| geneid | 6772 |
|---|---|
| ensemblid | ENSG00000115415.21 |
| hgncid | 11362 |
| symbol | STAT1 |
| name | signal transducer and activator of transcription 1 |
| refseq_nuc | NM_007315.4 |
| refseq_prot | NP_009330.1 |
| ensembl_nuc | ENST00000361099.8 |
| ensembl_prot | ENSP00000354394.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 190969149 |
| end | 191014171 |
| strand | - |
| ver | v1.2 |
| region | chr2:190969149-191014171 |
| region5000 | chr2:190964149-191019171 |
| regionname0 | STAT1_chr2_190969149_191014171 |
| regionname5000 | STAT1_chr2_190964149_191019171 |
| 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 | 750 | 412 | 92 | 74 | 194 | 14 | 36 | 154 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0002 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0003 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| 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 | 2253 | 325 | 79 | 66 | 136 | 12 | 30 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0002 | 0/0 | 2253 | 66 | 9 | 4 | 45 | 2 | 6 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0003 | 0/0 | 2253 | 6 | 0 | 0 | 6 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0004 | 0/0 | 2253 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0005 | 0/0 | 2253 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0006 | 0/0 | 2253 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0007 | 0/0 | 2253 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0008 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0009 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0010 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0011 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| c0012 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| 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 | 1863 | 364 | 54 | 68 | 192 | 14 | 34 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0002 | 0/0 | 1863 | 19 | 18 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0003 | 0/0 | 1863 | 8 | 8 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0004 | 0/0 | 1863 | 4 | 4 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0005 | 0/0 | 1859 | 3 | 3 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0006 | 0/0 | 1863 | 3 | 2 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0007 | 0/0 | 1863 | 2 | 0 | 1 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0008 | 0/0 | 1863 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0009 | 0/0 | 1863 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0010 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0011 | 0/0 | 1863 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0012 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0013 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0014 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0015 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| t0016 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| 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 | 6 | 0 | 4 | 1 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0024 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| 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 | 2253 | 325 | 79 | 66 | 136 | 12 | 30 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0002 | 0/0 | 2253 | 66 | 9 | 4 | 45 | 2 | 6 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0003 | 0/0 | 2253 | 6 | 0 | 0 | 6 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0004 | 0/0 | 2253 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0005 | 0/0 | 2253 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0006 | 0/0 | 2253 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0007 | 0/0 | 2253 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0008 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0010 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0011 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0002c0012 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0003c0009 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4115 | 281 | 42 | 61 | 136 | 12 | 28 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0002 | 0/0 | 4115 | 18 | 17 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0003 | 0/0 | 4115 | 8 | 8 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0004 | 0/0 | 4115 | 4 | 4 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0005 | 0/0 | 4111 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0006 | 0/0 | 4115 | 3 | 2 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0008 | 0/0 | 4115 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0009 | 0/0 | 4115 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0011 | 0/0 | 4115 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0012 | 0/0 | 4115 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0013 | 0/0 | 4115 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0014 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0015 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0001t0016 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0002t0001 | 0/0 | 4115 | 62 | 8 | 3 | 43 | 2 | 6 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0002t0002 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0002t0007 | 0/0 | 4115 | 2 | 0 | 1 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0002t0010 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0003t0001 | 0/0 | 4115 | 6 | 0 | 0 | 6 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0004t0001 | 0/0 | 4115 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0005t0001 | 0/0 | 4115 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0006t0001 | 0/0 | 4115 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0007t0005 | 0/0 | 4111 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0008t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0010t0001 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0001c0011t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0002c0012t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| a0003c0009t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | copy fasta | chr2 | 190964149 | 191019171 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 4 | 1 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0009g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0013g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0014g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0015g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0016g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0007g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0010g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0004t0001g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0005t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0006t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0007t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0007t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0008t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0010t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0011t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0002c0012t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0003c0009t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0248 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00438 | hp2 | a0001 | c0002 | t0010 | g0155 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0090 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0007 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01074 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01433 | hp2 | a0001 | c0002 | t0007 | g0153 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0091 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0199 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02135 | hp2 | a0001 | c0002 | t0007 | g0154 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02145 | hp2 | a0003 | c0009 | t0001 | g0327 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0131 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02622 | hp2 | a0001 | c0007 | t0005 | g0145 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0258 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0326 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0325 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02922 | hp2 | a0001 | c0008 | t0001 | g0265 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02970 | hp1 | a0001 | c0001 | t0016 | g0335 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02976 | hp1 | a0002 | c0012 | t0001 | g0142 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02976 | hp2 | a0001 | c0011 | t0001 | g0271 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0070 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0334 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03491 | hp2 | a0001 | c0001 | t0012 | g0156 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0319 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0230 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04115 | hp2 | a0001 | c0001 | t0013 | g0185 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0250 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18962 | hp1 | a0001 | c0010 | t0001 | g0170 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18968 | hp2 | a0001 | c0005 | t0001 | g0014 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0282 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18987 | hp2 | a0001 | c0006 | t0001 | g0283 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19055 | hp2 | a0001 | c0005 | t0001 | g0014 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19057 | hp1 | a0001 | c0006 | t0001 | g0280 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ASW | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ASW | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0254 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | GIH | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | GIH | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02109 | hp1 | a0001 | c0007 | t0005 | g0144 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0323 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18955 | hp2 | a0001 | c0005 | t0001 | g0014 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0301 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190983739
|
G | A | 1 | a0002 | 1 | HG02976.hp1 | missense_variant&splice_region_variant | MODERATE | c.1349C>T | p.Thr450Met | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/25 | 1658/4116 | 1349/2253 | 450/750 | chr2 | 190983739 | ||
| chr2:191001125
|
G | T | 1 | a0003 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.411C>A | p.Asp137Glu | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/25 | 720/4116 | 411/2253 | 137/750 | chr2 | 191001125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190974932
|
A | C | 2 | a0001c0008a0001c0011 | 2 | HG02922.hp2 HG02976.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2136T>G | p.Val712Val | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/25 | 2445/4116 | 2136/2253 | 712/750 | chr2 | 190974932 | ||
| chr2:190976880
|
T | C | 1 | a0001c0007 | 2 | HG02109.hp1 HG02622.hp2 |
synonymous_variant | LOW | c.2019A>G | p.Lys673Lys | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/25 | 2328/4116 | 2019/2253 | 673/750 | chr2 | 190976880 | ||
| chr2:190987050
|
A | G | 1 | a0001c0006 | 3 | NA18979.hp1 NA18987.hp2 NA19057.hp1 |
synonymous_variant | LOW | c.1116T>C | p.Asn372Asn | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 13/25 | 1425/4116 | 1116/2253 | 372/750 | chr2 | 190987050 | ||
| chr2:190991275
|
C | T | 1 | a0001c0004 | 4 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
synonymous_variant | LOW | c.990G>A | p.Gln330Gln | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/25 | 1299/4116 | 990/2253 | 330/750 | chr2 | 190991275 | ||
| chr2:190995204
|
C | T | 1 | a0001c0005 | 3 | NA18955.hp2 NA18968.hp2 NA19055.hp2 |
synonymous_variant | LOW | c.801G>A | p.Ala267Ala | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/25 | 1110/4116 | 801/2253 | 267/750 | chr2 | 190995204 | ||
| chr2:191001110
|
A | G | 1 | a0001c0010 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.426T>C | p.Leu142Leu | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/25 | 735/4116 | 426/2253 | 142/750 | chr2 | 191001110 | ||
| chr2:191007581
|
G | A | 1 | a0001c0003 | 6 | HG02027.hp2 HG02080.hp1 NA18949.hp2 others(3): Show |
synonymous_variant | LOW | c.354C>T | p.Asn118Asn | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/25 | 663/4116 | 354/2253 | 118/750 | chr2 | 191007581 | ||
| chr2:191009941
|
A | G | 3 | a0001c0002a0001c0004a0001c0008 | 71 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(68): Show |
synonymous_variant | LOW | c.63T>C | p.Leu21Leu | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/25 | 372/4116 | 63/2253 | 21/750 | chr2 | 191009941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190969176
|
CTTCT | C | 2 | a0001c0001t0005a0001c0007t0005 | 3 | HG02109.hp1 HG02622.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1523_*1526delAGAA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1523 | chr2 | 190969176 | |||||
| chr2:190969286
|
A | G | 1 | a0001c0001t0013 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1417T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1417 | chr2 | 190969286 | |||||
| chr2:190969298
|
A | G | 1 | a0001c0001t0012 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1405 | chr2 | 190969298 | |||||
| chr2:190969304
|
T | C | 2 | a0001c0001t0002a0001c0002t0002 | 19 | HG01261.hp2 HG02109.hp2 HG02486.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1399A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1399 | chr2 | 190969304 | |||||
| chr2:190969750
|
C | A | 1 | a0001c0001t0008 | 2 | HG02258.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*953G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 953 | chr2 | 190969750 | |||||
| chr2:190969754
|
C | T | 1 | a0001c0001t0011 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 949 | chr2 | 190969754 | |||||
| chr2:190969761
|
T | C | 1 | a0001c0001t0003 | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*942A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 942 | chr2 | 190969761 | |||||
| chr2:190969926
|
T | C | 1 | a0001c0001t0004 | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*777A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 777 | chr2 | 190969926 | |||||
| chr2:190970168
|
G | A | 1 | a0001c0001t0006 | 3 | HG00642.hp2 HG02723.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 535 | chr2 | 190970168 | |||||
| chr2:190970601
|
T | C | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 102 | chr2 | 190970601 | |||||
| chr2:191013555
|
G | A | 1 | a0001c0002t0010 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/25 | 3552 | chr2 | 191013555 | |||||
| chr2:191013663
|
C | G | 2 | a0001c0002t0007a0001c0002t0010 | 3 | HG00438.hp2 HG01433.hp2 HG02135.hp2 |
5_prime_UTR_variant | MODIFIER | c.-140G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/25 | 3660 | chr2 | 191013663 | |||||
| chr2:191014024
|
C | A | 1 | a0001c0001t0015 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4021 | chr2 | 191014024 | |||||
| chr2:191014083
|
G | C | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-221C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4080 | chr2 | 191014083 | |||||
| chr2:191014146
|
G | A | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-284C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4143 | chr2 | 191014146 | |||||
| chr2:191014149
|
G | C | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4146 | chr2 | 191014149 | |||||
| chr2:191014160
|
G | A | 1 | a0001c0001t0009 | 2 | HG00741.hp1 HG01074.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-298C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | chr2 | 191014160 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190970847
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2239-130C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970847 | ||||||
| chr2:190970870
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.2239-153A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970870 | ||||||
| chr2:190970919
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2239-202G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970919 | ||||||
| chr2:190970923
|
C | T | 1 | a0001c0001t0002g0308 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2239-206G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970923 | ||||||
| chr2:190971192
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(267): Show | 337 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(334): Show |
intron_variant | MODIFIER | c.2239-475A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971192 | ||||||
| chr2:190971286
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0331a0001c0001t0001g0332others(1): Show | 4 | HG01192.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2239-569G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971286 | ||||||
| chr2:190971334
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2239-617T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971334 | ||||||
| chr2:190971341
|
A | G | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2239-624T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971341 | ||||||
| chr2:190971353
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2239-636G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971353 | ||||||
| chr2:190971440
|
G | C | 3 | a0001c0001t0008g0070a0001c0001t0008g0131a0001c0008t0001g0265 | 3 | HG02258.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2239-723C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971440 | ||||||
| chr2:190971460
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2239-743C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971460 | ||||||
| chr2:190971599
|
A | G | 1 | a0001c0001t0001g0048 | 2 | NA19060.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2239-882T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971599 | ||||||
| chr2:190971656
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2239-939A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971656 | ||||||
| chr2:190971702
|
CTT | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(7): Show | 10 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2239-987_2239-986d others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971702 | ||||||
| chr2:190971704
|
T | TTC | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(273): Show | 345 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(342): Show |
intron_variant | MODIFIER | c.2239-988_2239-987i others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971704 | ||||||
| chr2:190971797
|
C | G | 14 | a0001c0001t0002g0039a0001c0001t0002g0122a0001c0001t0002g0126others(11): Show | 15 | HG02109.hp2 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2239-1080G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971797 | ||||||
| chr2:190971822
|
C | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0218a0001c0002t0001g0236others(3): Show | 7 | NA18947.hp2 NA18961.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.2239-1105G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971822 | ||||||
| chr2:190971827
|
C | T | 194 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 243 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.2239-1110G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971827 | ||||||
| chr2:190971835
|
C | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0218a0001c0002t0001g0236others(3): Show | 7 | NA18947.hp2 NA18961.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.2239-1118G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971835 | ||||||
| chr2:190971836
|
C | G | 178 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 224 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.2239-1119G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971836 | ||||||
| chr2:190971851
|
T | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0152a0001c0001t0016g0335 | 3 | HG01884.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2239-1134A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971851 | ||||||
| chr2:190971858
|
A | G | 1 | a0001c0008t0001g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2239-1141T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971858 | ||||||
| chr2:190971945
|
G | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(253): Show | 320 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.2239-1228C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971945 | ||||||
| chr2:190971964
|
C | T | 81 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 109 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.2239-1247G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971964 | ||||||
| chr2:190971965
|
G | A | 1 | a0001c0008t0001g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2239-1248C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971965 | ||||||
| chr2:190972008
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0143a0001c0001t0002g0320 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2239-1291G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972008 | ||||||
| chr2:190972045
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(154): Show | 191 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.2239-1328A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972045 | ||||||
| chr2:190972130
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2239-1413G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972130 | ||||||
| chr2:190972302
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2239-1585A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972302 | ||||||
| chr2:190972480
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2239-1763G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972480 | ||||||
| chr2:190972487
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0333 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2239-1770G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972487 | ||||||
| chr2:190972721
|
T | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0331a0001c0001t0001g0332others(4): Show | 7 | HG00642.hp2 HG01192.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2239-2004A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972721 | ||||||
| chr2:190972733
|
C | CT | 11 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0160others(8): Show | 11 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.2239-2017dupA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972733 | ||||||
| chr2:190972733
|
CT | C | 7 | a0001c0001t0001g0120a0001c0001t0001g0184a0001c0001t0001g0203others(4): Show | 7 | HG01070.hp2 HG01255.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2239-2017delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972733 | ||||||
| chr2:190972808
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2238+2022C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972808 | ||||||
| chr2:190972816
|
G | GGT | 101 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(98): Show | 128 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.2238+2012_2238+201 others(6): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
G | GGTGT | 33 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0042others(30): Show | 38 | HG00597.hp2 HG01099.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.2238+2010_2238+201 others(8): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
G | GGTGTGT | 6 | a0001c0001t0001g0051a0001c0001t0001g0207a0001c0001t0001g0212others(3): Show | 6 | HG03927.hp1 HG04204.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2238+2008_2238+201 others(10): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0138a0001c0001t0001g0152a0001c0001t0001g0157others(3): Show | 6 | HG00597.hp1 HG01884.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2238+2006_2238+201 others(12): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
G | GGTGTGTG others(3): Show |
2 | a0001c0001t0001g0314a0001c0001t0012g0156 | 2 | HG03491.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2238+2004_2238+201 others(14): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
G | GT | 3 | a0001c0001t0001g0137a0001c0001t0001g0161a0001c0001t0001g0186 | 3 | HG03927.hp2 HG04115.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2238+2013_2238+201 others(5): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
GGT | G | 29 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 35 | HG00642.hp2 HG01069.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.2238+2012_2238+201 others(6): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
GGTGT | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0059a0001c0001t0001g0140others(15): Show | 21 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2238+2010_2238+201 others(8): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
GGTGTGT | G | 4 | a0001c0001t0002g0125a0001c0001t0002g0143a0001c0001t0002g0320others(1): Show | 4 | HG02622.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2238+2008_2238+201 others(10): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0158a0001c0001t0001g0333 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2238+2004_2238+201 others(14): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972816
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2238+2002_2238+201 others(16): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | ||||||
| chr2:190972855
|
A | G | 1 | a0001c0001t0003g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2238+1975T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972855 | ||||||
| chr2:190972859
|
G | T | 39 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0059others(36): Show | 41 | HG00597.hp1 HG00735.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.2238+1971C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972859 | ||||||
| chr2:190972908
|
C | T | 53 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0059others(50): Show | 59 | HG00597.hp1 HG00735.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.2238+1922G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972908 | ||||||
| chr2:190972936
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0137 | 3 | HG03490.hp2 HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2238+1894G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972936 | ||||||
| chr2:190972949
|
T | C | 1 | a0001c0001t0004g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2238+1881A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972949 | ||||||
| chr2:190973115
|
T | C | 142 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 177 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(174): Show |
intron_variant | MODIFIER | c.2238+1715A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973115 | ||||||
| chr2:190973249
|
A | G | 13 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(10): Show | 17 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2238+1581T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973249 | ||||||
| chr2:190973303
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2238+1527G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973303 | ||||||
| chr2:190973372
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2238+1458C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973372 | ||||||
| chr2:190973458
|
T | C | 1 | a0001c0002t0001g0032 | 2 | NA18959.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.2238+1372A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973458 | ||||||
| chr2:190973478
|
C | T | 83 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 112 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.2238+1352G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973478 | ||||||
| chr2:190973616
|
T | C | 5 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0002g0126others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2238+1214A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973616 | ||||||
| chr2:190973624
|
C | T | 10 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0160others(7): Show | 10 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2238+1206G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973624 | ||||||
| chr2:190973788
|
G | A | 142 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 177 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(174): Show |
intron_variant | MODIFIER | c.2238+1042C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973788 | ||||||
| chr2:190973818
|
G | A | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2238+1012C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973818 | ||||||
| chr2:190973899
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2238+931C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973899 | ||||||
| chr2:190973933
|
C | T | 12 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0072others(9): Show | 16 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2238+897G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973933 | ||||||
| chr2:190973984
|
A | G | 2 | a0001c0001t0008g0070a0001c0001t0008g0131 | 2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2238+846T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973984 | ||||||
| chr2:190974041
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2238+789A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974041 | ||||||
| chr2:190974062
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2238+768T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974062 | ||||||
| chr2:190974210
|
AG | A | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(329): Show | 410 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(407): Show |
intron_variant | MODIFIER | c.2238+619delC | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974210 | ||||||
| chr2:190974252
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0333 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2238+578A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974252 | ||||||
| chr2:190974272
|
A | G | 14 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0080others(11): Show | 16 | HG01257.hp1 HG02083.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.2238+558T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974272 | ||||||
| chr2:190974311
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2238+519C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974311 | ||||||
| chr2:190974446
|
C | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 55 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2238+384G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974446 | ||||||
| chr2:190974733
|
C | A | 10 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0160others(7): Show | 10 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2238+97G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974733 | ||||||
| chr2:190974738
|
G | A | 14 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0064others(11): Show | 14 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2238+92C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974738 | ||||||
| chr2:190974813
|
C | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0333 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2238+17G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974813 | ||||||
| chr2:190975100
|
G | C | 1 | a0001c0002t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2136-168C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975100 | ||||||
| chr2:190975151
|
A | C | 2 | a0001c0001t0001g0124a0001c0002t0001g0264 | 2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2136-219T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975151 | ||||||
| chr2:190975164
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2136-232A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975164 | ||||||
| chr2:190975250
|
C | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 77 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.2136-318G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975250 | ||||||
| chr2:190975408
|
C | A | 1 | a0001c0002t0001g0055 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2135+404G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975408 | ||||||
| chr2:190975626
|
CT | C | 14 | a0001c0001t0001g0100a0001c0001t0001g0128a0001c0001t0001g0138others(11): Show | 17 | HG00597.hp1 HG00642.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.2135+185delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975626 | ||||||
| chr2:190975643
|
A | T | 14 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0080others(11): Show | 16 | HG01257.hp1 HG02083.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.2135+169T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975643 | ||||||
| chr2:190975957
|
G | A | 12 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0080others(9): Show | 14 | HG01257.hp1 HG02083.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.2060-70C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975957 | ||||||
| chr2:190975969
|
GTTC | G | 14 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0080others(11): Show | 16 | HG01257.hp1 HG02083.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.2060-85_2060-83del others(3): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975969 | ||||||
| chr2:190975977
|
G | A | 1 | a0001c0002t0001g0252 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2060-90C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975977 | ||||||
| chr2:190975983
|
C | G | 6 | a0001c0001t0001g0041a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 7 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.2060-96G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975983 | ||||||
| chr2:190976052
|
T | A | 2 | a0001c0001t0001g0124a0001c0002t0001g0264 | 2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2060-165A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976052 | ||||||
| chr2:190976064
|
A | G | 7 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(4): Show | 11 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2060-177T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976064 | ||||||
| chr2:190976167
|
G | C | 1 | a0001c0001t0001g0009 | 3 | NA18970.hp1 NA18986.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2060-280C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976167 | ||||||
| chr2:190976290
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2060-403C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976290 | ||||||
| chr2:190976698
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0143a0001c0001t0002g0320 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2059+142G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976698 | ||||||
| chr2:190976796
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2059+44C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976796 | ||||||
| chr2:190977033
|
G | A | 81 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 109 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(106): Show |
splice_region_variant&intron_variant | LOW | c.1874-8C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977033 | ||||||
| chr2:190977153
|
A | G | 83 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 111 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.1874-128T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977153 | ||||||
| chr2:190977287
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1874-262T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977287 | ||||||
| chr2:190977387
|
G | T | 1 | a0001c0001t0001g0330 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1874-362C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977387 | ||||||
| chr2:190977389
|
T | C | 7 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(4): Show | 11 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1874-364A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977389 | ||||||
| chr2:190977557
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1874-532G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977557 | ||||||
| chr2:190977714
|
G | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0128others(7): Show | 11 | HG02559.hp2 HG02615.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1874-689C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977714 | ||||||
| chr2:190977884
|
C | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1874-859G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977884 | ||||||
| chr2:190977897
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1874-872A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977897 | ||||||
| chr2:190978189
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1873+667A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978189 | ||||||
| chr2:190978200
|
C | A | 12 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0080others(9): Show | 14 | HG01257.hp1 HG02083.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.1873+656G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978200 | ||||||
| chr2:190978206
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1873+650G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978206 | ||||||
| chr2:190978216
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1873+640C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978216 | ||||||
| chr2:190978465
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1873+391G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978465 | ||||||
| chr2:190978480
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1873+376A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978480 | ||||||
| chr2:190978558
|
C | T | 1 | a0001c0010t0001g0170 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1873+298G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978558 | ||||||
| chr2:190978637
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1873+219A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978637 | ||||||
| chr2:190978719
|
G | A | 13 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0064others(10): Show | 13 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1873+137C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978719 | ||||||
| chr2:190978767
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1873+89G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978767 | ||||||
| chr2:190979093
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1728-92C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979093 | ||||||
| chr2:190979104
|
A | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(96): Show | 129 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.1728-103T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979104 | ||||||
| chr2:190979249
|
C | T | 1 | a0001c0002t0001g0256 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1728-248G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979249 | ||||||
| chr2:190979543
|
GT | G | 12 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0160others(9): Show | 12 | HG00597.hp1 HG02071.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1727+228delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979543 | ||||||
| chr2:190979679
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0117a0001c0002t0001g0052 | 3 | NA18612.hp1 NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1727+93G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979679 | ||||||
| chr2:190979760
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1727+12C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979760 | ||||||
| chr2:190980019
|
T | C | 12 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0160others(9): Show | 12 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1633-153A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980019 | ||||||
| chr2:190980035
|
C | T | 1 | a0001c0002t0001g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1633-169G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980035 | ||||||
| chr2:190980234
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1633-368T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980234 | ||||||
| chr2:190980251
|
G | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0148others(3): Show | 9 | HG02015.hp1 NA18612.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1632+369C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980251 | ||||||
| chr2:190980396
|
T | A | 1 | a0001c0001t0001g0288 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1632+224A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980396 | ||||||
| chr2:190980563
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1632+57C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980563 | ||||||
| chr2:190980614
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01106.hp2 | splice_region_variant&intron_variant | LOW | c.1632+6G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980614 | ||||||
| chr2:190980732
|
G | A | 4 | a0001c0002t0001g0053a0001c0002t0001g0256a0001c0002t0001g0257others(1): Show | 4 | NA18939.hp2 NA18968.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1583-63C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980732 | ||||||
| chr2:190980849
|
T | C | 1 | a0001c0002t0001g0053 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1583-180A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980849 | ||||||
| chr2:190980985
|
C | T | 17 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0079others(14): Show | 19 | HG01257.hp1 HG02056.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1583-316G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980985 | ||||||
| chr2:190980999
|
C | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(220): Show | 282 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1583-330G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980999 | ||||||
| chr2:190981007
|
C | T | 3 | a0001c0001t0002g0143a0001c0001t0002g0320a0001c0008t0001g0265 | 3 | HG02622.hp1 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1583-338G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981007 | ||||||
| chr2:190981022
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0012g0156 | 2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1583-353A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981022 | ||||||
| chr2:190981058
|
T | G | 1 | a0001c0002t0001g0267 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1583-389A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981058 | ||||||
| chr2:190981059
|
G | GC | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(204): Show | 254 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.1583-391dupG | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981059 | ||||||
| chr2:190981089
|
C | T | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1583-420G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981089 | ||||||
| chr2:190981104
|
C | T | 1 | a0001c0001t0001g0030 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1583-435G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981104 | ||||||
| chr2:190981195
|
G | C | 1 | a0001c0002t0007g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1583-526C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981195 | ||||||
| chr2:190981265
|
C | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0018others(62): Show | 83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1583-596G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981265 | ||||||
| chr2:190981365
|
C | G | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(329): Show | 410 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(407): Show |
intron_variant | MODIFIER | c.1583-696G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981365 | ||||||
| chr2:190981373
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1583-704A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981373 | ||||||
| chr2:190981411
|
A | C | 6 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-742T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981411 | ||||||
| chr2:190981416
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1583-747C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981416 | ||||||
| chr2:190981477
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 6 | HG02074.hp2 HG02129.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-808C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981477 | ||||||
| chr2:190981500
|
G | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0158others(16): Show | 21 | HG01257.hp1 HG01928.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.1583-831C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981500 | ||||||
| chr2:190981609
|
C | T | 12 | a0001c0001t0001g0330a0001c0001t0002g0039a0001c0001t0002g0122others(9): Show | 13 | HG02572.hp1 HG02809.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1582+774G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981609 | ||||||
| chr2:190981791
|
G | A | 2 | a0001c0001t0001g0307a0001c0011t0001g0271 | 2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1582+592C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981791 | ||||||
| chr2:190981966
|
C | T | 1 | a0001c0002t0001g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1582+417G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981966 | ||||||
| chr2:190982173
|
G | GA | 17 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0158others(14): Show | 19 | HG01257.hp1 HG01928.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1582+209dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190982173 | ||||||
| chr2:190982776
|
G | T | 2 | a0001c0001t0001g0307a0001c0011t0001g0271 | 2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1447-258C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982776 | ||||||
| chr2:190982780
|
ACACACAG others(3): Show |
A | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1447-272_1447-263d others(12): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982780 | ||||||
| chr2:190982935
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1447-417G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982935 | ||||||
| chr2:190982968
|
C | T | 1 | a0001c0010t0001g0170 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1447-450G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982968 | ||||||
| chr2:190983314
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0221 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1446+328G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983314 | ||||||
| chr2:190983409
|
A | G | 10 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(7): Show | 14 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1446+233T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983409 | ||||||
| chr2:190983419
|
T | C | 2 | a0001c0001t0001g0307a0001c0011t0001g0271 | 2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1446+223A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983419 | ||||||
| chr2:190983480
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG01099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1446+162T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983480 | ||||||
| chr2:190983560
|
T | C | 27 | a0001c0001t0001g0330a0001c0001t0002g0028a0001c0001t0002g0039others(24): Show | 32 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.1446+82A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983560 | ||||||
| chr2:190983586
|
T | C | 334 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(331): Show | 413 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(410): Show |
intron_variant | MODIFIER | c.1446+56A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983586 | ||||||
| chr2:190983877
|
G | T | 1 | a0001c0001t0004g0323 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1348-137C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190983877 | ||||||
| chr2:190983893
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1348-153G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190983893 | ||||||
| chr2:190984002
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1348-262A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190984002 | ||||||
| chr2:190984067
|
T | TA | 73 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(70): Show | 89 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1347+242dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190984067 | ||||||
| chr2:190984545
|
A | G | 1 | a0001c0008t0001g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1264-152T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984545 | ||||||
| chr2:190984550
|
T | C | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-157A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984550 | ||||||
| chr2:190984596
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1264-203C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984596 | ||||||
| chr2:190984603
|
G | A | 1 | a0001c0006t0001g0280 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1264-210C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984603 | ||||||
| chr2:190984954
|
G | A | 2 | a0001c0001t0006g0090a0001c0001t0006g0133 | 2 | HG00642.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1264-561C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984954 | ||||||
| chr2:190984963
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1264-570C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984963 | ||||||
| chr2:190985120
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1263+499A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985120 | ||||||
| chr2:190985127
|
T | C | 1 | a0001c0003t0001g0200 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1263+492A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985127 | ||||||
| chr2:190985240
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1263+379T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985240 | ||||||
| chr2:190985373
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(99): Show | 121 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1263+246T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985373 | ||||||
| chr2:190985374
|
C | T | 2 | a0001c0001t0001g0307a0001c0011t0001g0271 | 2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1263+245G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985374 | ||||||
| chr2:190985503
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1263+116G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985503 | ||||||
| chr2:190985669
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1222-9G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985669 | ||||||
| chr2:190985840
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(76): Show | 95 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1222-180A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985840 | ||||||
| chr2:190985895
|
C | A | 5 | a0001c0001t0001g0307a0001c0001t0002g0136a0001c0001t0002g0143others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-235G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985895 | ||||||
| chr2:190985974
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1222-314C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985974 | ||||||
| chr2:190986040
|
C | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 321 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.1222-380G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986040 | ||||||
| chr2:190986056
|
C | T | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-396G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986056 | ||||||
| chr2:190986119
|
C | T | 20 | a0001c0001t0001g0160a0001c0001t0001g0330a0001c0001t0002g0028others(17): Show | 25 | HG01261.hp2 HG02109.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1222-459G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986119 | ||||||
| chr2:190986224
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1222-564T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986224 | ||||||
| chr2:190986267
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1221+587C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986267 | ||||||
| chr2:190986351
|
C | A | 1 | a0001c0011t0001g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1221+503G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986351 | ||||||
| chr2:190986375
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1221+479C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986375 | ||||||
| chr2:190986474
|
A | G | 34 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0036others(31): Show | 39 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1221+380T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986474 | ||||||
| chr2:190986496
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1221+358C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986496 | ||||||
| chr2:190986536
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1221+318G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986536 | ||||||
| chr2:190986555
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1221+299C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986555 | ||||||
| chr2:190986569
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1221+285C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986569 | ||||||
| chr2:190986712
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1221+142G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986712 | ||||||
| chr2:190986759
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0159a0001c0001t0001g0163others(32): Show | 44 | HG00323.hp1 HG00438.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1221+95G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986759 | ||||||
| chr2:190986980
|
C | A | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1128-33G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 13/24 | chr2 | 190986980 | ||||||
| chr2:190987013
|
A | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1127+26T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 13/24 | chr2 | 190987013 | ||||||
| chr2:190987079
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0299 | 2 | HG02074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1098-11T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987079 | ||||||
| chr2:190987085
|
T | C | 1 | a0001c0001t0001g0030 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1098-17A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987085 | ||||||
| chr2:190987171
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0061others(78): Show | 94 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1098-103C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987171 | ||||||
| chr2:190987271
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(86): Show | 106 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.1098-203A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987271 | ||||||
| chr2:190987274
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0140 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1098-206G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987274 | ||||||
| chr2:190987720
|
T | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098-652A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987720 | ||||||
| chr2:190987737
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1098-669C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987737 | ||||||
| chr2:190987899
|
T | G | 20 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0046others(17): Show | 29 | HG01496.hp2 HG02004.hp1 HG02135.hp1 others(26): Show |
intron_variant | MODIFIER | c.1098-831A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987899 | ||||||
| chr2:190987952
|
C | T | 2 | a0001c0001t0001g0307a0001c0011t0001g0271 | 2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1098-884G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987952 | ||||||
| chr2:190987996
|
G | A | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1098-928C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987996 | ||||||
| chr2:190988218
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1098-1150A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988218 | ||||||
| chr2:190988310
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1098-1242A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988310 | ||||||
| chr2:190988426
|
T | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1097+1189A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988426 | ||||||
| chr2:190988444
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1097+1171A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988444 | ||||||
| chr2:190988496
|
G | A | 2 | a0001c0001t0002g0136a0001c0002t0001g0261 | 2 | HG02486.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1097+1119C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988496 | ||||||
| chr2:190988541
|
G | T | 1 | a0001c0001t0001g0021 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1097+1074C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988541 | ||||||
| chr2:190988561
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(131): Show | 159 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1097+1054C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988561 | ||||||
| chr2:190988569
|
G | A | 4 | a0001c0001t0001g0020a0001c0002t0001g0234a0001c0007t0005g0144others(1): Show | 5 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097+1046C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988569 | ||||||
| chr2:190988598
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1097+1017A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988598 | ||||||
| chr2:190988599
|
C | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0284others(6): Show | 13 | HG02004.hp1 HG02135.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1097+1016G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988599 | ||||||
| chr2:190988693
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0049others(9): Show | 18 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1097+922A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988693 | ||||||
| chr2:190988836
|
A | C | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1097+779T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988836 | ||||||
| chr2:190988865
|
A | G | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1097+750T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988865 | ||||||
| chr2:190988891
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1097+724T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988891 | ||||||
| chr2:190988966
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0316 | 4 | HG02155.hp1 NA19004.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097+649C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988966 | ||||||
| chr2:190989050
|
A | C | 1 | a0001c0001t0001g0020 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1097+565T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989050 | ||||||
| chr2:190989118
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1097+497T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989118 | ||||||
| chr2:190989118
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1097+497T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989118 | ||||||
| chr2:190989159
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1097+456G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989159 | ||||||
| chr2:190989165
|
G | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0049others(16): Show | 29 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1097+450C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989165 | ||||||
| chr2:190989172
|
G | T | 1 | a0001c0001t0002g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1097+443C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989172 | ||||||
| chr2:190989213
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(133): Show | 161 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1097+402C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989213 | ||||||
| chr2:190989516
|
G | A | 1 | a0001c0011t0001g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1097+99C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989516 | ||||||
| chr2:190989551
|
C | A | 1 | a0001c0001t0001g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1097+64G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989551 | ||||||
| chr2:190989605
|
G | C | 2 | a0001c0001t0001g0300a0001c0002t0001g0233 | 2 | HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1097+10C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989605 | ||||||
| chr2:190989697
|
T | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0074others(58): Show | 73 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1038-23A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190989697 | ||||||
| chr2:190989876
|
C | G | 1 | a0001c0001t0002g0308 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1038-202G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190989876 | ||||||
| chr2:190989913
|
C | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(96): Show | 122 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1038-239G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190989913 | ||||||
| chr2:190990000
|
C | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1038-326G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990000 | ||||||
| chr2:190990143
|
G | C | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1038-469C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990143 | ||||||
| chr2:190990148
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(133): Show | 161 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1038-474T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990148 | ||||||
| chr2:190990168
|
T | C | 2 | a0001c0001t0002g0320a0001c0008t0001g0265 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1038-494A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990168 | ||||||
| chr2:190990391
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1038-717G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990391 | ||||||
| chr2:190990795
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(100): Show | 121 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1037+433A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990795 | ||||||
| chr2:190991419
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0281others(3): Show | 8 | HG01496.hp2 NA18940.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.945-99G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991419 | ||||||
| chr2:190991516
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0331a0001c0001t0001g0332others(2): Show | 5 | HG01192.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.945-196G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991516 | ||||||
| chr2:190991586
|
C | T | 1 | a0001c0002t0007g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.945-266G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991586 | ||||||
| chr2:190991685
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0074others(56): Show | 71 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.945-365G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991685 | ||||||
| chr2:190991698
|
T | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(96): Show | 122 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.945-378A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991698 | ||||||
| chr2:190991700
|
TG | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(82): Show | 99 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.945-381delC | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991700 | ||||||
| chr2:190991701
|
G | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0020others(46): Show | 60 | HG00597.hp1 HG00735.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.945-381C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991701 | ||||||
| chr2:190991705
|
T | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 12 | HG04184.hp1 NA18747.hp2 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.945-385A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991705 | ||||||
| chr2:190991869
|
T | TA | 8 | a0001c0001t0001g0002a0001c0001t0001g0163a0001c0001t0001g0165others(5): Show | 12 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.945-550dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991869 | ||||||
| chr2:190991886
|
G | A | 10 | a0001c0001t0001g0330a0001c0001t0002g0122a0001c0001t0002g0126others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.945-566C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991886 | ||||||
| chr2:190991946
|
A | G | 12 | a0001c0001t0001g0307a0001c0001t0001g0330a0001c0001t0002g0122others(9): Show | 12 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.945-626T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991946 | ||||||
| chr2:190992018
|
G | T | 17 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(14): Show | 18 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.945-698C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992018 | ||||||
| chr2:190992022
|
AT | A | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG01943.hp1 HG01981.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.945-703delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992022 | ||||||
| chr2:190992029
|
T | A | 23 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0164others(20): Show | 25 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.945-709A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992029 | ||||||
| chr2:190992160
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0063others(73): Show | 89 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.945-840G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992160 | ||||||
| chr2:190992229
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.945-909T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992229 | ||||||
| chr2:190992474
|
TA | T | 10 | a0001c0001t0001g0330a0001c0001t0002g0122a0001c0001t0002g0126others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.945-1155delT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992474 | ||||||
| chr2:190992625
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0049others(12): Show | 21 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.945-1305C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992625 | ||||||
| chr2:190992772
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.945-1452A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992772 | ||||||
| chr2:190992793
|
C | CT | 12 | a0001c0001t0001g0307a0001c0001t0001g0330a0001c0001t0002g0122others(9): Show | 12 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.945-1474dupA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992793 | ||||||
| chr2:190992793
|
CT | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0065a0001c0001t0001g0069others(3): Show | 7 | HG00639.hp1 HG01069.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.945-1474delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992793 | ||||||
| chr2:190992820
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0115 | 5 | HG02129.hp1 NA18942.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.945-1500A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992820 | ||||||
| chr2:190992875
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.945-1555G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992875 | ||||||
| chr2:190992978
|
T | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 107 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.945-1658A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992978 | ||||||
| chr2:190993079
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.945-1759G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993079 | ||||||
| chr2:190993085
|
G | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.945-1765C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993085 | ||||||
| chr2:190993116
|
A | C | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.945-1796T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993116 | ||||||
| chr2:190993120
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.945-1800T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993120 | ||||||
| chr2:190993220
|
G | A | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+1841C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993220 | ||||||
| chr2:190993240
|
C | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | NA18998.hp2 NA19006.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+1821G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993240 | ||||||
| chr2:190993298
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.944+1763G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993298 | ||||||
| chr2:190993395
|
T | C | 5 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(2): Show | 9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.944+1666A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993395 | ||||||
| chr2:190993439
|
T | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0002t0001g0269 | 3 | HG02145.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.944+1622A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993439 | ||||||
| chr2:190993449
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.944+1612A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993449 | ||||||
| chr2:190993790
|
T | TA | 5 | a0001c0001t0001g0020a0001c0002t0001g0234a0001c0007t0005g0144others(2): Show | 6 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.944+1270dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993790 | ||||||
| chr2:190993910
|
A | C | 20 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0063others(17): Show | 21 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.944+1151T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993910 | ||||||
| chr2:190994016
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.944+1045G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994016 | ||||||
| chr2:190994104
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 109 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.944+957C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994104 | ||||||
| chr2:190994188
|
A | C | 1 | a0001c0001t0001g0286 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.944+873T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994188 | ||||||
| chr2:190994263
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+798G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994263 | ||||||
| chr2:190994264
|
G | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0074others(54): Show | 69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.944+797C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994264 | ||||||
| chr2:190994620
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0222a0001c0001t0016g0335 | 3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.944+441A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994620 | ||||||
| chr2:190994635
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.944+426A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994635 | ||||||
| chr2:190994695
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.944+366G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994695 | ||||||
| chr2:190994781
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.944+280A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994781 | ||||||
| chr2:190994914
|
C | CA | 14 | a0001c0001t0001g0024a0001c0001t0001g0064a0001c0001t0001g0065others(11): Show | 15 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.944+146dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994914 | ||||||
| chr2:190994914
|
C | CAA | 18 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0019others(15): Show | 27 | HG00408.hp2 HG00597.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.944+145_944+146dup others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994914 | ||||||
| chr2:190994925
|
A | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0275a0001c0001t0002g0122others(6): Show | 9 | HG01981.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.944+136T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994925 | ||||||
| chr2:190994927
|
A | AAT | 13 | a0001c0001t0001g0015a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 16 | HG01433.hp1 HG02155.hp2 HG03130.hp2 others(13): Show |
intron_variant | MODIFIER | c.944+132_944+133dup others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | ||||||
| chr2:190994927
|
A | AATATAT | 6 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG00621.hp2 HG01099.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.944+128_944+133dup others(6): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | ||||||
| chr2:190994927
|
A | T | 15 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(12): Show | 15 | HG01981.hp2 HG02109.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.944+134T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | ||||||
| chr2:190994927
|
AAT | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0134a0001c0001t0001g0175others(5): Show | 9 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.944+132_944+133del others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | ||||||
| chr2:190994927
|
AATAT | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(51): Show | 68 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.944+130_944+133del others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | ||||||
| chr2:190994927
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+122_944+133del others(12): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | ||||||
| chr2:190994928
|
ATAT | A | 5 | a0001c0001t0001g0202a0001c0001t0001g0220a0001c0002t0001g0237others(2): Show | 5 | HG01943.hp2 HG02300.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+130_944+132del others(3): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | ||||||
| chr2:190994928
|
ATATAT | A | 12 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0137others(9): Show | 13 | HG00323.hp1 HG00733.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.944+128_944+132del others(5): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | ||||||
| chr2:190994928
|
ATATATAT others(2): Show |
A | 12 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0049others(9): Show | 18 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.944+124_944+132del others(9): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | ||||||
| chr2:190994928
|
ATATATAT others(8): Show |
A | 5 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(2): Show | 9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.944+118_944+132del others(15): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | ||||||
| chr2:190994929
|
T | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0020others(113): Show | 139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.944+132A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994929 | ||||||
| chr2:190994929
|
T | TAC | 3 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0101 | 4 | NA18952.hp1 NA18962.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+131_944+132ins others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994929 | ||||||
| chr2:190994931
|
T | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0071others(53): Show | 70 | HG00438.hp2 HG00642.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.944+130A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994931 | ||||||
| chr2:190994933
|
T | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(66): Show | 86 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.944+128A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994933 | ||||||
| chr2:190994935
|
T | A | 17 | a0001c0001t0001g0061a0001c0001t0001g0135a0001c0001t0001g0202others(14): Show | 17 | HG00323.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.944+126A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994935 | ||||||
| chr2:190994937
|
T | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0305a0001c0001t0016g0335others(1): Show | 4 | HG02135.hp2 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+124A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994937 | ||||||
| chr2:190994939
|
T | A | 2 | a0001c0001t0001g0222a0001c0001t0016g0335 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.944+122A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994939 | ||||||
| chr2:190994941
|
T | A | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+120A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994941 | ||||||
| chr2:190994943
|
T | A | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+118A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994943 | ||||||
| chr2:190994945
|
T | A | 1 | a0002c0012t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.944+116A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994945 | ||||||
| chr2:190994949
|
TATATATA others(3): Show |
T | 8 | a0001c0001t0001g0216a0001c0001t0001g0298a0001c0001t0001g0333others(5): Show | 8 | HG00408.hp1 HG00438.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.944+102_944+111del others(10): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994949 | ||||||
| chr2:190994951
|
TATATATA others(1): Show |
T | 17 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0042others(14): Show | 20 | HG01257.hp1 HG01884.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.944+102_944+109del others(8): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994951 | ||||||
| chr2:190994955
|
TATAA | T | 37 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0075others(34): Show | 45 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.944+102_944+105del others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994955 | ||||||
| chr2:190994957
|
TAA | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0048others(24): Show | 34 | HG00280.hp1 HG00438.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.944+102_944+103del others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994957 | ||||||
| chr2:190994959
|
A | T | 68 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(65): Show | 81 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.944+102T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994959 | ||||||
| chr2:190995286
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.786-67T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995286 | ||||||
| chr2:190995294
|
A | G | 1 | a0001c0002t0007g0154 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.786-75T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995294 | ||||||
| chr2:190995327
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0222a0001c0001t0016g0335 | 3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.786-108T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995327 | ||||||
| chr2:190995327
|
A | T | 1 | a0001c0002t0001g0267 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.786-108T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995327 | ||||||
| chr2:190995341
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0222a0001c0001t0016g0335 | 3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.786-122T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995341 | ||||||
| chr2:190995504
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0074others(54): Show | 69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.786-285G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995504 | ||||||
| chr2:190995633
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.786-414G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995633 | ||||||
| chr2:190995655
|
A | G | 2 | a0001c0001t0002g0320a0001c0008t0001g0265 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.786-436T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995655 | ||||||
| chr2:190995667
|
G | A | 3 | a0001c0001t0002g0136a0001c0001t0002g0320a0001c0008t0001g0265 | 3 | HG02486.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.786-448C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995667 | ||||||
| chr2:190995684
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02630.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.786-465T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995684 | ||||||
| chr2:190995719
|
A | T | 23 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0164others(20): Show | 25 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.786-500T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995719 | ||||||
| chr2:190995776
|
C | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0037others(116): Show | 138 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.786-557G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995776 | ||||||
| chr2:190995803
|
C | T | 81 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 107 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.786-584G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995803 | ||||||
| chr2:190995851
|
T | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0163a0001c0001t0001g0165others(5): Show | 12 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-632A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995851 | ||||||
| chr2:190996029
|
AT | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0064others(14): Show | 18 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.786-811delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996029 | ||||||
| chr2:190996033
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.786-814C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996033 | ||||||
| chr2:190996043
|
G | A | 1 | a0001c0002t0001g0259 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.786-824C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996043 | ||||||
| chr2:190996111
|
G | T | 5 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(2): Show | 9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.786-892C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996111 | ||||||
| chr2:190996265
|
GCAGTAAT others(6): Show |
G | 3 | a0001c0001t0002g0136a0001c0001t0002g0320a0001c0008t0001g0265 | 3 | HG02486.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.786-1059_786-1047d others(15): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996265 | ||||||
| chr2:190996308
|
T | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0049others(10): Show | 19 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.786-1089A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996308 | ||||||
| chr2:190996453
|
C | T | 4 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(1): Show | 8 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.786-1234G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996453 | ||||||
| chr2:190996651
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(12): Show | 24 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+1205G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996651 | ||||||
| chr2:190996726
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.785+1130A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996726 | ||||||
| chr2:190996755
|
G | A | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.785+1101C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996755 | ||||||
| chr2:190997025
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(12): Show | 24 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+831G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997025 | ||||||
| chr2:190997080
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.785+776G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997080 | ||||||
| chr2:190997099
|
G | A | 1 | a0001c0002t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.785+757C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997099 | ||||||
| chr2:190997165
|
G | A | 2 | a0001c0001t0002g0125a0001c0001t0005g0319 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.785+691C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997165 | ||||||
| chr2:190997357
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 5 | HG02615.hp2 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+499G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997357 | ||||||
| chr2:190997365
|
C | A | 23 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0164others(20): Show | 25 | HG00438.hp1 HG01257.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.785+491G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997365 | ||||||
| chr2:190997430
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG00639.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.785+426A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997430 | ||||||
| chr2:190997459
|
A | G | 60 | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0001g0074others(57): Show | 69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.785+397T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997459 | ||||||
| chr2:190997502
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.785+354T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997502 | ||||||
| chr2:190997609
|
C | G | 5 | a0001c0001t0001g0222a0001c0001t0002g0136a0001c0001t0002g0320others(2): Show | 5 | HG02486.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+247G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997609 | ||||||
| chr2:190997672
|
G | A | 49 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0075others(46): Show | 57 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.785+184C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997672 | ||||||
| chr2:190997722
|
C | T | 5 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(2): Show | 9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+134G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997722 | ||||||
| chr2:190998023
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG01099.hp1 HG02056.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.634-16C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998023 | ||||||
| chr2:190998044
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.634-37T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998044 | ||||||
| chr2:190998050
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.634-43T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998050 | ||||||
| chr2:190998060
|
T | C | 22 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0164others(19): Show | 24 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.634-53A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998060 | ||||||
| chr2:190998175
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(9): Show | 21 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.633+42A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998175 | ||||||
| chr2:190998464
|
C | G | 2 | a0001c0002t0001g0043a0001c0002t0001g0242 | 3 | NA18971.hp1 NA19084.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.542-156G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998464 | ||||||
| chr2:190998522
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0222a0001c0001t0002g0136others(3): Show | 6 | HG02486.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-214G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998522 | ||||||
| chr2:190998618
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | NA18965.hp2 NA18973.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.542-310G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998618 | ||||||
| chr2:190998672
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.542-364G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998672 | ||||||
| chr2:190998672
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0279 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.542-375_542-365del others(11): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998672 | ||||||
| chr2:190998683
|
A | G | 12 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 12 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-375T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998683 | ||||||
| chr2:190998833
|
A | G | 5 | a0001c0001t0001g0020a0001c0002t0001g0233a0001c0002t0001g0234others(2): Show | 6 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-525T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998833 | ||||||
| chr2:190998914
|
T | C | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 11 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.542-606A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998914 | ||||||
| chr2:190998969
|
A | G | 1 | a0001c0008t0001g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.541+657T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998969 | ||||||
| chr2:190999064
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.541+562A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999064 | ||||||
| chr2:190999179
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.541+447C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999179 | ||||||
| chr2:190999227
|
C | T | 1 | a0001c0011t0001g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.541+399G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999227 | ||||||
| chr2:190999472
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.541+154T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999472 | ||||||
| chr2:190999558
|
T | A | 2 | a0001c0007t0005g0144a0001c0007t0005g0145 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.541+68A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999558 | ||||||
| chr2:190999568
|
C | A | 1 | a0001c0002t0001g0267 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.541+58G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999568 | ||||||
| chr2:190999576
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0171 | 3 | HG01167.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.541+50T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999576 | ||||||
| chr2:190999712
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.463-8G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999712 | ||||||
| chr2:190999841
|
C | A | 1 | a0001c0002t0001g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.463-137G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999841 | ||||||
| chr2:190999858
|
A | G | 3 | a0001c0001t0001g0020a0001c0002t0001g0233a0001c0002t0001g0234 | 4 | HG02257.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-154T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999858 | ||||||
| chr2:190999914
|
C | A | 1 | a0001c0001t0002g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463-210G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999914 | ||||||
| chr2:191000047
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.463-343G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000047 | ||||||
| chr2:191000048
|
G | A | 10 | a0001c0001t0001g0330a0001c0001t0002g0122a0001c0001t0002g0126others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.463-344C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000048 | ||||||
| chr2:191000160
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.463-456A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000160 | ||||||
| chr2:191000217
|
T | C | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.463-513A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000217 | ||||||
| chr2:191000231
|
A | C | 64 | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0001g0074others(61): Show | 74 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.463-527T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000231 | ||||||
| chr2:191000278
|
C | T | 3 | a0001c0001t0001g0020a0001c0002t0001g0233a0001c0002t0001g0234 | 4 | HG02257.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-574G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000278 | ||||||
| chr2:191000448
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0310others(1): Show | 8 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.462+626G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000448 | ||||||
| chr2:191000481
|
G | GGCCTCT | 30 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(27): Show | 36 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.462+587_462+592dup others(6): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000481 | ||||||
| chr2:191000495
|
A | G | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.462+579T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000495 | ||||||
| chr2:191000548
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.462+526G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000548 | ||||||
| chr2:191000548
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0171 | 3 | HG01167.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.462+526G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000548 | ||||||
| chr2:191000723
|
C | T | 1 | a0001c0001t0003g0004 | 4 | HG02258.hp2 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+351G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000723 | ||||||
| chr2:191000802
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.462+272C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000802 | ||||||
| chr2:191000999
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0137 | 3 | HG03490.hp2 HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.462+75G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000999 | ||||||
| chr2:191001010
|
A | G | 1 | a0001c0003t0001g0197 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.462+64T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191001010 | ||||||
| chr2:191001051
|
G | T | 5 | a0001c0001t0001g0020a0001c0002t0001g0233a0001c0002t0001g0234others(2): Show | 6 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.462+23C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191001051 | ||||||
| chr2:191001066
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.462+8T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191001066 | ||||||
| chr2:191001187
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.373-24A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001187 | ||||||
| chr2:191001445
|
T | C | 6 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(3): Show | 10 | HG01261.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-282A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001445 | ||||||
| chr2:191001684
|
A | G | 1 | a0001c0002t0007g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.373-521T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001684 | ||||||
| chr2:191001717
|
T | C | 1 | a0001c0001t0014g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.373-554A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001717 | ||||||
| chr2:191001751
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0222a0001c0001t0004g0323others(3): Show | 6 | HG02486.hp1 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-588A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001751 | ||||||
| chr2:191001804
|
C | G | 1 | a0001c0001t0002g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-641G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001804 | ||||||
| chr2:191001821
|
A | C | 1 | a0001c0002t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.373-658T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001821 | ||||||
| chr2:191001889
|
C | T | 37 | a0001c0001t0001g0020a0001c0001t0001g0167a0001c0001t0001g0168others(34): Show | 46 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.373-726G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001889 | ||||||
| chr2:191001932
|
T | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(90): Show | 118 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.373-769A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001932 | ||||||
| chr2:191001952
|
C | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-789G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001952 | ||||||
| chr2:191001995
|
T | C | 2 | a0001c0007t0005g0144a0001c0007t0005g0145 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.373-832A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001995 | ||||||
| chr2:191001997
|
C | T | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.373-834G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001997 | ||||||
| chr2:191002012
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.373-849C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002012 | ||||||
| chr2:191002119
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0162 | 3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.373-956A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002119 | ||||||
| chr2:191002140
|
T | C | 1 | a0001c0001t0002g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-977A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002140 | ||||||
| chr2:191002268
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.373-1105T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002268 | ||||||
| chr2:191002329
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.373-1166C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002329 | ||||||
| chr2:191002426
|
T | C | 2 | a0001c0001t0001g0302a0001c0002t0001g0262 | 2 | HG00597.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.373-1263A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002426 | ||||||
| chr2:191002558
|
T | G | 1 | a0001c0001t0001g0332 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.373-1395A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002558 | ||||||
| chr2:191002606
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.373-1443G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002606 | ||||||
| chr2:191002627
|
A | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(34): Show | 43 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.373-1464T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002627 | ||||||
| chr2:191002635
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.373-1472A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002635 | ||||||
| chr2:191002703
|
G | A | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1540C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002703 | ||||||
| chr2:191002790
|
T | G | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.373-1627A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002790 | ||||||
| chr2:191002809
|
T | C | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1646A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002809 | ||||||
| chr2:191002811
|
C | G | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG01943.hp1 HG01981.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1648G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002811 | ||||||
| chr2:191002820
|
T | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(27): Show | 36 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.373-1657A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002820 | ||||||
| chr2:191002988
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.373-1825T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002988 | ||||||
| chr2:191003060
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.373-1897A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003060 | ||||||
| chr2:191003068
|
A | G | 1 | a0001c0007t0005g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.373-1905T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003068 | ||||||
| chr2:191003105
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01346.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.373-1942A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003105 | ||||||
| chr2:191003141
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.373-1978A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003141 | ||||||
| chr2:191003143
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.373-1980C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003143 | ||||||
| chr2:191003305
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.373-2142G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003305 | ||||||
| chr2:191003379
|
T | C | 5 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-2216A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003379 | ||||||
| chr2:191003410
|
A | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(13): Show | 29 | HG01257.hp2 HG01258.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.373-2247T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003410 | ||||||
| chr2:191003418
|
C | G | 1 | a0001c0002t0001g0241 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.373-2255G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003418 | ||||||
| chr2:191003473
|
T | A | 2 | a0001c0001t0001g0307a0001c0011t0001g0271 | 2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.373-2310A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003473 | ||||||
| chr2:191003510
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.373-2347G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003510 | ||||||
| chr2:191003632
|
A | G | 1 | a0001c0004t0001g0007 | 4 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2469T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003632 | ||||||
| chr2:191003694
|
TA | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.373-2532delT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003694 | ||||||
| chr2:191003764
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(28): Show | 37 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.373-2601A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003764 | ||||||
| chr2:191003802
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(8): Show | 20 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.373-2639G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003802 | ||||||
| chr2:191003857
|
C | A | 52 | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0001g0074others(49): Show | 62 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.373-2694G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003857 | ||||||
| chr2:191003868
|
G | C | 1 | a0001c0002t0001g0263 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.373-2705C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003868 | ||||||
| chr2:191003973
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.373-2810A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003973 | ||||||
| chr2:191004197
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.373-3034G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004197 | ||||||
| chr2:191004216
|
T | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(27): Show | 36 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.373-3053A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004216 | ||||||
| chr2:191004248
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0222a0001c0001t0016g0335 | 3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.373-3085T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004248 | ||||||
| chr2:191004268
|
A | G | 1 | a0001c0001t0002g0320 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-3105T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004268 | ||||||
| chr2:191004437
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.372+3126C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004437 | ||||||
| chr2:191004527
|
A | G | 1 | a0001c0002t0001g0236 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.372+3036T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004527 | ||||||
| chr2:191004754
|
G | A | 1 | a0001c0002t0010g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.372+2809C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004754 | ||||||
| chr2:191004896
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.372+2667A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004896 | ||||||
| chr2:191005185
|
A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(73): Show | 95 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.372+2378T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005185 | ||||||
| chr2:191005223
|
T | C | 10 | a0001c0001t0001g0330a0001c0001t0002g0122a0001c0001t0002g0143others(7): Show | 10 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+2340A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005223 | ||||||
| chr2:191005251
|
C | T | 4 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(1): Show | 8 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+2312G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005251 | ||||||
| chr2:191005252
|
T | A | 51 | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0001g0074others(48): Show | 61 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.372+2311A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005252 | ||||||
| chr2:191005259
|
G | C | 2 | a0001c0001t0001g0307a0001c0011t0001g0271 | 2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.372+2304C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005259 | ||||||
| chr2:191005284
|
A | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0222others(12): Show | 16 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.372+2279T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005284 | ||||||
| chr2:191005437
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(31): Show | 44 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.372+2126G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005437 | ||||||
| chr2:191005594
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(124): Show | 156 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.372+1969C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005594 | ||||||
| chr2:191005786
|
G | T | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.372+1777C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005786 | ||||||
| chr2:191005898
|
C | T | 60 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0075others(57): Show | 69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.372+1665G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005898 | ||||||
| chr2:191006010
|
G | C | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.372+1553C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006010 | ||||||
| chr2:191006082
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.372+1481C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006082 | ||||||
| chr2:191006138
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.372+1425A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006138 | ||||||
| chr2:191006224
|
C | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(26): Show | 35 | HG00438.hp1 HG01167.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.372+1339G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006224 | ||||||
| chr2:191006225
|
G | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(26): Show | 35 | HG00438.hp1 HG01167.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.372+1338C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006225 | ||||||
| chr2:191006231
|
A | G | 5 | a0001c0002t0001g0236a0001c0002t0001g0237a0001c0002t0001g0238others(2): Show | 5 | NA18947.hp2 NA18966.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1332T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006231 | ||||||
| chr2:191006317
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.372+1246A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006317 | ||||||
| chr2:191006416
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.372+1147A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006416 | ||||||
| chr2:191006561
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(8): Show | 20 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.372+1002G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006561 | ||||||
| chr2:191006812
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.372+751G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006812 | ||||||
| chr2:191006862
|
G | A | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+701C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006862 | ||||||
| chr2:191006913
|
T | C | 2 | a0001c0003t0001g0201a0001c0003t0001g0217 | 2 | NA18949.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.372+650A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006913 | ||||||
| chr2:191007160
|
G | A | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+403C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007160 | ||||||
| chr2:191007343
|
G | C | 4 | a0001c0001t0002g0028a0001c0001t0003g0004a0001c0001t0003g0068others(1): Show | 8 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+220C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007343 | ||||||
| chr2:191007450
|
C | T | 5 | a0001c0001t0002g0122a0001c0001t0002g0143a0001c0001t0002g0224others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+113G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007450 | ||||||
| chr2:191007459
|
TAG | T | 51 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0075others(48): Show | 60 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.372+102_372+103del others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007459 | ||||||
| chr2:191007716
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.274-55A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007716 | ||||||
| chr2:191007756
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-95C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007756 | ||||||
| chr2:191007826
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.274-165G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007826 | ||||||
| chr2:191007852
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.274-191A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007852 | ||||||
| chr2:191007860
|
T | C | 7 | a0001c0001t0002g0122a0001c0001t0002g0143a0001c0001t0002g0146others(4): Show | 7 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-199A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007860 | ||||||
| chr2:191007873
|
C | T | 1 | a0001c0001t0005g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-212G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007873 | ||||||
| chr2:191008240
|
G | GA | 213 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(210): Show | 268 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.274-580dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008240 | ||||||
| chr2:191008240
|
G | GAA | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0166others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-581_274-580dup others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008240 | ||||||
| chr2:191008353
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.273+610T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008353 | ||||||
| chr2:191008827
|
A | T | 184 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(181): Show | 233 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.273+136T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008827 | ||||||
| chr2:191008900
|
G | A | 1 | a0001c0001t0001g0020 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.273+63C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008900 | ||||||
| chr2:191009395
|
A | G | 8 | a0001c0001t0001g0333a0001c0002t0001g0052a0001c0002t0001g0053others(5): Show | 8 | HG00438.hp1 NA18990.hp1 NA19004.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-288T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009395 | ||||||
| chr2:191009414
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.129-307G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009414 | ||||||
| chr2:191009429
|
AAAT | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0013others(75): Show | 95 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.129-325_129-323del others(3): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009429 | ||||||
| chr2:191009463
|
T | TA | 47 | a0001c0001t0001g0218a0001c0001t0001g0309a0001c0002t0001g0003others(44): Show | 58 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.129-357dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009463 | ||||||
| chr2:191009521
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.128+355A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009521 | ||||||
| chr2:191009591
|
G | T | 49 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0309others(46): Show | 61 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.128+285C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009591 | ||||||
| chr2:191009682
|
T | A | 4 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+194A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009682 | ||||||
| chr2:191010027
|
T | C | 12 | a0001c0001t0001g0059a0001c0001t0001g0140a0001c0001t0001g0307others(9): Show | 12 | HG01192.hp2 HG02145.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-23A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010027 | ||||||
| chr2:191010094
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0012g0156 | 2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-1-90T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010094 | ||||||
| chr2:191010309
|
C | T | 73 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(70): Show | 83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-1-305G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010309 | ||||||
| chr2:191010416
|
A | C | 1 | a0001c0001t0004g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-1-412T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010416 | ||||||
| chr2:191010581
|
C | T | 1 | a0001c0002t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1-577G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010581 | ||||||
| chr2:191010642
|
TTC | T | 109 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(106): Show | 138 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.-1-640_-1-639delGA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010642 | ||||||
| chr2:191010744
|
G | C | 1 | a0001c0001t0004g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-1-740C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010744 | ||||||
| chr2:191011175
|
C | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(285): Show | 357 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(354): Show |
intron_variant | MODIFIER | c.-1-1171G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011175 | ||||||
| chr2:191011342
|
C | T | 1 | a0001c0011t0001g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-1-1338G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011342 | ||||||
| chr2:191011343
|
G | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0049others(28): Show | 37 | HG01192.hp2 HG01257.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.-1-1339C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011343 | ||||||
| chr2:191011383
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-1-1379C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011383 | ||||||
| chr2:191011422
|
T | C | 6 | a0001c0001t0002g0143a0001c0001t0002g0146a0001c0002t0001g0141others(3): Show | 6 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-1418A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011422 | ||||||
| chr2:191011689
|
G | A | 8 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(5): Show | 8 | HG01192.hp2 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1685C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011689 | ||||||
| chr2:191011773
|
G | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 14 | HG00621.hp1 HG02015.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+1752C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011773 | ||||||
| chr2:191012138
|
C | T | 7 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0054others(4): Show | 7 | HG00438.hp1 NA18990.hp1 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+1387G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012138 | ||||||
| chr2:191012158
|
A | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0069 | 3 | NA18952.hp1 NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-2+1367T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012158 | ||||||
| chr2:191012347
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0151 | 4 | HG00621.hp1 NA18972.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+1178G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012347 | ||||||
| chr2:191012416
|
T | TA | 116 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 145 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.-2+1108dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012416 | ||||||
| chr2:191012440
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2+1085A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012440 | ||||||
| chr2:191012626
|
T | C | 1 | a0001c0002t0010g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-2+899A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012626 | ||||||
| chr2:191013164
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0051 | 4 | NA18970.hp1 NA18986.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+361T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191013164 | ||||||
| chr2:191013368
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-2+157A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191013368 | ||||||
| chr2:191013389
|
TG | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(77): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-2+135delC | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191013389 | ||||||
| chr2:191013683
|
G | A | 1 | a0001c0011t0001g0271 | 1 | HG02976.hp2 | splice_region_variant&intron_variant | LOW | c.-155-5C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013683 | ||||||
| chr2:191013761
|
T | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(69): Show | 87 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-155-83A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013761 | ||||||
| chr2:191013928
|
C | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(123): Show | 158 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(155): Show |
intron_variant | MODIFIER | c.-156+90G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013928 | ||||||
| chr2:191013964
|
G | A | 1 | a0001c0001t0001g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-156+54C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013964 |