||||
| chrX:71406031
|
T | A | 13 | a0002c0003t0001g0049a0002c0003t0001g0050a0002c0003t0001g0051others(10): Show | 13 | HG01109.hp1 HG01169.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3999-607T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71406031 | ||||||
| chrX:71406174
|
C | T | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3999-464C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71406174 | ||||||
| chrX:71406286
|
G | A | 1 | a0001c0001t0005g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3999-352G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | chrX | 71406286 | ||||||
| chrX:71406326
|
C | CA | 9 | a0001c0001t0001g0018a0001c0001t0001g0076a0001c0001t0001g0132others(6): Show | 9 | HG01978.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3999-292dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71406326 | |||||
| chrX:71406326
|
CA | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0154a0001c0002t0001g0196others(3): Show | 6 | HG01167.hp1 HG01257.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3999-292delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71406326 | |||||
| chrX:71406343
|
AAAAG | A | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3999-293_3999-290d others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71406343 | |||||
| chrX:71406344
|
AAAG | A | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3999-292_3999-290d others(5): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71406344 | |||||
| chrX:71406556
|
C | CT | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3999-74dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chrX | 71406556 | |||||
| chrX:71406916
|
A | AT | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(8): Show | 11 | HG01978.hp2 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.4107+187dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | INFO_REALIGN_3_PRIME | chrX | 71406916 | |||||
| chrX:71406916
|
A | G | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4107+170A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | chrX | 71406916 | ||||||
| chrX:71406916
|
AT | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0147a0001c0001t0005g0109others(1): Show | 4 | HG02809.hp2 HG03453.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.4107+187delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | INFO_REALIGN_3_PRIME | chrX | 71406916 | |||||
| chrX:71406954
|
C | T | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4107+208C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | chrX | 71406954 | ||||||
| chrX:71406955
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4107+209G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | chrX | 71406955 | ||||||
| chrX:71407151
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4107+405G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | chrX | 71407151 | ||||||
| chrX:71407156
|
T | G | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4107+410T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | chrX | 71407156 | ||||||
| chrX:71407214
|
A | AT | 30 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0045others(27): Show | 30 | HG00438.hp1 HG01167.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.4108-339dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | INFO_REALIGN_3_PRIME | chrX | 71407214 | |||||
| chrX:71407214
|
AT | A | 2 | a0001c0001t0001g0039a0002c0003t0001g0059 | 2 | HG01943.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.4108-339delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 26/37 | INFO_REALIGN_3_PRIME | chrX | 71407214 | |||||
| chrX:71407724
|
C | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0127a0001c0001t0001g0162 | 3 | HG00609.hp1 NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.4206+52C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 27/37 | chrX | 71407724 | ||||||
| chrX:71407770
|
AC | A | 1 | a0001c0001t0001g0113 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4206+99delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 27/37 | chrX | 71407770 | ||||||
| chrX:71407870
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4207-104T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 27/37 | chrX | 71407870 | ||||||
| chrX:71408363
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4384+212G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71408363 | ||||||
| chrX:71408403
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4384+252C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71408403 | ||||||
| chrX:71408752
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4384+601G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71408752 | ||||||
| chrX:71408974
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4384+823A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71408974 | ||||||
| chrX:71408980
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4384+829C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71408980 | ||||||
| chrX:71409013
|
C | CA | 2 | a0001c0001t0001g0124a0001c0002t0001g0198 | 2 | HG02055.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.4384+878dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71409013 | |||||
| chrX:71409013
|
CA | C | 4 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0005g0109others(1): Show | 4 | HG02109.hp1 NA18960.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.4384+878delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71409013 | |||||
| chrX:71409028
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4384+877A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409028 | ||||||
| chrX:71409073
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.4384+922C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409073 | ||||||
| chrX:71409315
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4384+1164A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409315 | ||||||
| chrX:71409365
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4384+1214C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409365 | ||||||
| chrX:71409472
|
G | A | 33 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0045others(30): Show | 33 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.4384+1321G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409472 | ||||||
| chrX:71409668
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4384+1517G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409668 | ||||||
| chrX:71409748
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0148 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4384+1597A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409748 | ||||||
| chrX:71409801
|
C | G | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4384+1650C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409801 | ||||||
| chrX:71409931
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4384+1780C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71409931 | ||||||
| chrX:71409944
|
G | GT | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+1794dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71409944 | |||||
| chrX:71410038
|
G | GC | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+1890dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410038 | |||||
| chrX:71410072
|
C | T | 23 | a0001c0001t0001g0159a0001c0002t0001g0177a0001c0002t0001g0178others(20): Show | 23 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4384+1921C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410072 | ||||||
| chrX:71410235
|
ACT | A | 1 | a0001c0001t0001g0041 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4384+2085_4384+208 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410235 | ||||||
| chrX:71410322
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4384+2171G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410322 | ||||||
| chrX:71410399
|
T | TA | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4384+2259dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410399 | |||||
| chrX:71410454
|
C | CT | 31 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0041others(28): Show | 31 | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(28): Show |
intron_variant | MODIFIER | c.4384+2324dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410454 | |||||
| chrX:71410454
|
C | CTT | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+2323_4384+232 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410454 | |||||
| chrX:71410454
|
CT | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0167a0001c0001t0005g0070 | 3 | HG01515.hp1 HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.4384+2324delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410454 | |||||
| chrX:71410458
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0121others(3): Show | 6 | NA18747.hp1 NA18994.hp1 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.4384+2307T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410458 | ||||||
| chrX:71410493
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4384+2342T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410493 | ||||||
| chrX:71410522
|
G | GT | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+2372dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410522 | |||||
| chrX:71410543
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0075 | 3 | NA18970.hp1 NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.4384+2392C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410543 | ||||||
| chrX:71410603
|
G | A | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4384+2452G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410603 | ||||||
| chrX:71410624
|
A | AT | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+2479dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410624 | |||||
| chrX:71410659
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0137a0001c0001t0001g0150others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.4384+2508G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410659 | ||||||
| chrX:71410765
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4384+2614G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71410765 | ||||||
| chrX:71410792
|
CT | C | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+2648delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71410792 | |||||
| chrX:71411151
|
T | TC | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+3001dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71411151 | |||||
| chrX:71411271
|
A | AG | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+3123dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71411271 | |||||
| chrX:71411323
|
T | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0101 | 2 | HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4384+3172T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71411323 | ||||||
| chrX:71411381
|
AG | A | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+3232delG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71411381 | |||||
| chrX:71411487
|
G | GA | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4384+3345dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71411487 | |||||
| chrX:71411495
|
AAGAT | A | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+3346_4384+334 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71411495 | |||||
| chrX:71411498
|
ATAAAG | A | 4 | a0003c0004t0001g0191a0003c0004t0001g0193a0003c0004t0001g0194others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4384+3350_4384+335 others(9): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71411498 | |||||
| chrX:71411502
|
A | G | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+3351A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71411502 | ||||||
| chrX:71411503
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4384+3352G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71411503 | ||||||
| chrX:71411538
|
G | A | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4384+3387G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71411538 | ||||||
| chrX:71411834
|
C | T | 2 | a0001c0001t0007g0037a0006c0007t0001g0112 | 2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.4384+3683C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71411834 | ||||||
| chrX:71412039
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4384+3888A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71412039 | ||||||
| chrX:71412122
|
G | GT | 4 | a0001c0001t0001g0009a0001c0001t0001g0132a0001c0001t0001g0168others(1): Show | 4 | HG02056.hp1 HG04199.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.4384+3991dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71412122 | |||||
| chrX:71412122
|
GT | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0162a0001c0001t0003g0023others(6): Show | 9 | HG00741.hp2 HG01256.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.4384+3991delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71412122 | |||||
| chrX:71412147
|
CAG | C | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4384+3997_4384+399 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71412147 | ||||||
| chrX:71412317
|
A | G | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4384+4166A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71412317 | ||||||
| chrX:71412440
|
T | A | 1 | a0001c0001t0002g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4384+4289T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71412440 | ||||||
| chrX:71412699
|
TG | T | 1 | a0001c0001t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4384+4549delG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71412699 | ||||||
| chrX:71412906
|
A | G | 1 | a0001c0002t0001g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4384+4755A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71412906 | ||||||
| chrX:71413095
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4384+4944A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71413095 | ||||||
| chrX:71413764
|
A | C | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4384+5613A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71413764 | ||||||
| chrX:71413883
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4384+5732C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71413883 | ||||||
| chrX:71413884
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4384+5733G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71413884 | ||||||
| chrX:71413920
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4384+5769C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71413920 | ||||||
| chrX:71414488
|
C | CA | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4384+6338dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71414488 | |||||
| chrX:71414547
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 81 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.4384+6396T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71414547 | ||||||
| chrX:71414744
|
C | T | 4 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0031others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.4385-6565C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71414744 | ||||||
| chrX:71415128
|
C | CG | 2 | a0001c0001t0001g0062a0002c0003t0001g0100 | 2 | HG02922.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.4385-6181_4385-618 others(5): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71415128 | ||||||
| chrX:71415128
|
C | CGT | 1 | a0001c0001t0001g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4385-6181_4385-618 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71415128 | ||||||
| chrX:71415128
|
C | CT | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.4385-6152dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71415128 | |||||
| chrX:71415128
|
C | CTT | 17 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0072others(14): Show | 17 | HG00438.hp1 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4385-6153_4385-615 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71415128 | |||||
| chrX:71415128
|
C | CTTT | 13 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0043others(10): Show | 13 | HG01243.hp1 HG02027.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.4385-6154_4385-615 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71415128 | |||||
| chrX:71415128
|
C | CTTTT | 1 | a0001c0001t0001g0010 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.4385-6155_4385-615 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71415128 | |||||
| chrX:71415128
|
C | CTTTTTTT | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4385-6158_4385-615 others(11): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71415128 | |||||
| chrX:71415128
|
CT | C | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0136others(1): Show | 4 | HG01069.hp1 HG02074.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.4385-6152delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71415128 | |||||
| chrX:71415128
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4385-6161_4385-615 others(14): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71415128 | |||||
| chrX:71415261
|
C | T | 2 | a0001c0002t0001g0188a0001c0002t0001g0190 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4385-6048C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71415261 | ||||||
| chrX:71415309
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4385-6000G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71415309 | ||||||
| chrX:71415965
|
A | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(6): Show | 9 | HG00280.hp1 HG01071.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.4385-5344A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71415965 | ||||||
| chrX:71416034
|
T | A | 1 | a0002c0003t0001g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4385-5275T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416034 | ||||||
| chrX:71416124
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4385-5185C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416124 | ||||||
| chrX:71416213
|
T | C | 18 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(15): Show | 18 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.4385-5096T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416213 | ||||||
| chrX:71416247
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0147 | 2 | HG02074.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.4385-5062G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416247 | ||||||
| chrX:71416394
|
AAAAAAAG | A | 2 | a0001c0001t0001g0117a0001c0001t0002g0042 | 2 | HG00738.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.4385-4912_4385-490 others(11): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71416394 | |||||
| chrX:71416547
|
C | G | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4385-4762C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416547 | ||||||
| chrX:71416619
|
A | C | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0121others(4): Show | 7 | HG04199.hp1 NA18747.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.4385-4690A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416619 | ||||||
| chrX:71416656
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(31): Show | 34 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.4385-4653A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416656 | ||||||
| chrX:71416682
|
T | TC | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18950.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.4385-4626dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71416682 | |||||
| chrX:71416837
|
AACAGTGC | A | 1 | a0001c0001t0006g0016 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4385-4470_4385-446 others(11): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71416837 | |||||
| chrX:71416896
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4385-4413C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71416896 | ||||||
| chrX:71417019
|
C | CA | 17 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0063others(14): Show | 17 | HG01261.hp1 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.4385-4270dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71417019 | |||||
| chrX:71417019
|
C | CAA | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4385-4271_4385-427 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71417019 | |||||
| chrX:71417019
|
CA | C | 10 | a0001c0001t0001g0047a0001c0001t0001g0113a0001c0001t0001g0116others(7): Show | 10 | HG01169.hp2 HG01255.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.4385-4270delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71417019 | |||||
| chrX:71417019
|
CAA | C | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4385-4271_4385-427 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71417019 | |||||
| chrX:71417040
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4385-4269T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417040 | ||||||
| chrX:71417167
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4385-4142G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417167 | ||||||
| chrX:71417428
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4385-3881C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417428 | ||||||
| chrX:71417454
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4385-3855C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417454 | ||||||
| chrX:71417624
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4385-3685A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417624 | ||||||
| chrX:71417700
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4385-3609A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417700 | ||||||
| chrX:71417875
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4385-3434A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417875 | ||||||
| chrX:71417958
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4385-3351T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417958 | ||||||
| chrX:71417969
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4385-3340G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71417969 | ||||||
| chrX:71418198
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4385-3111A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71418198 | ||||||
| chrX:71418233
|
A | G | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4385-3076A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71418233 | ||||||
| chrX:71418252
|
TC | T | 4 | a0003c0004t0001g0191a0003c0004t0001g0193a0003c0004t0001g0194others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4385-3055delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71418252 | |||||
| chrX:71418326
|
G | T | 9 | a0002c0003t0001g0049a0002c0003t0001g0050a0002c0003t0001g0051others(6): Show | 9 | HG01169.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4385-2983G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71418326 | ||||||
| chrX:71418339
|
C | T | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4385-2970C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71418339 | ||||||
| chrX:71418404
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4385-2905A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71418404 | ||||||
| chrX:71418761
|
A | AT | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0025others(11): Show | 14 | HG00735.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.4385-2524dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71418761 | |||||
| chrX:71418761
|
A | ATT | 15 | a0001c0001t0001g0134a0001c0001t0001g0153a0001c0001t0001g0155others(12): Show | 15 | HG01255.hp1 HG01257.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4385-2525_4385-252 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71418761 | |||||
| chrX:71418761
|
A | ATTT | 1 | a0001c0002t0001g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4385-2526_4385-252 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71418761 | |||||
| chrX:71418761
|
AT | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0161 | 2 | NA18906.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.4385-2524delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71418761 | |||||
| chrX:71418943
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4385-2366T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71418943 | ||||||
| chrX:71418956
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4385-2353G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71418956 | ||||||
| chrX:71419017
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4385-2292T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71419017 | ||||||
| chrX:71419266
|
T | TA | 1 | a0001c0001t0006g0016 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4385-2034dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71419266 | |||||
| chrX:71419381
|
G | GA | 2 | a0001c0001t0001g0123a0001c0002t0001g0198 | 2 | HG02055.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.4385-1919dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71419381 | |||||
| chrX:71419533
|
AAAAG | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(28): Show | 31 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.4385-1772_4385-176 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71419533 | |||||
| chrX:71419671
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4385-1638A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71419671 | ||||||
| chrX:71419825
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.4385-1484C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71419825 | ||||||
| chrX:71419861
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4385-1448C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71419861 | ||||||
| chrX:71420086
|
A | AG | 1 | a0001c0001t0001g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4385-1219dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71420086 | |||||
| chrX:71420214
|
C | G | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4385-1095C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71420214 | ||||||
| chrX:71420728
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4385-581C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71420728 | ||||||
| chrX:71420844
|
A | AG | 1 | a0001c0001t0006g0016 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4385-464dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71420844 | |||||
| chrX:71420880
|
C | CG | 1 | a0001c0001t0006g0016 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4385-425dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71420880 | |||||
| chrX:71420930
|
A | AC | 2 | a0001c0001t0001g0162a0001c0001t0006g0016 | 2 | NA18977.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.4385-377dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71420930 | |||||
| chrX:71420954
|
C | CG | 1 | a0001c0001t0006g0016 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4385-354dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71420954 | |||||
| chrX:71420971
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4385-338G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71420971 | ||||||
| chrX:71420971
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4385-338G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71420971 | ||||||
| chrX:71420992
|
CTT | C | 1 | a0001c0002t0001g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4385-315_4385-314d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chrX | 71420992 | |||||
| chrX:71421147
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4385-162C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71421147 | ||||||
| chrX:71421160
|
A | G | 1 | a0002c0003t0001g0059 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4385-149A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71421160 | ||||||
| chrX:71421171
|
G | A | 23 | a0001c0001t0001g0159a0001c0002t0001g0177a0001c0002t0001g0178others(20): Show | 23 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4385-138G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 28/37 | chrX | 71421171 | ||||||
| chrX:71421956
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4452+580G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | chrX | 71421956 | ||||||
| chrX:71422125
|
A | G | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4452+749A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | chrX | 71422125 | ||||||
| chrX:71422217
|
A | G | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4452+841A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | chrX | 71422217 | ||||||
| chrX:71422322
|
A | AT | 3 | a0001c0001t0001g0110a0001c0001t0003g0094a0003c0004t0001g0193 | 3 | HG00673.hp1 HG01358.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4453-777dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chrX | 71422322 | |||||
| chrX:71422322
|
AT | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0103others(17): Show | 20 | HG01169.hp1 HG01255.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.4453-777delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chrX | 71422322 | |||||
| chrX:71422331
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4453-786T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | chrX | 71422331 | ||||||
| chrX:71422482
|
A | AT | 1 | a0001c0001t0001g0008 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4453-620dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chrX | 71422482 | |||||
| chrX:71422906
|
G | GT | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4453-202dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chrX | 71422906 | |||||
| chrX:71423020
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4453-97G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 29/37 | chrX | 71423020 | ||||||
| chrX:71423696
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4576-278C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 30/37 | chrX | 71423696 | ||||||
| chrX:71424296
|
A | G | 1 | a0002c0003t0001g0050 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4753+58A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71424296 | ||||||
| chrX:71424318
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4753+80T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71424318 | ||||||
| chrX:71424414
|
C | CT | 1 | a0001c0002t0001g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4753+202dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71424414 | |||||
| chrX:71424414
|
C | CTT | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4753+201_4753+202d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71424414 | |||||
| chrX:71424414
|
CT | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0121others(12): Show | 15 | HG01071.hp2 HG01256.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4753+202delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71424414 | |||||
| chrX:71424414
|
CTT | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 168 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.4753+201_4753+202d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71424414 | |||||
| chrX:71424414
|
CTTT | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0116a0001c0001t0001g0145others(2): Show | 5 | HG02622.hp1 HG03017.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4753+200_4753+202d others(5): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71424414 | |||||
| chrX:71424768
|
G | A | 1 | a0001c0001t0006g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4753+530G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71424768 | ||||||
| chrX:71424797
|
G | T | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4753+559G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71424797 | ||||||
| chrX:71424928
|
C | CTT | 1 | a0001c0001t0001g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4753+698_4753+699d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71424928 | |||||
| chrX:71424976
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4753+738A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71424976 | ||||||
| chrX:71424981
|
T | C | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4753+743T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71424981 | ||||||
| chrX:71425469
|
T | G | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+1231T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71425469 | ||||||
| chrX:71425737
|
TGA | T | 1 | a0001c0001t0001g0005 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4753+1503_4753+150 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71425737 | |||||
| chrX:71425740
|
GAGTT | G | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4753+1505_4753+150 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71425740 | |||||
| chrX:71426095
|
G | GA | 2 | a0001c0001t0001g0077a0001c0005t0001g0186 | 2 | HG03492.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4753+1870dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71426095 | |||||
| chrX:71426095
|
GA | G | 1 | a0001c0002t0001g0188 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4753+1870delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71426095 | |||||
| chrX:71426383
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4753+2145C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71426383 | ||||||
| chrX:71426396
|
C | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4753+2158C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71426396 | ||||||
| chrX:71426672
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0137a0001c0001t0001g0150others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.4753+2434G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71426672 | ||||||
| chrX:71426673
|
C | T | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4753+2435C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71426673 | ||||||
| chrX:71426715
|
C | CA | 4 | a0001c0001t0001g0046a0001c0001t0001g0105a0002c0003t0001g0055others(1): Show | 4 | HG00621.hp1 HG01169.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.4753+2490dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71426715 | |||||
| chrX:71426767
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4753+2529A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71426767 | ||||||
| chrX:71426932
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01257.hp1 HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4753+2694C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71426932 | ||||||
| chrX:71426957
|
T | C | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4753+2719T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71426957 | ||||||
| chrX:71427133
|
T | C | 1 | a0002c0003t0001g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4753+2895T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71427133 | ||||||
| chrX:71427529
|
A | G | 5 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0108others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+3291A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71427529 | ||||||
| chrX:71427710
|
A | C | 1 | a0001c0001t0005g0070 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4753+3472A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71427710 | ||||||
| chrX:71427947
|
G | GA | 4 | a0001c0001t0005g0109a0001c0002t0001g0188a0001c0002t0001g0189others(1): Show | 4 | HG02615.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4753+3721dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71427947 | |||||
| chrX:71427980
|
C | CT | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4753+3752dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71427980 | |||||
| chrX:71428011
|
A | AT | 1 | a0001c0002t0001g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4753+3793dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71428011 | |||||
| chrX:71428011
|
AT | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(96): Show | 99 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.4753+3793delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71428011 | |||||
| chrX:71428164
|
C | T | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+3926C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71428164 | ||||||
| chrX:71428170
|
C | T | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+3932C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71428170 | ||||||
| chrX:71428524
|
A | AC | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4753+4292dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71428524 | |||||
| chrX:71428582
|
C | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4753+4344C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71428582 | ||||||
| chrX:71428864
|
T | C | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4753+4626T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71428864 | ||||||
| chrX:71429253
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4753+5015C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71429253 | ||||||
| chrX:71429274
|
C | CA | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4753+5046dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71429274 | |||||
| chrX:71429398
|
A | G | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+5160A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71429398 | ||||||
| chrX:71429547
|
G | A | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4753+5309G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71429547 | ||||||
| chrX:71429570
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4753+5332C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71429570 | ||||||
| chrX:71430377
|
C | A | 13 | a0002c0003t0001g0049a0002c0003t0001g0050a0002c0003t0001g0051others(10): Show | 13 | HG01109.hp1 HG01169.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4753+6139C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71430377 | ||||||
| chrX:71430385
|
C | CA | 18 | a0001c0001t0001g0028a0001c0001t0001g0043a0001c0001t0001g0045others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.4753+6167dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71430385 | |||||
| chrX:71430385
|
C | CAA | 3 | a0001c0001t0001g0164a0001c0002t0001g0188a0001c0002t0001g0189 | 3 | HG02027.hp1 HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4753+6166_4753+616 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71430385 | |||||
| chrX:71430385
|
C | CAAA | 1 | a0001c0002t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4753+6165_4753+616 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71430385 | |||||
| chrX:71430385
|
CA | C | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4753+6167delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71430385 | |||||
| chrX:71430385
|
CAAAA | C | 1 | a0001c0001t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4753+6164_4753+616 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71430385 | |||||
| chrX:71431003
|
A | AT | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(40): Show | 43 | HG00642.hp1 HG00673.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.4753+6794dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431003
|
A | ATT | 5 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0005g0199others(2): Show | 5 | HG00140.hp1 HG01109.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+6793_4753+679 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431003
|
A | ATTT | 1 | a0001c0001t0001g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4753+6792_4753+679 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431003
|
AT | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0039others(9): Show | 12 | HG01255.hp1 HG02135.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.4753+6794delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431003
|
ATT | A | 7 | a0001c0001t0001g0021a0001c0001t0001g0159a0001c0002t0001g0187others(4): Show | 7 | HG02055.hp1 HG02622.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.4753+6793_4753+679 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431003
|
ATTT | A | 6 | a0001c0002t0001g0184a0001c0002t0001g0192a0003c0004t0001g0191others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4753+6792_4753+679 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431003
|
ATTTT | A | 6 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0185others(3): Show | 6 | HG02615.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4753+6791_4753+679 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431003
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4753+6785_4753+679 others(14): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431003 | |||||
| chrX:71431032
|
T | TG | 1 | a0001c0001t0002g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4753+6795dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431032 | |||||
| chrX:71431183
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4753+6945C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71431183 | ||||||
| chrX:71431218
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4753+6980A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71431218 | ||||||
| chrX:71431618
|
T | A | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4753+7380T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71431618 | ||||||
| chrX:71431914
|
C | CA | 8 | a0001c0001t0001g0014a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4753+7694dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431914 | |||||
| chrX:71431914
|
CAAA | C | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4753+7692_4753+769 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71431914 | |||||
| chrX:71431917
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4753+7679A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71431917 | ||||||
| chrX:71432237
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4753+7999G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71432237 | ||||||
| chrX:71432347
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4753+8109A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71432347 | ||||||
| chrX:71432499
|
C | CT | 6 | a0001c0001t0001g0028a0001c0001t0001g0132a0001c0002t0001g0182others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4753+8275dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71432499 | |||||
| chrX:71432499
|
CT | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.4753+8275delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71432499 | |||||
| chrX:71433168
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4753+8930A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71433168 | ||||||
| chrX:71433656
|
A | AT | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4753+9425dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71433656 | |||||
| chrX:71433762
|
A | AT | 21 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(18): Show | 21 | HG02027.hp1 HG02486.hp1 NA18943.hp1 others(18): Show |
intron_variant | MODIFIER | c.4753+9535dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71433762 | |||||
| chrX:71434054
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4753+9816G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71434054 | ||||||
| chrX:71434414
|
T | A | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4753+10176T>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71434414 | ||||||
| chrX:71434579
|
A | T | 4 | a0003c0004t0001g0191a0003c0004t0001g0193a0003c0004t0001g0194others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4753+10341A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71434579 | ||||||
| chrX:71435482
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4753+11244C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71435482 | ||||||
| chrX:71435615
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4753+11377T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71435615 | ||||||
| chrX:71435845
|
C | T | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4753+11607C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71435845 | ||||||
| chrX:71436038
|
C | CT | 26 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0033others(23): Show | 26 | HG01109.hp1 HG01255.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.4753+11827dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436038 | |||||
| chrX:71436038
|
C | CTT | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167others(2): Show | 5 | HG02145.hp1 HG04204.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+11826_4753+11 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436038 | |||||
| chrX:71436038
|
CT | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0069a0001c0001t0001g0075others(6): Show | 9 | HG01256.hp1 HG02132.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.4753+11827delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436038 | |||||
| chrX:71436038
|
CTTTTTTT | C | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4753+11821_4753+11 others(13): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436038 | |||||
| chrX:71436038
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0111a0001c0002t0001g0188a0001c0002t0001g0189others(1): Show | 4 | HG02040.hp1 HG02615.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4753+11812_4753+11 others(22): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436038 | |||||
| chrX:71436214
|
A | AT | 9 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0123others(6): Show | 9 | HG01109.hp1 HG02738.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.4753+11995dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436214 | |||||
| chrX:71436214
|
A | ATT | 7 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4753+11994_4753+11 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436214 | |||||
| chrX:71436214
|
A | ATTT | 1 | a0003c0004t0001g0193 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4753+11993_4753+11 others(9): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436214 | |||||
| chrX:71436214
|
AT | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0103a0001c0001t0001g0143others(2): Show | 5 | HG02451.hp2 NA18955.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+11995delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436214 | |||||
| chrX:71436450
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4753+12212C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71436450 | ||||||
| chrX:71436467
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4753+12229G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71436467 | ||||||
| chrX:71436576
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4753+12338G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71436576 | ||||||
| chrX:71436874
|
T | TA | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4753+12639dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71436874 | |||||
| chrX:71437382
|
CTT | C | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4753+13151_4753+13 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71437382 | |||||
| chrX:71437649
|
CA | C | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4753+13425delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71437649 | |||||
| chrX:71437726
|
T | C | 1 | a0002c0003t0001g0052 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4753+13488T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71437726 | ||||||
| chrX:71437779
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0106others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.4753+13541A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71437779 | ||||||
| chrX:71437799
|
G | GA | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4753+13565dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71437799 | |||||
| chrX:71437834
|
C | CT | 9 | a0001c0001t0001g0091a0001c0001t0001g0165a0001c0001t0001g0168others(6): Show | 9 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4753+13615dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71437834 | |||||
| chrX:71437834
|
CT | C | 5 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0121others(2): Show | 5 | NA18747.hp1 NA18960.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+13615delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71437834 | |||||
| chrX:71437943
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4753+13705C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71437943 | ||||||
| chrX:71438025
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0081a0001c0001t0001g0084others(2): Show | 5 | NA18945.hp1 NA18953.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.4753+13787G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71438025 | ||||||
| chrX:71438149
|
A | G | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4753+13911A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71438149 | ||||||
| chrX:71438282
|
TC | T | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4753+14047delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71438282 | |||||
| chrX:71438493
|
GT | G | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4753+14256delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71438493 | ||||||
| chrX:71438783
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0148 | 3 | HG02922.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4753+14545T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71438783 | ||||||
| chrX:71439220
|
T | C | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4754-14950T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439220 | ||||||
| chrX:71439297
|
CT | C | 1 | a0001c0001t0001g0143 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4754-14864delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71439297 | |||||
| chrX:71439333
|
C | T | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4754-14837C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439333 | ||||||
| chrX:71439370
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4754-14800C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439370 | ||||||
| chrX:71439437
|
CAGGT | C | 1 | a0001c0001t0002g0042 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4754-14730_4754-14 others(10): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71439437 | |||||
| chrX:71439456
|
AC | A | 1 | a0001c0001t0001g0136 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4754-14713delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439456 | ||||||
| chrX:71439503
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 69 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.4754-14667C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439503 | ||||||
| chrX:71439505
|
TA | T | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4754-14661delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71439505 | |||||
| chrX:71439517
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4754-14653T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439517 | ||||||
| chrX:71439541
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4754-14629C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439541 | ||||||
| chrX:71439639
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4754-14531C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71439639 | ||||||
| chrX:71439773
|
CT | C | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4754-14392delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71439773 | |||||
| chrX:71440022
|
C | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4754-14148C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71440022 | ||||||
| chrX:71440308
|
G | GT | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4754-13860dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71440308 | |||||
| chrX:71440489
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4754-13681C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71440489 | ||||||
| chrX:71440490
|
G | A | 1 | a0001c0008t0001g0034 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4754-13680G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71440490 | ||||||
| chrX:71440501
|
AT | A | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4754-13657delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71440501 | |||||
| chrX:71440528
|
G | GA | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4754-13634dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71440528 | |||||
| chrX:71440766
|
AT | A | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4754-13400delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71440766 | |||||
| chrX:71441062
|
G | A | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4754-13108G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71441062 | ||||||
| chrX:71441174
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.4754-12996C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71441174 | ||||||
| chrX:71441229
|
G | GT | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4754-12931dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71441229 | |||||
| chrX:71441371
|
T | C | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4754-12799T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71441371 | ||||||
| chrX:71441549
|
CA | C | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4754-12620delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71441549 | ||||||
| chrX:71441733
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0196others(2): Show | 5 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4754-12437A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71441733 | ||||||
| chrX:71441811
|
TC | T | 1 | a0001c0001t0005g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.4754-12354delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71441811 | |||||
| chrX:71442116
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4754-12054C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442116 | ||||||
| chrX:71442125
|
CAT | C | 1 | a0001c0001t0001g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4754-12044_4754-12 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442125 | ||||||
| chrX:71442270
|
A | G | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4754-11900A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442270 | ||||||
| chrX:71442290
|
A | G | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4754-11880A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442290 | ||||||
| chrX:71442461
|
C | T | 1 | a0001c0008t0001g0034 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4754-11709C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442461 | ||||||
| chrX:71442716
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4754-11454T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442716 | ||||||
| chrX:71442838
|
A | G | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4754-11332A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442838 | ||||||
| chrX:71442879
|
C | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 23 | HG02027.hp1 HG02559.hp1 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.4754-11291C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442879 | ||||||
| chrX:71442886
|
A | C | 11 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(8): Show | 11 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.4754-11284A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442886 | ||||||
| chrX:71442977
|
G | A | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4754-11193G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71442977 | ||||||
| chrX:71443177
|
G | GT | 1 | a0001c0001t0001g0125 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4754-10987dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71443177 | |||||
| chrX:71443322
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4754-10848C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71443322 | ||||||
| chrX:71443411
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4754-10759A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71443411 | ||||||
| chrX:71443946
|
A | G | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4754-10224A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71443946 | ||||||
| chrX:71444082
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4754-10088A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71444082 | ||||||
| chrX:71444315
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4754-9855T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71444315 | ||||||
| chrX:71444391
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0002g0107 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4754-9779C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71444391 | ||||||
| chrX:71444532
|
A | AAT | 1 | a0001c0001t0001g0083 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4754-9634_4754-963 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71444532 | |||||
| chrX:71444735
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4754-9435G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71444735 | ||||||
| chrX:71444883
|
G | A | 2 | a0001c0001t0004g0031a0001c0001t0004g0163 | 2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.4754-9287G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71444883 | ||||||
| chrX:71444969
|
C | T | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4754-9201C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71444969 | ||||||
| chrX:71445112
|
A | G | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4754-9058A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71445112 | ||||||
| chrX:71445140
|
C | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG01257.hp1 HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4754-9030C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71445140 | ||||||
| chrX:71445298
|
C | CA | 4 | a0001c0001t0001g0008a0001c0001t0001g0117a0001c0001t0001g0132others(1): Show | 4 | HG01934.hp1 HG02602.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.4754-8852dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71445298 | |||||
| chrX:71445298
|
CA | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0045others(3): Show | 6 | HG01074.hp1 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4754-8852delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71445298 | |||||
| chrX:71445356
|
G | GT | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4754-8808dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71445356 | |||||
| chrX:71445428
|
G | GTAATTAA | 2 | a0001c0001t0001g0007a0001c0001t0001g0103 | 2 | NA18960.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.4754-8742_4754-874 others(11): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71445428 | ||||||
| chrX:71445455
|
C | CT | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4754-8708dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71445455 | |||||
| chrX:71445658
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4754-8512A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71445658 | ||||||
| chrX:71445915
|
A | AT | 1 | a0001c0002t0001g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4754-8239dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71445915 | |||||
| chrX:71445915
|
A | ATT | 8 | a0001c0002t0001g0192a0001c0002t0001g0196a0001c0002t0001g0197others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4754-8240_4754-823 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71445915 | |||||
| chrX:71446132
|
AAC | A | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4754-8037_4754-803 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71446132 | ||||||
| chrX:71446299
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4754-7871G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71446299 | ||||||
| chrX:71446306
|
C | G | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4754-7864C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71446306 | ||||||
| chrX:71447058
|
T | TG | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4754-7111dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71447058 | |||||
| chrX:71447430
|
TGGTGGCT others(37): Show |
T | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02083.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.4754-6736_4754-669 others(48): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71447430 | |||||
| chrX:71447640
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4754-6530T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71447640 | ||||||
| chrX:71447653
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4754-6517C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71447653 | ||||||
| chrX:71447683
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4754-6487C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71447683 | ||||||
| chrX:71447696
|
C | CA | 4 | a0001c0001t0001g0013a0001c0001t0001g0173a0001c0001t0001g0200others(1): Show | 4 | HG02135.hp1 HG02615.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.4754-6458dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71447696 | |||||
| chrX:71447696
|
CA | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0064others(26): Show | 29 | HG01081.hp1 HG01109.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.4754-6458delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71447696 | |||||
| chrX:71447731
|
T | TC | 1 | a0001c0001t0001g0125 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4754-6433dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71447731 | |||||
| chrX:71448303
|
C | CA | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4754-5863dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71448303 | |||||
| chrX:71448401
|
G | C | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4754-5769G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71448401 | ||||||
| chrX:71448642
|
G | C | 1 | a0001c0001t0002g0042 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4754-5528G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71448642 | ||||||
| chrX:71448752
|
GT | G | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4754-5408delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71448752 | |||||
| chrX:71448763
|
A | T | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4754-5407A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71448763 | ||||||
| chrX:71448820
|
C | CT | 2 | a0001c0001t0001g0120a0001c0001t0005g0122 | 2 | HG02559.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.4754-5335dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71448820 | |||||
| chrX:71448820
|
CT | C | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4754-5335delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71448820 | |||||
| chrX:71448843
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4754-5327A>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71448843 | ||||||
| chrX:71448951
|
T | TG | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4754-5216dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71448951 | |||||
| chrX:71449279
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0046others(1): Show | 4 | HG00621.hp1 HG00741.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.4754-4891C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71449279 | ||||||
| chrX:71449686
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4754-4484A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71449686 | ||||||
| chrX:71449854
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4754-4316C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71449854 | ||||||
| chrX:71449956
|
A | G | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4754-4214A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71449956 | ||||||
| chrX:71450051
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4754-4119C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71450051 | ||||||
| chrX:71450206
|
C | CT | 1 | a0001c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4754-3950dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71450206 | |||||
| chrX:71450206
|
CT | C | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4754-3950delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71450206 | |||||
| chrX:71450684
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4754-3486C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71450684 | ||||||
| chrX:71450737
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4754-3433A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71450737 | ||||||
| chrX:71450890
|
T | C | 23 | a0001c0001t0001g0159a0001c0002t0001g0177a0001c0002t0001g0178others(20): Show | 23 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4754-3280T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71450890 | ||||||
| chrX:71450978
|
G | C | 7 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(4): Show | 7 | HG01255.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4754-3192G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71450978 | ||||||
| chrX:71451059
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 183 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.4754-3111T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71451059 | ||||||
| chrX:71451309
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4754-2861G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71451309 | ||||||
| chrX:71451475
|
A | AT | 2 | a0001c0001t0001g0038a0001c0001t0001g0125 | 2 | HG00741.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4754-2686dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71451475 | |||||
| chrX:71451475
|
AT | A | 11 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(8): Show | 11 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.4754-2686delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71451475 | |||||
| chrX:71451578
|
G | T | 23 | a0001c0001t0001g0159a0001c0002t0001g0177a0001c0002t0001g0178others(20): Show | 23 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4754-2592G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71451578 | ||||||
| chrX:71451617
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4754-2553C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71451617 | ||||||
| chrX:71451957
|
T | C | 1 | a0001c0001t0005g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4754-2213T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71451957 | ||||||
| chrX:71452031
|
C | G | 1 | a0002c0003t0001g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4754-2139C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452031 | ||||||
| chrX:71452109
|
A | AC | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(42): Show | 45 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.4754-2050dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452109 | |||||
| chrX:71452109
|
AC | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0092others(15): Show | 18 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.4754-2050delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452109 | |||||
| chrX:71452162
|
A | AC | 1 | a0001c0001t0004g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4754-2001dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452162 | |||||
| chrX:71452304
|
C | CG | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4754-1862dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452304 | |||||
| chrX:71452309
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0025 | 2 | HG00735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4754-1861C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452309 | ||||||
| chrX:71452317
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18940.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.4754-1853G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452317 | ||||||
| chrX:71452344
|
C | CG | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4754-1822dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452344 | |||||
| chrX:71452348
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4754-1822G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452348 | ||||||
| chrX:71452353
|
C | CG | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4754-1814dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452353 | |||||
| chrX:71452363
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4754-1807C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452363 | ||||||
| chrX:71452421
|
C | CG | 3 | a0001c0001t0001g0169a0001c0005t0001g0186a0004c0009t0001g0142 | 3 | HG03669.hp1 NA19030.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.4754-1745dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452421 | |||||
| chrX:71452429
|
C | CG | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4754-1737dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71452429 | |||||
| chrX:71452441
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.4754-1729G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452441 | ||||||
| chrX:71452469
|
T | C | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4754-1701T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452469 | ||||||
| chrX:71452474
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4754-1696A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452474 | ||||||
| chrX:71452486
|
C | T | 1 | a0003c0004t0001g0193 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4754-1684C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452486 | ||||||
| chrX:71452621
|
C | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4754-1549C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452621 | ||||||
| chrX:71452653
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4754-1517C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452653 | ||||||
| chrX:71452762
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4754-1408C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452762 | ||||||
| chrX:71452862
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4754-1308C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452862 | ||||||
| chrX:71452953
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4754-1217C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71452953 | ||||||
| chrX:71453027
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4754-1143G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71453027 | ||||||
| chrX:71453030
|
C | G | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4754-1140C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71453030 | ||||||
| chrX:71453048
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4754-1122G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71453048 | ||||||
| chrX:71453084
|
G | GGA | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4754-1076_4754-107 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71453084 | |||||
| chrX:71453092
|
A | AGAGGGAG others(2): Show |
1 | a0001c0001t0001g0095 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4754-1067_4754-105 others(13): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71453092 | |||||
| chrX:71453101
|
GGAGGGA | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0067others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.4754-1046_4754-104 others(10): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71453101 | |||||
| chrX:71453383
|
A | AC | 15 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(12): Show | 15 | HG00741.hp1 HG01496.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.4754-777dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71453383 | |||||
| chrX:71453383
|
AC | A | 29 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0092others(26): Show | 29 | HG00609.hp1 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.4754-777delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chrX | 71453383 | |||||
| chrX:71453385
|
C | T | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4754-785C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71453385 | ||||||
| chrX:71453391
|
C | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0121a0001c0001t0001g0123others(2): Show | 5 | NA18747.hp1 NA18994.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.4754-779C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71453391 | ||||||
| chrX:71454124
|
G | C | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4754-46G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 32/37 | chrX | 71454124 | ||||||
| chrX:71454386
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4821+149G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 33/37 | chrX | 71454386 | ||||||
| chrX:71454571
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0108 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4822-170C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 33/37 | chrX | 71454571 | ||||||
| chrX:71454629
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4822-112C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 33/37 | chrX | 71454629 | ||||||
| chrX:71455725
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4938+868A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71455725 | ||||||
| chrX:71455748
|
C | T | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4938+891C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71455748 | ||||||
| chrX:71456060
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4938+1203G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71456060 | ||||||
| chrX:71456118
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4938+1261G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71456118 | ||||||
| chrX:71456231
|
G | GC | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4938+1376dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456231 | |||||
| chrX:71456234
|
T | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0150a0001c0001t0001g0152others(1): Show | 4 | HG02258.hp1 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4938+1377T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71456234 | ||||||
| chrX:71456266
|
A | G | 1 | a0001c0002t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4938+1409A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71456266 | ||||||
| chrX:71456649
|
C | CT | 8 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0076others(5): Show | 8 | HG01081.hp1 HG01192.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.4939-1549dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTT | 3 | a0001c0001t0001g0033a0001c0001t0002g0065a0001c0008t0001g0034 | 3 | HG01071.hp1 HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4939-1550_4939-154 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTT | 2 | a0001c0001t0001g0028a0001c0001t0001g0137 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4939-1551_4939-154 others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTT | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0200 | 3 | HG01257.hp1 HG01496.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4939-1552_4939-154 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTT | 3 | a0001c0001t0001g0020a0001c0001t0001g0062a0001c0002t0001g0180 | 3 | HG01255.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4939-1553_4939-154 others(9): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTT | 9 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0110others(6): Show | 9 | HG00673.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4939-1554_4939-154 others(10): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0153others(2): Show | 5 | HG02647.hp1 NA19056.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.4939-1555_4939-154 others(11): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(1): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0170 | 2 | HG00642.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.4939-1556_4939-154 others(12): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(2): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0088a0001c0002t0001g0177 | 3 | HG01884.hp1 HG02071.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.4939-1557_4939-154 others(13): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0102a0001c0001t0001g0114a0001c0001t0001g0117others(1): Show | 4 | HG00438.hp1 HG02602.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.4939-1558_4939-154 others(14): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0116 | 2 | HG01891.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.4939-1559_4939-154 others(15): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0174a0001c0002t0001g0181 | 2 | HG03471.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.4939-1560_4939-154 others(16): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0145 | 2 | HG02622.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4939-1561_4939-154 others(17): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0010g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4939-1563_4939-154 others(19): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0175 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4939-1564_4939-154 others(20): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4939-1565_4939-154 others(21): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0106a0001c0001t0001g0173 | 2 | HG03195.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.4939-1566_4939-154 others(22): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CT | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG00735.hp1 HG01099.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.4939-1549delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTT | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0148 | 2 | HG00735.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4939-1550_4939-154 others(6): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTT | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0046others(1): Show | 4 | HG00621.hp1 HG01074.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.4939-1553_4939-154 others(9): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTT | C | 1 | a0001c0002t0001g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4939-1554_4939-154 others(10): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(1): Show |
C | 1 | a0001c0001t0001g0113 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4939-1556_4939-154 others(12): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(2): Show |
C | 2 | a0001c0001t0001g0007a0001c0001t0001g0111 | 2 | HG02040.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.4939-1557_4939-154 others(13): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0002t0001g0183a0001c0002t0001g0184a0003c0004t0001g0191others(1): Show | 4 | HG02109.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.4939-1559_4939-154 others(15): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(5): Show |
C | 8 | a0001c0002t0001g0182a0001c0002t0001g0185a0001c0002t0001g0188others(5): Show | 8 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.4939-1560_4939-154 others(16): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0079a0001c0001t0001g0159 | 2 | NA18906.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.4939-1562_4939-154 others(18): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(8): Show |
C | 7 | a0001c0001t0001g0018a0001c0001t0001g0075a0001c0001t0001g0130others(4): Show | 7 | HG02523.hp1 HG02523.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4939-1563_4939-154 others(19): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(9): Show |
C | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(29): Show | 32 | HG00140.hp1 HG01433.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.4939-1564_4939-154 others(20): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(10): Show |
C | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4939-1565_4939-154 others(21): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0061a0001c0001t0006g0115 | 2 | HG02129.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4939-1566_4939-154 others(22): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(12): Show |
C | 5 | a0001c0001t0002g0042a0001c0001t0004g0029a0001c0001t0004g0030others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.4939-1567_4939-154 others(23): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(13): Show |
C | 5 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0048others(2): Show | 5 | HG02109.hp2 HG02698.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.4939-1568_4939-154 others(24): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(14): Show |
C | 43 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0089others(40): Show | 43 | HG00438.hp2 HG00609.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.4939-1569_4939-154 others(25): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0001g0019a0001c0001t0001g0021 | 2 | NA18948.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.4939-1570_4939-154 others(26): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(16): Show |
C | 3 | a0001c0001t0001g0038a0001c0002t0001g0187a0001c0005t0001g0186 | 3 | HG00741.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4939-1571_4939-154 others(27): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(19): Show |
C | 1 | a0001c0002t0001g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4939-1574_4939-154 others(30): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(21): Show |
C | 1 | a0001c0001t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.4939-1576_4939-154 others(32): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456649
|
CTTTTTTT others(22): Show |
C | 1 | a0001c0002t0001g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4939-1577_4939-154 others(33): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71456649 | |||||
| chrX:71456824
|
G | A | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198 | 3 | HG02055.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4939-1417G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71456824 | ||||||
| chrX:71456958
|
G | T | 1 | a0002c0003t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4939-1283G>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71456958 | ||||||
| chrX:71457026
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01884.hp2 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4939-1215C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71457026 | ||||||
| chrX:71457077
|
T | C | 1 | a0002c0003t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4939-1164T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71457077 | ||||||
| chrX:71457314
|
C | G | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4939-927C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71457314 | ||||||
| chrX:71457470
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4939-771A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71457470 | ||||||
| chrX:71457947
|
A | G | 11 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(8): Show | 11 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.4939-294A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | chrX | 71457947 | ||||||
| chrX:71457988
|
T | TA | 1 | a0001c0001t0002g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4939-249dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chrX | 71457988 | |||||
| chrX:71458422
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(8): Show | 11 | HG00673.hp1 HG01257.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.5064+56G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | chrX | 71458422 | ||||||
| chrX:71458448
|
T | C | 11 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(8): Show | 11 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5064+82T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | chrX | 71458448 | ||||||
| chrX:71458732
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.5064+366A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | chrX | 71458732 | ||||||
| chrX:71458852
|
TC | T | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5064+489delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chrX | 71458852 | |||||
| chrX:71459278
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | NA18955.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.5065-274G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | chrX | 71459278 | ||||||
| chrX:71459381
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0046 | 2 | HG00621.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.5065-171A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | chrX | 71459381 | ||||||
| chrX:71459465
|
C | G | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5065-87C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | chrX | 71459465 | ||||||
| chrX:71459470
|
A | AG | 4 | a0001c0001t0001g0038a0001c0001t0001g0146a0001c0001t0003g0144others(1): Show | 4 | HG00741.hp1 HG01261.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.5065-75dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chrX | 71459470 | |||||
| chrX:71459874
|
C | G | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5221+166C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 36/37 | chrX | 71459874 | ||||||
| chrX:71460024
|
A | AG | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5221+317dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 36/37 | INFO_REALIGN_3_PRIME | chrX | 71460024 | |||||
| chrX:71460487
|
AG | A | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5222-137delG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 36/37 | INFO_REALIGN_3_PRIME | chrX | 71460487 | |||||
| chrX:71460488
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5222-138G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 36/37 | chrX | 71460488 | ||||||
| chrX:71460592
|
C | T | 1 | a0001c0001t0010g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5222-34C>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 36/37 | chrX | 71460592 | ||||||
| chrX:71460918
|
G | C | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+115G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71460918 | ||||||
| chrX:71460919
|
C | G | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+116C>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71460919 | ||||||
| chrX:71460957
|
C | CA | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+158dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71460957 | |||||
| chrX:71461053
|
A | T | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+250A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71461053 | ||||||
| chrX:71461084
|
AG | A | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+284delG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71461084 | |||||
| chrX:71461090
|
TGTCTC | T | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+288_5399+292d others(7): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71461090 | ||||||
| chrX:71461431
|
A | AG | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+630dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71461431 | |||||
| chrX:71461582
|
GA | G | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+782delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71461582 | |||||
| chrX:71461624
|
TA | T | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+824delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71461624 | |||||
| chrX:71461640
|
A | G | 3 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190 | 3 | HG02615.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.5399+837A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71461640 | ||||||
| chrX:71461701
|
A | T | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+898A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71461701 | ||||||
| chrX:71461702
|
C | A | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+899C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71461702 | ||||||
| chrX:71461703
|
T | C | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+900T>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71461703 | ||||||
| chrX:71461838
|
A | AC | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+1037dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71461838 | |||||
| chrX:71461842
|
C | CA | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+1040dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71461842 | |||||
| chrX:71461952
|
G | GC | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+1150dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71461952 | |||||
| chrX:71461990
|
G | C | 1 | a0001c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5399+1187G>C | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71461990 | ||||||
| chrX:71462046
|
T | TG | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5399+1244dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462046 | |||||
| chrX:71462189
|
A | AT | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+1390dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462189 | |||||
| chrX:71462248
|
A | AT | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+1445_5399+144 others(5): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71462248 | ||||||
| chrX:71462254
|
GA | G | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+1454delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462254 | |||||
| chrX:71462294
|
CCAGCCGG others(19): Show |
C | 6 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0046others(3): Show | 6 | HG00621.hp1 HG00741.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.5399+1492_5400-150 others(30): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71462294 | ||||||
| chrX:71462299
|
C | CG | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5399+1499dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462299 | |||||
| chrX:71462324
|
TC | T | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5400-1497delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462324 | |||||
| chrX:71462344
|
G | A | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5400-1480G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71462344 | ||||||
| chrX:71462345
|
A | AG | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5400-1477dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462345 | |||||
| chrX:71462349
|
A | AG | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-1473dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462349 | |||||
| chrX:71462445
|
A | AC | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5400-1377dupC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462445 | |||||
| chrX:71462617
|
T | TAAAG | 22 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.5400-1204_5400-120 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462617 | |||||
| chrX:71462651
|
AC | A | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5400-1171delC | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462651 | |||||
| chrX:71462777
|
CTTAT | C | 5 | a0001c0002t0001g0192a0003c0004t0001g0191a0003c0004t0001g0193others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5400-1038_5400-103 others(8): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462777 | |||||
| chrX:71462809
|
T | TA | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-1010dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462809 | |||||
| chrX:71462851
|
GA | G | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-970delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462851 | |||||
| chrX:71462866
|
G | GA | 1 | a0004c0009t0001g0142 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.5400-956dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71462866 | |||||
| chrX:71462881
|
C | A | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-943C>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71462881 | ||||||
| chrX:71462967
|
A | AC | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-857_5400-856i others(3): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71462967 | ||||||
| chrX:71462969
|
ACT | A | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-854_5400-853d others(4): Show |
TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71462969 | ||||||
| chrX:71463022
|
A | AT | 2 | a0001c0001t0001g0136a0001c0001t0001g0147 | 2 | HG02074.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.5400-801dupT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463022 | |||||
| chrX:71463128
|
T | TA | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5400-688dupA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463128 | |||||
| chrX:71463128
|
TA | T | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5400-688delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463128 | |||||
| chrX:71463248
|
AT | A | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5400-569delT | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463248 | |||||
| chrX:71463267
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5400-557G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71463267 | ||||||
| chrX:71463286
|
T | G | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-538T>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71463286 | ||||||
| chrX:71463329
|
TA | T | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-492delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463329 | |||||
| chrX:71463369
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0032others(1): Show | 4 | HG01099.hp1 HG01106.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.5400-455G>A | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71463369 | ||||||
| chrX:71463376
|
A | AG | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-447dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463376 | |||||
| chrX:71463451
|
A | AG | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-370dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463451 | |||||
| chrX:71463461
|
A | T | 1 | a0005c0006t0001g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5400-363A>T | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71463461 | ||||||
| chrX:71463464
|
A | AG | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5400-356dupG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463464 | |||||
| chrX:71463508
|
A | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0088a0001c0001t0001g0106others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.5400-316A>G | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | chrX | 71463508 | ||||||
| chrX:71463514
|
TA | T | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5400-308delA | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463514 | |||||
| chrX:71463722
|
AG | A | 1 | a0001c0001t0001g0018 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5400-98delG | TAF1 | ENSG00000147133.17 | transcript | ENST00000423759.6 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chrX | 71463722 |