Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6775 |
|---|---|
| ensemblid | ENSG00000138378.19 |
| hgncid | 11365 |
| symbol | STAT4 |
| name | signal transducer and activator of transcription 4 |
| refseq_nuc | NM_003151.4 |
| refseq_prot | NP_003142.1 |
| ensembl_nuc | ENST00000392320.7 |
| ensembl_prot | ENSP00000376134.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 191029576 |
| end | 191150994 |
| strand | - |
| ver | v1.2 |
| region | chr2:191029576-191150994 |
| region5000 | chr2:191024576-191155994 |
| regionname0 | STAT4_chr2_191029576_191150994 |
| regionname5000 | STAT4_chr2_191024576_191155994 |
| 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 | 748 | 287 | 93 | 44 | 107 | 14 | 27 | 72 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0002 | 0/0 | 748 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0003 | 0/0 | 748 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0004 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| 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 | 2247 | 281 | 91 | 43 | 104 | 14 | 27 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| c0002 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| c0003 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| c0004 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| c0005 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| c0006 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| c0007 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| c0008 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| 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 | 313 | 288 | 93 | 44 | 108 | 13 | 28 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| t0002 | 0/0 | 313 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| t0003 | 0/0 | 313 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| 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 | 2 | 0 | 0 | 0 | 2 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| 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 | 2247 | 281 | 91 | 43 | 104 | 14 | 27 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0002 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0003 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0004 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0006 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0002c0005 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0003c0007 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0004c0008 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2559 | 279 | 90 | 43 | 104 | 13 | 27 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0001t0002 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0001t0003 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0002t0001 | 0/0 | 2559 | 2 | 2 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0003t0001 | 0/0 | 2559 | 2 | 0 | 0 | 2 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0004t0001 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0001c0006t0001 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0002c0005t0001 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0003c0007t0001 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| a0004c0008t0001 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | copy fasta | chr2 | 191024576 | 191155994 |
| 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 | 2 | 0 | 0 | 0 | 2 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0004t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0002c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0003c0007t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0004c0008t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0071 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0188 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01884 | hp1 | a0004 | c0008 | t0001 | g0248 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02080 | hp2 | a0002 | c0005 | t0001 | g0238 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04184 | hp2 | a0003 | c0007 | t0001 | g0034 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18940 | hp2 | a0001 | c0006 | t0001 | g0082 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ASW | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0026 | REF | REF | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0158 | REF | REF | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:191039285
|
G | C | 1 | a0003 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1348C>G | p.Pro450Ala | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/24 | 1397/2560 | 1348/2247 | 450/748 | chr2 | 191039285 | ||
| chr2:191062782
|
C | G | 1 | a0002 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.921G>C | p.Leu307Phe | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 9/24 | 970/2560 | 921/2247 | 307/748 | chr2 | 191062782 | ||
| chr2:191076256
|
T | C | 1 | a0004 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.343A>G | p.Ile115Val | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/24 | 392/2560 | 343/2247 | 115/748 | chr2 | 191076256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:191033030
|
G | A | 1 | a0001c0006 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.1972C>T | p.Leu658Leu | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/24 | 2021/2560 | 1972/2247 | 658/748 | chr2 | 191033030 | ||
| chr2:191041116
|
G | A | 1 | a0001c0003 | 2 | NA19002.hp2 NA19085.hp2 |
synonymous_variant | LOW | c.1284C>T | p.Ser428Ser | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/24 | 1333/2560 | 1284/2247 | 428/748 | chr2 | 191041116 | ||
| chr2:191062887
|
C | T | 1 | a0001c0004 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.816G>A | p.Leu272Leu | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 9/24 | 865/2560 | 816/2247 | 272/748 | chr2 | 191062887 | ||
| chr2:191148090
|
A | G | 1 | a0001c0002 | 2 | HG01891.hp1 HG02145.hp1 |
synonymous_variant | LOW | c.114T>C | p.Ile38Ile | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/24 | 163/2560 | 114/2247 | 38/748 | chr2 | 191148090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:191029679
|
T | C | 1 | a0001c0001t0003 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 24/24 | 161 | chr2 | 191029679 | |||||
| chr2:191150967
|
G | T | 1 | a0001c0001t0002 | 1 | NA20129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/24 | 2764 | chr2 | 191150967 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:191029957
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2221-91G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 23/23 | chr2 | 191029957 | ||||||
| chr2:191030081
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2221-215C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 23/23 | chr2 | 191030081 | ||||||
| chr2:191030444
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0136others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2220+528G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 23/23 | chr2 | 191030444 | ||||||
| chr2:191030476
|
T | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 43 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2220+496A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 23/23 | chr2 | 191030476 | ||||||
| chr2:191030601
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2220+371C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 23/23 | chr2 | 191030601 | ||||||
| chr2:191030650
|
G | C | 6 | a0001c0001t0001g0120a0001c0001t0001g0156a0001c0001t0001g0208others(3): Show | 6 | HG00609.hp1 HG02074.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2220+322C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 23/23 | chr2 | 191030650 | ||||||
| chr2:191030881
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 43 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2220+91G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 23/23 | chr2 | 191030881 | ||||||
| chr2:191031164
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2112-84A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031164 | ||||||
| chr2:191031167
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2112-87T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031167 | ||||||
| chr2:191031209
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0197 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2112-129A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031209 | ||||||
| chr2:191031245
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2112-165A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031245 | ||||||
| chr2:191031315
|
C | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 43 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2111+135G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031315 | ||||||
| chr2:191031319
|
T | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0013others(104): Show | 108 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.2111+131A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031319 | ||||||
| chr2:191031328
|
G | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0123others(1): Show | 4 | HG01081.hp1 HG01496.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2111+122C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031328 | ||||||
| chr2:191031440
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2111+10G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 22/23 | chr2 | 191031440 | ||||||
| chr2:191031628
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(16): Show | 19 | HG01257.hp1 HG01346.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.2045-112G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191031628 | ||||||
| chr2:191031629
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2045-113C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191031629 | ||||||
| chr2:191031838
|
G | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 43 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2045-322C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191031838 | ||||||
| chr2:191031861
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2045-345T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191031861 | ||||||
| chr2:191031990
|
C | T | 57 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0026others(54): Show | 57 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.2045-474G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191031990 | ||||||
| chr2:191032111
|
G | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0136others(7): Show | 10 | HG01192.hp1 HG02145.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2045-595C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032111 | ||||||
| chr2:191032155
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2045-639T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032155 | ||||||
| chr2:191032306
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2044+652C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032306 | ||||||
| chr2:191032310
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2044+648T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032310 | ||||||
| chr2:191032312
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2044+646C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032312 | ||||||
| chr2:191032455
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2044+503C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032455 | ||||||
| chr2:191032735
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2044+223C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032735 | ||||||
| chr2:191032814
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(118): Show | 123 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.2044+144G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 21/23 | chr2 | 191032814 | ||||||
| chr2:191033306
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0042others(7): Show | 10 | HG01891.hp2 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1853-157C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 20/23 | chr2 | 191033306 | ||||||
| chr2:191033444
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1852+46A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 20/23 | chr2 | 191033444 | ||||||
| chr2:191034136
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1621-131A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034136 | ||||||
| chr2:191034150
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1621-145A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034150 | ||||||
| chr2:191034160
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1621-155A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034160 | ||||||
| chr2:191034161
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0240a0001c0001t0001g0254 | 3 | HG02922.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1621-156C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034161 | ||||||
| chr2:191034202
|
T | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0055others(12): Show | 15 | HG01192.hp1 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621-197A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034202 | ||||||
| chr2:191034218
|
T | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0273a0001c0001t0001g0276 | 3 | HG00280.hp2 HG01106.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1621-213A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034218 | ||||||
| chr2:191034223
|
C | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1621-218G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034223 | ||||||
| chr2:191034223
|
C | T | 49 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0026others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.1621-218G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034223 | ||||||
| chr2:191034231
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1621-226T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034231 | ||||||
| chr2:191034287
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1620+261C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034287 | ||||||
| chr2:191034289
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1620+259C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034289 | ||||||
| chr2:191034291
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1620+257A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034291 | ||||||
| chr2:191034295
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0057others(1): Show | 4 | HG01169.hp2 HG02027.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1620+253A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034295 | ||||||
| chr2:191034372
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1620+176C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034372 | ||||||
| chr2:191034422
|
C | CA | 8 | a0001c0001t0001g0029a0001c0001t0001g0107a0001c0001t0001g0170others(5): Show | 8 | HG00438.hp2 HG03831.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1620+125dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034422 | ||||||
| chr2:191034422
|
CA | C | 7 | a0001c0001t0001g0102a0001c0001t0001g0148a0001c0001t0001g0160others(4): Show | 7 | HG00639.hp2 HG01517.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1620+125delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034422 | ||||||
| chr2:191034509
|
A | G | 2 | a0001c0001t0001g0233a0001c0001t0001g0236 | 2 | HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1620+39T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 18/23 | chr2 | 191034509 | ||||||
| chr2:191034620
|
A | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(4): Show | 7 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.1571-23T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191034620 | ||||||
| chr2:191035152
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1571-555C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191035152 | ||||||
| chr2:191035723
|
G | A | 93 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(90): Show | 93 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1570+441C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191035723 | ||||||
| chr2:191035795
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1570+369T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191035795 | ||||||
| chr2:191035801
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1570+363A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191035801 | ||||||
| chr2:191035839
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1570+325T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191035839 | ||||||
| chr2:191036082
|
G | T | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(4): Show | 7 | HG00438.hp2 HG02055.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1570+82C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191036082 | ||||||
| chr2:191036096
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1570+68C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 17/23 | chr2 | 191036096 | ||||||
| chr2:191036385
|
C | G | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1435-86G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191036385 | ||||||
| chr2:191036732
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1435-433C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191036732 | ||||||
| chr2:191036873
|
T | C | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1435-574A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191036873 | ||||||
| chr2:191036917
|
C | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0055others(10): Show | 13 | HG01192.hp1 HG02145.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1435-618G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191036917 | ||||||
| chr2:191037102
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0197 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1435-803A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191037102 | ||||||
| chr2:191037134
|
T | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1435-835A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191037134 | ||||||
| chr2:191037458
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0037others(28): Show | 32 | HG00639.hp2 HG01496.hp1 HG01981.hp2 others(29): Show |
intron_variant | MODIFIER | c.1435-1159T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191037458 | ||||||
| chr2:191037476
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1435-1177T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191037476 | ||||||
| chr2:191037620
|
G | A | 4 | a0001c0001t0001g0161a0001c0001t0001g0182a0001c0001t0001g0235others(1): Show | 4 | HG01071.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1435-1321C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191037620 | ||||||
| chr2:191037744
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1435-1445C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191037744 | ||||||
| chr2:191038032
|
G | A | 93 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(90): Show | 93 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1434+1167C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038032 | ||||||
| chr2:191038164
|
C | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(6): Show | 9 | HG00438.hp2 HG01884.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1434+1035G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038164 | ||||||
| chr2:191038230
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1434+969G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038230 | ||||||
| chr2:191038243
|
T | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1434+956A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038243 | ||||||
| chr2:191038264
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1434+935G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038264 | ||||||
| chr2:191038273
|
C | T | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1434+926G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038273 | ||||||
| chr2:191038447
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1434+752G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038447 | ||||||
| chr2:191038502
|
T | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0233 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1434+697A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038502 | ||||||
| chr2:191038525
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1434+674G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038525 | ||||||
| chr2:191038630
|
A | G | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(7): Show | 10 | HG00438.hp2 HG01884.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1434+569T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038630 | ||||||
| chr2:191038675
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1434+524G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038675 | ||||||
| chr2:191038864
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1434+335T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038864 | ||||||
| chr2:191038939
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1434+260G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 16/23 | chr2 | 191038939 | ||||||
| chr2:191039312
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1336-15T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039312 | ||||||
| chr2:191039561
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336-264G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039561 | ||||||
| chr2:191039735
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1336-438G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039735 | ||||||
| chr2:191039766
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1336-469A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039766 | ||||||
| chr2:191039796
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1336-499C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039796 | ||||||
| chr2:191039830
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(238): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1336-533T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039830 | ||||||
| chr2:191039873
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1336-576G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039873 | ||||||
| chr2:191039944
|
G | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0113others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1336-647C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191039944 | ||||||
| chr2:191040163
|
C | T | 122 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1336-866G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040163 | ||||||
| chr2:191040185
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0232 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1335+880C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040185 | ||||||
| chr2:191040291
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1335+774A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040291 | ||||||
| chr2:191040342
|
T | C | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1335+723A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040342 | ||||||
| chr2:191040412
|
C | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1335+653G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040412 | ||||||
| chr2:191040526
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0232 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1335+539G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040526 | ||||||
| chr2:191040609
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1335+456A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040609 | ||||||
| chr2:191040638
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0150a0001c0001t0001g0165others(2): Show | 5 | HG02486.hp1 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335+427G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040638 | ||||||
| chr2:191040867
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1335+198G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040867 | ||||||
| chr2:191040988
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1335+77G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 15/23 | chr2 | 191040988 | ||||||
| chr2:191041352
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1252-204A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191041352 | ||||||
| chr2:191041473
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1252-325G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191041473 | ||||||
| chr2:191041504
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1252-356T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191041504 | ||||||
| chr2:191041730
|
AG | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0123others(2): Show | 5 | HG00140.hp2 HG01081.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-583delC | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191041730 | ||||||
| chr2:191041854
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1252-706C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191041854 | ||||||
| chr2:191041855
|
A | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0021others(10): Show | 14 | HG00323.hp1 HG00733.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1252-707T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191041855 | ||||||
| chr2:191042033
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1252-885G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042033 | ||||||
| chr2:191042182
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1252-1034G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042182 | ||||||
| chr2:191042184
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1252-1036G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042184 | ||||||
| chr2:191042362
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1252-1214T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042362 | ||||||
| chr2:191042777
|
C | CT | 118 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 118 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1252-1630dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042777 | ||||||
| chr2:191042801
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(239): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1252-1653A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042801 | ||||||
| chr2:191042826
|
CTGGAGTG others(3): Show |
C | 3 | a0001c0001t0001g0100a0001c0001t0001g0237a0001c0001t0001g0254 | 3 | HG02809.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1252-1688_1252-167 others(14): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042826 | ||||||
| chr2:191042929
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 72 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1252-1781C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042929 | ||||||
| chr2:191042946
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1252-1798T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191042946 | ||||||
| chr2:191043135
|
T | C | 15 | a0001c0001t0001g0028a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1252-1987A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043135 | ||||||
| chr2:191043257
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1252-2109C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043257 | ||||||
| chr2:191043422
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1252-2274T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043422 | ||||||
| chr2:191043436
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0182others(3): Show | 6 | HG01071.hp2 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1252-2288A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043436 | ||||||
| chr2:191043480
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1252-2332T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043480 | ||||||
| chr2:191043539
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1252-2391G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043539 | ||||||
| chr2:191043664
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1252-2516A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043664 | ||||||
| chr2:191043754
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1252-2606G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043754 | ||||||
| chr2:191043755
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1252-2607C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043755 | ||||||
| chr2:191043831
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1252-2683C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191043831 | ||||||
| chr2:191044030
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1252-2882C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044030 | ||||||
| chr2:191044040
|
T | TG | 5 | a0001c0001t0001g0049a0001c0001t0001g0161a0001c0001t0001g0184others(2): Show | 5 | HG00621.hp1 HG02055.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-2893dupC | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044040 | ||||||
| chr2:191044232
|
T | C | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1252-3084A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044232 | ||||||
| chr2:191044618
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1252-3470C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044618 | ||||||
| chr2:191044848
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1252-3700A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044848 | ||||||
| chr2:191044857
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1252-3709A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044857 | ||||||
| chr2:191044872
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1252-3724A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044872 | ||||||
| chr2:191044977
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1252-3829T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191044977 | ||||||
| chr2:191045138
|
A | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(27): Show | 31 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(28): Show |
intron_variant | MODIFIER | c.1252-3990T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191045138 | ||||||
| chr2:191045570
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1252-4422C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191045570 | ||||||
| chr2:191045837
|
T | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1252-4689A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191045837 | ||||||
| chr2:191045915
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1252-4767G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191045915 | ||||||
| chr2:191045980
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1252-4832C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191045980 | ||||||
| chr2:191046017
|
C | G | 7 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0113others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1252-4869G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191046017 | ||||||
| chr2:191046292
|
C | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1252-5144G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191046292 | ||||||
| chr2:191046341
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1252-5193T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191046341 | ||||||
| chr2:191046411
|
C | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0055others(10): Show | 13 | HG01192.hp1 HG02145.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1252-5263G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191046411 | ||||||
| chr2:191046462
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1252-5314G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191046462 | ||||||
| chr2:191046554
|
G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0182others(2): Show | 5 | HG01071.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-5406C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191046554 | ||||||
| chr2:191046636
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1252-5488A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191046636 | ||||||
| chr2:191047077
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1252-5929A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047077 | ||||||
| chr2:191047121
|
G | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0123others(2): Show | 5 | HG00140.hp2 HG01081.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-5973C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047121 | ||||||
| chr2:191047124
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1252-5976T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047124 | ||||||
| chr2:191047126
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG01256.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1252-5978C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047126 | ||||||
| chr2:191047484
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1252-6336A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047484 | ||||||
| chr2:191047590
|
A | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0055others(10): Show | 13 | HG01192.hp1 HG02145.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1252-6442T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047590 | ||||||
| chr2:191047694
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1252-6546G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047694 | ||||||
| chr2:191047734
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1252-6586A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047734 | ||||||
| chr2:191047806
|
T | C | 122 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1252-6658A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047806 | ||||||
| chr2:191047814
|
C | T | 92 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 92 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1252-6666G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047814 | ||||||
| chr2:191047958
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251+6532C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191047958 | ||||||
| chr2:191048186
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0126 | 2 | HG02027.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1251+6304A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048186 | ||||||
| chr2:191048308
|
A | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(27): Show | 31 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251+6182T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048308 | ||||||
| chr2:191048479
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1251+6011T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048479 | ||||||
| chr2:191048513
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0161a0001c0001t0001g0182others(6): Show | 9 | HG01071.hp2 HG02145.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251+5977G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048513 | ||||||
| chr2:191048613
|
CA | C | 64 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1251+5876delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048613 | ||||||
| chr2:191048627
|
A | G | 5 | a0001c0001t0001g0161a0001c0001t0001g0182a0001c0001t0001g0235others(2): Show | 5 | HG01071.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251+5863T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048627 | ||||||
| chr2:191048631
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1251+5859T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048631 | ||||||
| chr2:191048743
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+5747C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048743 | ||||||
| chr2:191048788
|
CA | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 68 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1251+5701delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048788 | ||||||
| chr2:191048788
|
CAA | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1251+5700_1251+570 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048788 | ||||||
| chr2:191048788
|
CAAA | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0038others(5): Show | 8 | HG00140.hp2 HG01074.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1251+5699_1251+570 others(7): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048788 | ||||||
| chr2:191048818
|
A | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+5672T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048818 | ||||||
| chr2:191048916
|
A | G | 92 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 92 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1251+5574T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048916 | ||||||
| chr2:191048922
|
T | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+5568A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191048922 | ||||||
| chr2:191049073
|
A | G | 114 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1251+5417T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049073 | ||||||
| chr2:191049099
|
C | CT | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp2 HG02698.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251+5390dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049099 | ||||||
| chr2:191049167
|
C | CT | 49 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(46): Show | 50 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1251+5322dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049167 | ||||||
| chr2:191049167
|
C | CTT | 13 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0015others(10): Show | 13 | HG00741.hp1 HG02080.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1251+5321_1251+532 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049167 | ||||||
| chr2:191049167
|
CT | C | 9 | a0001c0001t0001g0026a0001c0001t0001g0060a0001c0001t0001g0064others(6): Show | 9 | HG00323.hp2 HG01081.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251+5322delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049167 | ||||||
| chr2:191049244
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1251+5246T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049244 | ||||||
| chr2:191049270
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1251+5220C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049270 | ||||||
| chr2:191049412
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1251+5078C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049412 | ||||||
| chr2:191049456
|
G | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0232 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1251+5034C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049456 | ||||||
| chr2:191049935
|
T | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0161others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1251+4555A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049935 | ||||||
| chr2:191049969
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1251+4521C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049969 | ||||||
| chr2:191050120
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1251+4370C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050120 | ||||||
| chr2:191050241
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1251+4249G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050241 | ||||||
| chr2:191050482
|
A | G | 22 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0021others(19): Show | 23 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1251+4008T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050482 | ||||||
| chr2:191050517
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1251+3973A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050517 | ||||||
| chr2:191050554
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251+3936C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050554 | ||||||
| chr2:191050633
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1251+3857A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050633 | ||||||
| chr2:191050661
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1251+3829T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050661 | ||||||
| chr2:191050817
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1251+3673T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050817 | ||||||
| chr2:191050842
|
C | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+3648G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050842 | ||||||
| chr2:191050947
|
T | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1251+3543A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050947 | ||||||
| chr2:191050989
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(190): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1251+3501C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050989 | ||||||
| chr2:191051012
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(24): Show | 28 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(25): Show |
intron_variant | MODIFIER | c.1251+3478C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051012 | ||||||
| chr2:191051195
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+3295T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051195 | ||||||
| chr2:191051638
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0190a0001c0001t0001g0233 | 3 | HG02717.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1251+2852A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051638 | ||||||
| chr2:191051743
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1251+2747G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051743 | ||||||
| chr2:191051800
|
AC | A | 74 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(71): Show | 74 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1251+2689delG | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051800 | ||||||
| chr2:191051834
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0282 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1251+2656G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051834 | ||||||
| chr2:191051980
|
T | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(5): Show | 8 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1251+2510A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051980 | ||||||
| chr2:191051991
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1251+2499G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191051991 | ||||||
| chr2:191052024
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1251+2466T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052024 | ||||||
| chr2:191052074
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251+2416A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052074 | ||||||
| chr2:191052225
|
C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1251+2265G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052225 | ||||||
| chr2:191052310
|
A | T | 1 | a0001c0001t0001g0286 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1251+2180T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052310 | ||||||
| chr2:191052389
|
G | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(5): Show | 8 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1251+2101C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052389 | ||||||
| chr2:191052480
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+2010T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052480 | ||||||
| chr2:191052509
|
C | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1251+1981G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052509 | ||||||
| chr2:191052591
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1251+1899A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052591 | ||||||
| chr2:191052618
|
C | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0021others(17): Show | 21 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1251+1872G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052618 | ||||||
| chr2:191052644
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1251+1846A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052644 | ||||||
| chr2:191052665
|
AGTTCAGG others(17): Show |
A | 33 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(30): Show | 34 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(31): Show |
intron_variant | MODIFIER | c.1251+1801_1251+182 others(28): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052665 | ||||||
| chr2:191052799
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0098 | 2 | NA18983.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1251+1691A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052799 | ||||||
| chr2:191052997
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251+1493C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052997 | ||||||
| chr2:191053059
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1251+1431G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053059 | ||||||
| chr2:191053135
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+1355T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053135 | ||||||
| chr2:191053305
|
C | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(29): Show | 33 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.1251+1185G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053305 | ||||||
| chr2:191053406
|
G | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0021others(15): Show | 19 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1251+1084C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053406 | ||||||
| chr2:191053536
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1251+954T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053536 | ||||||
| chr2:191053925
|
C | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02486.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1251+565G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053925 | ||||||
| chr2:191053925
|
C | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+565G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053925 | ||||||
| chr2:191053965
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1251+525C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053965 | ||||||
| chr2:191053978
|
A | C | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1251+512T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191053978 | ||||||
| chr2:191054045
|
T | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+445A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054045 | ||||||
| chr2:191054126
|
C | CA | 17 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0067others(14): Show | 17 | HG01074.hp2 HG01192.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1251+363dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054126 | ||||||
| chr2:191054140
|
AAAAGAAA others(85): Show |
A | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1251+258_1251+349d others(94): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054140 | ||||||
| chr2:191054142
|
AAGAAAGA others(83): Show |
A | 2 | a0001c0001t0001g0042a0001c0001t0001g0197 | 2 | HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1251+258_1251+347d others(92): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054142 | ||||||
| chr2:191054144
|
GAAAGAAA others(84): Show |
G | 29 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(26): Show | 30 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1251+255_1251+345d others(93): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054144 | ||||||
| chr2:191054235
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0059a0001c0001t0001g0197 | 3 | HG02897.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1251+255T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054235 | ||||||
| chr2:191054249
|
G | T | 1 | a0001c0001t0001g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1251+241C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054249 | ||||||
| chr2:191054261
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1251+229C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191054261 | ||||||
| chr2:191054566
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1207-32C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191054566 | ||||||
| chr2:191054628
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(29): Show | 33 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.1207-94T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191054628 | ||||||
| chr2:191054814
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1207-280G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191054814 | ||||||
| chr2:191055012
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02486.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1207-478C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055012 | ||||||
| chr2:191055096
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1207-562T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055096 | ||||||
| chr2:191055278
|
A | G | 5 | a0001c0001t0001g0100a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG02258.hp1 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-744T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055278 | ||||||
| chr2:191055365
|
AT | A | 33 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(30): Show | 33 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.1207-832delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055365 | ||||||
| chr2:191055365
|
ATT | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(28): Show | 32 | HG00639.hp2 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1207-833_1207-832d others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055365 | ||||||
| chr2:191055365
|
ATTT | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(15): Show | 18 | HG01192.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1207-834_1207-832d others(5): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055365 | ||||||
| chr2:191055365
|
ATTTT | A | 22 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0066others(19): Show | 22 | HG01891.hp1 HG02027.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.1207-835_1207-832d others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055365 | ||||||
| chr2:191055365
|
ATTTTT | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(154): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1207-836_1207-832d others(7): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055365 | ||||||
| chr2:191055365
|
ATTTTTT | A | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0038others(6): Show | 9 | HG00323.hp1 HG00673.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-837_1207-832d others(8): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055365 | ||||||
| chr2:191055365
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0001g0116a0001c0001t0001g0190a0001c0001t0001g0233 | 3 | HG02717.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1207-843_1207-832d others(14): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055365 | ||||||
| chr2:191055465
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1207-931G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055465 | ||||||
| chr2:191055485
|
CTGGGATT others(127): Show |
C | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1207-1085_1207-952 others(3): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055485 | ||||||
| chr2:191055544
|
G | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207-1010C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055544 | ||||||
| chr2:191055596
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1207-1062T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055596 | ||||||
| chr2:191055635
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1207-1101C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055635 | ||||||
| chr2:191055700
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1207-1166T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055700 | ||||||
| chr2:191055717
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0167 | 2 | NA18952.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1207-1183A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055717 | ||||||
| chr2:191055906
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-1372T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055906 | ||||||
| chr2:191055987
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0282 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1207-1453A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191055987 | ||||||
| chr2:191056045
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(29): Show | 33 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.1207-1511T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056045 | ||||||
| chr2:191056062
|
C | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1207-1528G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056062 | ||||||
| chr2:191056222
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-1688C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056222 | ||||||
| chr2:191056370
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1206+1648T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056370 | ||||||
| chr2:191056507
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1206+1511A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056507 | ||||||
| chr2:191056560
|
T | G | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1206+1458A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056560 | ||||||
| chr2:191056564
|
T | C | 7 | a0001c0001t0001g0080a0001c0001t0001g0151a0001c0001t0001g0171others(4): Show | 7 | HG02135.hp2 HG02155.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+1454A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056564 | ||||||
| chr2:191056610
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1206+1408T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056610 | ||||||
| chr2:191056702
|
T | C | 1 | a0001c0004t0001g0188 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1206+1316A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056702 | ||||||
| chr2:191056779
|
A | AT | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0019others(48): Show | 53 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1206+1238dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056779 | ||||||
| chr2:191056779
|
AT | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1206+1238delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056779 | ||||||
| chr2:191056876
|
G | T | 1 | a0001c0001t0001g0214 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1206+1142C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056876 | ||||||
| chr2:191056972
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1206+1046C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056972 | ||||||
| chr2:191057065
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1206+953C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057065 | ||||||
| chr2:191057073
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(171): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1206+945C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057073 | ||||||
| chr2:191057141
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1206+877G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057141 | ||||||
| chr2:191057148
|
C | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(71): Show | 74 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1206+870G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057148 | ||||||
| chr2:191057331
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0242 | 2 | HG02280.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1206+687G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057331 | ||||||
| chr2:191057350
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1206+668G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057350 | ||||||
| chr2:191057410
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1206+608A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057410 | ||||||
| chr2:191057423
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1206+595G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057423 | ||||||
| chr2:191057581
|
CT | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1206+436delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057581 | ||||||
| chr2:191057582
|
TTTTTTTT others(13): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1206+416_1206+435d others(22): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057582 | ||||||
| chr2:191057593
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1206+425A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057593 | ||||||
| chr2:191057602
|
C | CT | 11 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01433.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1206+415dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057602 | ||||||
| chr2:191057629
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(3): Show | 7 | HG00140.hp2 HG01081.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1206+389G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057629 | ||||||
| chr2:191057894
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1206+124C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057894 | ||||||
| chr2:191057959
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1206+59T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191057959 | ||||||
| chr2:191058115
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
splice_region_variant&intron_variant | LOW | c.1113-4C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 12/23 | chr2 | 191058115 | ||||||
| chr2:191058300
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(136): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1095-81A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 11/23 | chr2 | 191058300 | ||||||
| chr2:191058338
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1095-119A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 11/23 | chr2 | 191058338 | ||||||
| chr2:191058795
|
A | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02486.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1035-26T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191058795 | ||||||
| chr2:191058817
|
G | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0021others(17): Show | 21 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1035-48C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191058817 | ||||||
| chr2:191058945
|
A | G | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1035-176T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191058945 | ||||||
| chr2:191058962
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1035-193T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191058962 | ||||||
| chr2:191059040
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1035-271G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059040 | ||||||
| chr2:191059170
|
G | C | 1 | a0001c0001t0001g0236 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1035-401C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059170 | ||||||
| chr2:191059614
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1035-845G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059614 | ||||||
| chr2:191059646
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1035-877G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059646 | ||||||
| chr2:191059678
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1035-909G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059678 | ||||||
| chr2:191059687
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1035-918C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059687 | ||||||
| chr2:191059744
|
G | C | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1035-975C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059744 | ||||||
| chr2:191059880
|
T | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1035-1111A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059880 | ||||||
| chr2:191059981
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1035-1212A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191059981 | ||||||
| chr2:191060038
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1035-1269T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060038 | ||||||
| chr2:191060092
|
C | A | 2 | a0001c0001t0001g0255a0001c0001t0002g0004 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1035-1323G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060092 | ||||||
| chr2:191060208
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035-1439T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060208 | ||||||
| chr2:191060260
|
T | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1034+1469A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060260 | ||||||
| chr2:191060363
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1034+1366C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060363 | ||||||
| chr2:191060375
|
G | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01257.hp2 NA18950.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1034+1354C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060375 | ||||||
| chr2:191060480
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1034+1249C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060480 | ||||||
| chr2:191060584
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1034+1145T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060584 | ||||||
| chr2:191060663
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+1066G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060663 | ||||||
| chr2:191060698
|
C | T | 54 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(51): Show | 54 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.1034+1031G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060698 | ||||||
| chr2:191060712
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1034+1017G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060712 | ||||||
| chr2:191060950
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(252): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1034+779A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191060950 | ||||||
| chr2:191061033
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG02145.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1034+696C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191061033 | ||||||
| chr2:191061079
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02486.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1034+650A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191061079 | ||||||
| chr2:191061279
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1034+450A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191061279 | ||||||
| chr2:191061314
|
C | T | 10 | a0001c0001t0001g0043a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1034+415G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191061314 | ||||||
| chr2:191061335
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1034+394C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191061335 | ||||||
| chr2:191061507
|
C | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0184a0001c0001t0001g0271others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+222G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191061507 | ||||||
| chr2:191061707
|
A | C | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1034+22T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 10/23 | chr2 | 191061707 | ||||||
| chr2:191061945
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.942-124T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 9/23 | chr2 | 191061945 | ||||||
| chr2:191062090
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.942-269A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 9/23 | chr2 | 191062090 | ||||||
| chr2:191062323
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.941+439A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 9/23 | chr2 | 191062323 | ||||||
| chr2:191062747
|
T | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0190a0001c0001t0001g0233 | 3 | HG02717.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.941+15A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 9/23 | chr2 | 191062747 | ||||||
| chr2:191063217
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.783-297T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063217 | ||||||
| chr2:191063381
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783-461A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063381 | ||||||
| chr2:191063480
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-560A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063480 | ||||||
| chr2:191063628
|
G | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-708C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063628 | ||||||
| chr2:191063629
|
C | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-709G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063629 | ||||||
| chr2:191063630
|
C | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-710G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063630 | ||||||
| chr2:191063635
|
A | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-715T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063635 | ||||||
| chr2:191063636
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-716C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063636 | ||||||
| chr2:191063637
|
T | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-717A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063637 | ||||||
| chr2:191063640
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-720G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063640 | ||||||
| chr2:191063641
|
T | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0115others(8): Show | 11 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.783-721A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063641 | ||||||
| chr2:191063894
|
A | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.782+913T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191063894 | ||||||
| chr2:191064096
|
A | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0042others(30): Show | 34 | HG00639.hp2 HG01496.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.782+711T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191064096 | ||||||
| chr2:191064256
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.782+551G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191064256 | ||||||
| chr2:191064335
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.782+472G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191064335 | ||||||
| chr2:191064552
|
G | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG00140.hp1 HG00280.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.782+255C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 8/23 | chr2 | 191064552 | ||||||
| chr2:191065051
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | NA18940.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.631-93G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065051 | ||||||
| chr2:191065184
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.631-226C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065184 | ||||||
| chr2:191065221
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.631-263G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065221 | ||||||
| chr2:191065222
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0100others(8): Show | 11 | HG00323.hp1 HG00733.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.631-264C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065222 | ||||||
| chr2:191065286
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.631-328T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065286 | ||||||
| chr2:191065464
|
T | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0117others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-506A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065464 | ||||||
| chr2:191065564
|
T | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.631-606A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065564 | ||||||
| chr2:191065637
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.631-679A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065637 | ||||||
| chr2:191065745
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.630+685A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191065745 | ||||||
| chr2:191066139
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0108 | 2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.630+291C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191066139 | ||||||
| chr2:191066201
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0112 | 2 | HG01346.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.630+229T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191066201 | ||||||
| chr2:191066207
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.630+223A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191066207 | ||||||
| chr2:191066281
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.630+149G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191066281 | ||||||
| chr2:191066311
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.630+119C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191066311 | ||||||
| chr2:191066403
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.630+27T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 7/23 | chr2 | 191066403 | ||||||
| chr2:191066738
|
A | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.545-223T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191066738 | ||||||
| chr2:191066885
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.545-370G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191066885 | ||||||
| chr2:191067031
|
A | C | 5 | a0001c0001t0001g0116a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02280.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.545-516T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067031 | ||||||
| chr2:191067053
|
T | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0273a0001c0001t0001g0276 | 3 | HG00280.hp2 HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.545-538A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067053 | ||||||
| chr2:191067089
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.545-574G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067089 | ||||||
| chr2:191067234
|
G | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0100others(8): Show | 11 | HG00323.hp1 HG00733.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.545-719C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067234 | ||||||
| chr2:191067316
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.545-801A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067316 | ||||||
| chr2:191067323
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.545-808G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067323 | ||||||
| chr2:191067370
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.545-855T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067370 | ||||||
| chr2:191067379
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.545-864T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067379 | ||||||
| chr2:191067638
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.545-1123A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067638 | ||||||
| chr2:191067830
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.545-1315T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191067830 | ||||||
| chr2:191068528
|
G | A | 54 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(51): Show | 54 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.544+1165C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191068528 | ||||||
| chr2:191068557
|
T | C | 8 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0122others(5): Show | 8 | HG00280.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.544+1136A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191068557 | ||||||
| chr2:191068963
|
T | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(108): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.544+730A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191068963 | ||||||
| chr2:191068966
|
A | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00621.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.544+727T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191068966 | ||||||
| chr2:191069147
|
A | G | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0100others(8): Show | 11 | HG00323.hp1 HG00733.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.544+546T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191069147 | ||||||
| chr2:191069176
|
GTATT | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0117others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+513_544+516del others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191069176 | ||||||
| chr2:191069221
|
T | G | 1 | a0001c0004t0001g0188 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.544+472A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191069221 | ||||||
| chr2:191069355
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.544+338T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191069355 | ||||||
| chr2:191069370
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.544+323A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191069370 | ||||||
| chr2:191069453
|
T | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.544+240A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 6/23 | chr2 | 191069453 | ||||||
| chr2:191069861
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01257.hp2 NA18950.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.466-90A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191069861 | ||||||
| chr2:191069901
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.466-130C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191069901 | ||||||
| chr2:191070105
|
C | T | 10 | a0001c0001t0001g0043a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-334G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070105 | ||||||
| chr2:191070179
|
C | G | 12 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-408G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070179 | ||||||
| chr2:191070197
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.466-426G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070197 | ||||||
| chr2:191070307
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0053others(25): Show | 29 | HG00639.hp2 HG01496.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-536T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070307 | ||||||
| chr2:191070325
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.466-554T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070325 | ||||||
| chr2:191070371
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.466-600G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070371 | ||||||
| chr2:191070380
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.466-609A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070380 | ||||||
| chr2:191070479
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.466-708A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070479 | ||||||
| chr2:191070480
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0275 | 3 | HG02015.hp2 HG02071.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.466-709C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191070480 | ||||||
| chr2:191071033
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.466-1262T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071033 | ||||||
| chr2:191071078
|
C | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.466-1307G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071078 | ||||||
| chr2:191071106
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.466-1335C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071106 | ||||||
| chr2:191071162
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0237 | 3 | HG02976.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.466-1391C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071162 | ||||||
| chr2:191071195
|
A | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0222 | 3 | NA18999.hp2 NA19009.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.466-1424T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071195 | ||||||
| chr2:191071283
|
C | T | 1 | a0001c0002t0001g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.466-1512G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071283 | ||||||
| chr2:191071563
|
C | T | 6 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0167others(3): Show | 6 | HG00408.hp1 HG02071.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+1535G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071563 | ||||||
| chr2:191071657
|
A | G | 8 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0243others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.465+1441T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071657 | ||||||
| chr2:191071709
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.465+1389T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071709 | ||||||
| chr2:191071872
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.465+1226C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191071872 | ||||||
| chr2:191072021
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0099others(11): Show | 14 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.465+1077T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191072021 | ||||||
| chr2:191072036
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.465+1062C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191072036 | ||||||
| chr2:191072489
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.465+609G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191072489 | ||||||
| chr2:191072620
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.465+478G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191072620 | ||||||
| chr2:191072750
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.465+348G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191072750 | ||||||
| chr2:191072936
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.465+162T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191072936 | ||||||
| chr2:191072997
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.465+101T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 5/23 | chr2 | 191072997 | ||||||
| chr2:191073215
|
T | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG02145.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.373-25A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073215 | ||||||
| chr2:191073268
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0117others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-78C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073268 | ||||||
| chr2:191073398
|
T | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.373-208A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073398 | ||||||
| chr2:191073481
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.373-291C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073481 | ||||||
| chr2:191073654
|
C | T | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.373-464G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073654 | ||||||
| chr2:191073685
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0117others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-495C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073685 | ||||||
| chr2:191073688
|
T | TCAAA | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(200): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.373-502_373-499dup others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073688 | ||||||
| chr2:191073762
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.373-572G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073762 | ||||||
| chr2:191073874
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(26): Show | 30 | HG00639.hp2 HG01496.hp1 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.373-684C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073874 | ||||||
| chr2:191073911
|
T | C | 6 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG02647.hp1 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-721A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073911 | ||||||
| chr2:191073979
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0117others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-789A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191073979 | ||||||
| chr2:191074047
|
T | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-857A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074047 | ||||||
| chr2:191074071
|
T | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.373-881A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074071 | ||||||
| chr2:191074158
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0115 | 2 | HG01192.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.373-968G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074158 | ||||||
| chr2:191074461
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(211): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.373-1271G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074461 | ||||||
| chr2:191074606
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.373-1416A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074606 | ||||||
| chr2:191074773
|
A | T | 8 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(5): Show | 9 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.372+1454T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074773 | ||||||
| chr2:191074818
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.372+1409C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074818 | ||||||
| chr2:191074888
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.372+1339G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191074888 | ||||||
| chr2:191075087
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.372+1140C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075087 | ||||||
| chr2:191075170
|
C | CA | 41 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(38): Show | 41 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.372+1056dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075170 | ||||||
| chr2:191075179
|
A | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0099others(11): Show | 14 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+1048T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075179 | ||||||
| chr2:191075534
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(22): Show | 26 | HG00639.hp2 HG01496.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.372+693C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075534 | ||||||
| chr2:191075609
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.372+618A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075609 | ||||||
| chr2:191075653
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.372+574T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075653 | ||||||
| chr2:191075725
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.372+502C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075725 | ||||||
| chr2:191075749
|
T | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+478A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075749 | ||||||
| chr2:191075833
|
CTTTCT | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0099others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.372+389_372+393del others(5): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075833 | ||||||
| chr2:191075837
|
C | CT | 47 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(44): Show | 48 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.372+389dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075837 | ||||||
| chr2:191075837
|
CT | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0060others(6): Show | 9 | HG01081.hp2 HG02080.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.372+389delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075837 | ||||||
| chr2:191075837
|
CTT | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+388_372+389del others(2): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075837 | ||||||
| chr2:191075840
|
T | TC | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0185 | 3 | HG02258.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.372+386_372+387ins others(1): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075840 | ||||||
| chr2:191075841
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0130a0001c0001t0001g0191 | 3 | HG01106.hp1 HG01256.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.372+386A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075841 | ||||||
| chr2:191075852
|
T | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0099others(17): Show | 20 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.372+375A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 4/23 | chr2 | 191075852 | ||||||
| chr2:191076648
|
C | CT | 32 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0037others(29): Show | 33 | HG01071.hp1 HG01496.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-324dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191076648 | ||||||
| chr2:191076715
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.274-390T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191076715 | ||||||
| chr2:191076979
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0282 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.274-654A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191076979 | ||||||
| chr2:191077051
|
G | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-726C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077051 | ||||||
| chr2:191077078
|
T | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0146others(2): Show | 5 | HG02258.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-753A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077078 | ||||||
| chr2:191077254
|
T | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-929A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077254 | ||||||
| chr2:191077285
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0282 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.274-960A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077285 | ||||||
| chr2:191077491
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0252 | 2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.274-1166G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077491 | ||||||
| chr2:191077693
|
G | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | NA18940.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.274-1368C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077693 | ||||||
| chr2:191077774
|
A | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0159others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-1449T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077774 | ||||||
| chr2:191077787
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.274-1462G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077787 | ||||||
| chr2:191077932
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-1607G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191077932 | ||||||
| chr2:191078101
|
T | TA | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(216): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.274-1777dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191078101 | ||||||
| chr2:191078458
|
T | C | 5 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 5 | HG02083.hp1 NA18944.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-2133A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191078458 | ||||||
| chr2:191078546
|
A | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0192 | 2 | HG00280.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.274-2221T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191078546 | ||||||
| chr2:191078903
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.274-2578A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191078903 | ||||||
| chr2:191079016
|
C | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.274-2691G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079016 | ||||||
| chr2:191079235
|
T | TCACACAC others(9): Show |
186 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(183): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.274-2911_274-2910i others(18): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079235 | ||||||
| chr2:191079235
|
T | TCACACAC others(11): Show |
2 | a0001c0001t0001g0133a0004c0008t0001g0248 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.274-2911_274-2910i others(20): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079235 | ||||||
| chr2:191079235
|
T | TCACACAC others(25): Show |
25 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(22): Show | 26 | HG00639.hp2 HG01496.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.274-2911_274-2910i others(34): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079235 | ||||||
| chr2:191079235
|
T | TCACGCAC others(9): Show |
1 | a0001c0001t0001g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274-2911_274-2910i others(18): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079235 | ||||||
| chr2:191079254
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 4 | HG02717.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-2929G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079254 | ||||||
| chr2:191079270
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0190others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-2945T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079270 | ||||||
| chr2:191079304
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0165others(2): Show | 5 | HG02486.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-2979C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079304 | ||||||
| chr2:191079583
|
A | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0221 | 2 | NA18966.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.274-3258T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079583 | ||||||
| chr2:191079847
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.274-3522G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079847 | ||||||
| chr2:191079992
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-3667A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191079992 | ||||||
| chr2:191080087
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0146others(2): Show | 5 | HG02258.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3762C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191080087 | ||||||
| chr2:191080419
|
T | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0146others(2): Show | 5 | HG02258.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-4094A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191080419 | ||||||
| chr2:191080591
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.274-4266A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191080591 | ||||||
| chr2:191080610
|
C | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG01169.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-4285G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191080610 | ||||||
| chr2:191080855
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274-4530T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191080855 | ||||||
| chr2:191080898
|
T | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-4573A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191080898 | ||||||
| chr2:191080931
|
T | G | 1 | a0001c0001t0001g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.274-4606A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191080931 | ||||||
| chr2:191081218
|
A | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0099others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.274-4893T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191081218 | ||||||
| chr2:191081431
|
C | T | 1 | a0003c0007t0001g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.274-5106G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191081431 | ||||||
| chr2:191081596
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(100): Show | 104 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.274-5271G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191081596 | ||||||
| chr2:191081853
|
C | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-5528G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191081853 | ||||||
| chr2:191081877
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(4): Show | 8 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-5552A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191081877 | ||||||
| chr2:191081933
|
TG | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0190others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-5609delC | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191081933 | ||||||
| chr2:191082455
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0099others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.274-6130G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191082455 | ||||||
| chr2:191082819
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-6494G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191082819 | ||||||
| chr2:191082898
|
T | C | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.274-6573A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191082898 | ||||||
| chr2:191083241
|
G | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-6916C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191083241 | ||||||
| chr2:191083318
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.274-6993G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191083318 | ||||||
| chr2:191083546
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(100): Show | 104 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.274-7221G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191083546 | ||||||
| chr2:191083911
|
G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(2): Show | 6 | HG00140.hp2 HG01081.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-7586C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191083911 | ||||||
| chr2:191083947
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.274-7622C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191083947 | ||||||
| chr2:191084013
|
C | T | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.274-7688G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191084013 | ||||||
| chr2:191084176
|
C | G | 1 | a0001c0001t0002g0004 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.274-7851G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191084176 | ||||||
| chr2:191084210
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.274-7885G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191084210 | ||||||
| chr2:191084211
|
G | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0197 | 3 | HG02895.hp1 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.274-7886C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191084211 | ||||||
| chr2:191084256
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02486.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-7931G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191084256 | ||||||
| chr2:191084260
|
T | TA | 29 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0037others(26): Show | 30 | HG00639.hp2 HG01496.hp1 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.274-7936dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191084260 | ||||||
| chr2:191084906
|
G | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0169others(1): Show | 4 | HG00323.hp1 HG00733.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-8581C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191084906 | ||||||
| chr2:191085054
|
C | CA | 14 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0030others(11): Show | 14 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.274-8730dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191085054 | ||||||
| chr2:191085506
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.274-9181G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191085506 | ||||||
| chr2:191085741
|
G | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0165others(2): Show | 5 | HG02486.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-9416C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191085741 | ||||||
| chr2:191085920
|
CT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0165others(2): Show | 5 | HG02486.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-9596delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191085920 | ||||||
| chr2:191086012
|
T | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-9687A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191086012 | ||||||
| chr2:191086183
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.274-9858C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191086183 | ||||||
| chr2:191086294
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0120 | 2 | HG02129.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.274-9969G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191086294 | ||||||
| chr2:191086295
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG01169.hp1 HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.274-9970C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191086295 | ||||||
| chr2:191086635
|
GATTCTAG others(8): Show |
G | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(89): Show | 94 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.274-10325_274-1031 others(19): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191086635 | ||||||
| chr2:191086899
|
C | T | 8 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0243others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-10574G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191086899 | ||||||
| chr2:191086915
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0166others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-10590T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191086915 | ||||||
| chr2:191087085
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-10760A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087085 | ||||||
| chr2:191087250
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-10925G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087250 | ||||||
| chr2:191087313
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0137others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-10988G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087313 | ||||||
| chr2:191087357
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.274-11032T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087357 | ||||||
| chr2:191087392
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0169others(1): Show | 4 | HG00323.hp1 HG00733.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-11067C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087392 | ||||||
| chr2:191087448
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.274-11123A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087448 | ||||||
| chr2:191087536
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.274-11211C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087536 | ||||||
| chr2:191087641
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-11316G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191087641 | ||||||
| chr2:191088068
|
T | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.274-11743A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088068 | ||||||
| chr2:191088069
|
C | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.274-11744G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088069 | ||||||
| chr2:191088124
|
C | T | 9 | a0001c0001t0001g0051a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 9 | HG03834.hp1 NA18952.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-11799G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088124 | ||||||
| chr2:191088183
|
A | C | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.274-11858T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088183 | ||||||
| chr2:191088201
|
A | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-11876T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088201 | ||||||
| chr2:191088215
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0086 | 2 | NA18959.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.274-11890C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088215 | ||||||
| chr2:191088302
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.274-11977C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088302 | ||||||
| chr2:191088663
|
C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 41 | HG00140.hp2 HG01081.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.274-12338G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088663 | ||||||
| chr2:191089138
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0019others(41): Show | 46 | HG00140.hp2 HG00639.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.274-12813C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089138 | ||||||
| chr2:191089208
|
AAAGC | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0095others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-12887_274-1288 others(8): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089208 | ||||||
| chr2:191089272
|
A | C | 55 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.274-12947T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089272 | ||||||
| chr2:191089286
|
A | T | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.274-12961T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089286 | ||||||
| chr2:191089321
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.274-12996C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089321 | ||||||
| chr2:191089428
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.274-13103T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089428 | ||||||
| chr2:191089724
|
A | G | 13 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0101others(10): Show | 13 | HG01884.hp1 HG02280.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-13399T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089724 | ||||||
| chr2:191089998
|
C | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-13673G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191089998 | ||||||
| chr2:191090005
|
G | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0181a0004c0008t0001g0248 | 3 | HG01884.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-13680C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090005 | ||||||
| chr2:191090090
|
A | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(21): Show | 25 | HG00639.hp2 HG01071.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.274-13765T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090090 | ||||||
| chr2:191090126
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 172 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.274-13801C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090126 | ||||||
| chr2:191090231
|
A | T | 1 | a0001c0001t0001g0269 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.274-13906T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090231 | ||||||
| chr2:191090463
|
TATA | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.274-14141_274-1413 others(7): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090463 | ||||||
| chr2:191090535
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-14210G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090535 | ||||||
| chr2:191090718
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.274-14393C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090718 | ||||||
| chr2:191090724
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.274-14399G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090724 | ||||||
| chr2:191090728
|
T | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0222 | 3 | NA18999.hp2 NA19009.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.274-14403A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090728 | ||||||
| chr2:191090778
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0137others(2): Show | 5 | HG02486.hp2 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-14453C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090778 | ||||||
| chr2:191090871
|
G | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | HG01071.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-14546C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090871 | ||||||
| chr2:191090910
|
T | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG02809.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-14585A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191090910 | ||||||
| chr2:191091404
|
AG | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(15): Show | 19 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.274-15080delC | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091404 | ||||||
| chr2:191091442
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-15117A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091442 | ||||||
| chr2:191091512
|
T | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-15187A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091512 | ||||||
| chr2:191091523
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0019others(27): Show | 31 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.274-15198G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091523 | ||||||
| chr2:191091632
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.274-15307A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091632 | ||||||
| chr2:191091677
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.274-15352A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091677 | ||||||
| chr2:191091793
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.274-15468A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091793 | ||||||
| chr2:191091799
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(4): Show | 8 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-15474C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091799 | ||||||
| chr2:191091811
|
G | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0181a0004c0008t0001g0248 | 3 | HG01884.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-15486C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091811 | ||||||
| chr2:191091843
|
T | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.274-15518A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191091843 | ||||||
| chr2:191092032
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.274-15707C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092032 | ||||||
| chr2:191092063
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274-15738A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092063 | ||||||
| chr2:191092513
|
TA | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(13): Show | 17 | HG01081.hp1 HG01261.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.274-16189delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092513 | ||||||
| chr2:191092687
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(19): Show | 23 | HG00639.hp2 HG01071.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.274-16362C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092687 | ||||||
| chr2:191092717
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.274-16392C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092717 | ||||||
| chr2:191092771
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.274-16446G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092771 | ||||||
| chr2:191092815
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.274-16490A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092815 | ||||||
| chr2:191092969
|
C | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(119): Show | 123 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.274-16644G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092969 | ||||||
| chr2:191092983
|
A | T | 1 | a0001c0002t0001g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274-16658T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191092983 | ||||||
| chr2:191093259
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.274-16934G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093259 | ||||||
| chr2:191093277
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.274-16952C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093277 | ||||||
| chr2:191093445
|
A | AGGGTCTG | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0146others(2): Show | 5 | HG02258.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-17127_274-1712 others(11): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093445 | ||||||
| chr2:191093792
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.274-17467G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093792 | ||||||
| chr2:191093804
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0137 | 3 | HG02486.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.274-17479C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093804 | ||||||
| chr2:191093855
|
C | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0032others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-17530G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093855 | ||||||
| chr2:191093908
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-17583G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093908 | ||||||
| chr2:191093930
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.274-17605G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191093930 | ||||||
| chr2:191094069
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.274-17744G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094069 | ||||||
| chr2:191094072
|
A | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-17747T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094072 | ||||||
| chr2:191094383
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274-18058G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094383 | ||||||
| chr2:191094384
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0263 | 2 | NA19077.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.274-18059C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094384 | ||||||
| chr2:191094722
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.274-18397A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094722 | ||||||
| chr2:191094763
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.274-18438T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094763 | ||||||
| chr2:191094885
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-18560C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094885 | ||||||
| chr2:191094917
|
C | CA | 102 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(99): Show | 103 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.274-18593dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094917 | ||||||
| chr2:191094917
|
C | CAAA | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(23): Show | 27 | HG00639.hp2 HG01071.hp2 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.274-18595_274-1859 others(7): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094917 | ||||||
| chr2:191094917
|
CA | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(69): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.274-18593delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094917 | ||||||
| chr2:191094951
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-18626T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094951 | ||||||
| chr2:191094987
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.274-18662T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094987 | ||||||
| chr2:191095018
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.274-18693A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095018 | ||||||
| chr2:191095122
|
C | CAA | 4 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-18798_274-1879 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095122 | ||||||
| chr2:191095207
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(159): Show | 164 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.274-18882G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095207 | ||||||
| chr2:191095244
|
A | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-18919T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095244 | ||||||
| chr2:191095253
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-18928T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095253 | ||||||
| chr2:191095383
|
T | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.274-19058A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095383 | ||||||
| chr2:191095482
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0189 | 2 | HG00140.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.274-19157A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095482 | ||||||
| chr2:191095662
|
G | C | 10 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-19337C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095662 | ||||||
| chr2:191095683
|
C | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(13): Show | 17 | HG00140.hp2 HG01081.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-19358G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095683 | ||||||
| chr2:191095729
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.274-19404G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095729 | ||||||
| chr2:191095804
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.274-19479G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095804 | ||||||
| chr2:191095816
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0137 | 3 | HG02486.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.274-19491G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095816 | ||||||
| chr2:191095874
|
C | T | 14 | a0001c0001t0001g0031a0001c0001t0001g0142a0001c0001t0001g0143others(11): Show | 14 | HG01346.hp2 HG01891.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-19549G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191095874 | ||||||
| chr2:191096161
|
G | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-19836C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096161 | ||||||
| chr2:191096189
|
T | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0202 | 3 | HG02818.hp2 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.274-19864A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096189 | ||||||
| chr2:191096401
|
C | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(9): Show | 13 | HG01496.hp1 HG02135.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-20076G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096401 | ||||||
| chr2:191096422
|
C | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-20097G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096422 | ||||||
| chr2:191096475
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0117others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-20150G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096475 | ||||||
| chr2:191096625
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-20300A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096625 | ||||||
| chr2:191096703
|
C | A | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-20378G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096703 | ||||||
| chr2:191096860
|
T | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-20535A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096860 | ||||||
| chr2:191096890
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(98): Show | 102 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.274-20565G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096890 | ||||||
| chr2:191096967
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.274-20642T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096967 | ||||||
| chr2:191096970
|
C | A | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.274-20645G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096970 | ||||||
| chr2:191096990
|
A | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0139others(6): Show | 9 | HG02258.hp1 HG02717.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-20665T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191096990 | ||||||
| chr2:191097021
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-20696A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097021 | ||||||
| chr2:191097081
|
T | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.274-20756A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097081 | ||||||
| chr2:191097242
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-20917T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097242 | ||||||
| chr2:191097244
|
T | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(48): Show | 53 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.274-20919A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097244 | ||||||
| chr2:191097249
|
T | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0060a0001c0001t0001g0063others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-20924A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097249 | ||||||
| chr2:191097370
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 197 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.274-21045A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097370 | ||||||
| chr2:191097486
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.274-21161G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097486 | ||||||
| chr2:191097502
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0190others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-21177T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097502 | ||||||
| chr2:191097514
|
TG | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-21190delC | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097514 | ||||||
| chr2:191097597
|
T | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0038others(4): Show | 8 | HG00140.hp2 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-21272A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097597 | ||||||
| chr2:191097866
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0137 | 3 | HG02486.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.274-21541G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097866 | ||||||
| chr2:191097889
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.274-21564T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097889 | ||||||
| chr2:191097914
|
G | GA | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 195 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.274-21590dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097914 | ||||||
| chr2:191097925
|
C | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0076a0001c0001t0001g0078 | 3 | HG00733.hp2 HG01516.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.274-21600G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097925 | ||||||
| chr2:191098015
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-21690G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098015 | ||||||
| chr2:191098024
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-21699T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098024 | ||||||
| chr2:191098087
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-21762A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098087 | ||||||
| chr2:191098268
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-21943G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098268 | ||||||
| chr2:191098523
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-22198T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098523 | ||||||
| chr2:191098579
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0286 | 2 | HG00323.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.274-22254C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098579 | ||||||
| chr2:191098581
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | NA18940.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.274-22256C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098581 | ||||||
| chr2:191098666
|
G | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-22341C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098666 | ||||||
| chr2:191098689
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.274-22364T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098689 | ||||||
| chr2:191098955
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.274-22630T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191098955 | ||||||
| chr2:191099208
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274-22883T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099208 | ||||||
| chr2:191099471
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.274-23146C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099471 | ||||||
| chr2:191099523
|
C | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0116a0001c0001t0001g0139others(6): Show | 9 | HG02258.hp1 HG02717.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-23198G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099523 | ||||||
| chr2:191099568
|
C | T | 1 | a0001c0002t0001g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274-23243G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099568 | ||||||
| chr2:191099583
|
CAA | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG02809.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-23260_274-2325 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099583 | ||||||
| chr2:191099597
|
A | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(18): Show | 22 | HG00639.hp2 HG01071.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.274-23272T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099597 | ||||||
| chr2:191099636
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG01891.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.274-23311A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099636 | ||||||
| chr2:191099672
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.274-23347A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099672 | ||||||
| chr2:191099907
|
T | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 221 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.274-23582A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099907 | ||||||
| chr2:191099952
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.274-23627A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191099952 | ||||||
| chr2:191100283
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.274-23958T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191100283 | ||||||
| chr2:191100365
|
T | C | 8 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0243others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-24040A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191100365 | ||||||
| chr2:191100592
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.274-24267C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191100592 | ||||||
| chr2:191100618
|
C | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(111): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.274-24293G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191100618 | ||||||
| chr2:191100989
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-24664T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191100989 | ||||||
| chr2:191101196
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.274-24871A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101196 | ||||||
| chr2:191101225
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274-24900G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101225 | ||||||
| chr2:191101348
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0181a0004c0008t0001g0248 | 3 | HG01884.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-25023G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101348 | ||||||
| chr2:191101426
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.274-25101G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101426 | ||||||
| chr2:191101473
|
C | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0243others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-25148G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101473 | ||||||
| chr2:191101500
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.274-25175C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101500 | ||||||
| chr2:191101608
|
C | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-25283G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101608 | ||||||
| chr2:191101685
|
G | A | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.274-25360C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101685 | ||||||
| chr2:191101726
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 211 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.274-25401C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101726 | ||||||
| chr2:191101904
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-25579T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191101904 | ||||||
| chr2:191102004
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-25679G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102004 | ||||||
| chr2:191102009
|
C | CT | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(41): Show | 46 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.274-25685dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102009 | ||||||
| chr2:191102118
|
A | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-25793T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102118 | ||||||
| chr2:191102149
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0137 | 3 | HG02486.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.274-25824C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102149 | ||||||
| chr2:191102194
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG02809.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-25869C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102194 | ||||||
| chr2:191102223
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.274-25898C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102223 | ||||||
| chr2:191102360
|
CTCTTTTG others(4): Show |
C | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.274-26046_274-2603 others(15): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102360 | ||||||
| chr2:191102453
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-26128G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102453 | ||||||
| chr2:191102513
|
A | T | 8 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0243others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-26188T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102513 | ||||||
| chr2:191102521
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.274-26196G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102521 | ||||||
| chr2:191102853
|
G | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0095others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-26528C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102853 | ||||||
| chr2:191102863
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0212 | 2 | HG04184.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.274-26538C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102863 | ||||||
| chr2:191102915
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00621.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.274-26590A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191102915 | ||||||
| chr2:191103164
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-26839A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103164 | ||||||
| chr2:191103167
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.274-26842C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103167 | ||||||
| chr2:191103431
|
G | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.274-27106C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103431 | ||||||
| chr2:191103471
|
C | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG02809.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-27146G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103471 | ||||||
| chr2:191103541
|
T | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0040others(8): Show | 11 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-27216A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103541 | ||||||
| chr2:191103642
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-27317A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103642 | ||||||
| chr2:191103694
|
T | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0046others(18): Show | 22 | HG00639.hp2 HG01071.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.274-27369A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103694 | ||||||
| chr2:191103742
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.274-27417G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103742 | ||||||
| chr2:191103789
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-27464A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103789 | ||||||
| chr2:191103940
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.274-27615G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191103940 | ||||||
| chr2:191104092
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.274-27767A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104092 | ||||||
| chr2:191104187
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.274-27862C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104187 | ||||||
| chr2:191104368
|
C | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0031others(10): Show | 13 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-28043G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104368 | ||||||
| chr2:191104462
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-28137G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104462 | ||||||
| chr2:191104585
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-28260A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104585 | ||||||
| chr2:191104615
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.274-28290G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104615 | ||||||
| chr2:191104744
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.274-28419A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104744 | ||||||
| chr2:191104779
|
G | T | 1 | a0004c0008t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.274-28454C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191104779 | ||||||
| chr2:191105011
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.274-28686T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105011 | ||||||
| chr2:191105029
|
G | A | 6 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG02647.hp1 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-28704C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105029 | ||||||
| chr2:191105090
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.274-28765C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105090 | ||||||
| chr2:191105153
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.274-28828C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105153 | ||||||
| chr2:191105203
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-28878G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105203 | ||||||
| chr2:191105394
|
C | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.274-29069G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105394 | ||||||
| chr2:191105449
|
C | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-29124G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105449 | ||||||
| chr2:191105538
|
T | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0243others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-29213A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105538 | ||||||
| chr2:191105597
|
TAA | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-29274_274-2927 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105597 | ||||||
| chr2:191105604
|
C | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0037others(19): Show | 23 | HG00639.hp2 HG01071.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.274-29279G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105604 | ||||||
| chr2:191105718
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.274-29393A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105718 | ||||||
| chr2:191105766
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0184 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.274-29441T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105766 | ||||||
| chr2:191105815
|
T | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0122 | 2 | HG01243.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.274-29490A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105815 | ||||||
| chr2:191105872
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-29547C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105872 | ||||||
| chr2:191105877
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.274-29552A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191105877 | ||||||
| chr2:191106071
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG02809.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-29746C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106071 | ||||||
| chr2:191106132
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-29807A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106132 | ||||||
| chr2:191106429
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 176 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.274-30104C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106429 | ||||||
| chr2:191106525
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.274-30200C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106525 | ||||||
| chr2:191106536
|
G | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-30211C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106536 | ||||||
| chr2:191106647
|
A | AAAAAT | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.274-30327_274-3032 others(9): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106647 | ||||||
| chr2:191106647
|
A | AAAAATAA others(3): Show |
42 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.274-30332_274-3032 others(14): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106647 | ||||||
| chr2:191106647
|
A | AAAAATAA others(8): Show |
20 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0144others(17): Show | 20 | HG00438.hp1 HG00621.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.274-30337_274-3032 others(19): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106647 | ||||||
| chr2:191106647
|
AAAAAT | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0132others(9): Show | 12 | HG01516.hp1 HG01517.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-30327_274-3032 others(9): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106647 | ||||||
| chr2:191106647
|
AAAAATAA others(3): Show |
A | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG01071.hp2 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-30332_274-3032 others(14): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106647 | ||||||
| chr2:191106647
|
AAAAATAA others(8): Show |
A | 62 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(59): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-30337_274-3032 others(19): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106647 | ||||||
| chr2:191106839
|
G | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.274-30514C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191106839 | ||||||
| chr2:191107008
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-30683T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191107008 | ||||||
| chr2:191107179
|
T | C | 8 | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0243others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-30854A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191107179 | ||||||
| chr2:191107485
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.274-31160C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191107485 | ||||||
| chr2:191107528
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0212 | 2 | HG04184.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.274-31203T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191107528 | ||||||
| chr2:191107878
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.274-31553T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191107878 | ||||||
| chr2:191107997
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0263 | 2 | NA19077.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.274-31672A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191107997 | ||||||
| chr2:191108048
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(109): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.274-31723A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108048 | ||||||
| chr2:191108063
|
G | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(99): Show | 103 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.274-31738C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108063 | ||||||
| chr2:191108088
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.274-31763G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108088 | ||||||
| chr2:191108290
|
CA | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(25): Show | 29 | HG00140.hp2 HG01081.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.274-31966delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108290 | ||||||
| chr2:191108308
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 188 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.274-31983C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108308 | ||||||
| chr2:191108336
|
A | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG01346.hp2 HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.274-32011T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108336 | ||||||
| chr2:191108450
|
T | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0155 | 2 | HG00673.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.274-32125A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108450 | ||||||
| chr2:191108469
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.274-32144C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108469 | ||||||
| chr2:191108716
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.274-32391T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108716 | ||||||
| chr2:191108729
|
G | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG00609.hp2 HG00673.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-32404C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108729 | ||||||
| chr2:191108751
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02886.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.274-32426G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108751 | ||||||
| chr2:191108837
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.274-32512T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108837 | ||||||
| chr2:191109252
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-32927C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109252 | ||||||
| chr2:191109308
|
G | GT | 14 | a0001c0001t0001g0100a0001c0001t0001g0163a0001c0001t0001g0164others(11): Show | 14 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-32984dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109308 | ||||||
| chr2:191109427
|
C | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-33102G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109427 | ||||||
| chr2:191109455
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0073others(3): Show | 6 | HG00408.hp1 HG02071.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-33130G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109455 | ||||||
| chr2:191109606
|
A | T | 14 | a0001c0001t0001g0100a0001c0001t0001g0163a0001c0001t0001g0164others(11): Show | 14 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-33281T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109606 | ||||||
| chr2:191109671
|
C | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.274-33346G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109671 | ||||||
| chr2:191109709
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 203 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.274-33384A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109709 | ||||||
| chr2:191109958
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.274-33633G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109958 | ||||||
| chr2:191109973
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0095others(7): Show | 11 | HG01261.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-33648C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191109973 | ||||||
| chr2:191110057
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0146 | 3 | HG01261.hp1 HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.274-33732C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110057 | ||||||
| chr2:191110069
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-33744A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110069 | ||||||
| chr2:191110122
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.274-33797T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110122 | ||||||
| chr2:191110214
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.274-33889C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110214 | ||||||
| chr2:191110475
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.274-34150C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110475 | ||||||
| chr2:191110500
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 202 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.274-34175A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110500 | ||||||
| chr2:191110557
|
A | T | 1 | a0001c0001t0001g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-34232T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110557 | ||||||
| chr2:191110632
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.274-34307A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110632 | ||||||
| chr2:191110826
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-34501G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110826 | ||||||
| chr2:191110841
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.274-34516A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110841 | ||||||
| chr2:191110937
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02886.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.274-34612G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191110937 | ||||||
| chr2:191111157
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0002g0004 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.274-34832C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111157 | ||||||
| chr2:191111244
|
C | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.274-34919G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111244 | ||||||
| chr2:191111309
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.274-34984G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111309 | ||||||
| chr2:191111316
|
C | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0095others(12): Show | 16 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.274-34991G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111316 | ||||||
| chr2:191111493
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0110others(7): Show | 10 | HG00140.hp1 HG00140.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.273+35120A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111493 | ||||||
| chr2:191111577
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0095others(12): Show | 16 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.273+35036C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111577 | ||||||
| chr2:191111663
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.273+34950C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111663 | ||||||
| chr2:191111667
|
A | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0110others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+34946T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111667 | ||||||
| chr2:191111735
|
G | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165 | 3 | HG02280.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.273+34878C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111735 | ||||||
| chr2:191111876
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 202 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.273+34737T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111876 | ||||||
| chr2:191111908
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(158): Show | 163 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.273+34705T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111908 | ||||||
| chr2:191111965
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.273+34648C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111965 | ||||||
| chr2:191112118
|
A | AAT | 5 | a0001c0001t0001g0101a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+34493_273+3449 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112118 | ||||||
| chr2:191112318
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.273+34295T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112318 | ||||||
| chr2:191112336
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.273+34277C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112336 | ||||||
| chr2:191112405
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34208A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112405 | ||||||
| chr2:191112495
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0237 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.273+34118T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112495 | ||||||
| chr2:191112670
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.273+33943T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112670 | ||||||
| chr2:191112739
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+33874C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112739 | ||||||
| chr2:191112832
|
G | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165 | 3 | HG02280.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.273+33781C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112832 | ||||||
| chr2:191112991
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.273+33622G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191112991 | ||||||
| chr2:191113005
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.273+33608G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191113005 | ||||||
| chr2:191113579
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.273+33034C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191113579 | ||||||
| chr2:191113612
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0095 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.273+33001C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191113612 | ||||||
| chr2:191113933
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165 | 3 | HG02280.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.273+32680C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191113933 | ||||||
| chr2:191113975
|
G | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+32638C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191113975 | ||||||
| chr2:191114018
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0073others(3): Show | 6 | HG00408.hp1 HG02071.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+32595T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191114018 | ||||||
| chr2:191114196
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.273+32417G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191114196 | ||||||
| chr2:191114452
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 180 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.273+32161C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191114452 | ||||||
| chr2:191114469
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.273+32144C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191114469 | ||||||
| chr2:191114519
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.273+32094C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191114519 | ||||||
| chr2:191114633
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(157): Show | 162 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.273+31980T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191114633 | ||||||
| chr2:191115120
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.273+31493A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115120 | ||||||
| chr2:191115160
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.273+31453T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115160 | ||||||
| chr2:191115239
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG02155.hp1 HG03831.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+31374G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115239 | ||||||
| chr2:191115332
|
C | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02886.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.273+31281G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115332 | ||||||
| chr2:191115388
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.273+31225T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115388 | ||||||
| chr2:191115638
|
C | T | 7 | a0001c0001t0001g0250a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG02083.hp1 NA18944.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+30975G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115638 | ||||||
| chr2:191115654
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.273+30959G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115654 | ||||||
| chr2:191115785
|
T | C | 13 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+30828A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115785 | ||||||
| chr2:191115787
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.273+30826C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191115787 | ||||||
| chr2:191116122
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.273+30491T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116122 | ||||||
| chr2:191116180
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.273+30433T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116180 | ||||||
| chr2:191116200
|
C | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+30413G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116200 | ||||||
| chr2:191116455
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+30158G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116455 | ||||||
| chr2:191116548
|
A | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165 | 3 | HG02280.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.273+30065T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116548 | ||||||
| chr2:191116644
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0057others(4): Show | 7 | HG01169.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+29969G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116644 | ||||||
| chr2:191116797
|
A | AT | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.273+29815_273+2981 others(5): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116797 | ||||||
| chr2:191116866
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.273+29747C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191116866 | ||||||
| chr2:191117254
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+29359G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117254 | ||||||
| chr2:191117342
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.273+29271C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117342 | ||||||
| chr2:191117348
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.273+29265G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117348 | ||||||
| chr2:191117411
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.273+29202G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117411 | ||||||
| chr2:191117479
|
G | T | 65 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.273+29134C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117479 | ||||||
| chr2:191117609
|
G | C | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.273+29004C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117609 | ||||||
| chr2:191117610
|
A | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+29003T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117610 | ||||||
| chr2:191117645
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.273+28968C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117645 | ||||||
| chr2:191117934
|
T | C | 10 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+28679A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191117934 | ||||||
| chr2:191118107
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.273+28506C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118107 | ||||||
| chr2:191118382
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.273+28231C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118382 | ||||||
| chr2:191118392
|
T | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0208others(3): Show | 6 | HG00609.hp1 HG03834.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+28221A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118392 | ||||||
| chr2:191118539
|
G | A | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+28074C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118539 | ||||||
| chr2:191118575
|
A | T | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.273+28038T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118575 | ||||||
| chr2:191118762
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.273+27851A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118762 | ||||||
| chr2:191118827
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.273+27786A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118827 | ||||||
| chr2:191118901
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.273+27712A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191118901 | ||||||
| chr2:191119009
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.273+27604A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119009 | ||||||
| chr2:191119230
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+27383G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119230 | ||||||
| chr2:191119288
|
T | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0087 | 2 | HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.273+27325A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119288 | ||||||
| chr2:191119414
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.273+27199A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119414 | ||||||
| chr2:191119480
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.273+27133T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119480 | ||||||
| chr2:191119560
|
A | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 187 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.273+27053T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119560 | ||||||
| chr2:191119602
|
C | A | 1 | a0001c0002t0001g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.273+27011G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119602 | ||||||
| chr2:191119607
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+27006A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119607 | ||||||
| chr2:191119716
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.273+26897G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119716 | ||||||
| chr2:191119946
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0130 | 2 | HG01106.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.273+26667T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191119946 | ||||||
| chr2:191120031
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0110others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+26582G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120031 | ||||||
| chr2:191120165
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.273+26448C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120165 | ||||||
| chr2:191120491
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.273+26122T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120491 | ||||||
| chr2:191120500
|
A | G | 8 | a0001c0001t0001g0031a0001c0001t0001g0253a0001c0001t0001g0254others(5): Show | 8 | HG01346.hp2 HG01978.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+26113T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120500 | ||||||
| chr2:191120601
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0243others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+26012T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120601 | ||||||
| chr2:191120733
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+25880C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120733 | ||||||
| chr2:191120733
|
G | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 178 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.273+25880C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120733 | ||||||
| chr2:191120763
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.273+25850A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120763 | ||||||
| chr2:191120970
|
C | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0083 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.273+25643G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191120970 | ||||||
| chr2:191121042
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0002g0004 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.273+25571G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121042 | ||||||
| chr2:191121108
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG03209.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+25505C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121108 | ||||||
| chr2:191121132
|
A | C | 64 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.273+25481T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121132 | ||||||
| chr2:191121241
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0110others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+25372T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121241 | ||||||
| chr2:191121245
|
T | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0110others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+25368A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121245 | ||||||
| chr2:191121246
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273+25367C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121246 | ||||||
| chr2:191121327
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+25286C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121327 | ||||||
| chr2:191121599
|
G | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+25014C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121599 | ||||||
| chr2:191121664
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.273+24949G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121664 | ||||||
| chr2:191121665
|
G | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | NA18954.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.273+24948C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121665 | ||||||
| chr2:191121699
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.273+24914G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121699 | ||||||
| chr2:191121708
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273+24905C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121708 | ||||||
| chr2:191121784
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+24829T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121784 | ||||||
| chr2:191121792
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+24821C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121792 | ||||||
| chr2:191121921
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.273+24692C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121921 | ||||||
| chr2:191121947
|
A | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 187 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.273+24666T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191121947 | ||||||
| chr2:191122138
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+24475G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122138 | ||||||
| chr2:191122157
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.273+24456A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122157 | ||||||
| chr2:191122251
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.273+24362G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122251 | ||||||
| chr2:191122265
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.273+24348T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122265 | ||||||
| chr2:191122267
|
G | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+24346C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122267 | ||||||
| chr2:191122327
|
G | GA | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0281others(3): Show | 6 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+24285dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122327 | ||||||
| chr2:191122327
|
GA | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 177 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.273+24285delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122327 | ||||||
| chr2:191122539
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.273+24074A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122539 | ||||||
| chr2:191122609
|
C | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(10): Show | 13 | HG01192.hp1 HG01981.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+24004G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122609 | ||||||
| chr2:191122640
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(3): Show | 6 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+23973T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122640 | ||||||
| chr2:191122785
|
C | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.273+23828G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191122785 | ||||||
| chr2:191123017
|
G | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 6 | HG01192.hp1 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+23596C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123017 | ||||||
| chr2:191123079
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.273+23534G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123079 | ||||||
| chr2:191123081
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.273+23532G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123081 | ||||||
| chr2:191123378
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+23235C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123378 | ||||||
| chr2:191123433
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0281others(3): Show | 6 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+23180C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123433 | ||||||
| chr2:191123583
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.273+23030A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123583 | ||||||
| chr2:191123663
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0281others(3): Show | 6 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+22950G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123663 | ||||||
| chr2:191123670
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.273+22943G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123670 | ||||||
| chr2:191123772
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.273+22841C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123772 | ||||||
| chr2:191123812
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.273+22801C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123812 | ||||||
| chr2:191123885
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00621.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.273+22728C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123885 | ||||||
| chr2:191123903
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+22710A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123903 | ||||||
| chr2:191123904
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+22709T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123904 | ||||||
| chr2:191123918
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0110others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+22695C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191123918 | ||||||
| chr2:191124058
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0281others(3): Show | 6 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+22555C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124058 | ||||||
| chr2:191124073
|
ACATGACA others(7): Show |
A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+22526_273+2253 others(18): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124073 | ||||||
| chr2:191124109
|
T | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0281others(3): Show | 6 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+22504A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124109 | ||||||
| chr2:191124185
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.273+22428T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124185 | ||||||
| chr2:191124185
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.273+22428T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124185 | ||||||
| chr2:191124204
|
C | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.273+22409G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124204 | ||||||
| chr2:191124433
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.273+22180C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124433 | ||||||
| chr2:191124453
|
C | CA | 9 | a0001c0001t0001g0041a0001c0001t0001g0073a0001c0001t0001g0109others(6): Show | 9 | HG02080.hp1 HG03579.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+22159dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124453 | ||||||
| chr2:191124453
|
CA | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.273+22159delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124453 | ||||||
| chr2:191124453
|
CAA | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0056others(3): Show | 6 | HG01975.hp2 HG02622.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+22158_273+2215 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124453 | ||||||
| chr2:191124524
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+22089T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124524 | ||||||
| chr2:191124630
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+21983T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124630 | ||||||
| chr2:191125197
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.273+21416T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125197 | ||||||
| chr2:191125210
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 179 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.273+21403G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125210 | ||||||
| chr2:191125220
|
T | A | 14 | a0001c0001t0001g0100a0001c0001t0001g0163a0001c0001t0001g0164others(11): Show | 14 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+21393A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125220 | ||||||
| chr2:191125246
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.273+21367G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125246 | ||||||
| chr2:191125317
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+21296T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125317 | ||||||
| chr2:191125380
|
C | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 159 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.273+21233G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125380 | ||||||
| chr2:191125471
|
C | CATATTAT others(10): Show |
3 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0184 | 3 | HG02055.hp2 NA18993.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.273+21141_273+2114 others(21): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125471 | ||||||
| chr2:191125471
|
C | CATATTTA others(5): Show |
1 | a0001c0001t0001g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.273+21141_273+2114 others(16): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125471 | ||||||
| chr2:191125476
|
T | TATTATTA others(9): Show |
1 | a0001c0001t0001g0220 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.273+21136_273+2113 others(20): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TATTATTA others(12): Show |
1 | a0001c0001t0001g0241 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.273+21136_273+2113 others(23): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTA | 4 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0127others(1): Show | 4 | HG02055.hp2 HG02895.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+21136_273+2113 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTATTATT others(13): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0218 | 2 | HG02135.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.273+21136_273+2113 others(24): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTA | 8 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0118others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+21134_273+2113 others(7): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTA | 12 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0032others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+21131_273+2113 others(10): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(2): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(9): Show | 13 | HG01346.hp2 HG01975.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+21128_273+2113 others(13): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(5): Show |
7 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG01192.hp2 HG01981.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+21125_273+2113 others(16): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(8): Show |
37 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0028others(34): Show | 37 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.273+21122_273+2113 others(19): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(11): Show |
49 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0016others(46): Show | 50 | HG00621.hp2 HG00639.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.273+21119_273+2113 others(22): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(14): Show |
47 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0025others(44): Show | 47 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.273+21116_273+2113 others(25): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(17): Show |
20 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0035others(17): Show | 21 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.273+21113_273+2113 others(28): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(20): Show |
4 | a0001c0001t0001g0012a0001c0001t0001g0077a0001c0001t0001g0078others(1): Show | 4 | HG00733.hp2 HG01257.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+21110_273+2113 others(31): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125476
|
T | TTTATTAT others(23): Show |
1 | a0001c0001t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273+21136_273+2113 others(34): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125476 | ||||||
| chr2:191125532
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+21081C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125532 | ||||||
| chr2:191125628
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.273+20985G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125628 | ||||||
| chr2:191125636
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+20977G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125636 | ||||||
| chr2:191125810
|
C | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.273+20803G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125810 | ||||||
| chr2:191125870
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.273+20743G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125870 | ||||||
| chr2:191125919
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+20694T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125919 | ||||||
| chr2:191126052
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+20561C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126052 | ||||||
| chr2:191126060
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+20553C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126060 | ||||||
| chr2:191126478
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+20135A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126478 | ||||||
| chr2:191126506
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+20107C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126506 | ||||||
| chr2:191126617
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.273+19996A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126617 | ||||||
| chr2:191126733
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 200 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.273+19880A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126733 | ||||||
| chr2:191126916
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+19697A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126916 | ||||||
| chr2:191126939
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+19674G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126939 | ||||||
| chr2:191126947
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.273+19666C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126947 | ||||||
| chr2:191127014
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+19599C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127014 | ||||||
| chr2:191127131
|
C | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0156a0001c0001t0001g0190others(1): Show | 4 | HG02074.hp2 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+19482G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127131 | ||||||
| chr2:191127165
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+19448G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127165 | ||||||
| chr2:191127434
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 198 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.273+19179A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127434 | ||||||
| chr2:191127511
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.273+19102A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127511 | ||||||
| chr2:191127514
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+19099G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127514 | ||||||
| chr2:191127698
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.273+18915T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127698 | ||||||
| chr2:191127733
|
A | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+18880T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127733 | ||||||
| chr2:191127829
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.273+18784G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127829 | ||||||
| chr2:191127885
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 198 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.273+18728G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127885 | ||||||
| chr2:191127961
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.273+18652G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127961 | ||||||
| chr2:191128095
|
A | ACAACACA others(7): Show |
195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 198 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.273+18517_273+1851 others(18): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191128095 | ||||||
| chr2:191128229
|
G | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165 | 3 | HG02280.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.273+18384C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191128229 | ||||||
| chr2:191128263
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 198 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.273+18350A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191128263 | ||||||
| chr2:191128438
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+18175C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191128438 | ||||||
| chr2:191128785
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+17828T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191128785 | ||||||
| chr2:191128822
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0131others(1): Show | 5 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+17791G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191128822 | ||||||
| chr2:191128900
|
G | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.273+17713C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191128900 | ||||||
| chr2:191129002
|
A | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+17611T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129002 | ||||||
| chr2:191129231
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.273+17382C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129231 | ||||||
| chr2:191129309
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.273+17304T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129309 | ||||||
| chr2:191129374
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.273+17239C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129374 | ||||||
| chr2:191129587
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.273+17026T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129587 | ||||||
| chr2:191129609
|
C | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 178 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.273+17004G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129609 | ||||||
| chr2:191129614
|
G | C | 13 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+16999C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129614 | ||||||
| chr2:191129670
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.273+16943C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129670 | ||||||
| chr2:191129689
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.273+16924C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129689 | ||||||
| chr2:191129716
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0280others(4): Show | 7 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+16897A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129716 | ||||||
| chr2:191129877
|
G | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(77): Show | 80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.273+16736C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129877 | ||||||
| chr2:191129980
|
T | G | 1 | a0002c0005t0001g0238 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.273+16633A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129980 | ||||||
| chr2:191129984
|
C | CTT | 7 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0243others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+16627_273+1662 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129984 | ||||||
| chr2:191130193
|
T | A | 13 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+16420A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130193 | ||||||
| chr2:191130210
|
GTCTA | G | 41 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.273+16399_273+1640 others(8): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130210 | ||||||
| chr2:191130213
|
TATC | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 4 | NA18944.hp2 NA18974.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+16397_273+1639 others(7): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130213 | ||||||
| chr2:191130217
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0001t0001g0258others(2): Show | 5 | NA18944.hp2 NA18974.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+16396A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130217 | ||||||
| chr2:191130219
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.273+16394G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130219 | ||||||
| chr2:191130220
|
C | CT | 15 | a0001c0001t0001g0014a0001c0001t0001g0100a0001c0001t0001g0116others(12): Show | 15 | HG02145.hp2 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.273+16392dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130220 | ||||||
| chr2:191130220
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0257a0001c0001t0001g0258others(2): Show | 5 | NA18944.hp2 NA18974.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+16393G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130220 | ||||||
| chr2:191130220
|
CT | C | 6 | a0001c0001t0001g0085a0001c0001t0001g0094a0001c0001t0001g0102others(3): Show | 6 | HG00609.hp2 HG00673.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+16392delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130220 | ||||||
| chr2:191130220
|
CTT | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(133): Show | 138 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.273+16391_273+1639 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130220 | ||||||
| chr2:191130220
|
CTTT | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(30): Show | 34 | HG00438.hp2 HG01261.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.273+16390_273+1639 others(7): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130220 | ||||||
| chr2:191130220
|
CTTTTT | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0243others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+16388_273+1639 others(9): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130220 | ||||||
| chr2:191130221
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0279 | 2 | HG03710.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.273+16392A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130221 | ||||||
| chr2:191130261
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.273+16352G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130261 | ||||||
| chr2:191130350
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0243others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+16263C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130350 | ||||||
| chr2:191130356
|
T | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0243others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+16257A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130356 | ||||||
| chr2:191130357
|
GGACTACA others(3565): Show |
G | 7 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0243others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+12684_273+1625 others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130357 | ||||||
| chr2:191130452
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.273+16161C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130452 | ||||||
| chr2:191130516
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 178 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.273+16097A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130516 | ||||||
| chr2:191130635
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 178 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.273+15978G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130635 | ||||||
| chr2:191130636
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0270 | 2 | HG00558.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.273+15977C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130636 | ||||||
| chr2:191130739
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.273+15874A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130739 | ||||||
| chr2:191130746
|
T | A | 1 | a0001c0001t0001g0240 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.273+15867A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130746 | ||||||
| chr2:191130748
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.273+15865T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130748 | ||||||
| chr2:191130956
|
A | AG | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.273+15656dupC | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130956 | ||||||
| chr2:191131019
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.273+15594C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131019 | ||||||
| chr2:191131254
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+15359G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131254 | ||||||
| chr2:191131280
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.273+15333C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131280 | ||||||
| chr2:191131315
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0028others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+15298C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131315 | ||||||
| chr2:191131406
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.273+15207C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131406 | ||||||
| chr2:191131412
|
C | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.273+15201G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131412 | ||||||
| chr2:191131536
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.273+15077C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131536 | ||||||
| chr2:191131588
|
A | C | 6 | a0001c0001t0001g0101a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+15025T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131588 | ||||||
| chr2:191131792
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.273+14821A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131792 | ||||||
| chr2:191131793
|
G | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0165 | 3 | HG02280.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.273+14820C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131793 | ||||||
| chr2:191131863
|
C | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+14750G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131863 | ||||||
| chr2:191131936
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.273+14677A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131936 | ||||||
| chr2:191131944
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0280others(4): Show | 7 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+14669C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131944 | ||||||
| chr2:191132145
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.273+14468A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132145 | ||||||
| chr2:191132551
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+14062A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132551 | ||||||
| chr2:191132755
|
C | CT | 17 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0094others(14): Show | 17 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+13857dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132755 | ||||||
| chr2:191132755
|
CT | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.273+13857delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132755 | ||||||
| chr2:191132777
|
C | T | 13 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+13836G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132777 | ||||||
| chr2:191132858
|
A | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 199 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.273+13755T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132858 | ||||||
| chr2:191132867
|
T | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0280others(4): Show | 7 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+13746A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132867 | ||||||
| chr2:191132914
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0280others(4): Show | 7 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+13699G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132914 | ||||||
| chr2:191132937
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0126a0001c0006t0001g0082 | 3 | NA18940.hp2 NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.273+13676C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132937 | ||||||
| chr2:191132955
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG03209.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+13658G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191132955 | ||||||
| chr2:191133043
|
T | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 197 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.273+13570A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133043 | ||||||
| chr2:191133061
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.273+13552A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133061 | ||||||
| chr2:191133064
|
T | A | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273+13549A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133064 | ||||||
| chr2:191133220
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 206 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.273+13393G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133220 | ||||||
| chr2:191133550
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.273+13063C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133550 | ||||||
| chr2:191133623
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0271others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+12990G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133623 | ||||||
| chr2:191133698
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0131others(1): Show | 5 | HG01192.hp2 HG01243.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+12915C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133698 | ||||||
| chr2:191133826
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 168 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.273+12787G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133826 | ||||||
| chr2:191133838
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.273+12775G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133838 | ||||||
| chr2:191133896
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.273+12717A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133896 | ||||||
| chr2:191133951
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.273+12662T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191133951 | ||||||
| chr2:191134310
|
T | C | 9 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(6): Show | 9 | HG00438.hp1 HG02015.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+12303A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191134310 | ||||||
| chr2:191134361
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.273+12252G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191134361 | ||||||
| chr2:191134508
|
G | T | 4 | a0001c0001t0001g0101a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG03209.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+12105C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191134508 | ||||||
| chr2:191134589
|
G | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+12024C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191134589 | ||||||
| chr2:191134614
|
A | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0184a0001c0001t0001g0249others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+11999T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191134614 | ||||||
| chr2:191135169
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+11444A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191135169 | ||||||
| chr2:191135356
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 155 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.273+11257C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191135356 | ||||||
| chr2:191135713
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.273+10900A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191135713 | ||||||
| chr2:191135742
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.273+10871G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191135742 | ||||||
| chr2:191135749
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0281others(3): Show | 6 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+10864C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191135749 | ||||||
| chr2:191135802
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.273+10811T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191135802 | ||||||
| chr2:191136005
|
G | GA | 116 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.273+10607dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136005 | ||||||
| chr2:191136005
|
G | GAA | 14 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0100others(11): Show | 14 | HG00673.hp2 HG01981.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+10606_273+1060 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136005 | ||||||
| chr2:191136005
|
GA | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0028others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+10607delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136005 | ||||||
| chr2:191136006
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.273+10607T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136006 | ||||||
| chr2:191136015
|
A | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0101others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+10598T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136015 | ||||||
| chr2:191136021
|
AAC | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 132 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.273+10590_273+1059 others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136021 | ||||||
| chr2:191136022
|
AC | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+10590delG | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136022 | ||||||
| chr2:191136023
|
C | A | 11 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0176others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+10590G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136023 | ||||||
| chr2:191136024
|
C | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0028others(13): Show | 16 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.273+10589G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136024 | ||||||
| chr2:191136031
|
C | A | 10 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+10582G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136031 | ||||||
| chr2:191136193
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 138 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.273+10420G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136193 | ||||||
| chr2:191136383
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.273+10230C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136383 | ||||||
| chr2:191136523
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 138 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.273+10090G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136523 | ||||||
| chr2:191136717
|
CTCTA | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 155 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.273+9892_273+9895d others(6): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136717 | ||||||
| chr2:191136812
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 138 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.273+9801T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136812 | ||||||
| chr2:191136850
|
G | T | 1 | a0001c0001t0001g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.273+9763C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136850 | ||||||
| chr2:191137023
|
GA | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 129 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.273+9589delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137023 | ||||||
| chr2:191137030
|
A | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 129 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.273+9583T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137030 | ||||||
| chr2:191137031
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 129 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.273+9582G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137031 | ||||||
| chr2:191137194
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.273+9419A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137194 | ||||||
| chr2:191137216
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.273+9397C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137216 | ||||||
| chr2:191137269
|
G | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 138 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.273+9344C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137269 | ||||||
| chr2:191137289
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(10): Show | 13 | HG01192.hp1 HG01981.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+9324A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137289 | ||||||
| chr2:191137326
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 138 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.273+9287G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137326 | ||||||
| chr2:191137422
|
T | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.273+9191A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137422 | ||||||
| chr2:191137432
|
C | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02886.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.273+9181G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137432 | ||||||
| chr2:191137432
|
C | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 152 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.273+9181G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137432 | ||||||
| chr2:191137479
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.273+9134G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137479 | ||||||
| chr2:191137527
|
T | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0028others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+9086A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137527 | ||||||
| chr2:191137556
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.273+9057C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137556 | ||||||
| chr2:191137684
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.273+8929T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137684 | ||||||
| chr2:191137812
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 160 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.273+8801C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137812 | ||||||
| chr2:191138002
|
A | AT | 3 | a0001c0001t0001g0030a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG00438.hp2 HG02698.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.273+8610dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138002 | ||||||
| chr2:191138044
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.273+8569T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138044 | ||||||
| chr2:191138305
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 163 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.273+8308A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138305 | ||||||
| chr2:191138343
|
T | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0249a0001c0001t0002g0004 | 3 | HG02055.hp2 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.273+8270A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138343 | ||||||
| chr2:191138400
|
T | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.273+8213A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138400 | ||||||
| chr2:191138612
|
T | TA | 11 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(8): Show | 11 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+8000dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138612 | ||||||
| chr2:191138646
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0035others(2): Show | 6 | HG00735.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+7967T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138646 | ||||||
| chr2:191138722
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0280others(4): Show | 7 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+7891T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138722 | ||||||
| chr2:191138744
|
C | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(10): Show | 13 | HG01192.hp1 HG01981.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+7869G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138744 | ||||||
| chr2:191138835
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+7778T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138835 | ||||||
| chr2:191138901
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+7712G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138901 | ||||||
| chr2:191138952
|
G | A | 10 | a0001c0001t0001g0153a0001c0001t0001g0170a0001c0001t0001g0203others(7): Show | 10 | HG00558.hp1 NA18940.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+7661C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191138952 | ||||||
| chr2:191139047
|
C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.273+7566G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191139047 | ||||||
| chr2:191139093
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0280others(4): Show | 7 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+7520G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191139093 | ||||||
| chr2:191139425
|
C | T | 9 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+7188G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191139425 | ||||||
| chr2:191139716
|
A | C | 10 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+6897T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191139716 | ||||||
| chr2:191139719
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(97): Show | 102 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.273+6894G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191139719 | ||||||
| chr2:191140170
|
C | G | 1 | a0001c0001t0001g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.273+6443G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191140170 | ||||||
| chr2:191140318
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.273+6295C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191140318 | ||||||
| chr2:191140792
|
G | A | 13 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG01071.hp1 HG02074.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+5821C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191140792 | ||||||
| chr2:191140825
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0181 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.273+5788T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191140825 | ||||||
| chr2:191140879
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.273+5734A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191140879 | ||||||
| chr2:191141003
|
C | G | 133 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.273+5610G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141003 | ||||||
| chr2:191141136
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0137 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+5477C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141136 | ||||||
| chr2:191141280
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | NA18959.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.273+5333C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141280 | ||||||
| chr2:191141351
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0280others(4): Show | 7 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+5262T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141351 | ||||||
| chr2:191141384
|
G | GTA | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+5227_273+5228d others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141384 | ||||||
| chr2:191141391
|
T | C | 1 | a0001c0001t0001g0274 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.273+5222A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141391 | ||||||
| chr2:191141406
|
CATATACA others(41): Show |
C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 151 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.273+5159_273+5206d others(50): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141406 | ||||||
| chr2:191141433
|
CATATACA others(14): Show |
C | 2 | a0001c0001t0001g0011a0001c0001t0001g0095 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.273+5159_273+5179d others(23): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141433 | ||||||
| chr2:191141492
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.273+5121C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141492 | ||||||
| chr2:191141540
|
G | GAT | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+5071_273+5072d others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141540 | ||||||
| chr2:191141597
|
GTA | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 141 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.273+5014_273+5015d others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141597 | ||||||
| chr2:191141604
|
T | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(11): Show | 14 | HG00438.hp2 HG01346.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+5009A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141604 | ||||||
| chr2:191141606
|
C | T | 56 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(53): Show | 56 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.273+5007G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141606 | ||||||
| chr2:191141614
|
CAT | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.273+4997_273+4998d others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141614 | ||||||
| chr2:191141616
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 201 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.273+4997A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141616 | ||||||
| chr2:191141700
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.273+4913C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141700 | ||||||
| chr2:191141895
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0115a0001c0001t0001g0243others(4): Show | 7 | HG01192.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+4718C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141895 | ||||||
| chr2:191141952
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.273+4661A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191141952 | ||||||
| chr2:191142180
|
T | C | 10 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+4433A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142180 | ||||||
| chr2:191142216
|
GAT | G | 13 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+4395_273+4396d others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142216 | ||||||
| chr2:191142226
|
T | TAC | 13 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0100others(10): Show | 13 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+4386_273+4387i others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142226 | ||||||
| chr2:191142228
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(265): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.273+4385A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142228 | ||||||
| chr2:191142244
|
T | C | 13 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0147others(10): Show | 13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+4369A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142244 | ||||||
| chr2:191142319
|
G | A | 10 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+4294C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142319 | ||||||
| chr2:191142422
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.273+4191C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142422 | ||||||
| chr2:191142607
|
T | C | 2 | a0001c0001t0001g0249a0001c0001t0002g0004 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.273+4006A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142607 | ||||||
| chr2:191142610
|
A | C | 2 | a0001c0001t0001g0249a0001c0001t0002g0004 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.273+4003T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142610 | ||||||
| chr2:191142644
|
A | T | 10 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+3969T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142644 | ||||||
| chr2:191142691
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.273+3922G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142691 | ||||||
| chr2:191142763
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.273+3850T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191142763 | ||||||
| chr2:191143008
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG02145.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+3605C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143008 | ||||||
| chr2:191143183
|
T | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0117a0001c0001t0001g0132others(18): Show | 21 | HG01891.hp1 HG02257.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.273+3430A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143183 | ||||||
| chr2:191143325
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+3288A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143325 | ||||||
| chr2:191143429
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02109.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+3184C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143429 | ||||||
| chr2:191143431
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+3182C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143431 | ||||||
| chr2:191143453
|
A | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0190 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+3160T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143453 | ||||||
| chr2:191143477
|
G | A | 53 | a0001c0001t0001g0018a0001c0001t0001g0097a0001c0001t0001g0098others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.273+3136C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143477 | ||||||
| chr2:191143792
|
A | AT | 98 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0013others(95): Show | 98 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.273+2820dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143792 | ||||||
| chr2:191143866
|
C | CA | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+2746dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143866 | ||||||
| chr2:191143910
|
A | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 25 | HG01081.hp1 HG01192.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.273+2703T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143910 | ||||||
| chr2:191144023
|
T | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0099others(59): Show | 63 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.273+2590A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144023 | ||||||
| chr2:191144120
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0133 | 4 | HG01261.hp1 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+2493A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144120 | ||||||
| chr2:191144216
|
T | C | 10 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(7): Show | 10 | HG01192.hp1 HG02145.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+2397A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144216 | ||||||
| chr2:191144380
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG00280.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.273+2233C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144380 | ||||||
| chr2:191144568
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.273+2045C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144568 | ||||||
| chr2:191144584
|
G | A | 60 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0118others(57): Show | 60 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.273+2029C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144584 | ||||||
| chr2:191144588
|
CTG | C | 36 | a0001c0001t0001g0120a0001c0001t0001g0136a0001c0001t0001g0138others(33): Show | 36 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.273+2023_273+2024d others(4): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144588 | ||||||
| chr2:191144620
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.273+1993C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144620 | ||||||
| chr2:191144629
|
T | TAGAAGAA others(903): Show |
1 | a0001c0001t0001g0280 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.273+1983_273+1984i others(912): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144629 | ||||||
| chr2:191144629
|
T | TAGAAGAA others(903): Show |
1 | a0001c0001t0001g0281 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.273+1983_273+1984i others(912): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144629 | ||||||
| chr2:191144629
|
T | TAGAAGAA others(907): Show |
4 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG01978.hp1 HG01981.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1983_273+1984i others(916): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144629 | ||||||
| chr2:191144655
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.273+1958A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144655 | ||||||
| chr2:191144729
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 142 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.273+1884A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144729 | ||||||
| chr2:191144791
|
T | C | 32 | a0001c0001t0001g0120a0001c0001t0001g0138a0001c0001t0001g0250others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.273+1822A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144791 | ||||||
| chr2:191144926
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(163): Show | 168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.273+1687T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144926 | ||||||
| chr2:191144932
|
A | AT | 4 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1680dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144932 | ||||||
| chr2:191145020
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.273+1593A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145020 | ||||||
| chr2:191145070
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.273+1543G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145070 | ||||||
| chr2:191145341
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.273+1272G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145341 | ||||||
| chr2:191145463
|
T | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.273+1150A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145463 | ||||||
| chr2:191145485
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.273+1128T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145485 | ||||||
| chr2:191145701
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+912C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145701 | ||||||
| chr2:191145762
|
A | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(126): Show | 131 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.273+851T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145762 | ||||||
| chr2:191145772
|
G | T | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.273+841C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145772 | ||||||
| chr2:191145798
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.273+815T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145798 | ||||||
| chr2:191145863
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(164): Show | 169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.273+750A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145863 | ||||||
| chr2:191146045
|
G | C | 94 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(91): Show | 95 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.273+568C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146045 | ||||||
| chr2:191146202
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.273+411T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146202 | ||||||
| chr2:191146221
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+392G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146221 | ||||||
| chr2:191146228
|
T | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00621.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.273+385A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146228 | ||||||
| chr2:191146234
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.273+379G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146234 | ||||||
| chr2:191146310
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.273+303C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146310 | ||||||
| chr2:191146329
|
A | G | 38 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0250others(35): Show | 38 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+284T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146329 | ||||||
| chr2:191146380
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG00558.hp1 HG00673.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+233G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146380 | ||||||
| chr2:191146392
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.273+221A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146392 | ||||||
| chr2:191146469
|
T | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | NA18950.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.273+144A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146469 | ||||||
| chr2:191146498
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+115T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146498 | ||||||
| chr2:191146558
|
C | T | 8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG02257.hp2 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+55G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191146558 | ||||||
| chr2:191146884
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.129-127T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191146884 | ||||||
| chr2:191146923
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.129-166A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191146923 | ||||||
| chr2:191147107
|
A | G | 38 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0250others(35): Show | 38 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.129-350T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191147107 | ||||||
| chr2:191147197
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.129-440G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191147197 | ||||||
| chr2:191147198
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0132a0001c0002t0001g0134others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-441T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191147198 | ||||||
| chr2:191147453
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.128+623C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191147453 | ||||||
| chr2:191147615
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.128+461C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191147615 | ||||||
| chr2:191147825
|
A | T | 1 | a0001c0001t0001g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.128+251T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191147825 | ||||||
| chr2:191148063
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.128+13A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 2/23 | chr2 | 191148063 | ||||||
| chr2:191148389
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-1-185G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191148389 | ||||||
| chr2:191148428
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-1-224A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191148428 | ||||||
| chr2:191148561
|
G | C | 6 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-357C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191148561 | ||||||
| chr2:191148649
|
GCTT | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02886.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-1-448_-1-446delAA others(1): Show |
STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191148649 | ||||||
| chr2:191148865
|
A | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0132others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-1-661T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191148865 | ||||||
| chr2:191148888
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-1-684A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191148888 | ||||||
| chr2:191149195
|
A | G | 30 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(27): Show | 30 | HG00280.hp2 HG00408.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1-991T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149195 | ||||||
| chr2:191149353
|
TA | T | 32 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0250others(29): Show | 32 | HG00280.hp2 HG00408.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1-1150delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149353 | ||||||
| chr2:191149411
|
G | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG02886.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-1-1207C>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149411 | ||||||
| chr2:191149490
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-1286A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149490 | ||||||
| chr2:191149538
|
T | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0132others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-1-1334A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149538 | ||||||
| chr2:191149643
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-2+1304A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149643 | ||||||
| chr2:191149664
|
C | A | 2 | a0001c0002t0001g0134a0001c0002t0001g0135 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-2+1283G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149664 | ||||||
| chr2:191149704
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0132others(4): Show | 7 | HG00323.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+1243C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149704 | ||||||
| chr2:191149754
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-2+1193T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149754 | ||||||
| chr2:191149923
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-2+1024T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191149923 | ||||||
| chr2:191150125
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+822A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191150125 | ||||||
| chr2:191150346
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(132): Show | 137 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.-2+601T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191150346 | ||||||
| chr2:191150724
|
C | A | 1 | a0001c0001t0001g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-2+223G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191150724 |