| geneid | 10735 |
|---|---|
| ensemblid | ENSG00000101972.20 |
| hgncid | 11355 |
| symbol | STAG2 |
| name | STAG2 cohesin complex component |
| refseq_nuc | NM_001042750.2 |
| refseq_prot | NP_001036215.1 |
| ensembl_nuc | ENST00000371145.8 |
| ensembl_prot | ENSP00000360187.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 123961706 |
| end | 124102656 |
| strand | + |
| ver | v1.2 |
| region | chrX:123961706-124102656 |
| region5000 | chrX:123956706-124107656 |
| regionname0 | STAG2_chrX_123961706_124102656 |
| regionname5000 | STAG2_chrX_123956706_124107656 |
| 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 | 1268 | 273 | 70 | 44 | 120 | 7 | 30 | 95 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0002 | 0/0 | 574 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0003 | 0/0 | 679 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0004 | 0/0 | 659 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| 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 | 3807 | 267 | 66 | 43 | 119 | 7 | 30 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| c0002 | 0/0 | 3807 | 3 | 2 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| c0003 | 0/0 | 3807 | 2 | 2 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| c0004 | 0/0 | 3806 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| c0005 | 0/0 | 3815 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| c0006 | 0/0 | 3808 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| c0007 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| 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 | 2373 | 209 | 57 | 34 | 96 | 2 | 18 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0002 | 0/0 | 2372 | 47 | 2 | 7 | 21 | 5 | 12 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0003 | 0/0 | 2373 | 5 | 5 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0004 | 0/0 | 2374 | 4 | 4 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0005 | 0/0 | 2372 | 3 | 0 | 0 | 3 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0006 | 0/0 | 2371 | 3 | 1 | 2 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0007 | 0/0 | 2373 | 2 | 0 | 0 | 2 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0008 | 0/0 | 2374 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0009 | 0/0 | 2372 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| t0010 | 0/0 | 2368 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| 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 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| 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 | 3807 | 267 | 66 | 43 | 119 | 7 | 30 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0002 | 0/0 | 3807 | 3 | 2 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0003 | 0/0 | 3807 | 2 | 2 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0007 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0002c0004 | 0/0 | 3806 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0003c0006 | 0/0 | 3808 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0004c0005 | 0/0 | 3815 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6179 | 201 | 53 | 33 | 93 | 2 | 18 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0002 | 0/0 | 6178 | 47 | 2 | 7 | 21 | 5 | 12 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0003 | 0/0 | 6179 | 5 | 5 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0004 | 0/0 | 6180 | 4 | 4 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0005 | 0/0 | 6178 | 3 | 0 | 0 | 3 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0006 | 0/0 | 6177 | 3 | 1 | 2 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0007 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0008 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0009 | 0/0 | 6178 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0001t0010 | 0/0 | 6174 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0002t0001 | 0/0 | 6179 | 3 | 2 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0003t0001 | 0/0 | 6179 | 2 | 2 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0001c0007t0001 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0002c0004t0001 | 0/0 | 6178 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0003c0006t0001 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| a0004c0005t0007 | 0/0 | 6187 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | copy fasta | chrX | 123956706 | 124107656 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0009g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0001c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0002c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0003c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| a0004c0005t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | GBR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | FIN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0139 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0058 | AMR | PEL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | MSL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | STU | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | YRI | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18941 | hp2 | a0004 | c0005 | t0007 | g0083 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18965 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0255 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19065 | hp2 | a0001 | c0007 | t0001 | g0165 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19091 | hp1 | a0003 | c0006 | t0001 | g0226 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | YRI | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0164 | AFR | ASW | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | GIH | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | MSL | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | USA | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | USA | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0128 | REF | REF | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | STAG2_chrX_123956706_124107656 | STAG2 | chrX | 123956706 | 124107656 |
| 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:124061852
|
TG | T | 1 | a0002 | 1 | NA18969.hp2 | frameshift_variant | HIGH | c.1619delG | p.Gly540fs | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 17/35 | 1932/6179 | 1619/3807 | 540/1268 | INFO_REALIGN_3_PRIME | chrX | 124061852 | |
| chrX:124063987
|
G | GAAGTCAA others(1): Show |
1 | a0004 | 1 | NA18941.hp2 | frameshift_variant | HIGH | c.1962_1969dupAAGTCA others(2): Show |
p.Leu657fs | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/35 | 2283/6179 | 1970/3807 | 657/1268 | INFO_REALIGN_3_PRIME | chrX | 124063987 | |
| chrX:124065879
|
G | GA | 1 | a0003 | 1 | NA19091.hp1 | frameshift_variant | HIGH | c.2031dupA | p.Glu678fs | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/35 | 2345/6179 | 2032/3807 | 678/1268 | INFO_REALIGN_3_PRIME | chrX | 124065879 |
| 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:124051156
|
A | G | 1 | a0001c0007 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.1053A>G | p.Leu351Leu | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 12/35 | 1366/6179 | 1053/3807 | 351/1268 | chrX | 124051156 | ||
| chrX:124065932
|
C | T | 1 | a0001c0003 | 2 | HG02886.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.2082C>T | p.Ile694Ile | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/35 | 2395/6179 | 2082/3807 | 694/1268 | chrX | 124065932 | ||
| chrX:124090657
|
A | G | 1 | a0001c0002 | 3 | HG01496.hp1 HG03225.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.3360A>G | p.Gln1120Gln | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 31/35 | 3673/6179 | 3360/3807 | 1120/1268 | chrX | 124090657 |
| 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:123961712
|
T | TC | 1 | a0001c0001t0008 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-305dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/35 | 60913 | INFO_REALIGN_3_PRIME | chrX | 123961712 | ||||
| chrX:124021376
|
G | A | 2 | a0001c0001t0007a0004c0005t0007 | 2 | NA18941.hp2 NA19068.hp1 |
5_prime_UTR_variant | MODIFIER | c.-153G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/35 | 1252 | chrX | 124021376 | |||||
| chrX:124100883
|
T | TA | 1 | a0001c0001t0004 | 4 | HG02280.hp1 HG02818.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*301dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 35/35 | 302 | INFO_REALIGN_3_PRIME | chrX | 124100883 | ||||
| chrX:124100883
|
TA | T | 2 | a0001c0001t0002a0001c0001t0005 | 50 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*301delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 35/35 | 301 | INFO_REALIGN_3_PRIME | chrX | 124100883 | ||||
| chrX:124100883
|
TAA | T | 1 | a0001c0001t0006 | 3 | HG01346.hp1 HG02273.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*300_*301delAA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 35/35 | 300 | INFO_REALIGN_3_PRIME | chrX | 124100883 | ||||
| chrX:124100892
|
A | C | 1 | a0001c0001t0003 | 5 | HG02055.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*295A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 35/35 | 295 | chrX | 124100892 | |||||
| chrX:124100894
|
AAAAAC | A | 1 | a0001c0001t0010 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*302_*306delCAAAA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 35/35 | 302 | INFO_REALIGN_3_PRIME | chrX | 124100894 | ||||
| chrX:124101171
|
A | G | 1 | a0001c0001t0005 | 3 | HG00597.hp1 NA18944.hp1 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*574A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 35/35 | 574 | chrX | 124101171 | |||||
| chrX:124101605
|
TA | T | 1 | a0001c0001t0009 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 35/35 | 1013 | INFO_REALIGN_3_PRIME | chrX | 124101605 |
| 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:123961869
|
CG | C | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+16delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123961869 | |||||
| chrX:123961903
|
C | T | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG00558.hp2 NA18966.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+47C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123961903 | ||||||
| chrX:123961966
|
AG | A | 2 | a0001c0001t0002g0002a0001c0001t0008g0001 | 2 | HG02896.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-163+116delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123961966 | |||||
| chrX:123962026
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-163+170T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123962026 | ||||||
| chrX:123962174
|
TC | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+322delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123962174 | |||||
| chrX:123962339
|
GC | G | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+485delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123962339 | |||||
| chrX:123962500
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-163+644G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123962500 | ||||||
| chrX:123962605
|
TC | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+752delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123962605 | |||||
| chrX:123962697
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-163+841C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123962697 | ||||||
| chrX:123962735
|
TA | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+882delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123962735 | |||||
| chrX:123962854
|
T | A | 1 | a0001c0001t0001g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-163+998T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123962854 | ||||||
| chrX:123963052
|
T | TC | 1 | a0001c0001t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-163+1198dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123963052 | |||||
| chrX:123963134
|
T | TG | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-163+1280dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123963134 | |||||
| chrX:123963373
|
A | G | 1 | a0001c0001t0004g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-163+1517A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123963373 | ||||||
| chrX:123963449
|
AT | A | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+1597delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123963449 | |||||
| chrX:123963488
|
G | C | 1 | a0001c0001t0001g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-163+1632G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123963488 | ||||||
| chrX:123963615
|
A | AT | 90 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0184others(87): Show | 90 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-163+1770dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123963615 | |||||
| chrX:123963615
|
AT | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0008g0001others(1): Show | 4 | HG00673.hp1 HG02015.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+1770delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123963615 | |||||
| chrX:123963732
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-163+1876C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123963732 | ||||||
| chrX:123964107
|
A | T | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-163+2251A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123964107 | ||||||
| chrX:123964250
|
C | CA | 52 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(49): Show | 52 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-163+2407dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964250 | |||||
| chrX:123964250
|
CA | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG01884.hp2 HG03471.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+2407delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964250 | |||||
| chrX:123964304
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-163+2448C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123964304 | ||||||
| chrX:123964319
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-163+2463A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123964319 | ||||||
| chrX:123964448
|
G | GT | 1 | a0001c0001t0001g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-163+2594dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964448 | |||||
| chrX:123964571
|
G | T | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+2715G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123964571 | ||||||
| chrX:123964597
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-163+2741T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123964597 | ||||||
| chrX:123964654
|
TC | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+2801delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964654 | |||||
| chrX:123964718
|
GT | G | 69 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 69 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-163+2875delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964718 | |||||
| chrX:123964891
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | HG01952.hp1 HG02071.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-163+3035A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123964891 | ||||||
| chrX:123964960
|
C | CT | 66 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(63): Show | 66 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-163+3122dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964960 | |||||
| chrX:123964960
|
C | CTT | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0190 | 3 | HG01891.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-163+3121_-163+312 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964960 | |||||
| chrX:123964960
|
CT | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG02129.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+3122delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964960 | |||||
| chrX:123964960
|
CTTTTTT | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0058 | 3 | HG01346.hp1 HG02273.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-163+3117_-163+312 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123964960 | |||||
| chrX:123965016
|
TC | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+3165delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123965016 | |||||
| chrX:123965055
|
C | T | 1 | a0001c0007t0001g0165 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-163+3199C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123965055 | ||||||
| chrX:123965102
|
AC | A | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+3250delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123965102 | |||||
| chrX:123965257
|
A | G | 1 | a0001c0001t0010g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-163+3401A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123965257 | ||||||
| chrX:123965411
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-163+3555C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123965411 | ||||||
| chrX:123965453
|
T | G | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG00558.hp2 NA18966.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+3597T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123965453 | ||||||
| chrX:123965478
|
TG | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+3627delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123965478 | |||||
| chrX:123965751
|
TG | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+3898delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123965751 | |||||
| chrX:123965772
|
TG | T | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+3922delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123965772 | |||||
| chrX:123965874
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-163+4018C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123965874 | ||||||
| chrX:123965997
|
C | CA | 1 | a0001c0001t0002g0193 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-163+4150dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123965997 | |||||
| chrX:123966132
|
G | C | 1 | a0001c0001t0001g0075 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-163+4276G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123966132 | ||||||
| chrX:123966160
|
T | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-163+4304T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123966160 | ||||||
| chrX:123966228
|
TGAGGCAG others(3): Show |
T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+4375_-163+438 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123966228 | |||||
| chrX:123966332
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+4476C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123966332 | ||||||
| chrX:123966334
|
C | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+4478C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123966334 | ||||||
| chrX:123966351
|
G | A | 167 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(164): Show | 167 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-163+4495G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123966351 | ||||||
| chrX:123966458
|
TA | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0169a0001c0001t0001g0260others(6): Show | 9 | HG01515.hp1 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-163+4615delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123966458 | |||||
| chrX:123966533
|
T | TC | 1 | a0001c0001t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-163+4680dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123966533 | |||||
| chrX:123966762
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-163+4906C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123966762 | ||||||
| chrX:123966975
|
C | G | 1 | a0001c0001t0002g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-163+5119C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123966975 | ||||||
| chrX:123967256
|
A | AT | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(36): Show | 39 | HG00673.hp1 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.-163+5426dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967256
|
A | ATT | 40 | a0001c0001t0001g0043a0001c0001t0001g0189a0001c0001t0002g0011others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-163+5425_-163+542 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967256
|
A | ATTT | 7 | a0001c0001t0001g0012a0001c0001t0001g0052a0001c0001t0002g0044others(4): Show | 7 | HG01175.hp2 HG02056.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.-163+5424_-163+542 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967256
|
A | ATTTT | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-163+5423_-163+542 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967256
|
AT | A | 15 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0166others(12): Show | 15 | HG00642.hp1 HG01884.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.-163+5426delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967256
|
ATT | A | 4 | a0001c0001t0004g0174a0001c0002t0001g0063a0001c0002t0001g0064others(1): Show | 4 | HG01496.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+5425_-163+542 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967256
|
ATTT | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-163+5424_-163+542 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967256
|
ATTTTTT | A | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+5421_-163+542 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967256 | |||||
| chrX:123967346
|
A | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+5490A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123967346 | ||||||
| chrX:123967397
|
CTGGGATT others(6960): Show |
C | 1 | a0001c0001t0001g0082 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-163+5556_-163+125 others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967397 | |||||
| chrX:123967493
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+5637C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123967493 | ||||||
| chrX:123967525
|
CA | C | 1 | a0001c0001t0002g0047 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-163+5672delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967525 | |||||
| chrX:123967839
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+5983C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123967839 | ||||||
| chrX:123967905
|
CT | C | 1 | a0001c0001t0001g0196 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-163+6063delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967905 | |||||
| chrX:123967905
|
CTT | C | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+6062_-163+606 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123967905 | |||||
| chrX:123967947
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-163+6091C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123967947 | ||||||
| chrX:123968142
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-163+6286G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123968142 | ||||||
| chrX:123968476
|
G | A | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+6620G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123968476 | ||||||
| chrX:123968765
|
AACTT | A | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+6911_-163+691 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123968765 | |||||
| chrX:123969203
|
CT | C | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+7349delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969203 | |||||
| chrX:123969218
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-163+7362G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123969218 | ||||||
| chrX:123969247
|
T | TG | 1 | a0001c0001t0001g0249 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-163+7399dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969247 | |||||
| chrX:123969247
|
TG | T | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+7399delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969247 | |||||
| chrX:123969255
|
G | A | 1 | a0004c0005t0007g0083 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-163+7399G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123969255 | ||||||
| chrX:123969469
|
CT | C | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+7615delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969469 | |||||
| chrX:123969567
|
T | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-163+7711T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123969567 | ||||||
| chrX:123969632
|
T | TC | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+7777dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969632 | |||||
| chrX:123969655
|
G | GT | 2 | a0001c0001t0001g0248a0001c0001t0001g0264 | 2 | HG00438.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-163+7809dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969655 | |||||
| chrX:123969693
|
G | A | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG00558.hp2 NA18966.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+7837G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123969693 | ||||||
| chrX:123969938
|
C | CA | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+8083dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969938 | |||||
| chrX:123969939
|
AC | A | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-163+8086delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969939 | |||||
| chrX:123969952
|
G | GT | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0055others(27): Show | 30 | HG01433.hp1 HG01496.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.-163+8123dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969952
|
G | GTT | 52 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 52 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-163+8122_-163+812 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969952
|
G | GTTT | 3 | a0001c0001t0001g0077a0001c0001t0002g0042a0001c0001t0002g0051 | 3 | HG02717.hp1 HG03942.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-163+8121_-163+812 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969952
|
G | GTTTT | 1 | a0001c0001t0001g0043 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-163+8120_-163+812 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969952
|
GT | G | 24 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0087others(21): Show | 24 | HG00280.hp1 HG00597.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-163+8123delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969952
|
GTT | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+8122_-163+812 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969952
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-163+8113_-163+812 others(15): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969952
|
GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0001g0084a0001c0001t0002g0151 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-163+8110_-163+812 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969952 | |||||
| chrX:123969979
|
TA | T | 6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 6 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-163+8125delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123969979 | |||||
| chrX:123969980
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-163+8124A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123969980 | ||||||
| chrX:123970022
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-163+8166T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123970022 | ||||||
| chrX:123970287
|
G | A | 1 | a0001c0001t0006g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-163+8431G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123970287 | ||||||
| chrX:123970373
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-163+8517G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123970373 | ||||||
| chrX:123970639
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-163+8783C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123970639 | ||||||
| chrX:123970819
|
TA | T | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+8968delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123970819 | |||||
| chrX:123971119
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-163+9263G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123971119 | ||||||
| chrX:123971403
|
G | A | 2 | a0001c0001t0001g0076a0001c0003t0001g0078 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-163+9547G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123971403 | ||||||
| chrX:123971460
|
TG | T | 1 | a0001c0001t0001g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-163+9607delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123971460 | |||||
| chrX:123971873
|
C | G | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-163+10017C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123971873 | ||||||
| chrX:123971941
|
A | G | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-163+10085A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123971941 | ||||||
| chrX:123972049
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+10193G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972049 | ||||||
| chrX:123972219
|
G | GT | 3 | a0001c0001t0001g0247a0001c0001t0001g0257a0001c0001t0001g0261 | 3 | HG02074.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-163+10374dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972219 | |||||
| chrX:123972276
|
AT | A | 8 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG00280.hp1 HG00642.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.-163+10432delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972276 | |||||
| chrX:123972289
|
C | CT | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-163+10442dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972289 | |||||
| chrX:123972291
|
T | G | 1 | a0001c0001t0008g0001 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-163+10435T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972291 | ||||||
| chrX:123972370
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-163+10514A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972370 | ||||||
| chrX:123972414
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+10558G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972414 | ||||||
| chrX:123972419
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-163+10563T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972419 | ||||||
| chrX:123972482
|
AG | A | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+10628delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972482 | |||||
| chrX:123972490
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-163+10634C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972490 | ||||||
| chrX:123972513
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0145 | 2 | NA18947.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-163+10657C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972513 | ||||||
| chrX:123972566
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+10710C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972566 | ||||||
| chrX:123972568
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-163+10712G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972568 | ||||||
| chrX:123972632
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-163+10776G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972632 | ||||||
| chrX:123972647
|
C | G | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-163+10791C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972647 | ||||||
| chrX:123972789
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+10933C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972789 | ||||||
| chrX:123972845
|
T | TC | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+10996dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972845 | |||||
| chrX:123972866
|
C | CA | 37 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0074others(34): Show | 37 | HG00280.hp1 HG00642.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.-163+11035dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
C | CAA | 55 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0094others(52): Show | 55 | HG00621.hp1 HG00639.hp2 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.-163+11034_-163+11 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
C | CAAA | 23 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0205others(20): Show | 23 | HG00438.hp2 HG01175.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-163+11033_-163+11 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
C | CAAAA | 5 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0002g0041others(2): Show | 5 | HG01257.hp2 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+11032_-163+11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
C | CAAAAA | 24 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0002g0011others(21): Show | 24 | HG00438.hp1 HG00609.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.-163+11031_-163+11 others(11): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
C | CAAAAAA | 21 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 21 | HG00140.hp1 HG00558.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-163+11030_-163+11 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
C | CAAAAAAA | 2 | a0001c0001t0001g0014a0001c0001t0001g0071 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-163+11029_-163+11 others(13): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
C | CAAAAAAA others(1): Show |
1 | a0001c0001t0005g0019 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-163+11028_-163+11 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
CA | C | 8 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0072others(5): Show | 8 | HG01496.hp1 HG01884.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.-163+11035delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972866
|
CAA | C | 1 | a0001c0001t0004g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-163+11034_-163+11 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972866 | |||||
| chrX:123972903
|
G | GC | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+11049dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123972903 | |||||
| chrX:123972941
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-163+11085C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123972941 | ||||||
| chrX:123973055
|
G | GA | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-163+11207dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973055 | |||||
| chrX:123973100
|
A | AT | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+11248dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973100 | |||||
| chrX:123973414
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+11558T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123973414 | ||||||
| chrX:123973479
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-163+11623T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123973479 | ||||||
| chrX:123973540
|
C | CA | 140 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(137): Show | 140 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-163+11704dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973540 | |||||
| chrX:123973540
|
C | CAA | 19 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0171others(16): Show | 19 | HG00621.hp1 HG01175.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.-163+11703_-163+11 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973540 | |||||
| chrX:123973540
|
C | CAAA | 1 | a0001c0001t0004g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-163+11702_-163+11 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973540 | |||||
| chrX:123973540
|
CA | C | 2 | a0001c0001t0001g0091a0001c0001t0002g0144 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-163+11704delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973540 | |||||
| chrX:123973561
|
T | A | 6 | a0001c0001t0001g0180a0001c0001t0001g0250a0001c0001t0001g0270others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-163+11705T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123973561 | ||||||
| chrX:123973688
|
T | C | 1 | a0001c0001t0003g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-163+11832T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123973688 | ||||||
| chrX:123973706
|
T | TG | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+11852dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973706 | |||||
| chrX:123973712
|
T | C | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-163+11856T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123973712 | ||||||
| chrX:123973739
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-163+11883G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123973739 | ||||||
| chrX:123973844
|
C | CA | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0002g0042 | 3 | HG03831.hp1 HG03942.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-163+12002dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973844 | |||||
| chrX:123973844
|
CA | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0189 | 3 | HG02258.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-163+12002delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973844 | |||||
| chrX:123973957
|
T | TA | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+12108dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123973957 | |||||
| chrX:123974138
|
AC | A | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+12284delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974138 | |||||
| chrX:123974166
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-163+12310G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974166 | ||||||
| chrX:123974236
|
C | CT | 46 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0181others(43): Show | 46 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-163+12394dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974236 | |||||
| chrX:123974236
|
C | CTT | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-163+12393_-163+12 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974236 | |||||
| chrX:123974236
|
CT | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0263 | 2 | NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-163+12394delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974236 | |||||
| chrX:123974354
|
TC | T | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+12501delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974354 | |||||
| chrX:123974364
|
T | C | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(271): Show | 274 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.-163+12508T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974364 | ||||||
| chrX:123974402
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-163+12546T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974402 | ||||||
| chrX:123974412
|
GA | G | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+12559delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974412 | |||||
| chrX:123974445
|
C | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+12589C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974445 | ||||||
| chrX:123974532
|
A | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+12676A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974532 | ||||||
| chrX:123974573
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-163+12717C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974573 | ||||||
| chrX:123974577
|
C | CT | 15 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0074others(12): Show | 15 | HG00597.hp2 HG00735.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-163+12740dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974577 | |||||
| chrX:123974577
|
CT | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0150others(2): Show | 5 | HG01993.hp2 HG03195.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+12740delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974577 | |||||
| chrX:123974577
|
CTT | C | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-163+12739_-163+12 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974577 | |||||
| chrX:123974577
|
CTTTT | C | 2 | a0001c0001t0001g0241a0001c0001t0003g0216 | 2 | HG02615.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.-163+12737_-163+12 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974577 | |||||
| chrX:123974577
|
CTTTTT | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0183others(77): Show | 80 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-163+12736_-163+12 others(11): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974577 | |||||
| chrX:123974577
|
CTTTTTT | C | 1 | a0001c0001t0001g0260 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-163+12735_-163+12 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974577 | |||||
| chrX:123974750
|
T | TG | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+12895dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974750 | |||||
| chrX:123974857
|
A | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0039a0001c0001t0002g0045 | 3 | NA18990.hp1 NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-163+13001A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974857 | ||||||
| chrX:123974886
|
AT | A | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+13034delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123974886 | |||||
| chrX:123974901
|
A | G | 53 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0184others(50): Show | 53 | HG00438.hp2 HG01123.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.-163+13045A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123974901 | ||||||
| chrX:123975042
|
A | T | 1 | a0001c0001t0001g0272 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-163+13186A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123975042 | ||||||
| chrX:123975052
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-163+13196G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123975052 | ||||||
| chrX:123975186
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+13330G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123975186 | ||||||
| chrX:123975226
|
AAAG | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0137others(1): Show | 4 | HG00639.hp1 HG01361.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+13378_-163+13 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123975226 | |||||
| chrX:123975300
|
G | GT | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+13447dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123975300 | |||||
| chrX:123975471
|
C | CT | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+13623dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123975471 | |||||
| chrX:123975519
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+13663A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123975519 | ||||||
| chrX:123975673
|
AG | A | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+13819delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123975673 | |||||
| chrX:123975744
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-163+13888A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123975744 | ||||||
| chrX:123975773
|
CT | C | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+13922delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123975773 | |||||
| chrX:123975823
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-163+13967A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123975823 | ||||||
| chrX:123976034
|
C | CA | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+14180dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123976034 | |||||
| chrX:123976041
|
T | C | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+14185T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976041 | ||||||
| chrX:123976077
|
CG | C | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+14223delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123976077 | |||||
| chrX:123976198
|
C | G | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+14342C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976198 | ||||||
| chrX:123976231
|
G | GC | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+14377dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123976231 | |||||
| chrX:123976235
|
C | CT | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+14380dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123976235 | |||||
| chrX:123976274
|
T | TA | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-163+14427dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123976274 | |||||
| chrX:123976293
|
ATGAAAT | A | 1 | a0001c0001t0002g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-163+14439_-163+14 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123976293 | |||||
| chrX:123976356
|
T | TA | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-163+14503dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123976356 | |||||
| chrX:123976379
|
C | T | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+14523C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976379 | ||||||
| chrX:123976533
|
A | T | 85 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 85 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-163+14677A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976533 | ||||||
| chrX:123976545
|
A | C | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-163+14689A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976545 | ||||||
| chrX:123976728
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-163+14872A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976728 | ||||||
| chrX:123976739
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+14883A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976739 | ||||||
| chrX:123976879
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-163+15023G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123976879 | ||||||
| chrX:123977016
|
T | G | 1 | a0001c0001t0002g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-163+15160T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977016 | ||||||
| chrX:123977123
|
C | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+15267C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977123 | ||||||
| chrX:123977131
|
AGAT | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+15279_-163+15 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977131 | |||||
| chrX:123977243
|
A | AT | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+15391dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977243 | |||||
| chrX:123977391
|
T | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-163+15535T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977391 | ||||||
| chrX:123977444
|
G | GT | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+15596dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977444 | |||||
| chrX:123977444
|
GT | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-163+15596delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977444 | |||||
| chrX:123977451
|
T | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+15595T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977451 | ||||||
| chrX:123977452
|
T | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+15596T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977452 | ||||||
| chrX:123977452
|
T | TC | 1 | a0001c0001t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-163+15603dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977452 | |||||
| chrX:123977463
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-163+15607G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977463 | ||||||
| chrX:123977506
|
G | GT | 1 | a0001c0001t0001g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-163+15654dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977506 | |||||
| chrX:123977646
|
G | GA | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+15798dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977646 | |||||
| chrX:123977743
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-163+15887G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977743 | ||||||
| chrX:123977765
|
C | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-163+15909C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977765 | ||||||
| chrX:123977832
|
G | GT | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0056others(34): Show | 37 | HG00558.hp2 HG00642.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.-163+16003dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977832 | |||||
| chrX:123977832
|
G | GTT | 12 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0101others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-163+16002_-163+16 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977832 | |||||
| chrX:123977832
|
G | GTTT | 2 | a0001c0001t0001g0052a0001c0001t0001g0148 | 2 | HG03688.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-163+16001_-163+16 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977832 | |||||
| chrX:123977832
|
GT | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 96 | HG00621.hp1 HG00639.hp2 HG01081.hp1 others(93): Show |
intron_variant | MODIFIER | c.-163+16003delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977832 | |||||
| chrX:123977832
|
GTT | G | 13 | a0001c0001t0001g0071a0001c0001t0001g0169a0001c0001t0001g0187others(10): Show | 13 | HG00280.hp1 HG01175.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-163+16002_-163+16 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977832 | |||||
| chrX:123977832
|
GTTTTTTT | G | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+15997_-163+16 others(13): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977832 | |||||
| chrX:123977839
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+15983T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123977839 | ||||||
| chrX:123977975
|
T | TG | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-163+16122dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123977975 | |||||
| chrX:123978070
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-163+16214G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123978070 | ||||||
| chrX:123978154
|
C | CT | 42 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0071others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-163+16317dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123978154 | |||||
| chrX:123978154
|
C | CTT | 2 | a0001c0001t0002g0038a0001c0001t0002g0046 | 2 | HG03710.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-163+16316_-163+16 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123978154 | |||||
| chrX:123978154
|
CT | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0101others(8): Show | 11 | HG01099.hp1 HG02015.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.-163+16317delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123978154 | |||||
| chrX:123978864
|
A | G | 43 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0002g0011others(40): Show | 43 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-163+17008A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123978864 | ||||||
| chrX:123979601
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-163+17745T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123979601 | ||||||
| chrX:123979802
|
T | G | 1 | a0001c0001t0001g0096 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-163+17946T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123979802 | ||||||
| chrX:123979907
|
A | G | 13 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-163+18051A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123979907 | ||||||
| chrX:123980028
|
C | T | 2 | a0001c0001t0001g0076a0001c0003t0001g0078 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-163+18172C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123980028 | ||||||
| chrX:123980280
|
T | TG | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+18429dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123980280 | |||||
| chrX:123980284
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-163+18428G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123980284 | ||||||
| chrX:123980346
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+18490G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123980346 | ||||||
| chrX:123980349
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0137others(1): Show | 4 | HG00639.hp1 HG01361.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+18493A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123980349 | ||||||
| chrX:123980587
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+18731G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123980587 | ||||||
| chrX:123980814
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+18958A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123980814 | ||||||
| chrX:123981109
|
T | TC | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+19254dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123981109 | |||||
| chrX:123981308
|
T | TC | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+19455dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123981308 | |||||
| chrX:123981320
|
T | TC | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+19467dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123981320 | |||||
| chrX:123981415
|
G | GT | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+19561dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123981415 | |||||
| chrX:123981486
|
C | CT | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+19635dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123981486 | |||||
| chrX:123981730
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+19874G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123981730 | ||||||
| chrX:123981761
|
G | GA | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+19910dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123981761 | |||||
| chrX:123982022
|
C | CT | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+20168dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982022 | |||||
| chrX:123982061
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-163+20205C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982061 | ||||||
| chrX:123982079
|
G | GC | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+20225dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982079 | |||||
| chrX:123982098
|
T | TG | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+20245dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982098 | |||||
| chrX:123982127
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+20271G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982127 | ||||||
| chrX:123982176
|
T | TA | 19 | a0001c0001t0001g0043a0001c0001t0001g0071a0001c0001t0001g0102others(16): Show | 19 | HG00597.hp1 HG00621.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-163+20338dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982176 | |||||
| chrX:123982176
|
TA | T | 2 | a0001c0001t0002g0222a0001c0003t0001g0008 | 2 | HG02683.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-163+20338delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982176 | |||||
| chrX:123982438
|
G | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+20582G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982438 | ||||||
| chrX:123982460
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-163+20604C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982460 | ||||||
| chrX:123982579
|
G | GT | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+20726dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982579 | |||||
| chrX:123982731
|
A | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+20875A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982731 | ||||||
| chrX:123982734
|
C | CT | 3 | a0001c0001t0001g0052a0001c0001t0001g0247a0001c0001t0002g0198 | 3 | HG03688.hp1 HG04199.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-163+20893dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982734 | |||||
| chrX:123982734
|
CT | C | 6 | a0001c0001t0001g0112a0001c0001t0001g0187a0001c0001t0001g0188others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-163+20893delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982734 | |||||
| chrX:123982752
|
CT | C | 1 | a0001c0001t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-163+20905delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982752 | |||||
| chrX:123982762
|
G | T | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-163+20906G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982762 | ||||||
| chrX:123982763
|
C | G | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-163+20907C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982763 | ||||||
| chrX:123982765
|
CT | C | 270 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 270 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(267): Show |
intron_variant | MODIFIER | c.-163+20923delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982765 | |||||
| chrX:123982765
|
CTT | C | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+20922_-163+20 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982765 | |||||
| chrX:123982766
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-163+20910T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982766 | ||||||
| chrX:123982795
|
A | C | 5 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(2): Show | 5 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-163+20939A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123982795 | ||||||
| chrX:123982956
|
G | GAA | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+21101_-163+21 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123982956 | |||||
| chrX:123983042
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-163+21186C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983042 | ||||||
| chrX:123983139
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-163+21283A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983139 | ||||||
| chrX:123983231
|
C | CT | 13 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-163+21387dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983231 | |||||
| chrX:123983259
|
C | T | 16 | a0001c0001t0001g0077a0001c0001t0001g0203a0001c0001t0001g0204others(13): Show | 16 | HG00639.hp2 HG01081.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.-163+21403C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983259 | ||||||
| chrX:123983345
|
AG | A | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+21491delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983345 | |||||
| chrX:123983439
|
A | T | 1 | a0001c0001t0001g0267 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-163+21583A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983439 | ||||||
| chrX:123983485
|
A | AT | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+21638dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983485 | |||||
| chrX:123983648
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-163+21792A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983648 | ||||||
| chrX:123983952
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-163+22096A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983952 | ||||||
| chrX:123983969
|
C | CTTTTTT | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-163+22117_-163+22 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983969 | |||||
| chrX:123983969
|
C | CTTTTTTT | 1 | a0001c0001t0002g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-163+22117_-163+22 others(13): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983969 | |||||
| chrX:123983969
|
CTTTTCTT | C | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-163+22118_-163+22 others(13): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983969 | |||||
| chrX:123983974
|
C | CT | 3 | a0001c0001t0001g0085a0001c0001t0001g0125a0001c0001t0001g0177 | 3 | HG02809.hp2 HG03486.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-163+22139dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTT | 3 | a0001c0001t0001g0105a0001c0001t0001g0155a0001c0001t0001g0225 | 3 | NA18949.hp2 NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-163+22138_-163+22 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTT | 2 | a0001c0003t0001g0008a0001c0003t0001g0078 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-163+22137_-163+22 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTCTT others(1): Show |
3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0062 | 3 | HG00280.hp1 HG01175.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-163+22122_-163+22 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTCTT others(2): Show |
2 | a0001c0001t0001g0242a0001c0001t0002g0061 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-163+22122_-163+22 others(15): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTCTT others(3): Show |
10 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0209others(7): Show | 10 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-163+22122_-163+22 others(16): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTCTT others(4): Show |
1 | a0001c0001t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-163+22122_-163+22 others(17): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(2): Show |
11 | a0001c0001t0001g0053a0001c0001t0001g0186a0001c0001t0001g0195others(8): Show | 11 | HG02080.hp1 HG02165.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-163+22131_-163+22 others(15): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(3): Show |
37 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0147others(34): Show | 37 | HG00438.hp2 HG01361.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.-163+22130_-163+22 others(16): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(4): Show |
16 | a0001c0001t0001g0149a0001c0001t0001g0200a0001c0001t0001g0202others(13): Show | 16 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-163+22129_-163+22 others(17): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0234 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-163+22128_-163+22 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-163+22126_-163+22 others(20): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0172others(2): Show | 5 | HG01952.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+22124_-163+22 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-163+22123_-163+22 others(23): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0171a0001c0001t0004g0174 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+22122_-163+22 others(24): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0004g0175a0001c0001t0004g0269 | 2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-163+22119_-163+22 others(27): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0162 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-163+22139_-163+22 others(29): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-163+22118C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983974 | ||||||
| chrX:123983974
|
CT | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(14): Show | 17 | HG01099.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-163+22139delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
CTT | C | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-163+22138_-163+22 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
CTTTT | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0205a0001c0001t0001g0217others(3): Show | 6 | HG00621.hp1 NA18943.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-163+22136_-163+22 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983974
|
CTTTTTT | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-163+22134_-163+22 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123983974 | |||||
| chrX:123983980
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-163+22124T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123983980 | ||||||
| chrX:123984000
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-163+22144C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123984000 | ||||||
| chrX:123984225
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-163+22369G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123984225 | ||||||
| chrX:123984385
|
A | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+22529A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123984385 | ||||||
| chrX:123984490
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+22634C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123984490 | ||||||
| chrX:123984547
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-163+22691G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123984547 | ||||||
| chrX:123984781
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-163+22925G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123984781 | ||||||
| chrX:123984941
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-163+23085C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123984941 | ||||||
| chrX:123985144
|
C | CT | 1 | a0001c0002t0001g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-163+23298dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123985144 | |||||
| chrX:123985317
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0200 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-163+23461C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985317 | ||||||
| chrX:123985340
|
C | T | 42 | a0001c0001t0001g0043a0001c0001t0002g0011a0001c0001t0002g0018others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-163+23484C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985340 | ||||||
| chrX:123985418
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-163+23562A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985418 | ||||||
| chrX:123985533
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-163+23677T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985533 | ||||||
| chrX:123985615
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-163+23759C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985615 | ||||||
| chrX:123985718
|
G | A | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-163+23862G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985718 | ||||||
| chrX:123985726
|
G | A | 238 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(235): Show | 238 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.-163+23870G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985726 | ||||||
| chrX:123985737
|
A | AT | 2 | a0001c0001t0001g0084a0001c0001t0002g0151 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-163+23895dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123985737 | |||||
| chrX:123985737
|
AT | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0238 | 2 | NA18986.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-163+23895delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123985737 | |||||
| chrX:123985797
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-163+23941C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123985797 | ||||||
| chrX:123986032
|
C | G | 1 | a0001c0001t0005g0027 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-163+24176C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123986032 | ||||||
| chrX:123986043
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-163+24187T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123986043 | ||||||
| chrX:123986052
|
A | T | 5 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049others(2): Show | 5 | NA18975.hp2 NA18979.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-163+24196A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123986052 | ||||||
| chrX:123986137
|
CAT | C | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-163+24286_-163+24 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123986137 | |||||
| chrX:123986567
|
CTG | C | 1 | a0001c0001t0001g0127 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-163+24716_-163+24 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123986567 | |||||
| chrX:123986844
|
A | AT | 1 | a0001c0001t0002g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-163+25001dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123986844 | |||||
| chrX:123986844
|
AT | A | 1 | a0001c0001t0001g0196 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-163+25001delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123986844 | |||||
| chrX:123986991
|
A | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0001g0264 | 3 | HG00438.hp2 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-163+25135A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123986991 | ||||||
| chrX:123986992
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-163+25136T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123986992 | ||||||
| chrX:123987043
|
AGTGCAG | A | 1 | a0001c0001t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-163+25188_-163+25 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123987043 | ||||||
| chrX:123987149
|
T | C | 238 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(235): Show | 238 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.-163+25293T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123987149 | ||||||
| chrX:123987218
|
C | G | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-163+25362C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123987218 | ||||||
| chrX:123987270
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-163+25414G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123987270 | ||||||
| chrX:123987553
|
A | AT | 1 | a0001c0001t0001g0221 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-163+25704dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123987553 | |||||
| chrX:123988009
|
A | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-163+26153A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123988009 | ||||||
| chrX:123988440
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-163+26584G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123988440 | ||||||
| chrX:123989235
|
TG | T | 42 | a0001c0001t0001g0043a0001c0001t0002g0011a0001c0001t0002g0018others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-163+27380delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123989235 | ||||||
| chrX:123989583
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-163+27727T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123989583 | ||||||
| chrX:123989607
|
C | CT | 6 | a0001c0001t0001g0134a0001c0001t0001g0190a0001c0001t0002g0046others(3): Show | 6 | HG02257.hp2 NA18975.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-163+27766dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123989607 | |||||
| chrX:123989607
|
CT | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0241 | 2 | NA19089.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-163+27766delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123989607 | |||||
| chrX:123989801
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-163+27945G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123989801 | ||||||
| chrX:123989931
|
A | AT | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-163+28084dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123989931 | |||||
| chrX:123989957
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-163+28101G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123989957 | ||||||
| chrX:123990285
|
T | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-163+28429T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990285 | ||||||
| chrX:123990286
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+28430T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990286 | ||||||
| chrX:123990357
|
A | G | 42 | a0001c0001t0001g0043a0001c0001t0002g0011a0001c0001t0002g0018others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-163+28501A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990357 | ||||||
| chrX:123990464
|
C | CT | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-163+28608_-163+28 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990464 | ||||||
| chrX:123990465
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-163+28609A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990465 | ||||||
| chrX:123990466
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-163+28610G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990466 | ||||||
| chrX:123990586
|
T | TG | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-163+28731dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123990586 | |||||
| chrX:123990676
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0047 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-163+28820A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990676 | ||||||
| chrX:123990686
|
G | C | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-163+28830G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990686 | ||||||
| chrX:123990790
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-163+28934C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990790 | ||||||
| chrX:123990805
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-163+28949G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990805 | ||||||
| chrX:123990817
|
C | G | 2 | a0001c0001t0001g0076a0001c0003t0001g0078 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-163+28961C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990817 | ||||||
| chrX:123990933
|
T | C | 32 | a0001c0001t0001g0055a0001c0001t0001g0079a0001c0001t0001g0081others(29): Show | 32 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.-163+29077T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990933 | ||||||
| chrX:123990986
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-163+29130G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123990986 | ||||||
| chrX:123991223
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-163+29367T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123991223 | ||||||
| chrX:123991248
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0200 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-163+29392G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123991248 | ||||||
| chrX:123991357
|
A | AT | 7 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0125others(4): Show | 7 | HG01167.hp1 HG02056.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-163+29514dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123991357 | |||||
| chrX:123991357
|
AT | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0189 | 2 | HG02258.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-163+29514delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123991357 | |||||
| chrX:123991439
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-163+29583G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123991439 | ||||||
| chrX:123991496
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-163+29640G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123991496 | ||||||
| chrX:123991666
|
C | CT | 11 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0086others(8): Show | 11 | HG01081.hp2 HG01167.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-162-29686dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123991666 | |||||
| chrX:123991801
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-29566A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123991801 | ||||||
| chrX:123991861
|
T | TAGTAGAG others(3): Show |
4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-29506_-162-29 others(16): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123991861 | ||||||
| chrX:123991862
|
C | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-29505C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123991862 | ||||||
| chrX:123992047
|
A | G | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-162-29320A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123992047 | ||||||
| chrX:123992505
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0085 | 3 | HG00673.hp1 HG02015.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-162-28862T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123992505 | ||||||
| chrX:123992647
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162-28720T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123992647 | ||||||
| chrX:123992730
|
G | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-28637G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123992730 | ||||||
| chrX:123992805
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-28562G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123992805 | ||||||
| chrX:123993031
|
TG | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-28333delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123993031 | |||||
| chrX:123993226
|
GAGGCTGA others(13): Show |
G | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-28138_-162-28 others(26): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123993226 | |||||
| chrX:123993378
|
AT | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-27985delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123993378 | |||||
| chrX:123993430
|
A | AT | 3 | a0001c0001t0001g0080a0001c0001t0001g0147a0001c0001t0001g0162 | 3 | HG00642.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-162-27927dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123993430 | |||||
| chrX:123993595
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-162-27772G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123993595 | ||||||
| chrX:123993810
|
A | G | 13 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-162-27557A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123993810 | ||||||
| chrX:123993921
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-162-27446G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123993921 | ||||||
| chrX:123994016
|
C | T | 9 | a0001c0001t0001g0054a0001c0001t0001g0137a0001c0001t0001g0166others(6): Show | 9 | HG00639.hp1 HG01952.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-162-27351C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123994016 | ||||||
| chrX:123994187
|
A | G | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-162-27180A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123994187 | ||||||
| chrX:123995147
|
A | G | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-162-26220A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995147 | ||||||
| chrX:123995196
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0076a0001c0001t0001g0167others(2): Show | 5 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162-26171A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995196 | ||||||
| chrX:123995209
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-162-26158A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995209 | ||||||
| chrX:123995383
|
T | G | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-162-25984T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995383 | ||||||
| chrX:123995423
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-25944A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995423 | ||||||
| chrX:123995563
|
G | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(167): Show | 170 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-162-25804G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995563 | ||||||
| chrX:123995567
|
G | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(167): Show | 170 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-162-25800G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995567 | ||||||
| chrX:123995695
|
G | GAA | 1 | a0001c0001t0001g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-162-25663_-162-25 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123995695 | |||||
| chrX:123995695
|
GA | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-162-25662delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123995695 | |||||
| chrX:123995739
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0243 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-162-25628C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123995739 | ||||||
| chrX:123996196
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-162-25171T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996196 | ||||||
| chrX:123996203
|
G | A | 5 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049others(2): Show | 5 | NA18975.hp2 NA18979.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-25164G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996203 | ||||||
| chrX:123996309
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-162-25058A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996309 | ||||||
| chrX:123996419
|
C | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0118a0001c0001t0001g0177 | 3 | HG02109.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-162-24948C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996419 | ||||||
| chrX:123996548
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162-24819T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996548 | ||||||
| chrX:123996558
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162-24809A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996558 | ||||||
| chrX:123996565
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-24802G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996565 | ||||||
| chrX:123996601
|
G | GT | 1 | a0001c0001t0002g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-162-24758dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123996601 | |||||
| chrX:123996748
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-162-24619T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123996748 | ||||||
| chrX:123997063
|
TC | T | 1 | a0001c0001t0002g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-162-24302delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123997063 | |||||
| chrX:123997181
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-24186C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123997181 | ||||||
| chrX:123997389
|
G | A | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(271): Show | 274 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.-162-23978G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123997389 | ||||||
| chrX:123997648
|
G | GT | 1 | a0001c0001t0001g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-162-23712dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123997648 | |||||
| chrX:123997664
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-23703G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123997664 | ||||||
| chrX:123997753
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-23614G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123997753 | ||||||
| chrX:123997892
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0137others(1): Show | 4 | HG00639.hp1 HG01361.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-23475C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123997892 | ||||||
| chrX:123997940
|
C | A | 1 | a0001c0001t0001g0262 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-162-23427C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123997940 | ||||||
| chrX:123998168
|
A | AT | 27 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(24): Show | 27 | HG00597.hp1 HG01891.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.-162-23181dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998168 | |||||
| chrX:123998168
|
AT | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0241a0001c0001t0002g0025 | 3 | HG03704.hp2 NA18982.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-162-23181delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998168 | |||||
| chrX:123998333
|
A | AT | 2 | a0001c0001t0001g0014a0001c0001t0001g0093 | 2 | HG01192.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-162-23018dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998333 | |||||
| chrX:123998333
|
AT | A | 1 | a0001c0001t0001g0212 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-162-23018delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998333 | |||||
| chrX:123998390
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-162-22977C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123998390 | ||||||
| chrX:123998485
|
G | GT | 4 | a0001c0001t0001g0053a0001c0001t0001g0080a0001c0001t0001g0093others(1): Show | 4 | HG00642.hp1 HG01192.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-22868dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998485 | |||||
| chrX:123998485
|
G | GTT | 2 | a0001c0001t0002g0060a0001c0003t0001g0008 | 2 | HG03471.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-162-22869_-162-22 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998485 | |||||
| chrX:123998485
|
GT | G | 2 | a0001c0001t0001g0214a0001c0001t0002g0151 | 2 | HG01891.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-162-22868delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998485 | |||||
| chrX:123998587
|
C | CATCT | 16 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0068others(13): Show | 16 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.-162-22734_-162-22 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998587 | |||||
| chrX:123998587
|
CATCT | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 145 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.-162-22734_-162-22 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998587 | |||||
| chrX:123998587
|
CATCTATC others(1): Show |
C | 61 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0077others(58): Show | 61 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-162-22738_-162-22 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998587 | |||||
| chrX:123998587
|
CATCTATC others(5): Show |
C | 4 | a0001c0001t0001g0179a0001c0001t0001g0203a0001c0001t0001g0207others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-22742_-162-22 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998587 | |||||
| chrX:123998587
|
CATCTATC others(9): Show |
C | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-162-22746_-162-22 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998587 | |||||
| chrX:123998613
|
T | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-162-22754T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123998613 | ||||||
| chrX:123998633
|
T | A | 8 | a0001c0001t0002g0018a0001c0001t0002g0023a0001c0001t0002g0026others(5): Show | 8 | HG00140.hp1 HG00735.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162-22734T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123998633 | ||||||
| chrX:123998724
|
CT | C | 1 | a0001c0001t0002g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-162-22640delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998724 | |||||
| chrX:123998892
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-162-22475G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123998892 | ||||||
| chrX:123998949
|
GA | G | 3 | a0001c0001t0002g0030a0001c0001t0002g0035a0001c0001t0002g0059 | 3 | HG00280.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-162-22407delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123998949 | |||||
| chrX:123999065
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0155 | 2 | NA18949.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-162-22302C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999065 | ||||||
| chrX:123999128
|
G | GT | 1 | a0001c0001t0002g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-162-22234dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123999128 | |||||
| chrX:123999134
|
A | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0105others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.-162-22233A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999134 | ||||||
| chrX:123999414
|
T | TCTCCCTC others(15): Show |
1 | a0004c0005t0007g0083 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-162-21947_-162-21 others(28): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123999414 | |||||
| chrX:123999425
|
C | A | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-162-21942C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999425 | ||||||
| chrX:123999515
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-162-21852C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999515 | ||||||
| chrX:123999609
|
T | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-21758T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999609 | ||||||
| chrX:123999704
|
T | G | 1 | a0001c0001t0002g0041 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-162-21663T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999704 | ||||||
| chrX:123999910
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-162-21457G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999910 | ||||||
| chrX:123999917
|
G | GT | 3 | a0001c0001t0001g0149a0001c0001t0001g0154a0001c0001t0001g0225 | 3 | HG02027.hp1 HG04184.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-162-21435dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 123999917 | |||||
| chrX:123999925
|
T | A | 43 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0002g0011others(40): Show | 43 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-162-21442T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999925 | ||||||
| chrX:123999935
|
T | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0075others(20): Show | 23 | HG00558.hp2 HG00642.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-162-21432T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 123999935 | ||||||
| chrX:124000129
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-162-21238G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124000129 | ||||||
| chrX:124000141
|
ATAT | A | 2 | a0001c0001t0001g0105a0003c0006t0001g0226 | 2 | NA19080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-162-21224_-162-21 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124000141 | |||||
| chrX:124000146
|
G | A | 83 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-162-21221G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124000146 | ||||||
| chrX:124000380
|
C | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-20987C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124000380 | ||||||
| chrX:124000472
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-162-20895T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124000472 | ||||||
| chrX:124000520
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-162-20847A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124000520 | ||||||
| chrX:124000925
|
A | T | 43 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0002g0011others(40): Show | 43 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-162-20442A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124000925 | ||||||
| chrX:124001095
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-162-20272T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124001095 | ||||||
| chrX:124001216
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0153 | 2 | NA18948.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-162-20151G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124001216 | ||||||
| chrX:124001223
|
TG | T | 1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162-20141delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124001223 | |||||
| chrX:124001247
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0125 | 3 | HG01167.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-162-20120C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124001247 | ||||||
| chrX:124001450
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-19917A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124001450 | ||||||
| chrX:124001586
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-162-19781T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124001586 | ||||||
| chrX:124001839
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-19528T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124001839 | ||||||
| chrX:124002004
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-162-19363G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002004 | ||||||
| chrX:124002070
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-162-19297A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002070 | ||||||
| chrX:124002320
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-162-19047T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002320 | ||||||
| chrX:124002339
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0068others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-19028C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002339 | ||||||
| chrX:124002353
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-19014C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002353 | ||||||
| chrX:124002792
|
TTTTC | T | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162-18555_-162-18 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124002792 | |||||
| chrX:124002811
|
TC | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0138a0001c0001t0001g0160 | 3 | HG02257.hp1 HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-162-18555delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002811 | ||||||
| chrX:124002812
|
C | CT | 16 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0001g0090others(13): Show | 16 | HG00609.hp1 HG01081.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-162-18540dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124002812 | |||||
| chrX:124002812
|
CT | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-18540delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124002812 | |||||
| chrX:124002830
|
AT | A | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-18532delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124002830 | |||||
| chrX:124002948
|
A | AC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-18416dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124002948 | |||||
| chrX:124002949
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162-18418C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002949 | ||||||
| chrX:124002968
|
T | TG | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-18399_-162-18 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124002968 | ||||||
| chrX:124003157
|
A | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0108a0001c0001t0001g0115others(2): Show | 5 | HG01934.hp1 HG02083.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162-18210A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003157 | ||||||
| chrX:124003289
|
AG | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162-18077delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003289 | ||||||
| chrX:124003308
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0002g0193 | 2 | NA18950.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-162-18059G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003308 | ||||||
| chrX:124003402
|
G | A | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-162-17965G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003402 | ||||||
| chrX:124003476
|
C | T | 4 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0028others(1): Show | 4 | HG00140.hp1 HG00735.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-17891C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003476 | ||||||
| chrX:124003502
|
C | A | 83 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-162-17865C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003502 | ||||||
| chrX:124003587
|
A | AT | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-17772dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124003587 | |||||
| chrX:124003704
|
G | T | 1 | a0001c0001t0002g0041 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-162-17663G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003704 | ||||||
| chrX:124003713
|
C | T | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162-17654C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003713 | ||||||
| chrX:124003979
|
T | A | 1 | a0001c0001t0001g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-162-17388T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124003979 | ||||||
| chrX:124004014
|
G | GA | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-17351dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124004014 | |||||
| chrX:124004194
|
A | AG | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-17172dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124004194 | |||||
| chrX:124004271
|
TA | T | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-17091delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124004271 | |||||
| chrX:124004369
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162-16998A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004369 | ||||||
| chrX:124004405
|
A | AC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-16961dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124004405 | |||||
| chrX:124004410
|
T | TG | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-16957_-162-16 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004410 | ||||||
| chrX:124004448
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-162-16919T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004448 | ||||||
| chrX:124004559
|
T | TC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-16806dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124004559 | |||||
| chrX:124004591
|
C | CCATT | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162-16767_-162-16 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124004591 | |||||
| chrX:124004727
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0065others(11): Show | 14 | HG01106.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.-162-16640G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004727 | ||||||
| chrX:124004742
|
C | CT | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-16617dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124004742 | |||||
| chrX:124004750
|
T | C | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-162-16617T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004750 | ||||||
| chrX:124004751
|
C | T | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-162-16616C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004751 | ||||||
| chrX:124004752
|
T | C | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-162-16615T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004752 | ||||||
| chrX:124004914
|
A | G | 7 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0001g0217others(4): Show | 7 | HG00621.hp1 HG02129.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162-16453A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124004914 | ||||||
| chrX:124005001
|
CTTAAGT | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | NA18981.hp2 NA18988.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-16362_-162-16 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124005001 | |||||
| chrX:124005079
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-162-16288C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124005079 | ||||||
| chrX:124005116
|
GTAAA | G | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-162-16248_-162-16 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124005116 | |||||
| chrX:124005178
|
G | GT | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-16183dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124005178 | |||||
| chrX:124005367
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-162-16000T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124005367 | ||||||
| chrX:124005452
|
A | AC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-15914dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124005452 | |||||
| chrX:124005460
|
A | AC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-15903dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124005460 | |||||
| chrX:124005853
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-15514T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124005853 | ||||||
| chrX:124005949
|
TC | T | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-15415delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124005949 | |||||
| chrX:124005976
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0235 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-162-15391G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124005976 | ||||||
| chrX:124006072
|
T | TG | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162-15294dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006072 | |||||
| chrX:124006124
|
TG | T | 1 | a0001c0001t0001g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-162-15238delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006124 | |||||
| chrX:124006323
|
G | GT | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-15039dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006323 | |||||
| chrX:124006341
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-162-15026A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006341 | ||||||
| chrX:124006387
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-162-14980T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006387 | ||||||
| chrX:124006436
|
A | AT | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-162-14911dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006436 | |||||
| chrX:124006436
|
AT | A | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 189 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(186): Show |
intron_variant | MODIFIER | c.-162-14911delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006436 | |||||
| chrX:124006436
|
ATT | A | 11 | a0001c0001t0001g0104a0001c0001t0001g0154a0001c0001t0001g0188others(8): Show | 11 | HG00597.hp1 HG02027.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-162-14912_-162-14 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006436 | |||||
| chrX:124006436
|
ATTT | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(41): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-162-14913_-162-14 others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006436 | |||||
| chrX:124006436
|
ATTTT | A | 1 | a0001c0001t0002g0036 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-162-14914_-162-14 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006436 | |||||
| chrX:124006583
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-162-14784T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006583 | ||||||
| chrX:124006605
|
A | AT | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-14755dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006605 | |||||
| chrX:124006629
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-162-14738C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006629 | ||||||
| chrX:124006660
|
T | C | 46 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0002g0011others(43): Show | 46 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-162-14707T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006660 | ||||||
| chrX:124006661
|
G | C | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-162-14706G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006661 | ||||||
| chrX:124006682
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-162-14685G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006682 | ||||||
| chrX:124006682
|
GC | G | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-14682delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006682 | |||||
| chrX:124006730
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0117 | 2 | HG02717.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-162-14637T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006730 | ||||||
| chrX:124006731
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162-14636G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006731 | ||||||
| chrX:124006832
|
G | GT | 1 | a0001c0001t0001g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-162-14531dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124006832 | |||||
| chrX:124006846
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-162-14521T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006846 | ||||||
| chrX:124006862
|
T | C | 2 | a0001c0001t0005g0019a0001c0001t0005g0027 | 2 | HG00597.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-162-14505T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006862 | ||||||
| chrX:124006919
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-14448T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006919 | ||||||
| chrX:124006978
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-162-14389G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124006978 | ||||||
| chrX:124007011
|
TA | T | 1 | a0001c0001t0003g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-162-14351delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007011 | |||||
| chrX:124007017
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-14350T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007017 | ||||||
| chrX:124007075
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-162-14292A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007075 | ||||||
| chrX:124007085
|
C | CGTACTCC others(1): Show |
1 | a0001c0007t0001g0165 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-162-14280_-162-14 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007085 | |||||
| chrX:124007092
|
C | CT | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-14274dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007092 | |||||
| chrX:124007095
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-162-14272G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007095 | ||||||
| chrX:124007118
|
T | TC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-14248dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007118 | |||||
| chrX:124007264
|
A | AC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-14101dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007264 | |||||
| chrX:124007305
|
TC | T | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-14059delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007305 | |||||
| chrX:124007414
|
T | TC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-13952dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007414 | |||||
| chrX:124007429
|
T | TC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-13938_-162-13 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007429 | ||||||
| chrX:124007445
|
G | GT | 2 | a0001c0001t0001g0114a0001c0001t0001g0153 | 2 | NA18994.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-162-13913dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007445 | |||||
| chrX:124007445
|
GT | G | 53 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0183others(50): Show | 53 | HG00438.hp2 HG01123.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.-162-13913delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007445 | |||||
| chrX:124007555
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-162-13812A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007555 | ||||||
| chrX:124007764
|
T | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-13603T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007764 | ||||||
| chrX:124007780
|
TA | T | 1 | a0001c0001t0001g0017 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-162-13586delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007780 | ||||||
| chrX:124007790
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-162-13577C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007790 | ||||||
| chrX:124007799
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-162-13568C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007799 | ||||||
| chrX:124007828
|
GT | G | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-13533delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124007828 | |||||
| chrX:124007959
|
C | CA | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-13408_-162-13 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124007959 | ||||||
| chrX:124008210
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-162-13157T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008210 | ||||||
| chrX:124008212
|
T | TC | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-13155_-162-13 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008212 | ||||||
| chrX:124008215
|
C | CT | 3 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0180 | 3 | HG03579.hp1 NA18959.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-162-13137dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124008215 | |||||
| chrX:124008215
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-13152C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008215 | ||||||
| chrX:124008215
|
CT | C | 1 | a0001c0001t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-162-13137delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124008215 | |||||
| chrX:124008216
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-13151T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008216 | ||||||
| chrX:124008300
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-162-13067G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008300 | ||||||
| chrX:124008353
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-162-13014A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008353 | ||||||
| chrX:124008362
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-162-13005C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008362 | ||||||
| chrX:124008393
|
A | G | 3 | a0001c0001t0005g0019a0001c0001t0005g0027a0001c0001t0005g0034 | 3 | HG00597.hp1 NA18944.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-162-12974A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008393 | ||||||
| chrX:124008718
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-162-12649A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008718 | ||||||
| chrX:124008802
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-162-12565A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008802 | ||||||
| chrX:124008907
|
T | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 107 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.-162-12460T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008907 | ||||||
| chrX:124008972
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-162-12395G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124008972 | ||||||
| chrX:124009081
|
ATATT | A | 1 | a0001c0001t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-162-12284_-162-12 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009081 | |||||
| chrX:124009392
|
C | CAGGT | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-162-11924_-162-11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009392 | |||||
| chrX:124009392
|
C | CAGGTAGG others(13): Show |
2 | a0001c0001t0001g0072a0001c0001t0001g0189 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-162-11940_-162-11 others(26): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009392 | |||||
| chrX:124009392
|
CAGGT | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(72): Show | 75 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.-162-11924_-162-11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009392 | |||||
| chrX:124009392
|
CAGGTAGG others(1): Show |
C | 9 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0196others(6): Show | 9 | HG02559.hp2 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162-11928_-162-11 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009392 | |||||
| chrX:124009392
|
CAGGTAGG others(5): Show |
C | 8 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162-11932_-162-11 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009392 | |||||
| chrX:124009397
|
A | AG | 1 | a0001c0001t0001g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-162-11968dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009397 | |||||
| chrX:124009427
|
G | GTAGA | 4 | a0001c0001t0001g0056a0001c0001t0001g0103a0001c0001t0001g0109others(1): Show | 4 | HG04228.hp1 NA18947.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-11937_-162-11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009427 | |||||
| chrX:124009427
|
G | GTAGATAG others(1): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0134 | 2 | NA18954.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-162-11937_-162-11 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009427 | |||||
| chrX:124009431
|
G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0096others(6): Show | 9 | HG00673.hp1 HG01109.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162-11936G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124009431 | ||||||
| chrX:124009431
|
G | GTAGA | 43 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0054others(40): Show | 43 | HG00597.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-162-11933_-162-11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009431 | |||||
| chrX:124009431
|
G | GTAGATAG others(1): Show |
19 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0094others(16): Show | 19 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-162-11933_-162-11 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009431 | |||||
| chrX:124009431
|
G | GTAGATAG others(5): Show |
6 | a0001c0001t0001g0082a0001c0001t0001g0108a0001c0001t0001g0111others(3): Show | 6 | HG02165.hp2 HG03239.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162-11933_-162-11 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009431 | |||||
| chrX:124009431
|
G | GTAGATAG others(9): Show |
2 | a0001c0001t0001g0146a0001c0001t0001g0161 | 2 | HG01433.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-162-11933_-162-11 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009431 | |||||
| chrX:124009431
|
GTAGGTAG others(9): Show |
G | 2 | a0001c0001t0002g0070a0001c0001t0006g0010 | 2 | HG00558.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-162-11932_-162-11 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009431 | |||||
| chrX:124009435
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 87 | HG00597.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.-162-11932G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124009435 | ||||||
| chrX:124009435
|
G | GTAGA | 12 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0205others(9): Show | 12 | HG02055.hp1 HG02486.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-162-11929_-162-11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009435 | |||||
| chrX:124009435
|
G | GTAGATAG others(1): Show |
6 | a0001c0001t0001g0087a0001c0001t0001g0092a0001c0001t0001g0107others(3): Show | 6 | HG00558.hp2 HG01099.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162-11929_-162-11 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009435 | |||||
| chrX:124009435
|
G | GTAGATAG others(5): Show |
2 | a0001c0001t0001g0123a0001c0001t0001g0140 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-162-11929_-162-11 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009435 | |||||
| chrX:124009435
|
G | GTAGATAG others(9): Show |
1 | a0001c0001t0001g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-162-11929_-162-11 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009435 | |||||
| chrX:124009435
|
GTAGGTAG others(5): Show |
G | 35 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0002g0011others(32): Show | 35 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.-162-11928_-162-11 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009435 | |||||
| chrX:124009435
|
GTAGGTAG others(9): Show |
G | 1 | a0001c0001t0002g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-162-11928_-162-11 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009435 | |||||
| chrX:124009439
|
G | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 132 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.-162-11928G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124009439 | ||||||
| chrX:124009439
|
G | GTAGA | 3 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0239 | 3 | HG01884.hp1 HG02723.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-162-11925_-162-11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009439 | |||||
| chrX:124009439
|
G | GTAGATAG others(5): Show |
1 | a0001c0001t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-162-11925_-162-11 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009439 | |||||
| chrX:124009439
|
G | GTAGATAG others(9): Show |
1 | a0001c0001t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-162-11925_-162-11 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009439 | |||||
| chrX:124009439
|
GTAGGTAG others(1): Show |
G | 6 | a0001c0001t0001g0190a0001c0001t0002g0020a0001c0001t0002g0022others(3): Show | 6 | HG01257.hp2 HG02080.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162-11924_-162-11 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009439 | |||||
| chrX:124009443
|
G | A | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(209): Show |
intron_variant | MODIFIER | c.-162-11924G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124009443 | ||||||
| chrX:124009443
|
G | GTAGATAG others(1): Show |
1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-162-11897_-162-11 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009443 | |||||
| chrX:124009443
|
G | GTAGATAG others(5): Show |
1 | a0001c0001t0001g0249 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-162-11901_-162-11 others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009443 | |||||
| chrX:124009443
|
G | GTAGATAG others(9): Show |
1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-11905_-162-11 others(22): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009443 | |||||
| chrX:124009443
|
G | GTAGGTAG others(21): Show |
1 | a0001c0001t0001g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-162-11921_-162-11 others(34): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009443 | |||||
| chrX:124009443
|
GTAGA | G | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-162-11893_-162-11 others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009443 | |||||
| chrX:124009447
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-162-11920A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124009447 | ||||||
| chrX:124009451
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-162-11916A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124009451 | ||||||
| chrX:124009455
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-162-11912A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124009455 | ||||||
| chrX:124009832
|
G | GT | 1 | a0001c0001t0001g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-162-11528dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124009832 | |||||
| chrX:124010094
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162-11273G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124010094 | ||||||
| chrX:124010253
|
A | T | 58 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-162-11114A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124010253 | ||||||
| chrX:124010789
|
G | A | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-10578G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124010789 | ||||||
| chrX:124010836
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-162-10531A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124010836 | ||||||
| chrX:124011079
|
G | GT | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162-10284dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124011079 | |||||
| chrX:124011103
|
G | C | 59 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-162-10264G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124011103 | ||||||
| chrX:124011216
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162-10151A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124011216 | ||||||
| chrX:124011382
|
C | T | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(270): Show | 273 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(270): Show |
intron_variant | MODIFIER | c.-162-9985C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124011382 | ||||||
| chrX:124011414
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-162-9953T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124011414 | ||||||
| chrX:124011504
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-162-9863A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124011504 | ||||||
| chrX:124011945
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-162-9422T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124011945 | ||||||
| chrX:124011971
|
C | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0206 | 3 | HG01884.hp1 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-162-9396C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124011971 | ||||||
| chrX:124012003
|
A | AG | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-162-9361dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124012003 | |||||
| chrX:124012078
|
G | A | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(270): Show | 273 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(270): Show |
intron_variant | MODIFIER | c.-162-9289G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124012078 | ||||||
| chrX:124012100
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-162-9267G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124012100 | ||||||
| chrX:124012221
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-162-9146C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124012221 | ||||||
| chrX:124012385
|
CTGT | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0148 | 2 | HG01081.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-162-8977_-162-897 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124012385 | |||||
| chrX:124012484
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-162-8883T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124012484 | ||||||
| chrX:124012962
|
T | TC | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-162-8400dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124012962 | |||||
| chrX:124013253
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-162-8114A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124013253 | ||||||
| chrX:124013322
|
CAA | C | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162-8043_-162-804 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124013322 | |||||
| chrX:124013324
|
A | AAC | 11 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0166others(8): Show | 11 | HG01099.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-162-8020_-162-801 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124013324 | |||||
| chrX:124013324
|
A | AACAC | 2 | a0001c0001t0001g0180a0001c0001t0010g0164 | 2 | NA18959.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-162-8022_-162-801 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124013324 | |||||
| chrX:124013324
|
AAC | A | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(50): Show | 53 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-162-8020_-162-801 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124013324 | |||||
| chrX:124013505
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-162-7862A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124013505 | ||||||
| chrX:124013644
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0048 | 2 | NA18975.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-162-7723C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124013644 | ||||||
| chrX:124013661
|
C | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-7706C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124013661 | ||||||
| chrX:124013722
|
CAA | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-162-7644_-162-764 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124013722 | ||||||
| chrX:124014159
|
A | T | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 262 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(259): Show |
intron_variant | MODIFIER | c.-162-7208A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014159 | ||||||
| chrX:124014319
|
C | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-7048C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014319 | ||||||
| chrX:124014367
|
A | AT | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-6987dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124014367 | |||||
| chrX:124014367
|
AT | A | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-162-6987delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124014367 | |||||
| chrX:124014424
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162-6943G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014424 | ||||||
| chrX:124014442
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-6925C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014442 | ||||||
| chrX:124014677
|
T | G | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-162-6690T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014677 | ||||||
| chrX:124014876
|
T | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-6491T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014876 | ||||||
| chrX:124014934
|
A | G | 1 | a0001c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-162-6433A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014934 | ||||||
| chrX:124014979
|
C | CT | 173 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0053others(170): Show | 173 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(170): Show |
intron_variant | MODIFIER | c.-162-6363dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124014979 | |||||
| chrX:124014979
|
C | CTT | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(23): Show | 26 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-162-6364_-162-636 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124014979 | |||||
| chrX:124014979
|
C | CTTT | 8 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0166others(5): Show | 8 | HG01952.hp1 HG02148.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162-6365_-162-636 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124014979 | |||||
| chrX:124014979
|
CT | C | 2 | a0001c0001t0001g0012a0001c0001t0002g0047 | 2 | HG01515.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-162-6363delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124014979 | |||||
| chrX:124014987
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG02451.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-162-6380T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014987 | ||||||
| chrX:124014988
|
T | TC | 1 | a0001c0001t0001g0266 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-162-6379_-162-637 others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124014988 | ||||||
| chrX:124015009
|
C | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-162-6358C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015009 | ||||||
| chrX:124015073
|
A | G | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 261 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.-162-6294A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015073 | ||||||
| chrX:124015207
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-162-6160C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015207 | ||||||
| chrX:124015233
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0270 | 2 | NA19064.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-162-6134G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015233 | ||||||
| chrX:124015388
|
C | CT | 3 | a0001c0001t0001g0067a0001c0001t0001g0103a0001c0001t0001g0149 | 3 | HG01243.hp1 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-162-5965dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124015388 | |||||
| chrX:124015388
|
CT | C | 6 | a0001c0001t0001g0081a0001c0001t0001g0194a0001c0001t0001g0199others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162-5965delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124015388 | |||||
| chrX:124015477
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162-5890C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015477 | ||||||
| chrX:124015669
|
G | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-5698G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015669 | ||||||
| chrX:124015758
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-5609T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015758 | ||||||
| chrX:124015956
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-162-5411T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124015956 | ||||||
| chrX:124016143
|
G | GT | 2 | a0001c0001t0001g0171a0001c0001t0002g0042 | 2 | HG02280.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-162-5214dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124016143 | |||||
| chrX:124016308
|
A | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0057 | 2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-162-5059A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124016308 | ||||||
| chrX:124016370
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-162-4997A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124016370 | ||||||
| chrX:124016398
|
T | TA | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-4963dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124016398 | |||||
| chrX:124016426
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-162-4941T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124016426 | ||||||
| chrX:124016932
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-162-4435A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124016932 | ||||||
| chrX:124017001
|
T | C | 4 | a0001c0001t0001g0243a0001c0002t0001g0063a0001c0002t0001g0064others(1): Show | 4 | HG01496.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-4366T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124017001 | ||||||
| chrX:124017095
|
C | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0235 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-162-4272C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124017095 | ||||||
| chrX:124017213
|
C | CT | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-162-4143dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124017213 | |||||
| chrX:124017279
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-162-4088G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124017279 | ||||||
| chrX:124017550
|
GA | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | NA18981.hp2 NA18988.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-3810delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124017550 | |||||
| chrX:124017569
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-3798C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124017569 | ||||||
| chrX:124018003
|
T | C | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-162-3364T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018003 | ||||||
| chrX:124018057
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-162-3310G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018057 | ||||||
| chrX:124018433
|
T | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0047 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-162-2934T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018433 | ||||||
| chrX:124018446
|
T | TTGGA | 6 | a0001c0001t0001g0243a0001c0001t0002g0032a0001c0001t0002g0033others(3): Show | 6 | HG00438.hp1 HG00558.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162-2884_-162-288 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124018446 | |||||
| chrX:124018446
|
T | TTGGATGG others(1): Show |
2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-162-2888_-162-288 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124018446 | |||||
| chrX:124018446
|
TTGGA | T | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 206 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(203): Show |
intron_variant | MODIFIER | c.-162-2884_-162-288 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124018446 | |||||
| chrX:124018446
|
TTGGATGG others(1): Show |
T | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-2888_-162-288 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124018446 | |||||
| chrX:124018446
|
TTGGATGG others(5): Show |
T | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-162-2892_-162-288 others(16): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124018446 | |||||
| chrX:124018478
|
ATGG | A | 1 | a0001c0001t0001g0110 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-162-2888_-162-288 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018478 | ||||||
| chrX:124018483
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-162-2884T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018483 | ||||||
| chrX:124018484
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-162-2883G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018484 | ||||||
| chrX:124018488
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-162-2879A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018488 | ||||||
| chrX:124018494
|
A | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-162-2873A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018494 | ||||||
| chrX:124018495
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-162-2872C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018495 | ||||||
| chrX:124018581
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-162-2786G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018581 | ||||||
| chrX:124018637
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-162-2730T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124018637 | ||||||
| chrX:124018872
|
AT | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.-162-2493delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124018872 | |||||
| chrX:124019052
|
C | CT | 90 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(87): Show | 90 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-162-2293dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124019052 | |||||
| chrX:124019052
|
C | CTT | 6 | a0001c0001t0001g0199a0001c0001t0001g0214a0001c0001t0001g0235others(3): Show | 6 | HG02559.hp1 HG04184.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162-2294_-162-229 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124019052 | |||||
| chrX:124019052
|
C | CTTT | 1 | a0001c0001t0001g0167 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-162-2295_-162-229 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124019052 | |||||
| chrX:124019052
|
C | CTTTT | 6 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162-2296_-162-229 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124019052 | |||||
| chrX:124019052
|
CT | C | 5 | a0001c0001t0001g0111a0001c0001t0001g0179a0001c0001t0002g0020others(2): Show | 5 | HG01257.hp2 HG02165.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162-2293delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124019052 | |||||
| chrX:124019149
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-162-2218C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124019149 | ||||||
| chrX:124019540
|
A | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162-1827A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124019540 | ||||||
| chrX:124019642
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-162-1725A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124019642 | ||||||
| chrX:124019913
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-162-1454G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124019913 | ||||||
| chrX:124019947
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-162-1420A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124019947 | ||||||
| chrX:124020209
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162-1158G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124020209 | ||||||
| chrX:124020256
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-162-1111C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124020256 | ||||||
| chrX:124020395
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0162 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-162-972C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124020395 | ||||||
| chrX:124020395
|
C | G | 104 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0054others(101): Show | 104 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.-162-972C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124020395 | ||||||
| chrX:124020458
|
G | A | 106 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0054others(103): Show | 106 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.-162-909G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124020458 | ||||||
| chrX:124020780
|
G | T | 2 | a0001c0001t0002g0222a0001c0001t0002g0271 | 2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-162-587G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124020780 | ||||||
| chrX:124020829
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-162-538A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | chrX | 124020829 | ||||||
| chrX:124021182
|
TATTA | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0265others(2): Show | 5 | HG02071.hp1 NA18991.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162-179_-162-176d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124021182 | |||||
| chrX:124021295
|
G | GT | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-162-69dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 1/34 | INFO_REALIGN_3_PRIME | chrX | 124021295 | |||||
| chrX:124021682
|
AT | A | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-98+257delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chrX | 124021682 | |||||
| chrX:124021705
|
A | G | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-98+274A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | chrX | 124021705 | ||||||
| chrX:124021776
|
C | T | 8 | a0001c0001t0001g0082a0001c0001t0001g0100a0001c0001t0001g0129others(5): Show | 8 | HG00738.hp1 HG01993.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98+345C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | chrX | 124021776 | ||||||
| chrX:124021807
|
G | GT | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-98+384dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chrX | 124021807 | |||||
| chrX:124021818
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-98+387T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | chrX | 124021818 | ||||||
| chrX:124022136
|
C | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-97-395C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | chrX | 124022136 | ||||||
| chrX:124022305
|
AG | A | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-97-224delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chrX | 124022305 | |||||
| chrX:124022370
|
CA | C | 252 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 252 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.-97-145delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chrX | 124022370 | |||||
| chrX:124022370
|
CAA | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0273a0001c0001t0002g0031others(1): Show | 4 | HG01993.hp1 HG03540.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-97-146_-97-145del others(2): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chrX | 124022370 | |||||
| chrX:124022382
|
AAAAAG | A | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-97-145_-97-141del others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chrX | 124022382 | |||||
| chrX:124022467
|
A | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0090others(3): Show | 6 | HG01167.hp1 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-97-64A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 2/34 | chrX | 124022467 | ||||||
| chrX:124022770
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.44+99C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124022770 | ||||||
| chrX:124022967
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0254 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.44+296G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124022967 | ||||||
| chrX:124023124
|
A | T | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+453A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023124 | ||||||
| chrX:124023252
|
G | A | 42 | a0001c0001t0001g0043a0001c0001t0002g0011a0001c0001t0002g0018others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.44+581G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023252 | ||||||
| chrX:124023304
|
C | T | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.44+633C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023304 | ||||||
| chrX:124023319
|
G | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0129a0001c0001t0001g0131others(1): Show | 4 | HG00738.hp1 HG02040.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+648G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023319 | ||||||
| chrX:124023424
|
CATTT | C | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.44+755_44+758delTT others(2): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chrX | 124023424 | |||||
| chrX:124023841
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0213 | 2 | HG02165.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.44+1170G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023841 | ||||||
| chrX:124023855
|
A | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+1184A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023855 | ||||||
| chrX:124023866
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.44+1195A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023866 | ||||||
| chrX:124023872
|
C | T | 2 | a0001c0003t0001g0008a0001c0003t0001g0078 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.44+1201C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124023872 | ||||||
| chrX:124024164
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.44+1493A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124024164 | ||||||
| chrX:124024324
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.45-1516G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124024324 | ||||||
| chrX:124024374
|
A | AT | 1 | a0001c0001t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.45-1456dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chrX | 124024374 | |||||
| chrX:124024374
|
AT | A | 1 | a0001c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45-1456delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chrX | 124024374 | |||||
| chrX:124024915
|
GC | G | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.45-923delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chrX | 124024915 | |||||
| chrX:124025029
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.45-811T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025029 | ||||||
| chrX:124025130
|
T | C | 53 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0183others(50): Show | 53 | HG00438.hp2 HG01123.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.45-710T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025130 | ||||||
| chrX:124025187
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.45-653T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025187 | ||||||
| chrX:124025461
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.45-379T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025461 | ||||||
| chrX:124025522
|
G | C | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 262 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(259): Show |
intron_variant | MODIFIER | c.45-318G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025522 | ||||||
| chrX:124025624
|
T | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.45-216T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025624 | ||||||
| chrX:124025683
|
A | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-157A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025683 | ||||||
| chrX:124025829
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45-11T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 3/34 | chrX | 124025829 | ||||||
| chrX:124025960
|
TCACA | T | 1 | a0001c0001t0010g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.123+51_123+54delCA others(2): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124025960 | |||||
| chrX:124026000
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123+82A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124026000 | ||||||
| chrX:124026128
|
A | AAAT | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(90): Show | 93 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.123+251_123+253dup others(3): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
A | AAATAAT | 49 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0056others(46): Show | 49 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.123+248_123+253dup others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
A | AAATAATA others(2): Show |
19 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0071others(16): Show | 19 | HG01167.hp1 HG02040.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+245_123+253dup others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
A | AAATAATA others(5): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0118a0001c0001t0001g0138others(2): Show | 5 | HG02622.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+242_123+253dup others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
A | AAATAATA others(11): Show |
1 | a0001c0001t0003g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.123+236_123+253dup others(18): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
A | AT | 1 | a0001c0001t0001g0241 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.123+210_123+211ins others(1): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124026128 | ||||||
| chrX:124026128
|
AAAT | A | 4 | a0001c0001t0001g0012a0001c0001t0002g0029a0001c0001t0004g0174others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+251_123+253del others(3): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
AAATAAT | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0053others(10): Show | 13 | HG01106.hp1 HG02071.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.123+248_123+253del others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
AAATAATA others(2): Show |
A | 72 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0105others(69): Show | 72 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.123+245_123+253del others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
AAATAATA others(5): Show |
A | 1 | a0001c0001t0001g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.123+242_123+253del others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026128
|
AAATAATA others(8): Show |
A | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.123+239_123+253del others(15): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026128 | |||||
| chrX:124026154
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123+236A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124026154 | ||||||
| chrX:124026165
|
A | T | 1 | a0001c0001t0001g0266 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.123+247A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124026165 | ||||||
| chrX:124026172
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123+254C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124026172 | ||||||
| chrX:124026366
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG00673.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.123+448A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124026366 | ||||||
| chrX:124026566
|
A | AT | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+651dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026566 | |||||
| chrX:124026885
|
AT | A | 1 | a0001c0001t0001g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.123+969delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124026885 | |||||
| chrX:124026908
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0118a0001c0001t0001g0177 | 3 | HG02109.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.123+990A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124026908 | ||||||
| chrX:124027162
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.123+1244C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124027162 | ||||||
| chrX:124027210
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.123+1292C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124027210 | ||||||
| chrX:124027656
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.123+1738A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124027656 | ||||||
| chrX:124027838
|
T | G | 2 | a0001c0001t0004g0174a0001c0001t0004g0175 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.123+1920T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124027838 | ||||||
| chrX:124027847
|
G | GT | 1 | a0001c0001t0001g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.123+1937dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124027847 | |||||
| chrX:124027876
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.123+1958G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124027876 | ||||||
| chrX:124027882
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.123+1964G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124027882 | ||||||
| chrX:124028083
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123+2165G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028083 | ||||||
| chrX:124028578
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-2383C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028578 | ||||||
| chrX:124028644
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.124-2317G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028644 | ||||||
| chrX:124028670
|
C | T | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-2291C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028670 | ||||||
| chrX:124028794
|
T | TTA | 2 | a0001c0001t0001g0043a0001c0001t0002g0018 | 2 | HG02148.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.124-2139_124-2138d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028794 | |||||
| chrX:124028794
|
T | TTATA | 2 | a0001c0001t0001g0066a0001c0002t0001g0064 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.124-2141_124-2138d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028794 | |||||
| chrX:124028794
|
T | TTATATA | 3 | a0001c0001t0001g0243a0001c0002t0001g0063a0001c0002t0001g0069 | 3 | HG01496.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.124-2143_124-2138d others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028794 | |||||
| chrX:124028794
|
TTA | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0196a0001c0001t0002g0259 | 3 | HG01358.hp1 HG03491.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.124-2139_124-2138d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028794 | |||||
| chrX:124028794
|
TTATA | T | 14 | a0001c0001t0001g0128a0001c0001t0001g0166a0001c0001t0001g0167others(11): Show | 14 | HG00438.hp2 HG01952.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.124-2141_124-2138d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028794 | |||||
| chrX:124028794
|
TTATATA | T | 179 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 179 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(176): Show |
intron_variant | MODIFIER | c.124-2143_124-2138d others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028794 | |||||
| chrX:124028812
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.124-2147_124-2134d others(16): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028812 | |||||
| chrX:124028813
|
TATA | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-2147_124-2145d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028813 | ||||||
| chrX:124028815
|
TATATATA | T | 2 | a0001c0001t0001g0160a0001c0001t0008g0001 | 2 | HG02257.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.124-2145_124-2139d others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028815 | ||||||
| chrX:124028816
|
ATATATAT others(1): Show |
A | 2 | a0001c0001t0001g0071a0001c0001t0001g0188 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.124-2143_124-2136d others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028816 | |||||
| chrX:124028818
|
A | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-2143A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028818 | ||||||
| chrX:124028818
|
ATATAT | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0162 | 2 | HG00597.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.124-2141_124-2137d others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028818 | |||||
| chrX:124028818
|
ATATATT | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0127a0001c0001t0001g0161 | 3 | HG01099.hp1 HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.124-2141_124-2136d others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028818 | |||||
| chrX:124028818
|
ATATATTT others(1): Show |
A | 6 | a0001c0001t0001g0187a0001c0001t0002g0002a0001c0001t0002g0059others(3): Show | 6 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-2141_124-2134d others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028818 | |||||
| chrX:124028820
|
A | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-2141A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028820 | ||||||
| chrX:124028820
|
ATATT | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-2139_124-2136d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028820 | |||||
| chrX:124028822
|
A | ATATATAT others(3): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0068others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-2138_124-2137i others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028822 | |||||
| chrX:124028822
|
A | ATATT | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.124-2138_124-2137i others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028822 | |||||
| chrX:124028822
|
A | T | 25 | a0001c0001t0001g0067a0001c0001t0001g0094a0001c0001t0001g0122others(22): Show | 25 | HG00639.hp2 HG01081.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.124-2139A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028822 | ||||||
| chrX:124028822
|
AT | A | 1 | a0001c0001t0002g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.124-2128delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028822 | |||||
| chrX:124028822
|
ATT | A | 29 | a0001c0001t0001g0017a0001c0001t0002g0011a0001c0001t0002g0020others(26): Show | 29 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.124-2129_124-2128d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028822 | |||||
| chrX:124028823
|
T | TATATA | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.124-2138_124-2137i others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028823 | ||||||
| chrX:124028823
|
T | TATATATA others(2): Show |
1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.124-2138_124-2137i others(11): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028823 | ||||||
| chrX:124028824
|
T | A | 13 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0066others(10): Show | 13 | HG01346.hp1 HG01515.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.124-2137T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028824 | ||||||
| chrX:124028825
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0190 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.124-2136T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028825 | ||||||
| chrX:124028826
|
T | A | 3 | a0001c0001t0002g0028a0001c0001t0002g0051a0001c0001t0002g0070 | 3 | HG00558.hp1 HG04115.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.124-2135T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028826 | ||||||
| chrX:124028934
|
G | A | 43 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0002g0011others(40): Show | 43 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.124-2027G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028934 | ||||||
| chrX:124028981
|
T | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0224 | 2 | NA18974.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.124-1980T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028981 | ||||||
| chrX:124028985
|
T | TTA | 2 | a0001c0001t0004g0174a0001c0001t0004g0175 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.124-1948_124-1947d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028985 | |||||
| chrX:124028985
|
TTA | T | 83 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0105others(80): Show | 83 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.124-1948_124-1947d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028985 | |||||
| chrX:124028985
|
TTATA | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.124-1950_124-1947d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028985 | |||||
| chrX:124028987
|
A | ATATT | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.124-1971_124-1970i others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028987 | |||||
| chrX:124028989
|
A | ATT | 16 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0081others(13): Show | 16 | HG00597.hp2 HG01106.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-1971_124-1970i others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124028989 | |||||
| chrX:124028990
|
TA | T | 2 | a0001c0001t0003g0106a0001c0007t0001g0165 | 2 | NA19065.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124-1970delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028990 | ||||||
| chrX:124028991
|
A | T | 155 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(152): Show | 155 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.124-1970A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028991 | ||||||
| chrX:124028993
|
A | T | 83 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0105others(80): Show | 83 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.124-1968A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028993 | ||||||
| chrX:124028995
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.124-1966A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028995 | ||||||
| chrX:124028995
|
A | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.124-1966A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124028995 | ||||||
| chrX:124029007
|
A | ATT | 2 | a0001c0001t0001g0066a0001c0001t0001g0243 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.124-1953_124-1952i others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029007 | |||||
| chrX:124029007
|
A | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00738.hp1 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.124-1954A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029007 | ||||||
| chrX:124029011
|
A | AT | 1 | a0001c0001t0001g0241 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.124-1949dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029011 | |||||
| chrX:124029011
|
A | ATATTTAT others(1): Show |
1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-1936_124-1929d others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029011 | |||||
| chrX:124029011
|
A | ATT | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.124-1949_124-1948i others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029011 | |||||
| chrX:124029011
|
A | T | 252 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 252 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.124-1950A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029011 | ||||||
| chrX:124029117
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-1844C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029117 | ||||||
| chrX:124029207
|
T | C | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.124-1754T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029207 | ||||||
| chrX:124029398
|
C | T | 8 | a0001c0001t0001g0220a0001c0001t0001g0227a0001c0001t0001g0229others(5): Show | 8 | NA18949.hp1 NA18950.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-1563C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029398 | ||||||
| chrX:124029456
|
G | T | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.124-1505G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029456 | ||||||
| chrX:124029530
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.124-1431C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029530 | ||||||
| chrX:124029541
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.124-1420G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029541 | ||||||
| chrX:124029787
|
AG | A | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.124-1170delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029787 | |||||
| chrX:124029789
|
G | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-1172G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029789 | ||||||
| chrX:124029795
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.124-1166G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124029795 | ||||||
| chrX:124029870
|
GT | G | 1 | a0001c0001t0001g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.124-1087delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029870 | |||||
| chrX:124029922
|
AG | A | 1 | a0001c0001t0001g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.124-1036delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029922 | |||||
| chrX:124029939
|
AT | A | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.124-1015delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124029939 | |||||
| chrX:124030092
|
CCTA | C | 1 | a0001c0001t0002g0021 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.124-866_124-864del others(3): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124030092 | |||||
| chrX:124030101
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0093 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.124-860A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124030101 | ||||||
| chrX:124030197
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.124-764T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124030197 | ||||||
| chrX:124030338
|
GT | G | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.124-618delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | INFO_REALIGN_3_PRIME | chrX | 124030338 | |||||
| chrX:124030596
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-365C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124030596 | ||||||
| chrX:124030921
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124-40G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 4/34 | chrX | 124030921 | ||||||
| chrX:124031368
|
A | T | 1 | a0001c0001t0001g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.288+243A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031368 | ||||||
| chrX:124031447
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.288+322C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031447 | ||||||
| chrX:124031528
|
G | GT | 1 | a0001c0001t0001g0241 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.288+409dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124031528 | |||||
| chrX:124031535
|
G | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(248): Show | 251 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.288+410G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031535 | ||||||
| chrX:124031550
|
TG | T | 1 | a0001c0001t0001g0257 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.288+426delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031550 | ||||||
| chrX:124031551
|
G | GT | 38 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0056others(35): Show | 38 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.288+434dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124031551 | |||||
| chrX:124031552
|
TTTTTTTT others(1): Show |
T | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.288+451_288+458del others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124031552 | |||||
| chrX:124031555
|
T | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0213 | 2 | HG02818.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.288+430T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031555 | ||||||
| chrX:124031577
|
T | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.288+452T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031577 | ||||||
| chrX:124031655
|
T | C | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.288+530T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031655 | ||||||
| chrX:124031741
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0042 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.288+616A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031741 | ||||||
| chrX:124031833
|
C | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.288+708C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031833 | ||||||
| chrX:124031879
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.288+754C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124031879 | ||||||
| chrX:124032091
|
A | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+966A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032091 | ||||||
| chrX:124032169
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.288+1044A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032169 | ||||||
| chrX:124032217
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.288+1092G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032217 | ||||||
| chrX:124032436
|
A | G | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.288+1311A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032436 | ||||||
| chrX:124032465
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.288+1340A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032465 | ||||||
| chrX:124032468
|
C | A | 59 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.288+1343C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032468 | ||||||
| chrX:124032775
|
T | C | 1 | a0001c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.288+1650T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032775 | ||||||
| chrX:124032905
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0213 | 2 | HG02165.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.288+1780A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032905 | ||||||
| chrX:124032992
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.288+1867G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124032992 | ||||||
| chrX:124033027
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.288+1902A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124033027 | ||||||
| chrX:124033186
|
CT | C | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.288+2065delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124033186 | |||||
| chrX:124033541
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.288+2416C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124033541 | ||||||
| chrX:124033677
|
A | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+2552A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124033677 | ||||||
| chrX:124033703
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.288+2578A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124033703 | ||||||
| chrX:124033767
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.288+2642A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124033767 | ||||||
| chrX:124033790
|
CAT | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.288+2667_288+2668d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124033790 | |||||
| chrX:124033847
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.288+2722C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124033847 | ||||||
| chrX:124033911
|
A | AT | 1 | a0001c0001t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.288+2787dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124033911 | |||||
| chrX:124034295
|
T | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.288+3170T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124034295 | ||||||
| chrX:124034400
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.289-3127C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124034400 | ||||||
| chrX:124034643
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.289-2884C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124034643 | ||||||
| chrX:124034649
|
A | G | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.289-2878A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124034649 | ||||||
| chrX:124034823
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.289-2704A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124034823 | ||||||
| chrX:124034856
|
AGTT | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0238a0001c0001t0002g0198 | 3 | NA18970.hp1 NA19006.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.289-2649_289-2647d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124034856 | |||||
| chrX:124034868
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.289-2659T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124034868 | ||||||
| chrX:124034875
|
G | GTTA | 24 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0117others(21): Show | 24 | HG01081.hp2 HG01123.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.289-2650_289-2649i others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124034875 | |||||
| chrX:124034875
|
G | GTTATTA | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.289-2650_289-2649i others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124034875 | |||||
| chrX:124034875
|
GTTGTTA | G | 49 | a0001c0001t0001g0043a0001c0001t0001g0166a0001c0001t0001g0167others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.289-2649_289-2644d others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124034875 | |||||
| chrX:124034878
|
G | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 206 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(203): Show |
intron_variant | MODIFIER | c.289-2649G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124034878 | ||||||
| chrX:124034878
|
G | GTTA | 2 | a0001c0001t0001g0178a0001c0003t0001g0008 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.289-2623_289-2621d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124034878 | |||||
| chrX:124034904
|
T | TATC | 1 | a0001c0001t0001g0182 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.289-2620_289-2618d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124034904 | |||||
| chrX:124035053
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-2474C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124035053 | ||||||
| chrX:124035055
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-2472C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124035055 | ||||||
| chrX:124035091
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.289-2436G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124035091 | ||||||
| chrX:124035500
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.289-2027G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124035500 | ||||||
| chrX:124035756
|
ATG | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(80): Show | 83 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.289-1768_289-1767d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | INFO_REALIGN_3_PRIME | chrX | 124035756 | |||||
| chrX:124035805
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-1722C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124035805 | ||||||
| chrX:124036215
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0153 | 2 | NA18948.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.289-1312A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036215 | ||||||
| chrX:124036293
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.289-1234C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036293 | ||||||
| chrX:124036476
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.289-1051C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036476 | ||||||
| chrX:124036609
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0138a0001c0001t0001g0160 | 3 | HG02257.hp1 HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.289-918C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036609 | ||||||
| chrX:124036658
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289-869G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036658 | ||||||
| chrX:124036701
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-826C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036701 | ||||||
| chrX:124036715
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.289-812C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036715 | ||||||
| chrX:124036816
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.289-711C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036816 | ||||||
| chrX:124036871
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.289-656A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124036871 | ||||||
| chrX:124037097
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.289-430G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124037097 | ||||||
| chrX:124037105
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.289-422C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124037105 | ||||||
| chrX:124037138
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.289-389G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 5/34 | chrX | 124037138 | ||||||
| chrX:124038018
|
TAAGC | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0239 | 2 | NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.385+407_385+410del others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124038018 | |||||
| chrX:124038022
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.385+399C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124038022 | ||||||
| chrX:124038203
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.385+580C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124038203 | ||||||
| chrX:124038750
|
TA | T | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.385+1133delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124038750 | |||||
| chrX:124038821
|
T | C | 2 | a0001c0001t0001g0105a0003c0006t0001g0226 | 2 | NA19080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.385+1198T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124038821 | ||||||
| chrX:124038881
|
T | A | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.385+1258T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124038881 | ||||||
| chrX:124039120
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.385+1497T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124039120 | ||||||
| chrX:124039137
|
T | TTTA | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(164): Show | 167 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.385+1544_385+1546d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039137 | |||||
| chrX:124039137
|
T | TTTATTA | 21 | a0001c0001t0001g0056a0001c0001t0001g0079a0001c0001t0001g0084others(18): Show | 21 | HG01261.hp1 HG01361.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.385+1541_385+1546d others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039137 | |||||
| chrX:124039137
|
T | TTTATTAT others(2): Show |
6 | a0001c0001t0001g0052a0001c0001t0001g0086a0001c0001t0001g0090others(3): Show | 6 | HG01099.hp1 HG01167.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+1538_385+1546d others(11): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039137 | |||||
| chrX:124039137
|
T | TTTATTAT others(8): Show |
2 | a0001c0001t0001g0076a0001c0003t0001g0078 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.385+1532_385+1546d others(17): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039137 | |||||
| chrX:124039223
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.385+1600A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124039223 | ||||||
| chrX:124039233
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.385+1610G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124039233 | ||||||
| chrX:124039397
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.385+1774C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124039397 | ||||||
| chrX:124039511
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.385+1888A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124039511 | ||||||
| chrX:124039586
|
A | AGTTT | 1 | a0001c0001t0002g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.385+1986_385+1989d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039586 | |||||
| chrX:124039609
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0118a0001c0001t0001g0177others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+1986T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124039609 | ||||||
| chrX:124039640
|
CT | C | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 188 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(185): Show |
intron_variant | MODIFIER | c.385+2032delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039640 | |||||
| chrX:124039640
|
CTT | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0245a0001c0001t0001g0248 | 3 | NA18955.hp1 NA18961.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.385+2031_385+2032d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039640 | |||||
| chrX:124039640
|
CTTTTT | C | 1 | a0001c0001t0001g0268 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.385+2028_385+2032d others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124039640 | |||||
| chrX:124039849
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.385+2226T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124039849 | ||||||
| chrX:124040286
|
G | T | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-2283G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040286 | ||||||
| chrX:124040389
|
C | A | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 261 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.386-2180C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040389 | ||||||
| chrX:124040522
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.386-2047G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040522 | ||||||
| chrX:124040543
|
G | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.386-2026G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040543 | ||||||
| chrX:124040838
|
T | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-1731T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040838 | ||||||
| chrX:124040841
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1728T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040841 | ||||||
| chrX:124040854
|
C | CT | 55 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0055others(52): Show | 55 | HG00597.hp2 HG00738.hp1 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.386-1695dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124040854 | |||||
| chrX:124040854
|
C | CTT | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0152 | 3 | HG02148.hp1 HG02735.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.386-1696_386-1695d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124040854 | |||||
| chrX:124040854
|
CT | C | 4 | a0001c0001t0001g0081a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1695delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124040854 | |||||
| chrX:124040856
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.386-1713T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040856 | ||||||
| chrX:124040934
|
C | T | 105 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0054others(102): Show | 105 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.386-1635C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124040934 | ||||||
| chrX:124041036
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.386-1533T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041036 | ||||||
| chrX:124041094
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.386-1475G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041094 | ||||||
| chrX:124041218
|
A | AT | 1 | a0001c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386-1336dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124041218 | |||||
| chrX:124041218
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.386-1351A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041218 | ||||||
| chrX:124041218
|
AT | A | 81 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0077others(78): Show | 81 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.386-1336delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124041218 | |||||
| chrX:124041218
|
ATT | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0238 | 2 | HG03017.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.386-1337_386-1336d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124041218 | |||||
| chrX:124041241
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.386-1328G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041241 | ||||||
| chrX:124041409
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386-1160A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041409 | ||||||
| chrX:124041419
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386-1150A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041419 | ||||||
| chrX:124041422
|
G | GGC | 1 | a0001c0001t0006g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.386-1140_386-1139d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | INFO_REALIGN_3_PRIME | chrX | 124041422 | |||||
| chrX:124041426
|
C | T | 2 | a0001c0001t0004g0174a0001c0001t0004g0175 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.386-1143C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041426 | ||||||
| chrX:124041466
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.386-1103C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041466 | ||||||
| chrX:124041472
|
A | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-1097A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041472 | ||||||
| chrX:124041650
|
A | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.386-919A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041650 | ||||||
| chrX:124041789
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG01952.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.386-780A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041789 | ||||||
| chrX:124041840
|
T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0068others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-729T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041840 | ||||||
| chrX:124041888
|
CAT | C | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386-680_386-679del others(2): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041888 | ||||||
| chrX:124041938
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-631A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124041938 | ||||||
| chrX:124042038
|
A | C | 1 | a0001c0001t0001g0273 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.386-531A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124042038 | ||||||
| chrX:124042263
|
G | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-306G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124042263 | ||||||
| chrX:124042402
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386-167C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124042402 | ||||||
| chrX:124042533
|
C | T | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.386-36C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 6/34 | chrX | 124042533 | ||||||
| chrX:124042786
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0235 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.462+141C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124042786 | ||||||
| chrX:124042857
|
C | CA | 1 | a0001c0001t0001g0263 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.462+220dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chrX | 124042857 | |||||
| chrX:124042872
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.462+227G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124042872 | ||||||
| chrX:124042946
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.462+301C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124042946 | ||||||
| chrX:124043012
|
C | CA | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.462+376dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chrX | 124043012 | |||||
| chrX:124043109
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0137others(1): Show | 4 | HG00639.hp1 HG01361.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+464G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124043109 | ||||||
| chrX:124043130
|
G | GT | 3 | a0001c0001t0001g0153a0001c0001t0001g0190a0001c0001t0002g0198 | 3 | HG02257.hp2 NA19006.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.462+496dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chrX | 124043130 | |||||
| chrX:124043195
|
A | G | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG00558.hp2 NA18966.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+550A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124043195 | ||||||
| chrX:124043207
|
C | CA | 1 | a0001c0001t0001g0248 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462+564dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chrX | 124043207 | |||||
| chrX:124043211
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.462+566C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124043211 | ||||||
| chrX:124043299
|
C | T | 1 | a0001c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.462+654C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124043299 | ||||||
| chrX:124043437
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.462+792C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124043437 | ||||||
| chrX:124043505
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+860G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124043505 | ||||||
| chrX:124043729
|
TA | T | 1 | a0001c0001t0001g0241 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.462+1089delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chrX | 124043729 | |||||
| chrX:124043779
|
T | TC | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.462+1141dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | INFO_REALIGN_3_PRIME | chrX | 124043779 | |||||
| chrX:124044076
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0232 | 2 | NA18970.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.463-1088T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124044076 | ||||||
| chrX:124044169
|
T | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.463-995T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124044169 | ||||||
| chrX:124044493
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.463-671C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 7/34 | chrX | 124044493 | ||||||
| chrX:124045897
|
C | T | 1 | a0001c0001t0005g0019 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.667+529C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124045897 | ||||||
| chrX:124045951
|
A | T | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.667+583A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124045951 | ||||||
| chrX:124045968
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.667+600T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124045968 | ||||||
| chrX:124046026
|
C | T | 2 | a0001c0001t0007g0141a0004c0005t0007g0083 | 2 | NA18941.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.667+658C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046026 | ||||||
| chrX:124046263
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667+895A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046263 | ||||||
| chrX:124046275
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0134 | 2 | NA19003.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.667+907G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046275 | ||||||
| chrX:124046410
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.668-944A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046410 | ||||||
| chrX:124046417
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.668-937C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046417 | ||||||
| chrX:124046484
|
ATTAAC | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.668-866_668-862del others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chrX | 124046484 | |||||
| chrX:124046724
|
G | GT | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG01952.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.668-626dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | INFO_REALIGN_3_PRIME | chrX | 124046724 | |||||
| chrX:124046737
|
G | A | 12 | a0001c0001t0002g0020a0001c0001t0002g0024a0001c0001t0002g0025others(9): Show | 12 | HG01515.hp1 HG01517.hp2 HG03490.hp1 others(9): Show |
intron_variant | MODIFIER | c.668-617G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046737 | ||||||
| chrX:124046931
|
T | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.668-423T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046931 | ||||||
| chrX:124046962
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.668-392G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046962 | ||||||
| chrX:124046997
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.668-357C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124046997 | ||||||
| chrX:124047027
|
G | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.668-327G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 8/34 | chrX | 124047027 | ||||||
| chrX:124047596
|
GT | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+96delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chrX | 124047596 | |||||
| chrX:124047694
|
C | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.819+189C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124047694 | ||||||
| chrX:124047701
|
G | A | 46 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 46 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.819+196G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124047701 | ||||||
| chrX:124047746
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.819+241C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124047746 | ||||||
| chrX:124047946
|
A | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+441A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124047946 | ||||||
| chrX:124048038
|
C | A | 1 | a0001c0001t0002g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.819+533C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048038 | ||||||
| chrX:124048073
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.819+568A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048073 | ||||||
| chrX:124048145
|
A | G | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 261 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.819+640A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048145 | ||||||
| chrX:124048174
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.819+669T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048174 | ||||||
| chrX:124048206
|
G | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+701G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048206 | ||||||
| chrX:124048320
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820-685A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048320 | ||||||
| chrX:124048443
|
G | GT | 1 | a0001c0001t0002g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.820-554dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chrX | 124048443 | |||||
| chrX:124048515
|
A | G | 1 | a0001c0001t0003g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.820-490A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048515 | ||||||
| chrX:124048626
|
T | C | 10 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-379T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048626 | ||||||
| chrX:124048725
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.820-280C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048725 | ||||||
| chrX:124048854
|
A | C | 2 | a0001c0001t0001g0159a0001c0001t0009g0139 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.820-151A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048854 | ||||||
| chrX:124048920
|
C | CT | 1 | a0001c0001t0001g0220 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.820-78dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | INFO_REALIGN_3_PRIME | chrX | 124048920 | |||||
| chrX:124048926
|
T | C | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.820-79T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 9/34 | chrX | 124048926 | ||||||
| chrX:124049252
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.893+174G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124049252 | ||||||
| chrX:124049377
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0002g0193 | 2 | NA18950.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.893+299G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124049377 | ||||||
| chrX:124049448
|
G | GT | 1 | a0001c0001t0001g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.893+371dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | INFO_REALIGN_3_PRIME | chrX | 124049448 | |||||
| chrX:124049871
|
T | G | 1 | a0001c0001t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.894-315T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124049871 | ||||||
| chrX:124049886
|
C | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.894-300C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124049886 | ||||||
| chrX:124049961
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.894-225G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124049961 | ||||||
| chrX:124050115
|
C | G | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.894-71C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124050115 | ||||||
| chrX:124050151
|
A | G | 5 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049others(2): Show | 5 | NA18975.hp2 NA18979.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.894-35A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124050151 | ||||||
| chrX:124050177
|
C | T | 10 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.894-9C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 10/34 | chrX | 124050177 | ||||||
| chrX:124050434
|
T | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1017+125T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 11/34 | chrX | 124050434 | ||||||
| chrX:124050634
|
TA | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1017+335delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chrX | 124050634 | |||||
| chrX:124050788
|
T | C | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1018-333T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 11/34 | chrX | 124050788 | ||||||
| chrX:124051099
|
C | CT | 20 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0085others(17): Show | 20 | HG00280.hp1 HG01106.hp1 HG01123.hp2 others(17): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1018-3dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chrX | 124051099 | |||||
| chrX:124051099
|
C | CTT | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1018-4_1018-3dupTT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chrX | 124051099 | |||||
| chrX:124051099
|
CT | C | 5 | a0001c0001t0001g0134a0001c0001t0001g0224a0001c0001t0001g0241others(2): Show | 5 | HG01069.hp1 NA18969.hp1 NA18974.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1018-3delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chrX | 124051099 | |||||
| chrX:124051099
|
CTT | C | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
splice_region_variant&intron_variant | LOW | c.1018-4_1018-3delTT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 11/34 | INFO_REALIGN_3_PRIME | chrX | 124051099 | |||||
| chrX:124051499
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1196+105G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124051499 | ||||||
| chrX:124051673
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1196+279C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124051673 | ||||||
| chrX:124051688
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1196+294T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124051688 | ||||||
| chrX:124052033
|
A | G | 1 | a0001c0001t0001g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1196+639A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124052033 | ||||||
| chrX:124052050
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1196+656A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124052050 | ||||||
| chrX:124052062
|
GTC | G | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1196+670_1196+671d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124052062 | |||||
| chrX:124052229
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1196+835C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124052229 | ||||||
| chrX:124052345
|
TC | T | 1 | a0001c0001t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1196+955delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124052345 | |||||
| chrX:124052424
|
C | T | 2 | a0001c0001t0002g0040a0001c0001t0002g0057 | 2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1196+1030C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124052424 | ||||||
| chrX:124052501
|
G | A | 7 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0001g0217others(4): Show | 7 | HG00621.hp1 HG02129.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196+1107G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124052501 | ||||||
| chrX:124052675
|
C | A | 1 | a0001c0001t0002g0021 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1196+1281C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124052675 | ||||||
| chrX:124052815
|
C | CT | 1 | a0001c0001t0001g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1196+1437dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124052815 | |||||
| chrX:124052938
|
TC | T | 1 | a0001c0001t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1196+1547delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124052938 | |||||
| chrX:124052973
|
C | T | 13 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(10): Show | 13 | NA18957.hp1 NA18965.hp1 NA18971.hp1 others(10): Show |
intron_variant | MODIFIER | c.1196+1579C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124052973 | ||||||
| chrX:124053051
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1196+1657A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124053051 | ||||||
| chrX:124053222
|
A | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0039a0001c0001t0002g0045 | 3 | NA18990.hp1 NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1196+1828A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124053222 | ||||||
| chrX:124053371
|
T | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196+1977T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124053371 | ||||||
| chrX:124053454
|
A | AT | 4 | a0001c0001t0001g0188a0001c0001t0001g0202a0001c0001t0001g0248others(1): Show | 4 | HG02723.hp1 HG03017.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196+2072dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124053454 | |||||
| chrX:124053454
|
AT | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1196+2072delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124053454 | |||||
| chrX:124053735
|
T | C | 1 | a0001c0001t0004g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1196+2341T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124053735 | ||||||
| chrX:124054082
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1197-2046A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124054082 | ||||||
| chrX:124054134
|
G | A | 81 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(78): Show | 81 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1197-1994G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124054134 | ||||||
| chrX:124054274
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | NA18981.hp2 NA18988.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197-1854T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124054274 | ||||||
| chrX:124054549
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1197-1579A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124054549 | ||||||
| chrX:124054764
|
G | GT | 1 | a0001c0001t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1197-1356dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124054764 | |||||
| chrX:124054902
|
A | ACT | 1 | a0001c0001t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1197-1225_1197-122 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124054902 | |||||
| chrX:124054927
|
A | AT | 1 | a0001c0001t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1197-1191dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124054927 | |||||
| chrX:124054944
|
G | GT | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1197-1178dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124054944 | |||||
| chrX:124054951
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1197-1177G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124054951 | ||||||
| chrX:124055128
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1197-1000T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055128 | ||||||
| chrX:124055139
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0118a0001c0001t0001g0177 | 3 | HG02109.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1197-989A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055139 | ||||||
| chrX:124055180
|
T | C | 3 | a0001c0001t0005g0019a0001c0001t0005g0027a0001c0001t0005g0034 | 3 | HG00597.hp1 NA18944.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1197-948T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055180 | ||||||
| chrX:124055517
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0207 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1197-611T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055517 | ||||||
| chrX:124055662
|
A | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1197-466A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055662 | ||||||
| chrX:124055663
|
CATGGTGT others(5): Show |
C | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1197-463_1197-452d others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124055663 | |||||
| chrX:124055727
|
A | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0162 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1197-401A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055727 | ||||||
| chrX:124055773
|
G | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1197-355G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055773 | ||||||
| chrX:124055948
|
T | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0153 | 2 | NA18948.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1197-180T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124055948 | ||||||
| chrX:124055996
|
G | GT | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 264 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.1197-122dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124055996 | |||||
| chrX:124055996
|
G | GTT | 10 | a0001c0001t0001g0052a0001c0001t0001g0153a0001c0001t0001g0180others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1197-123_1197-122d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124055996 | |||||
| chrX:124055996
|
G | GTTT | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1197-124_1197-122d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | INFO_REALIGN_3_PRIME | chrX | 124055996 | |||||
| chrX:124056082
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1197-46A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 13/34 | chrX | 124056082 | ||||||
| chrX:124056455
|
TG | T | 1 | a0001c0001t0002g0028 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1304+223delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056455 | |||||
| chrX:124056500
|
G | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+265G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124056500 | ||||||
| chrX:124056589
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0002g0151 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1304+354C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124056589 | ||||||
| chrX:124056650
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1304+415G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124056650 | ||||||
| chrX:124056676
|
T | TGAGCC | 2 | a0001c0001t0001g0071a0001c0001t0001g0091 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1304+445_1304+449d others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056676 | |||||
| chrX:124056731
|
T | TA | 230 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 230 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.1304+519dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056731 | |||||
| chrX:124056731
|
T | TAA | 22 | a0001c0001t0001g0074a0001c0001t0001g0133a0001c0001t0001g0140others(19): Show | 22 | HG01074.hp1 HG01109.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1304+518_1304+519d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056731 | |||||
| chrX:124056731
|
T | TAAA | 2 | a0001c0001t0001g0134a0001c0001t0001g0252 | 2 | HG03831.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1304+517_1304+519d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056731 | |||||
| chrX:124056731
|
T | TAAAA | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1304+516_1304+519d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056731 | |||||
| chrX:124056731
|
T | TAAAAA | 1 | a0001c0001t0001g0268 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1304+515_1304+519d others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056731 | |||||
| chrX:124056797
|
T | C | 2 | a0001c0001t0002g0038a0001c0001t0002g0042 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1304+562T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124056797 | ||||||
| chrX:124056896
|
C | CT | 2 | a0001c0001t0001g0178a0001c0001t0001g0192 | 2 | HG01884.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1304+673dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056896 | |||||
| chrX:124056896
|
CT | C | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(173): Show | 176 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1304+673delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | INFO_REALIGN_3_PRIME | chrX | 124056896 | |||||
| chrX:124056956
|
G | A | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1304+721G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124056956 | ||||||
| chrX:124057037
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1304+802C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124057037 | ||||||
| chrX:124057165
|
A | G | 1 | a0001c0001t0002g0198 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1305-701A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124057165 | ||||||
| chrX:124057453
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1305-413G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124057453 | ||||||
| chrX:124057760
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305-106T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124057760 | ||||||
| chrX:124057815
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305-51A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 14/34 | chrX | 124057815 | ||||||
| chrX:124058072
|
A | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416+95A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124058072 | ||||||
| chrX:124058099
|
ACCCACTC others(1): Show |
A | 5 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0068others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416+135_1416+142d others(10): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124058099 | |||||
| chrX:124058124
|
T | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0075others(3): Show | 6 | HG00673.hp1 HG02015.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1416+147T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124058124 | ||||||
| chrX:124058154
|
C | CT | 64 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0043others(61): Show | 64 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1416+198dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124058154 | |||||
| chrX:124058154
|
C | CTT | 7 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0111others(4): Show | 7 | HG02080.hp2 HG02165.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1416+197_1416+198d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124058154 | |||||
| chrX:124058154
|
C | CTTT | 1 | a0001c0001t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1416+196_1416+198d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124058154 | |||||
| chrX:124058154
|
CT | C | 6 | a0001c0001t0001g0094a0001c0001t0001g0118a0001c0001t0001g0177others(3): Show | 6 | HG01361.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416+198delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124058154 | |||||
| chrX:124058157
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1416+180T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124058157 | ||||||
| chrX:124058446
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1416+469C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124058446 | ||||||
| chrX:124058569
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1416+592A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124058569 | ||||||
| chrX:124058874
|
T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1416+897T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124058874 | ||||||
| chrX:124059088
|
G | A | 37 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0082others(34): Show | 37 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1416+1111G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059088 | ||||||
| chrX:124059133
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0002g0151 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1416+1156A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059133 | ||||||
| chrX:124059145
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1416+1168C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059145 | ||||||
| chrX:124059241
|
G | A | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1416+1264G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059241 | ||||||
| chrX:124059291
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1416+1314T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059291 | ||||||
| chrX:124059576
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1416+1599A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059576 | ||||||
| chrX:124059687
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1417-1537G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059687 | ||||||
| chrX:124059941
|
C | CATAA | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1417-1281_1417-127 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124059941 | |||||
| chrX:124059999
|
A | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1417-1225A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124059999 | ||||||
| chrX:124060145
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1417-1079T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124060145 | ||||||
| chrX:124060375
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1417-849C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124060375 | ||||||
| chrX:124060887
|
TC | T | 1 | a0002c0004t0001g0255 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1417-334delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124060887 | |||||
| chrX:124060926
|
A | AC | 10 | a0001c0001t0001g0056a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG00735.hp1 HG01069.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417-291dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124060926 | |||||
| chrX:124060981
|
T | TA | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1417-237dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | INFO_REALIGN_3_PRIME | chrX | 124060981 | |||||
| chrX:124060987
|
A | T | 1 | a0001c0001t0001g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1417-237A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124060987 | ||||||
| chrX:124061017
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0105others(57): Show | 60 | HG00438.hp2 HG00621.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.1417-207T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124061017 | ||||||
| chrX:124061183
|
T | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0232 | 2 | NA18970.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1417-41T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124061183 | ||||||
| chrX:124061185
|
A | C | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1417-39A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 15/34 | chrX | 124061185 | ||||||
| chrX:124061401
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1534+60A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | chrX | 124061401 | ||||||
| chrX:124061417
|
CT | C | 1 | a0002c0004t0001g0255 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1534+80delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061417 | |||||
| chrX:124061743
|
C | CT | 16 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0055others(13): Show | 16 | HG01106.hp1 HG01167.hp1 HG01496.hp2 others(13): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1535-3dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124061743
|
C | CTT | 21 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00140.hp1 HG00735.hp2 HG01257.hp2 others(18): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1535-4_1535-3dupTT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124061743
|
C | CTTT | 40 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0071others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1535-5_1535-3dupTT others(1): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124061743
|
C | CTTTT | 5 | a0001c0001t0002g0028a0001c0001t0002g0042a0001c0001t0002g0050others(2): Show | 5 | HG00558.hp1 HG01175.hp2 HG03942.hp1 others(2): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1535-6_1535-3dupTT others(2): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124061743
|
CT | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0072others(72): Show | 75 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(72): Show |
splice_region_variant&intron_variant | LOW | c.1535-3delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124061743
|
CTT | C | 5 | a0001c0001t0001g0077a0001c0001t0001g0254a0001c0001t0001g0266others(2): Show | 5 | HG02109.hp2 HG02683.hp1 HG02717.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1535-4_1535-3delTT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124061743
|
CTTTTT | C | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.1535-7_1535-3delTT others(3): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124061743
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.1535-12_1535-3delT others(9): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 16/34 | INFO_REALIGN_3_PRIME | chrX | 124061743 | |||||
| chrX:124062578
|
T | TTA | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1639-317_1639-316d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 17/34 | INFO_REALIGN_3_PRIME | chrX | 124062578 | |||||
| chrX:124062690
|
A | AT | 2 | a0001c0001t0002g0011a0001c0003t0001g0008 | 2 | HG03471.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1639-203dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 17/34 | INFO_REALIGN_3_PRIME | chrX | 124062690 | |||||
| chrX:124062690
|
AT | A | 1 | a0002c0004t0001g0255 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1639-203delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 17/34 | INFO_REALIGN_3_PRIME | chrX | 124062690 | |||||
| chrX:124062791
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1639-111C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 17/34 | chrX | 124062791 | ||||||
| chrX:124063083
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0057 | 2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1732-33T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 18/34 | chrX | 124063083 | ||||||
| chrX:124063222
|
T | TA | 1 | a0001c0001t0001g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1821+25dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 19/34 | INFO_REALIGN_3_PRIME | chrX | 124063222 | |||||
| chrX:124063390
|
CA | C | 1 | a0002c0004t0001g0255 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1821+186delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 19/34 | chrX | 124063390 | ||||||
| chrX:124063457
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821+252G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 19/34 | chrX | 124063457 | ||||||
| chrX:124063495
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1821+290G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 19/34 | chrX | 124063495 | ||||||
| chrX:124063687
|
G | C | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1822-161G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 19/34 | chrX | 124063687 | ||||||
| chrX:124063707
|
T | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 107 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.1822-141T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 19/34 | chrX | 124063707 | ||||||
| chrX:124064128
|
T | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2025+77T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124064128 | ||||||
| chrX:124064296
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2025+245A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124064296 | ||||||
| chrX:124064411
|
G | GT | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2025+364dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chrX | 124064411 | |||||
| chrX:124064444
|
G | GT | 5 | a0001c0001t0001g0261a0001c0001t0002g0050a0001c0001t0002g0136others(2): Show | 5 | HG02074.hp1 HG02683.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2025+409dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chrX | 124064444 | |||||
| chrX:124064618
|
A | AC | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2025+567_2025+568i others(3): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124064618 | ||||||
| chrX:124064724
|
G | A | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2025+673G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124064724 | ||||||
| chrX:124064860
|
ACAC | A | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2025+810_2025+812d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124064860 | ||||||
| chrX:124064914
|
C | A | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 261 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.2025+863C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124064914 | ||||||
| chrX:124064988
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2026-888A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124064988 | ||||||
| chrX:124065029
|
T | TC | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2026-847_2026-846i others(3): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124065029 | ||||||
| chrX:124065159
|
T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0180 | 2 | HG03540.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.2026-717T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124065159 | ||||||
| chrX:124065171
|
ACTCTT | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026-704_2026-700d others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124065171 | ||||||
| chrX:124065295
|
C | CA | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2026-579dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chrX | 124065295 | |||||
| chrX:124065494
|
GAT | G | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2026-377_2026-376d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chrX | 124065494 | |||||
| chrX:124065501
|
G | GT | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2026-372dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chrX | 124065501 | |||||
| chrX:124065516
|
A | AT | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026-356dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | INFO_REALIGN_3_PRIME | chrX | 124065516 | |||||
| chrX:124065547
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2026-329T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124065547 | ||||||
| chrX:124065695
|
C | CA | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2026-181_2026-180i others(3): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124065695 | ||||||
| chrX:124065826
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2026-50C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 20/34 | chrX | 124065826 | ||||||
| chrX:124066049
|
T | TG | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2096+108dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chrX | 124066049 | |||||
| chrX:124066143
|
A | AT | 101 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(98): Show |
splice_region_variant&intron_variant | LOW | c.2097-5dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chrX | 124066143 | |||||
| chrX:124066143
|
A | ATT | 17 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0076others(14): Show | 17 | HG00639.hp1 HG01361.hp2 HG01496.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.2097-6_2097-5dupTT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chrX | 124066143 | |||||
| chrX:124066143
|
AT | A | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(50): Show | 53 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
splice_region_variant&intron_variant | LOW | c.2097-5delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chrX | 124066143 | |||||
| chrX:124066143
|
ATT | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0071others(76): Show | 79 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
splice_region_variant&intron_variant | LOW | c.2097-6_2097-5delTT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chrX | 124066143 | |||||
| chrX:124066143
|
ATTT | A | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | splice_region_variant&intron_variant | LOW | c.2097-7_2097-5delTT others(1): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 21/34 | INFO_REALIGN_3_PRIME | chrX | 124066143 | |||||
| chrX:124066583
|
G | GGA | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2265+151_2265+152d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124066583 | |||||
| chrX:124066632
|
ATTG | A | 130 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(127): Show | 130 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2265+202_2265+204d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124066632 | |||||
| chrX:124066805
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2265+369T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124066805 | ||||||
| chrX:124066813
|
ATC | A | 131 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(128): Show | 131 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2265+383_2265+384d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124066813 | |||||
| chrX:124066893
|
A | AT | 1 | a0003c0006t0001g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2265+458dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124066893 | |||||
| chrX:124067010
|
G | A | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(270): Show | 273 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(270): Show |
intron_variant | MODIFIER | c.2265+574G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124067010 | ||||||
| chrX:124067039
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2265+603C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124067039 | ||||||
| chrX:124067055
|
TCA | T | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2265+624_2265+625d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124067055 | |||||
| chrX:124067207
|
C | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2265+771C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124067207 | ||||||
| chrX:124067265
|
G | GC | 4 | a0001c0001t0001g0052a0001c0001t0001g0203a0001c0001t0002g0011others(1): Show | 4 | HG02572.hp1 HG03688.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2265+836dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124067265 | |||||
| chrX:124067321
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0002g0151 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2265+885T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124067321 | ||||||
| chrX:124067373
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2265+937A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124067373 | ||||||
| chrX:124067404
|
A | G | 61 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2265+968A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124067404 | ||||||
| chrX:124067685
|
C | A | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(272): Show | 275 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(272): Show |
intron_variant | MODIFIER | c.2266-879C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124067685 | ||||||
| chrX:124068034
|
C | CA | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2266-518dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124068034 | |||||
| chrX:124068034
|
CA | C | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2266-518delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124068034 | |||||
| chrX:124068185
|
A | C | 60 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2266-379A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124068185 | ||||||
| chrX:124068224
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0096a0001c0001t0001g0119others(3): Show | 6 | HG01261.hp1 NA18947.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.2266-340C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124068224 | ||||||
| chrX:124068468
|
C | CTATA | 10 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(7): Show | 10 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.2266-93_2266-92ins others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | INFO_REALIGN_3_PRIME | chrX | 124068468 | |||||
| chrX:124068506
|
A | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2266-58A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 23/34 | chrX | 124068506 | ||||||
| chrX:124068920
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2358+264G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124068920 | ||||||
| chrX:124069137
|
C | T | 5 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0199others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2358+481C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124069137 | ||||||
| chrX:124069182
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2358+526C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124069182 | ||||||
| chrX:124069222
|
C | CATGTTCA others(23): Show |
1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2358+569_2358+598d others(32): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chrX | 124069222 | |||||
| chrX:124069292
|
TG | T | 1 | a0001c0001t0001g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2358+639delG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chrX | 124069292 | |||||
| chrX:124069398
|
G | GT | 1 | a0001c0001t0001g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2358+748dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chrX | 124069398 | |||||
| chrX:124069617
|
C | CT | 1 | a0001c0001t0001g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2358+968dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chrX | 124069617 | |||||
| chrX:124069833
|
CA | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0153 | 2 | NA18948.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2358+1178delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124069833 | ||||||
| chrX:124070119
|
TC | T | 1 | a0001c0001t0001g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2359-1027delC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chrX | 124070119 | |||||
| chrX:124070332
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2359-817C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070332 | ||||||
| chrX:124070564
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2359-585A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070564 | ||||||
| chrX:124070588
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2359-561G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070588 | ||||||
| chrX:124070636
|
G | T | 68 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0054others(65): Show | 68 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2359-513G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070636 | ||||||
| chrX:124070799
|
A | G | 1 | a0001c0001t0010g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2359-350A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070799 | ||||||
| chrX:124070820
|
G | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2359-329G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070820 | ||||||
| chrX:124070898
|
A | T | 1 | a0001c0001t0002g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2359-251A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070898 | ||||||
| chrX:124070921
|
T | TA | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2359-227dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chrX | 124070921 | |||||
| chrX:124070983
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2359-166C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124070983 | ||||||
| chrX:124071086
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2359-63G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | chrX | 124071086 | ||||||
| chrX:124071128
|
CT | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0002g0041others(1): Show | 4 | HG01257.hp2 HG01943.hp1 HG02976.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2359-7delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 24/34 | INFO_REALIGN_3_PRIME | chrX | 124071128 | |||||
| chrX:124071540
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2533+217A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124071540 | ||||||
| chrX:124071628
|
T | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2533+305T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124071628 | ||||||
| chrX:124071745
|
C | T | 4 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0002g0040others(1): Show | 4 | HG00609.hp1 HG02080.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.2533+422C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124071745 | ||||||
| chrX:124071940
|
A | G | 84 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(81): Show | 84 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2533+617A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124071940 | ||||||
| chrX:124072024
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2533+701A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072024 | ||||||
| chrX:124072076
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0235 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2533+753T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072076 | ||||||
| chrX:124072256
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2533+933C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072256 | ||||||
| chrX:124072257
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2533+934G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072257 | ||||||
| chrX:124072393
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2533+1070A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072393 | ||||||
| chrX:124072450
|
C | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0035 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2533+1127C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072450 | ||||||
| chrX:124072501
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2533+1178T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072501 | ||||||
| chrX:124072682
|
G | GC | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2533+1359_2533+136 others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072682 | ||||||
| chrX:124072683
|
T | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.2533+1360T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072683 | ||||||
| chrX:124072691
|
G | GT | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2533+1370dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072691 | |||||
| chrX:124072691
|
G | GTTGT | 73 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(70): Show | 73 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2533+1391_2533+139 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072691 | |||||
| chrX:124072691
|
GTTGTTTG others(1): Show |
G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2533+1387_2533+139 others(12): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072691 | |||||
| chrX:124072873
|
CT | C | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2533+1560delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072873 | |||||
| chrX:124072880
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG00597.hp2 HG02135.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2533+1557T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072880 | ||||||
| chrX:124072880
|
TTTTC | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG02027.hp1 NA18950.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2533+1581_2533+158 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072880 | |||||
| chrX:124072901
|
TTTC | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0256 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2533+1581_2533+158 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072901 | |||||
| chrX:124072904
|
C | CT | 12 | a0001c0001t0001g0056a0001c0001t0001g0079a0001c0001t0001g0113others(9): Show | 12 | HG01123.hp1 HG01175.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.2533+1601dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072904 | |||||
| chrX:124072904
|
C | CTTT | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2533+1599_2533+160 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072904 | |||||
| chrX:124072904
|
CT | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0065others(20): Show | 23 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2533+1601delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072904 | |||||
| chrX:124072904
|
CTT | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2533+1600_2533+160 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072904 | |||||
| chrX:124072905
|
T | TTTC | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2533+1584_2533+158 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072905 | |||||
| chrX:124072905
|
T | TTTCTTTC | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2533+1584_2533+158 others(11): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072905 | |||||
| chrX:124072906
|
T | TTC | 3 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0002g0029 | 3 | HG03209.hp1 HG03669.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2533+1584_2533+158 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124072906 | |||||
| chrX:124072907
|
T | TC | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2533+1584_2533+158 others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072907 | ||||||
| chrX:124072960
|
G | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0140 | 3 | HG01074.hp1 HG01256.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2533+1637G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072960 | ||||||
| chrX:124072975
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2533+1652C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124072975 | ||||||
| chrX:124073031
|
CA | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG02027.hp1 NA18950.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2533+1709delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073031 | ||||||
| chrX:124073040
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2533+1717C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073040 | ||||||
| chrX:124073148
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2533+1825C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073148 | ||||||
| chrX:124073154
|
A | T | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 263 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.2533+1831A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073154 | ||||||
| chrX:124073192
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2533+1869A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073192 | ||||||
| chrX:124073378
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2533+2055G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073378 | ||||||
| chrX:124073437
|
T | TG | 1 | a0001c0001t0001g0238 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2533+2115dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124073437 | |||||
| chrX:124073566
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2533+2243C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073566 | ||||||
| chrX:124073611
|
C | G | 1 | a0001c0001t0002g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2533+2288C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073611 | ||||||
| chrX:124073693
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0140 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2533+2370G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073693 | ||||||
| chrX:124073982
|
T | C | 3 | a0001c0001t0003g0106a0001c0001t0003g0208a0001c0001t0003g0244 | 3 | HG02055.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2534-2350T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124073982 | ||||||
| chrX:124074069
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2534-2263A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124074069 | ||||||
| chrX:124074105
|
G | C | 1 | a0001c0001t0001g0212 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2534-2227G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124074105 | ||||||
| chrX:124074393
|
C | CA | 1 | a0001c0001t0001g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2534-1936dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124074393 | |||||
| chrX:124074581
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2534-1751A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124074581 | ||||||
| chrX:124074714
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2534-1618T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124074714 | ||||||
| chrX:124074832
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2534-1500T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124074832 | ||||||
| chrX:124074880
|
G | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2534-1452G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124074880 | ||||||
| chrX:124074900
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2534-1432A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124074900 | ||||||
| chrX:124075368
|
G | A | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2534-964G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124075368 | ||||||
| chrX:124075396
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2534-936C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124075396 | ||||||
| chrX:124075591
|
T | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0068others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2534-741T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | chrX | 124075591 | ||||||
| chrX:124075656
|
C | CT | 1 | a0001c0001t0001g0004 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2534-666dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124075656 | |||||
| chrX:124075656
|
CT | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2534-666delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 25/34 | INFO_REALIGN_3_PRIME | chrX | 124075656 | |||||
| chrX:124076795
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2673+324A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 26/34 | chrX | 124076795 | ||||||
| chrX:124077168
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2673+697C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 26/34 | chrX | 124077168 | ||||||
| chrX:124077250
|
G | GT | 13 | a0001c0001t0001g0012a0001c0001t0001g0055a0001c0001t0001g0095others(10): Show | 13 | HG01496.hp2 HG01928.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2674-694dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chrX | 124077250 | |||||
| chrX:124077250
|
GT | G | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2674-694delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 26/34 | INFO_REALIGN_3_PRIME | chrX | 124077250 | |||||
| chrX:124077517
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0235 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2674-440A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 26/34 | chrX | 124077517 | ||||||
| chrX:124077822
|
T | A | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2674-135T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 26/34 | chrX | 124077822 | ||||||
| chrX:124078349
|
CTT | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2775+294_2775+295d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chrX | 124078349 | |||||
| chrX:124078577
|
G | A | 192 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(189): Show | 192 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.2775+519G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124078577 | ||||||
| chrX:124078798
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2775+740G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124078798 | ||||||
| chrX:124078851
|
C | T | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2775+793C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124078851 | ||||||
| chrX:124078876
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2775+818C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124078876 | ||||||
| chrX:124079133
|
C | CT | 3 | a0001c0001t0001g0224a0001c0001t0002g0045a0001c0001t0002g0198 | 3 | NA18974.hp1 NA19006.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2775+1087dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chrX | 124079133 | |||||
| chrX:124079141
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2775+1083T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124079141 | ||||||
| chrX:124079379
|
T | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2775+1321T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124079379 | ||||||
| chrX:124079432
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2775+1374C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124079432 | ||||||
| chrX:124079777
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2776-1603C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124079777 | ||||||
| chrX:124079933
|
CT | C | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2776-1435delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chrX | 124079933 | |||||
| chrX:124080105
|
ATACT | A | 1 | a0001c0001t0002g0020 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2776-1269_2776-126 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chrX | 124080105 | |||||
| chrX:124080206
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2776-1174T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124080206 | ||||||
| chrX:124080391
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2776-989T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124080391 | ||||||
| chrX:124080603
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2776-777G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124080603 | ||||||
| chrX:124080741
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2776-639A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124080741 | ||||||
| chrX:124080865
|
G | GT | 2 | a0001c0001t0002g0030a0001c0001t0002g0035 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2776-508dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chrX | 124080865 | |||||
| chrX:124081061
|
G | A | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0058 | 3 | HG01346.hp1 HG02273.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2776-319G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124081061 | ||||||
| chrX:124081097
|
T | TC | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 193 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.2776-279dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | INFO_REALIGN_3_PRIME | chrX | 124081097 | |||||
| chrX:124081097
|
T | TTC | 1 | a0001c0001t0001g0273 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2776-283_2776-282i others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 27/34 | chrX | 124081097 | ||||||
| chrX:124081689
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2924+161A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | chrX | 124081689 | ||||||
| chrX:124081721
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2924+193C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | chrX | 124081721 | ||||||
| chrX:124082147
|
CAGAT | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2924+623_2924+626d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chrX | 124082147 | |||||
| chrX:124082267
|
A | G | 1 | a0001c0001t0003g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2924+739A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | chrX | 124082267 | ||||||
| chrX:124082474
|
G | C | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2924+946G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | chrX | 124082474 | ||||||
| chrX:124082983
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2925-438G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | chrX | 124082983 | ||||||
| chrX:124083017
|
G | A | 59 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2925-404G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | chrX | 124083017 | ||||||
| chrX:124083206
|
T | TTG | 113 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 113 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.2925-199_2925-198d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | INFO_REALIGN_3_PRIME | chrX | 124083206 | |||||
| chrX:124083238
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2925-183A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 28/34 | chrX | 124083238 | ||||||
| chrX:124083560
|
G | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3053+11G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124083560 | ||||||
| chrX:124083677
|
A | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3053+128A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124083677 | ||||||
| chrX:124083928
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3053+379G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124083928 | ||||||
| chrX:124084021
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3053+472C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084021 | ||||||
| chrX:124084149
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3053+600C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084149 | ||||||
| chrX:124084279
|
C | T | 5 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049others(2): Show | 5 | NA18975.hp2 NA18979.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.3053+730C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084279 | ||||||
| chrX:124084320
|
G | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3053+771G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084320 | ||||||
| chrX:124084338
|
C | CT | 1 | a0001c0001t0001g0239 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3053+802dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124084338 | |||||
| chrX:124084338
|
CT | C | 1 | a0001c0001t0001g0135 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3053+802delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124084338 | |||||
| chrX:124084354
|
A | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3053+805A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084354 | ||||||
| chrX:124084393
|
ACTGCAAA others(2): Show |
A | 42 | a0001c0001t0001g0043a0001c0001t0002g0011a0001c0001t0002g0018others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.3053+849_3053+857d others(11): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124084393 | |||||
| chrX:124084544
|
G | C | 262 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 262 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(259): Show |
intron_variant | MODIFIER | c.3053+995G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084544 | ||||||
| chrX:124084565
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3053+1016A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084565 | ||||||
| chrX:124084669
|
T | G | 83 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(80): Show | 83 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.3053+1120T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084669 | ||||||
| chrX:124084884
|
T | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3053+1335T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084884 | ||||||
| chrX:124084958
|
A | G | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3053+1409A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124084958 | ||||||
| chrX:124085064
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG00642.hp1 HG01192.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3054-1483A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085064 | ||||||
| chrX:124085183
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3054-1364A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085183 | ||||||
| chrX:124085387
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0182 | 2 | HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.3054-1160G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085387 | ||||||
| chrX:124085556
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0181a0001c0001t0001g0261 | 3 | HG02074.hp1 NA18612.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.3054-991A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085556 | ||||||
| chrX:124085572
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3054-975C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085572 | ||||||
| chrX:124085593
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3054-954G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085593 | ||||||
| chrX:124085641
|
A | G | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 263 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.3054-906A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085641 | ||||||
| chrX:124085655
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0265others(1): Show | 4 | HG02071.hp1 NA18991.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.3054-892A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085655 | ||||||
| chrX:124085676
|
G | A | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3054-871G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085676 | ||||||
| chrX:124085773
|
C | CA | 2 | a0001c0001t0001g0068a0001c0001t0001g0190 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3054-751dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124085773 | |||||
| chrX:124085773
|
C | CAA | 1 | a0001c0002t0001g0069 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3054-752_3054-751d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124085773 | |||||
| chrX:124085773
|
CA | C | 104 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0074others(101): Show | 104 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.3054-751delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124085773 | |||||
| chrX:124085773
|
CAA | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0012others(140): Show | 143 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.3054-752_3054-751d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124085773 | |||||
| chrX:124085773
|
CAAA | C | 2 | a0001c0001t0001g0087a0001c0001t0009g0139 | 2 | HG01069.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.3054-753_3054-751d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124085773 | |||||
| chrX:124085834
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0105others(57): Show | 60 | HG00438.hp2 HG00621.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.3054-713T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124085834 | ||||||
| chrX:124086135
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0177 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3054-412A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124086135 | ||||||
| chrX:124086154
|
A | AG | 2 | a0001c0001t0004g0174a0001c0001t0004g0175 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3054-391dupG | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124086154 | |||||
| chrX:124086156
|
G | GA | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 259 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.3054-381dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124086156 | |||||
| chrX:124086281
|
C | CT | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3054-260dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | INFO_REALIGN_3_PRIME | chrX | 124086281 | |||||
| chrX:124086533
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3054-14G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 29/34 | chrX | 124086533 | ||||||
| chrX:124087247
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0068others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3277+477A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124087247 | ||||||
| chrX:124087600
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3277+830C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124087600 | ||||||
| chrX:124087658
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3277+888G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124087658 | ||||||
| chrX:124088054
|
TA | T | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3277+1289delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088054 | |||||
| chrX:124088148
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3277+1378T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124088148 | ||||||
| chrX:124088170
|
ATC | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3277+1412_3277+141 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088170 | |||||
| chrX:124088182
|
C | CT | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3277+1421dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088182 | |||||
| chrX:124088240
|
C | CT | 1 | a0001c0001t0010g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3277+1480dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088240 | |||||
| chrX:124088417
|
T | C | 46 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 46 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.3277+1647T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124088417 | ||||||
| chrX:124088424
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3277+1654A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124088424 | ||||||
| chrX:124088614
|
T | TC | 2 | a0001c0001t0001g0043a0001c0001t0002g0049 | 2 | NA19082.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.3277+1845dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088614 | |||||
| chrX:124088615
|
C | CT | 103 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(100): Show | 103 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.3277+1863dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088615 | |||||
| chrX:124088615
|
C | CTT | 4 | a0001c0001t0001g0100a0001c0001t0001g0152a0001c0001t0001g0190others(1): Show | 4 | HG02148.hp1 HG02257.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.3277+1862_3277+186 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088615 | |||||
| chrX:124088615
|
CT | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0183others(66): Show | 69 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.3277+1863delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088615 | |||||
| chrX:124088615
|
CTT | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0191 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3277+1862_3277+186 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088615 | |||||
| chrX:124088616
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 45 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.3277+1846T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124088616 | ||||||
| chrX:124088617
|
T | C | 1 | a0001c0001t0006g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3277+1847T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124088617 | ||||||
| chrX:124088741
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3278-1834A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124088741 | ||||||
| chrX:124088913
|
C | CT | 256 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 256 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.3278-1647dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088913 | |||||
| chrX:124088913
|
C | CTT | 4 | a0001c0001t0001g0092a0001c0001t0002g0028a0001c0001t0002g0198others(1): Show | 4 | HG02273.hp1 HG02738.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3278-1648_3278-164 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088913 | |||||
| chrX:124088913
|
CT | C | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3278-1647delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088913 | |||||
| chrX:124088920
|
T | TTTTTTTT others(3): Show |
1 | a0001c0001t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3278-1647_3278-164 others(14): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124088920 | |||||
| chrX:124089154
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3278-1421C>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124089154 | ||||||
| chrX:124089435
|
T | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 105 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.3278-1140T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124089435 | ||||||
| chrX:124089475
|
A | G | 4 | a0001c0001t0002g0023a0001c0001t0002g0026a0001c0001t0002g0028others(1): Show | 4 | HG00140.hp1 HG00735.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.3278-1100A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124089475 | ||||||
| chrX:124089486
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3278-1089G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124089486 | ||||||
| chrX:124089729
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3278-846T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124089729 | ||||||
| chrX:124089782
|
A | G | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0052others(67): Show | 70 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.3278-793A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124089782 | ||||||
| chrX:124090114
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3278-461T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124090114 | ||||||
| chrX:124090160
|
C | CA | 45 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0065others(42): Show | 45 | HG00597.hp2 HG01175.hp2 HG01358.hp1 others(42): Show |
intron_variant | MODIFIER | c.3278-389dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
C | CAA | 6 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG01928.hp1 HG02280.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.3278-390_3278-389d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
C | CAAA | 8 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.3278-391_3278-389d others(5): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
C | CAAAA | 82 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0054others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.3278-392_3278-389d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
C | CAAAAA | 30 | a0001c0001t0001g0056a0001c0001t0001g0100a0001c0001t0001g0107others(27): Show | 30 | HG01099.hp1 HG01175.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.3278-393_3278-389d others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
C | CAAAAAA | 3 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0002g0193 | 3 | HG03017.hp1 NA18950.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.3278-394_3278-389d others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
CA | C | 14 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0071others(11): Show | 14 | HG01993.hp1 HG02056.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.3278-389delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
CAA | C | 35 | a0001c0001t0002g0011a0001c0001t0002g0020a0001c0001t0002g0021others(32): Show | 35 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.3278-390_3278-389d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
CAAAAAAA others(2): Show |
C | 1 | a0001c0001t0001g0096 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3278-397_3278-389d others(11): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090160
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3278-399_3278-389d others(13): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chrX | 124090160 | |||||
| chrX:124090187
|
G | T | 37 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0082others(34): Show | 37 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.3278-388G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 30/34 | chrX | 124090187 | ||||||
| chrX:124091609
|
C | CA | 2 | a0001c0001t0001g0080a0001c0001t0001g0093 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3578+646dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chrX | 124091609 | |||||
| chrX:124092175
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3578+1211T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124092175 | ||||||
| chrX:124092415
|
G | A | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.3578+1451G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124092415 | ||||||
| chrX:124092555
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3579-1463C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124092555 | ||||||
| chrX:124092640
|
A | G | 47 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(44): Show | 47 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.3579-1378A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124092640 | ||||||
| chrX:124092668
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3579-1350C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124092668 | ||||||
| chrX:124092794
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3579-1224T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124092794 | ||||||
| chrX:124092984
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0077a0001c0001t0001g0081others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3579-1034G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124092984 | ||||||
| chrX:124093017
|
T | C | 1 | a0001c0001t0004g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3579-1001T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124093017 | ||||||
| chrX:124093225
|
T | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0105others(57): Show | 60 | HG00438.hp2 HG00621.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.3579-793T>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124093225 | ||||||
| chrX:124093472
|
C | CT | 5 | a0001c0001t0001g0093a0001c0001t0001g0135a0001c0001t0001g0203others(2): Show | 5 | HG01192.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3579-526dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chrX | 124093472 | |||||
| chrX:124093472
|
CT | C | 63 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(60): Show | 63 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.3579-526delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chrX | 124093472 | |||||
| chrX:124093472
|
CTT | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0036a0001c0001t0002g0041 | 3 | HG01257.hp2 HG01517.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3579-527_3579-526d others(4): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | INFO_REALIGN_3_PRIME | chrX | 124093472 | |||||
| chrX:124093525
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3579-493G>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124093525 | ||||||
| chrX:124093598
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3579-420A>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124093598 | ||||||
| chrX:124093745
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3579-273A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124093745 | ||||||
| chrX:124093754
|
T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.3579-264T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 32/34 | chrX | 124093754 | ||||||
| chrX:124094198
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3705+54A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | chrX | 124094198 | ||||||
| chrX:124094442
|
TTTTA | T | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3705+303_3705+306d others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chrX | 124094442 | |||||
| chrX:124094678
|
C | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3705+534C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | chrX | 124094678 | ||||||
| chrX:124094731
|
C | G | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.3705+587C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | chrX | 124094731 | ||||||
| chrX:124094806
|
T | C | 1 | a0001c0001t0007g0141 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3706-566T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | chrX | 124094806 | ||||||
| chrX:124094903
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3706-469C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | chrX | 124094903 | ||||||
| chrX:124094935
|
G | GT | 52 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(49): Show | 52 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3706-427dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | INFO_REALIGN_3_PRIME | chrX | 124094935 | |||||
| chrX:124095174
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3706-198G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | chrX | 124095174 | ||||||
| chrX:124095216
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3706-156C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 33/34 | chrX | 124095216 | ||||||
| chrX:124095545
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0162 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3783+96T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124095545 | ||||||
| chrX:124095943
|
G | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3783+494G>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124095943 | ||||||
| chrX:124096018
|
C | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG01361.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3783+569C>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124096018 | ||||||
| chrX:124096092
|
G | A | 254 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 254 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.3783+643G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124096092 | ||||||
| chrX:124096176
|
AT | A | 50 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.3783+734delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124096176 | |||||
| chrX:124096183
|
T | TC | 10 | a0001c0001t0001g0013a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3783+741dupC | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124096183 | |||||
| chrX:124096227
|
A | C | 1 | a0001c0001t0001g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3783+778A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124096227 | ||||||
| chrX:124096475
|
A | AT | 2 | a0001c0001t0001g0147a0001c0001t0001g0162 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3783+1035dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124096475 | |||||
| chrX:124096500
|
T | C | 1 | a0001c0001t0002g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3783+1051T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124096500 | ||||||
| chrX:124096900
|
C | T | 3 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0269 | 3 | HG02280.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3783+1451C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124096900 | ||||||
| chrX:124097057
|
C | T | 46 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 46 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.3783+1608C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124097057 | ||||||
| chrX:124097144
|
A | C | 3 | a0001c0001t0002g0059a0001c0001t0002g0061a0001c0001t0002g0062 | 3 | HG00280.hp1 HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.3783+1695A>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124097144 | ||||||
| chrX:124097179
|
C | CA | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(166): Show | 169 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.3783+1755dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124097179 | |||||
| chrX:124097179
|
C | CAA | 75 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0068others(72): Show | 75 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.3783+1754_3783+175 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124097179 | |||||
| chrX:124097179
|
C | CAAA | 17 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(14): Show | 17 | HG00558.hp1 HG00735.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.3783+1753_3783+175 others(7): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124097179 | |||||
| chrX:124097179
|
C | CAAAA | 1 | a0001c0001t0001g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3783+1752_3783+175 others(8): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124097179 | |||||
| chrX:124097179
|
CA | C | 1 | a0001c0001t0001g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3783+1755delA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124097179 | |||||
| chrX:124097861
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0061 | 2 | HG00280.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.3783+2412C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124097861 | ||||||
| chrX:124097903
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3783+2454G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124097903 | ||||||
| chrX:124097956
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3783+2507T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124097956 | ||||||
| chrX:124098065
|
T | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3784-2509T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124098065 | ||||||
| chrX:124098085
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3784-2489T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124098085 | ||||||
| chrX:124098342
|
G | A | 48 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.3784-2232G>A | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124098342 | ||||||
| chrX:124098354
|
CTT | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0002 | 3 | HG02723.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3784-2218_3784-221 others(6): Show |
STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124098354 | |||||
| chrX:124098392
|
A | AT | 1 | a0001c0001t0010g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3784-2176dupT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124098392 | |||||
| chrX:124098743
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3784-1826delT | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124098743 | |||||
| chrX:124099259
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3784-1315C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124099259 | ||||||
| chrX:124099307
|
T | C | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG00280.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3784-1267T>C | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124099307 | ||||||
| chrX:124099577
|
T | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 109 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.3784-997T>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124099577 | ||||||
| chrX:124100224
|
T | TA | 2 | a0001c0001t0001g0159a0001c0001t0009g0139 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.3784-349dupA | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | INFO_REALIGN_3_PRIME | chrX | 124100224 | |||||
| chrX:124100425
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3784-149A>G | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124100425 | ||||||
| chrX:124100542
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0162 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3784-32C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124100542 | ||||||
| chrX:124100555
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3784-19C>T | STAG2 | ENSG00000101972.20 | transcript | ENST00000371145.8 | protein_coding | 34/34 | chrX | 124100555 |