Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MSQWN others(743): Show |
chr2 | 191024576 | 191155994 |
| a0002 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | MSQWN others(743): Show |
chr2 | 191024576 | 191155994 |
| a0003 | 0/0 | 748 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | MSQWN others(743): Show |
chr2 | 191024576 | 191155994 |
| a0004 | 0/0 | 748 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | MSQWN others(743): Show |
chr2 | 191024576 | 191155994 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2244 | 281 | 91 | 43 | 104 | 14 | 27 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
chr2 | 191024576 | 191155994 | ||
| a0001c0002 | 0/0 | 2244 | 2 | 2 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
chr2 | 191024576 | 191155994 | ||
| a0001c0003 | 0/0 | 2244 | 2 | 0 | 0 | 2 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
chr2 | 191024576 | 191155994 | ||
| a0001c0004 | 0/0 | 2244 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
chr2 | 191024576 | 191155994 | ||
| a0001c0006 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
chr2 | 191024576 | 191155994 | ||
| a0002c0008 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
chr2 | 191024576 | 191155994 | ||
| a0003c0005 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
chr2 | 191024576 | 191155994 | ||
| a0004c0007 | 0/0 | 2244 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | ATGTC others(2239): Show |
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 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0001c0001t0002 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0001c0001t0003 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0001c0002t0001 | 0/0 | 2559 | 2 | 2 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0001c0003t0001 | 0/0 | 2559 | 2 | 0 | 0 | 2 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0001c0004t0001 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0001c0006t0001 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0002c0008t0001 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0003c0005t0001 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| a0004c0007t0001 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | GACTT others(2554): Show |
chr2 | 191024576 | 191155994 |
| actghapid | grch38/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 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0134 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 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 | 1/0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0001c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0002c0008t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0003c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| a0004c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | g0097 | EUR | GBR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0070 | EUR | FIN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0170 | 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 | g0034 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | 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 | g0189 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | 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 | g0069 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0104 | 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 | g0197 | 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 | g0196 | EUR | IBS | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01884 | hp1 | a0002 | c0008 | t0001 | g0249 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0067 | 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 | g0185 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0274 | 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 | g0157 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02080 | hp2 | a0003 | c0005 | t0001 | g0239 | 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 | g0156 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0176 | 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 | g0136 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0247 | 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 | g0133 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | 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 | g0199 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0181 | 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 | g0045 | 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 | g0072 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0180 | 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 | g0015 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0145 | 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 | g0271 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0248 | 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 | g0110 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0212 | 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 | g0198 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0218 | 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 | g0049 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04184 | hp2 | a0004 | c0007 | t0001 | g0032 | SAS | BEB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0103 | 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 | g0238 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18940 | hp2 | a0001 | c0006 | t0001 | g0065 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0204 | 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 | g0168 | 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 | g0260 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0035 | 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 | g0224 | 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 | g0119 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0222 | 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 | g0084 | 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 | g0276 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0279 | 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 | g0099 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0171 | 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 | g0207 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | 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 | g0184 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | USA | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0028 | REF | REF | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0161 | REF | REF | STAT4_chr2_191024576_191155994 | STAT4 | chr2 | 191024576 | 191155994 |
| view | 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 | a0004 | 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 | a0003 | 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 | a0002 | 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 |
| view | 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 |
| view | 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 |
| view | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0137 others(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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(38): 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0157 a0001c0001t0001g0209 others(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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(38): 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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0257 | 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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(38): 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 | 106 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0014 others(103): Show |
107 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(104): 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 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0198 | 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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(38): 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 | a0001c0001t0001g0230 | 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 | 56 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(53): Show |
56 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0031 | 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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(119): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0230 | 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 | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): 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 | a0001c0001t0001g0225 a0001c0001t0001g0241 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0272 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | 48 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0034 others(45): Show |
48 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(45): 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0109 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0149 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0234 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0064 | 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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | 30 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0021 others(27): 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0185 | 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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0234 |
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 | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): 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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0002c0008t0001g0249 | 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 | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): 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 | a0001c0001t0001g0163 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0151 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0166 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(237): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): 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 | a0001c0001t0001g0101 a0001c0001t0001g0238 a0001c0001t0001g0254 |
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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(68): 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0162 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0162 a0001c0001t0001g0185 others(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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0166 a0001c0001t0001g0270 others(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 | 29 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(26): 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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
81 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(78): 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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0162 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0166 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0127 |
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 | 29 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(26): 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0001g0236 others(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 | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
81 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(78): 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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(179): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): 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 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0016 others(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 | 8 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0076 others(5): Show |
8 | HG00323.hp2 HG01081.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1251+5322delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191049167 | |||||||
| chr2:191049244 | A | G | 1 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(184): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1251+3543A>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050947 | |||||||
| chr2:191050989 | G | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(189): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1251+3501C>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191050989 | |||||||
| chr2:191051012 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(23): 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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0191 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0095 others(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 | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1251+1981G>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 14/23 | chr2 | 191052509 | |||||||
| chr2:191052591 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): 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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0134 | 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 | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0039 others(29): 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 | a0001c0001t0001g0041 a0001c0001t0001g0099 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0095 others(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 | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0039 others(28): 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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0134 | 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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0198 |
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 | 28 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(25): 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 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0147 | 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 | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0039 others(28): 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0140 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0087 others(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 | 30 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0039 others(27): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0064 others(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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(153): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0191 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(184): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0168 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0281 |
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 | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0039 others(28): 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0124 | 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 | 6 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0152 others(3): 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 | a0001c0001t0001g0015 | 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 | a0001c0004t0001g0189 | 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 | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): 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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1206+1238delA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 13/23 | chr2 | 191056779 | |||||||
| chr2:191056876 | G | T | 1 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0006 | 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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(170): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0243 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0183 | 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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(135): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1095-81A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 11/23 | chr2 | 191058300 | |||||||
| chr2:191058338 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): 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 | a0001c0001t0001g0166 a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0120 | 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 | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): 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 | a0002c0008t0001g0249 | 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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(116): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0256 a0001c0001t0002g0005 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0134 | 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 | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): 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 | a0001c0001t0001g0162 a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0185 a0001c0001t0001g0270 others(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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0191 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0163 a0001c0001t0001g0164 others(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 | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0039 others(29): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0118 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(97): 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0110 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0113 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0151 | 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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
102 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(99): 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0159 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0272 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0134 | 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(97): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0104 a0001c0001t0001g0123 others(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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0118 others(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 | a0001c0004t0001g0189 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0134 | 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 | 27 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(24): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0223 |
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 | a0001c0002t0001g0136 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0073 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0118 others(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 | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): 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 | a0001c0001t0001g0253 | 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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0118 others(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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): 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 | a0001c0001t0001g0188 | 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 | 28 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(25): 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0116 |
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 | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): 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 | a0001c0001t0001g0017 | 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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(158): Show |
163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0186 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0131 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0042 others(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 | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): 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 | a0001c0001t0001g0096 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0253 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.274-1777dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191078101 | |||||||
| chr2:191078458 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): 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 | a0001c0001t0001g0074 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 |
184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(181): Show |
186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): 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 | a0001c0001t0001g0134 a0002c0008t0001g0249 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0222 |
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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0100 others(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 | a0004c0007t0001g0032 | 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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(98): Show |
103 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(100): 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0165 | 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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(98): Show |
103 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(100): 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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0181 | 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 | a0002c0008t0001g0249 | 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 | a0001c0001t0002g0005 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0122 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0163 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0099 | 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 | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.274-11743A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191088068 | |||||||
| chr2:191088069 | C | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): 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 | a0001c0001t0001g0049 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0086 |
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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(172): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 a0002c0008t0001g0249 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
171 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(168): 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 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0223 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 a0002c0008t0001g0249 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0223 | 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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(117): Show |
122 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(119): 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 | a0001c0002t0001g0136 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0134 others(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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(211): 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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0262 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(211): 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(97): Show |
102 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.274-18593dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191094917 | |||||||
| chr2:191094917 | C | CAAA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0270 others(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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): 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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(187): 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 | a0001c0001t0001g0097 a0001c0001t0001g0190 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0134 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(96): Show |
101 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(98): 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(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 | 5 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0076 others(2): Show |
5 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-20924A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097249 | |||||||
| chr2:191097370 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
196 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(193): 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0134 | 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 | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
194 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.274-21590dupT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097914 | |||||||
| chr2:191097925 | C | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG00733.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.274-21600G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191097925 | |||||||
| chr2:191098015 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0170 a0001c0001t0001g0285 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0140 others(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 | a0001c0002t0001g0136 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0094 |
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 | a0001c0001t0001g0106 | 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 | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
220 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(217): 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0154 | 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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
114 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(111): 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 a0002c0008t0001g0249 |
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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0002c0008t0001g0249 | 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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
210 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(207): 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0255 | 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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(211): 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0002c0008t0001g0249 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(211): 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0134 others(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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(211): 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0185 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0255 | 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 | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
175 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(172): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): 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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
182 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(179): 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0111 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0262 |
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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(108): Show |
112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.274-31723A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191108048 | |||||||
| chr2:191108063 | G | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(97): Show |
102 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(99): 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
187 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(184): 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 | a0001c0001t0001g0096 a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(77): 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
202 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(199): 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0284 | 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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
201 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(198): 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0250 a0001c0001t0002g0005 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.274-34832C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111157 | |||||||
| chr2:191111309 | C | T | 1 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
201 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.273+34737T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191111876 | |||||||
| chr2:191111908 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(157): Show |
162 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(159): 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0031 |
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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
179 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(176): 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 | a0001c0001t0001g0012 | 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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
161 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(158): 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0263 | 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 | 6 | a0001c0001t0001g0004 a0001c0001t0001g0251 a0001c0001t0001g0258 others(3): 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | |||||||
| chr2:191116866 | G | A | 1 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0100 | 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 | 64 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(61): 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0049 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 |
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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0087 |
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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0231 | 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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
186 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(183): 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 | a0001c0002t0001g0136 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
177 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(174): 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0082 |
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 | a0001c0001t0001g0250 a0001c0001t0002g0005 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | 63 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(60): 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 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0171 | 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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
186 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(183): 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 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0280 others(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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
176 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(173): 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0015 others(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 | |||||||
| chr2:191123017 | G | A | 6 | a0001c0001t0001g0116 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0280 others(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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0166 | 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 | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0111 others(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 | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.273+22159delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124453 | |||||||
| chr2:191124453 | CAA | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0054 others(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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.273+22089T>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191124524 | |||||||
| chr2:191124630 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): 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 | a0001c0001t0001g0134 | 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 | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
178 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(175): 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 | a0001c0001t0001g0101 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.273+21296T>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125317 | |||||||
| chr2:191125380 | C | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
158 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(155): 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 | a0001c0001t0001g0030 a0001c0001t0001g0129 a0001c0001t0001g0185 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0219 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0095 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0017 others(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 |
46 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0026 others(43): Show |
46 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(43): 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 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0033 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0174 | 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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.273+20977G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125636 | |||||||
| chr2:191125870 | C | T | 1 | a0001c0001t0001g0279 | 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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.273+20694T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191125919 | |||||||
| chr2:191126052 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): 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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): 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 | a0001c0001t0001g0026 | 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 | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
199 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.273+19880A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126733 | |||||||
| chr2:191126916 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.273+19697A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191126916 | |||||||
| chr2:191126939 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0157 a0001c0001t0001g0191 others(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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.273+19448G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127165 | |||||||
| chr2:191127434 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
197 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.273+19179A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191127434 | |||||||
| chr2:191127511 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
184 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(181): 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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0168 | 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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
197 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(194): 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 |
194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
197 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(194): 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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
197 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(194): 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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0132 others(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 | 72 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0029 | 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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
190 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.273+17239C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129374 | |||||||
| chr2:191129609 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
177 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(174): 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.273+16943C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191129670 | |||||||
| chr2:191129716 | T | C | 7 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0279 others(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 | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(76): 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 | a0003c0005t0001g0239 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | 3 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0259 |
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 | 4 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0258 others(1): 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0117 others(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 | 4 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0258 others(1): 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0103 others(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 | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(132): Show |
137 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(134): 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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0208 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0168 | 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 | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
177 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.273+16097A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130516 | |||||||
| chr2:191130635 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
177 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(174): 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 | a0001c0001t0001g0154 a0001c0001t0001g0267 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0241 | 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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
190 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.273+15656dupC | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191130956 | |||||||
| chr2:191131019 | G | A | 1 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0270 others(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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
190 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(187): 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0029 others(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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
190 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.273+15207C>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191131406 | |||||||
| chr2:191131412 | C | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): 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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
190 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(187): 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 | a0001c0001t0001g0102 a0001c0001t0001g0133 a0001c0001t0001g0134 others(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 | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
183 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(180): 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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0084 others(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 | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(66): 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
198 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(195): 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0127 a0001c0006t0001g0065 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
196 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(193): 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 | a0001c0001t0001g0133 | 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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
205 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(202): 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0132 others(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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
167 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(164): 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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0185 a0001c0001t0001g0250 others(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 | a0001c0001t0001g0162 | 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 | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
154 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(151): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0103 | 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 | 115 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0019 others(112): 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 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0102 others(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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
131 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(128): 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0101 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
137 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(134): 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 | a0001c0001t0001g0020 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
137 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.273+10090G>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191136523 | |||||||
| chr2:191136717 | CTCTA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
154 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(151): 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
137 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(134): 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 | a0001c0001t0001g0252 | 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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
128 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.273+9589delT | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137023 | |||||||
| chr2:191137030 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
128 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.273+9583T>A | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191137030 | |||||||
| chr2:191137031 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
128 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(125): 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0134 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
137 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(134): 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
137 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(134): 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 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
151 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(148): 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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0029 | 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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
159 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(156): 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 | a0001c0001t0001g0095 a0001c0001t0001g0279 a0001c0001t0001g0280 |
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 | a0001c0001t0001g0035 | 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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
162 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(159): 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 | a0001c0001t0001g0185 a0001c0001t0001g0250 a0001c0001t0002g0005 |
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 | 122 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(119): 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 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0171 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0011 |
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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(96): Show |
101 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(98): 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0100 | 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 | 132 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(129): 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 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0273 | 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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
150 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(147): 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 | a0001c0001t0001g0012 a0001c0001t0001g0031 |
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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
140 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(137): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(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 | 55 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(52): 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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(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 | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
200 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(197): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0244 others(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 | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): 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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0101 others(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 | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): 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 | a0001c0001t0001g0250 a0001c0001t0002g0005 |
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 | a0001c0001t0001g0250 a0001c0001t0002g0005 |
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 | a0001c0001t0001g0101 a0001c0001t0001g0177 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0118 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 |
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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0098 a0001c0001t0001g0099 others(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 | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(93): Show |
97 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.273+2820dupA | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191143792 | |||||||
| chr2:191143866 | C | CA | 6 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0119 others(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 | 35 | a0001c0001t0001g0004 a0001c0001t0001g0121 a0001c0001t0001g0137 others(32): 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(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 | a0001c0001t0001g0120 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
141 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.273+1884A>G | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191144729 | |||||||
| chr2:191144791 | T | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0121 a0001c0001t0001g0139 others(28): 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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
167 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(164): 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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.273+1150A>C | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 3/23 | chr2 | 191145463 | |||||||
| chr2:191145485 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): 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 | a0001c0001t0001g0285 | 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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(125): Show |
130 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(127): 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0012 | 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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(162): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): 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 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0127 | 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 | 37 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(34): 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0278 | 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 | 37 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(34): 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0133 a0001c0002t0001g0135 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | 44 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): 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 | a0001c0001t0001g0131 | 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 | 29 | a0001c0001t0001g0004 a0001c0001t0001g0251 a0001c0001t0001g0252 others(26): 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 | 31 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(28): 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 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0250 | 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 | 44 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): 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 | a0001c0001t0001g0132 | 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 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
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 | a0001c0001t0001g0137 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
136 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(133): 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 | a0001c0001t0001g0286 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-2+223G>T | STAT4 | ENSG00000138378.19 | transcript | ENST00000392320.7 | protein_coding | 1/23 | chr2 | 191150724 |