Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6772 |
| ensemblid | ENSG00000115415.21 |
| hgncid | 11362 |
| symbol | STAT1 |
| name | signal transducer and activator of transcription 1 |
| refseq_nuc | NM_007315.4 |
| refseq_prot | NP_009330.1 |
| ensembl_nuc | ENST00000361099.8 |
| ensembl_prot | ENSP00000354394.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 190969149 |
| end | 191014171 |
| strand | - |
| ver | v1.2 |
| region | chr2:190969149-191014171 |
| region5000 | chr2:190964149-191019171 |
| regionname0 | STAT1_chr2_190969149_191014171 |
| regionname5000 | STAT1_chr2_190964149_191019171 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 750 | 412 | 92 | 74 | 194 | 14 | 36 | 154 | STAT1_chr2_190964149_191019171 | STAT1 | MSQWY others(745): Show |
chr2 | 190964149 | 191019171 |
| a0002 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | MSQWY others(745): Show |
chr2 | 190964149 | 191019171 |
| a0003 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | MSQWY others(745): Show |
chr2 | 190964149 | 191019171 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2250 | 325 | 79 | 66 | 136 | 12 | 30 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0002 | 0/0 | 2250 | 66 | 9 | 4 | 45 | 2 | 6 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0003 | 0/0 | 2250 | 6 | 0 | 0 | 6 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0004 | 0/0 | 2250 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0005 | 0/0 | 2250 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0006 | 0/0 | 2250 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0007 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0008 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0010 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0001c0011 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0002c0009 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 | ||
| a0003c0012 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | ATGTC others(2245): Show |
chr2 | 190964149 | 191019171 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4115 | 281 | 42 | 61 | 136 | 12 | 28 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0002 | 0/0 | 4115 | 18 | 17 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0003 | 0/0 | 4115 | 8 | 8 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0004 | 0/0 | 4115 | 4 | 4 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0005 | 0/0 | 4111 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4106): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0006 | 0/0 | 4115 | 3 | 2 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0008 | 0/0 | 4115 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0009 | 0/0 | 4115 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0011 | 0/0 | 4115 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0012 | 0/0 | 4115 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0013 | 0/0 | 4115 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0014 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0015 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0001t0016 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0002t0001 | 0/0 | 4115 | 62 | 8 | 3 | 43 | 2 | 6 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0002t0002 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0002t0007 | 0/0 | 4115 | 2 | 0 | 1 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0002t0010 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0003t0001 | 0/0 | 4115 | 6 | 0 | 0 | 6 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0004t0001 | 0/0 | 4115 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0005t0001 | 0/0 | 4115 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0006t0001 | 0/0 | 4115 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0007t0005 | 0/0 | 4111 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4106): Show |
chr2 | 190964149 | 191019171 |
| a0001c0008t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0010t0001 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0001c0011t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0002c0009t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| a0003c0012t0001 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | GTTTC others(4110): Show |
chr2 | 190964149 | 191019171 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 1 | 2 | 3 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 4 | 1 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0009g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0011g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0014g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0015g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0001t0016g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0002t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0004t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0005t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0006t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0007t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0007t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0008t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0010t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0001c0011t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0002c0009t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| a0003c0012t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0242 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00438 | hp2 | a0001 | c0002 | t0010 | g0147 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0009 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0086 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0052 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0009 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0009 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01074 | hp1 | a0001 | c0001 | t0009 | g0052 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0009 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01433 | hp2 | a0001 | c0002 | t0007 | g0145 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0088 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0189 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02135 | hp2 | a0001 | c0002 | t0007 | g0146 | EAS | KHV | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02145 | hp2 | a0002 | c0009 | t0001 | g0315 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0127 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02622 | hp2 | a0001 | c0007 | t0005 | g0138 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0249 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0313 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02922 | hp2 | a0001 | c0008 | t0001 | g0256 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02970 | hp1 | a0001 | c0001 | t0016 | g0321 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02976 | hp1 | a0003 | c0012 | t0001 | g0135 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02976 | hp2 | a0001 | c0011 | t0001 | g0262 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0077 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0320 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03491 | hp2 | a0001 | c0001 | t0012 | g0148 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0312 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0222 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04115 | hp2 | a0001 | c0001 | t0013 | g0177 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0240 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18962 | hp1 | a0001 | c0010 | t0001 | g0162 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18968 | hp2 | a0001 | c0005 | t0001 | g0017 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18979 | hp1 | a0001 | c0006 | t0001 | g0275 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18987 | hp2 | a0001 | c0006 | t0001 | g0276 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19055 | hp2 | a0001 | c0005 | t0001 | g0017 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19057 | hp1 | a0001 | c0006 | t0001 | g0277 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ASW | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0245 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | GIH | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02109 | hp1 | a0001 | c0007 | t0005 | g0137 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0311 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA18955 | hp2 | a0001 | c0005 | t0001 | g0017 | EAS | JPT | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | USA | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0289 | AFR | LWK | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0104 | REF | REF | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0219 | REF | REF | STAT1_chr2_190964149_191019171 | STAT1 | chr2 | 190964149 | 191019171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190983739 | G | A | 1 | a0003 | 1 | HG02976.hp1 | missense_variant&splice_region_variant | MODERATE | c.1349C>T | p.Thr450Met | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/25 | 1658/4116 | 1349/2253 | 450/750 | chr2 | 190983739 | |||
| chr2:191001125 | G | T | 1 | a0002 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.411C>A | p.Asp137Glu | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/25 | 720/4116 | 411/2253 | 137/750 | chr2 | 191001125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190974932 | A | C | 2 | a0001c0008 a0001c0011 |
2 | HG02922.hp2 HG02976.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2136T>G | p.Val712Val | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/25 | 2445/4116 | 2136/2253 | 712/750 | chr2 | 190974932 | |||
| chr2:190976880 | T | C | 1 | a0001c0007 | 2 | HG02109.hp1 HG02622.hp2 |
synonymous_variant | LOW | c.2019A>G | p.Lys673Lys | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/25 | 2328/4116 | 2019/2253 | 673/750 | chr2 | 190976880 | |||
| chr2:190987050 | A | G | 1 | a0001c0006 | 3 | NA18979.hp1 NA18987.hp2 NA19057.hp1 |
synonymous_variant | LOW | c.1116T>C | p.Asn372Asn | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 13/25 | 1425/4116 | 1116/2253 | 372/750 | chr2 | 190987050 | |||
| chr2:190991275 | C | T | 1 | a0001c0004 | 4 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
synonymous_variant | LOW | c.990G>A | p.Gln330Gln | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/25 | 1299/4116 | 990/2253 | 330/750 | chr2 | 190991275 | |||
| chr2:190995204 | C | T | 1 | a0001c0005 | 3 | NA18955.hp2 NA18968.hp2 NA19055.hp2 |
synonymous_variant | LOW | c.801G>A | p.Ala267Ala | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/25 | 1110/4116 | 801/2253 | 267/750 | chr2 | 190995204 | |||
| chr2:191001110 | A | G | 1 | a0001c0010 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.426T>C | p.Leu142Leu | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/25 | 735/4116 | 426/2253 | 142/750 | chr2 | 191001110 | |||
| chr2:191007581 | G | A | 1 | a0001c0003 | 6 | HG02027.hp2 HG02080.hp1 NA18949.hp2 others(3): Show |
synonymous_variant | LOW | c.354C>T | p.Asn118Asn | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/25 | 663/4116 | 354/2253 | 118/750 | chr2 | 191007581 | |||
| chr2:191009941 | A | G | 3 | a0001c0002 a0001c0004 a0001c0008 |
71 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(68): Show |
synonymous_variant | LOW | c.63T>C | p.Leu21Leu | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/25 | 372/4116 | 63/2253 | 21/750 | chr2 | 191009941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190969176 | CTTCT | C | 2 | a0001c0001t0005 a0001c0007t0005 |
3 | HG02109.hp1 HG02622.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1523_*1526delAGAA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1523 | chr2 | 190969176 | ||||||
| chr2:190969286 | A | G | 1 | a0001c0001t0013 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1417T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1417 | chr2 | 190969286 | ||||||
| chr2:190969298 | A | G | 1 | a0001c0001t0012 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1405 | chr2 | 190969298 | ||||||
| chr2:190969304 | T | C | 2 | a0001c0001t0002 a0001c0002t0002 |
19 | HG01261.hp2 HG02109.hp2 HG02486.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1399A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 1399 | chr2 | 190969304 | ||||||
| chr2:190969750 | C | A | 1 | a0001c0001t0008 | 2 | HG02258.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*953G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 953 | chr2 | 190969750 | ||||||
| chr2:190969754 | C | T | 1 | a0001c0001t0011 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 949 | chr2 | 190969754 | ||||||
| chr2:190969761 | T | C | 1 | a0001c0001t0003 | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*942A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 942 | chr2 | 190969761 | ||||||
| chr2:190969926 | T | C | 1 | a0001c0001t0004 | 4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*777A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 777 | chr2 | 190969926 | ||||||
| chr2:190970168 | G | A | 1 | a0001c0001t0006 | 3 | HG00642.hp2 HG02723.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 535 | chr2 | 190970168 | ||||||
| chr2:190970601 | T | C | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 25/25 | 102 | chr2 | 190970601 | ||||||
| chr2:191013555 | G | A | 1 | a0001c0002t0010 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/25 | 3552 | chr2 | 191013555 | ||||||
| chr2:191013663 | C | G | 2 | a0001c0002t0007 a0001c0002t0010 |
3 | HG00438.hp2 HG01433.hp2 HG02135.hp2 |
5_prime_UTR_variant | MODIFIER | c.-140G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/25 | 3660 | chr2 | 191013663 | ||||||
| chr2:191014024 | C | A | 1 | a0001c0001t0015 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4021 | chr2 | 191014024 | ||||||
| chr2:191014083 | G | C | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-221C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4080 | chr2 | 191014083 | ||||||
| chr2:191014146 | G | A | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-284C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4143 | chr2 | 191014146 | ||||||
| chr2:191014149 | G | C | 1 | a0001c0001t0016 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | 4146 | chr2 | 191014149 | ||||||
| chr2:191014160 | G | A | 1 | a0001c0001t0009 | 2 | HG00741.hp1 HG01074.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-298C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/25 | chr2 | 191014160 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190970847 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0218 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2239-130C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970847 | |||||||
| chr2:190970870 | T | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(132): Show |
172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.2239-153A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970870 | |||||||
| chr2:190970919 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2239-202G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970919 | |||||||
| chr2:190970923 | C | T | 1 | a0001c0001t0002g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2239-206G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190970923 | |||||||
| chr2:190971192 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
337 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(334): Show |
intron_variant | MODIFIER | c.2239-475A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971192 | |||||||
| chr2:190971286 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0317 a0001c0001t0001g0318 others(1): Show |
4 | HG01192.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2239-569G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971286 | |||||||
| chr2:190971334 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2239-617T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971334 | |||||||
| chr2:190971341 | A | G | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2239-624T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971341 | |||||||
| chr2:190971353 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2239-636G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971353 | |||||||
| chr2:190971440 | G | C | 3 | a0001c0001t0008g0077 a0001c0001t0008g0127 a0001c0008t0001g0256 |
3 | HG02258.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2239-723C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971440 | |||||||
| chr2:190971460 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2239-743C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971460 | |||||||
| chr2:190971599 | A | G | 1 | a0001c0001t0001g0048 | 2 | NA19060.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2239-882T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971599 | |||||||
| chr2:190971656 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2239-939A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971656 | |||||||
| chr2:190971702 | CTT | C | 10 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
10 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2239-987_2239-986d others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971702 | |||||||
| chr2:190971704 | T | TTC | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
345 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(342): Show |
intron_variant | MODIFIER | c.2239-988_2239-987i others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971704 | |||||||
| chr2:190971797 | C | G | 14 | a0001c0001t0002g0041 a0001c0001t0002g0115 a0001c0001t0002g0119 others(11): Show |
15 | HG02109.hp2 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2239-1080G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971797 | |||||||
| chr2:190971822 | C | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0210 a0001c0002t0001g0228 others(3): Show |
7 | NA18947.hp2 NA18961.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.2239-1105G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971822 | |||||||
| chr2:190971827 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(180): Show |
243 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.2239-1110G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971827 | |||||||
| chr2:190971835 | C | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0210 a0001c0002t0001g0228 others(3): Show |
7 | NA18947.hp2 NA18961.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.2239-1118G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971835 | |||||||
| chr2:190971836 | C | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(164): Show |
224 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.2239-1119G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971836 | |||||||
| chr2:190971851 | T | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0144 a0001c0001t0016g0321 |
3 | HG01884.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2239-1134A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971851 | |||||||
| chr2:190971858 | A | G | 1 | a0001c0008t0001g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2239-1141T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971858 | |||||||
| chr2:190971945 | G | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
320 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.2239-1228C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971945 | |||||||
| chr2:190971964 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(69): Show |
109 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.2239-1247G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971964 | |||||||
| chr2:190971965 | G | A | 1 | a0001c0008t0001g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2239-1248C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190971965 | |||||||
| chr2:190972008 | C | T | 3 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0002g0308 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2239-1291G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972008 | |||||||
| chr2:190972045 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(150): Show |
191 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.2239-1328A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972045 | |||||||
| chr2:190972130 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2239-1413G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972130 | |||||||
| chr2:190972302 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2239-1585A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972302 | |||||||
| chr2:190972480 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2239-1763G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972480 | |||||||
| chr2:190972487 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0319 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2239-1770G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972487 | |||||||
| chr2:190972721 | T | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0317 a0001c0001t0001g0318 others(4): Show |
7 | HG00642.hp2 HG01192.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2239-2004A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972721 | |||||||
| chr2:190972733 | C | CT | 11 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0001g0152 others(8): Show |
11 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.2239-2017dupA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972733 | |||||||
| chr2:190972733 | CT | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0176 a0001c0001t0001g0195 others(4): Show |
7 | HG01070.hp2 HG01255.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.2239-2017delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972733 | |||||||
| chr2:190972808 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2238+2022C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972808 | |||||||
| chr2:190972816 | G | GGT | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(88): Show |
127 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.2238+2012_2238+201 others(6): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | G | GGTGT | 33 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0044 others(30): Show |
38 | HG00597.hp2 HG01099.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.2238+2010_2238+201 others(8): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | G | GGTGTGT | 6 | a0001c0001t0001g0053 a0001c0001t0001g0199 a0001c0001t0001g0204 others(3): Show |
6 | HG03927.hp1 HG04204.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2238+2008_2238+201 others(10): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0131 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG00597.hp1 HG01884.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2238+2006_2238+201 others(12): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | G | GGTGTGTG others(3): Show |
2 | a0001c0001t0001g0302 a0001c0001t0012g0148 |
2 | HG03491.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2238+2004_2238+201 others(14): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | G | GT | 3 | a0001c0001t0001g0130 a0001c0001t0001g0153 a0001c0001t0001g0178 |
3 | HG03927.hp2 HG04115.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2238+2013_2238+201 others(5): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | GGT | G | 29 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(26): Show |
35 | HG00642.hp2 HG01069.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.2238+2012_2238+201 others(6): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | GGTGT | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0061 others(14): Show |
21 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2238+2010_2238+201 others(8): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | GGTGTGT | G | 4 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0002g0308 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2238+2008_2238+201 others(10): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0319 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2238+2004_2238+201 others(14): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972816 | GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0169 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2238+2002_2238+201 others(16): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972816 | |||||||
| chr2:190972855 | A | G | 1 | a0001c0001t0003g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2238+1975T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972855 | |||||||
| chr2:190972859 | G | T | 39 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0061 others(36): Show |
41 | HG00597.hp1 HG00735.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.2238+1971C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972859 | |||||||
| chr2:190972908 | C | T | 53 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0061 others(50): Show |
59 | HG00597.hp1 HG00735.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.2238+1922G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972908 | |||||||
| chr2:190972936 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0130 |
3 | HG03490.hp2 HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2238+1894G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972936 | |||||||
| chr2:190972949 | T | C | 1 | a0001c0001t0004g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2238+1881A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190972949 | |||||||
| chr2:190973115 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
177 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(174): Show |
intron_variant | MODIFIER | c.2238+1715A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973115 | |||||||
| chr2:190973249 | A | G | 13 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(10): Show |
17 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2238+1581T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973249 | |||||||
| chr2:190973303 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2238+1527G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973303 | |||||||
| chr2:190973372 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2238+1458C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973372 | |||||||
| chr2:190973458 | T | C | 1 | a0001c0002t0001g0035 | 2 | NA18959.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.2238+1372A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973458 | |||||||
| chr2:190973478 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
112 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.2238+1352G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973478 | |||||||
| chr2:190973616 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0002g0119 a0001c0002t0001g0224 others(1): Show |
5 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2238+1214A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973616 | |||||||
| chr2:190973624 | C | T | 10 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0001g0152 others(7): Show |
10 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2238+1206G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973624 | |||||||
| chr2:190973788 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
177 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(174): Show |
intron_variant | MODIFIER | c.2238+1042C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973788 | |||||||
| chr2:190973818 | G | A | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2238+1012C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973818 | |||||||
| chr2:190973899 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2238+931C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973899 | |||||||
| chr2:190973933 | C | T | 12 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0073 others(9): Show |
16 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2238+897G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973933 | |||||||
| chr2:190973984 | A | G | 2 | a0001c0001t0008g0077 a0001c0001t0008g0127 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2238+846T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190973984 | |||||||
| chr2:190974041 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2238+789A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974041 | |||||||
| chr2:190974062 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2238+768T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974062 | |||||||
| chr2:190974210 | AG | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
409 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(406): Show |
intron_variant | MODIFIER | c.2238+619delC | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974210 | |||||||
| chr2:190974252 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0319 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2238+578A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974252 | |||||||
| chr2:190974272 | A | G | 14 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0083 others(11): Show |
16 | HG01257.hp1 HG02083.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.2238+558T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974272 | |||||||
| chr2:190974311 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2238+519C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974311 | |||||||
| chr2:190974446 | C | T | 40 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
55 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2238+384G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974446 | |||||||
| chr2:190974733 | C | A | 10 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0001g0152 others(7): Show |
10 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2238+97G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974733 | |||||||
| chr2:190974738 | G | A | 14 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
14 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2238+92C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974738 | |||||||
| chr2:190974813 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0319 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2238+17G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 24/24 | chr2 | 190974813 | |||||||
| chr2:190975100 | G | C | 1 | a0001c0002t0001g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2136-168C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975100 | |||||||
| chr2:190975151 | A | C | 2 | a0001c0001t0001g0117 a0001c0002t0001g0255 |
2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2136-219T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975151 | |||||||
| chr2:190975164 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2136-232A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975164 | |||||||
| chr2:190975250 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(50): Show |
77 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.2136-318G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975250 | |||||||
| chr2:190975408 | C | A | 1 | a0001c0002t0001g0057 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2135+404G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975408 | |||||||
| chr2:190975626 | CT | C | 14 | a0001c0001t0001g0101 a0001c0001t0001g0121 a0001c0001t0001g0131 others(11): Show |
17 | HG00597.hp1 HG00642.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.2135+185delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975626 | |||||||
| chr2:190975643 | A | T | 14 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0083 others(11): Show |
16 | HG01257.hp1 HG02083.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.2135+169T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 23/24 | chr2 | 190975643 | |||||||
| chr2:190975957 | G | A | 12 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0083 others(9): Show |
14 | HG01257.hp1 HG02083.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.2060-70C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975957 | |||||||
| chr2:190975969 | GTTC | G | 14 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0083 others(11): Show |
16 | HG01257.hp1 HG02083.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.2060-85_2060-83del others(3): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975969 | |||||||
| chr2:190975977 | G | A | 1 | a0001c0002t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2060-90C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975977 | |||||||
| chr2:190975983 | C | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
7 | HG00280.hp2 HG00735.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.2060-96G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190975983 | |||||||
| chr2:190976052 | T | A | 2 | a0001c0001t0001g0117 a0001c0002t0001g0255 |
2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2060-165A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976052 | |||||||
| chr2:190976064 | A | G | 7 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(4): Show |
11 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2060-177T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976064 | |||||||
| chr2:190976167 | G | C | 1 | a0001c0001t0001g0011 | 3 | NA18970.hp1 NA18986.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2060-280C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976167 | |||||||
| chr2:190976290 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2060-403C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976290 | |||||||
| chr2:190976698 | C | T | 3 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0002g0308 |
3 | HG02622.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2059+142G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976698 | |||||||
| chr2:190976796 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2059+44C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 22/24 | chr2 | 190976796 | |||||||
| chr2:190977033 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(69): Show |
109 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(106): Show |
splice_region_variant&intron_variant | LOW | c.1874-8C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977033 | |||||||
| chr2:190977153 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
111 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.1874-128T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977153 | |||||||
| chr2:190977287 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1874-262T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977287 | |||||||
| chr2:190977387 | G | T | 1 | a0001c0001t0001g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1874-362C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977387 | |||||||
| chr2:190977389 | T | C | 7 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(4): Show |
11 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1874-364A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977389 | |||||||
| chr2:190977557 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1874-532G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977557 | |||||||
| chr2:190977714 | G | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
11 | HG02559.hp2 HG02615.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.1874-689C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977714 | |||||||
| chr2:190977884 | C | G | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1874-859G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977884 | |||||||
| chr2:190977897 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1874-872A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190977897 | |||||||
| chr2:190978189 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1873+667A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978189 | |||||||
| chr2:190978200 | C | A | 12 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0083 others(9): Show |
14 | HG01257.hp1 HG02083.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.1873+656G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978200 | |||||||
| chr2:190978206 | C | G | 1 | a0001c0001t0001g0087 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1873+650G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978206 | |||||||
| chr2:190978216 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1873+640C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978216 | |||||||
| chr2:190978465 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1873+391G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978465 | |||||||
| chr2:190978480 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1873+376A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978480 | |||||||
| chr2:190978558 | C | T | 1 | a0001c0010t0001g0162 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1873+298G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978558 | |||||||
| chr2:190978637 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1873+219A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978637 | |||||||
| chr2:190978719 | G | A | 13 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
13 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1873+137C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978719 | |||||||
| chr2:190978767 | C | T | 1 | a0001c0001t0006g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1873+89G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 21/24 | chr2 | 190978767 | |||||||
| chr2:190979093 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1728-92C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979093 | |||||||
| chr2:190979104 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(87): Show |
129 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.1728-103T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979104 | |||||||
| chr2:190979249 | C | T | 1 | a0001c0002t0001g0246 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1728-248G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979249 | |||||||
| chr2:190979543 | GT | G | 12 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0001g0152 others(9): Show |
12 | HG00597.hp1 HG02071.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1727+228delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979543 | |||||||
| chr2:190979679 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0002t0001g0054 |
3 | NA18612.hp1 NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1727+93G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979679 | |||||||
| chr2:190979760 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1727+12C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 20/24 | chr2 | 190979760 | |||||||
| chr2:190980019 | T | C | 12 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0001g0152 others(9): Show |
12 | HG00597.hp1 HG02071.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1633-153A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980019 | |||||||
| chr2:190980035 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1633-169G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980035 | |||||||
| chr2:190980234 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1633-368T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980234 | |||||||
| chr2:190980251 | G | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0141 others(2): Show |
9 | HG02015.hp1 NA18612.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1632+369C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980251 | |||||||
| chr2:190980396 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1632+224A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980396 | |||||||
| chr2:190980563 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1632+57C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980563 | |||||||
| chr2:190980614 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01106.hp2 | splice_region_variant&intron_variant | LOW | c.1632+6G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 19/24 | chr2 | 190980614 | |||||||
| chr2:190980732 | G | A | 4 | a0001c0002t0001g0055 a0001c0002t0001g0246 a0001c0002t0001g0247 others(1): Show |
4 | NA18939.hp2 NA18968.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1583-63C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980732 | |||||||
| chr2:190980849 | T | C | 1 | a0001c0002t0001g0055 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1583-180A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980849 | |||||||
| chr2:190980985 | C | T | 17 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0081 others(14): Show |
19 | HG01257.hp1 HG02056.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1583-316G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980985 | |||||||
| chr2:190980999 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(208): Show |
282 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1583-330G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190980999 | |||||||
| chr2:190981007 | C | T | 3 | a0001c0001t0002g0136 a0001c0001t0002g0308 a0001c0008t0001g0256 |
3 | HG02622.hp1 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1583-338G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981007 | |||||||
| chr2:190981022 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0012g0148 |
2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1583-353A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981022 | |||||||
| chr2:190981058 | T | G | 1 | a0001c0002t0001g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1583-389A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981058 | |||||||
| chr2:190981059 | G | GC | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(193): Show |
254 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.1583-391dupG | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981059 | |||||||
| chr2:190981089 | C | T | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1583-420G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981089 | |||||||
| chr2:190981104 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1583-435G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981104 | |||||||
| chr2:190981195 | G | C | 1 | a0001c0002t0007g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1583-526C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981195 | |||||||
| chr2:190981265 | C | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(60): Show |
83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1583-596G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981265 | |||||||
| chr2:190981365 | C | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
409 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(406): Show |
intron_variant | MODIFIER | c.1583-696G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981365 | |||||||
| chr2:190981373 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1583-704A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981373 | |||||||
| chr2:190981411 | A | C | 6 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
6 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-742T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981411 | |||||||
| chr2:190981416 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1583-747C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981416 | |||||||
| chr2:190981477 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0100 others(1): Show |
6 | HG02074.hp2 HG02129.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-808C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981477 | |||||||
| chr2:190981500 | G | A | 19 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0150 others(16): Show |
21 | HG01257.hp1 HG01928.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.1583-831C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981500 | |||||||
| chr2:190981609 | C | T | 12 | a0001c0001t0001g0316 a0001c0001t0002g0041 a0001c0001t0002g0115 others(9): Show |
13 | HG02572.hp1 HG02809.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1582+774G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981609 | |||||||
| chr2:190981791 | G | A | 2 | a0001c0001t0001g0295 a0001c0011t0001g0262 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1582+592C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981791 | |||||||
| chr2:190981966 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1582+417G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190981966 | |||||||
| chr2:190982173 | G | GA | 17 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0150 others(14): Show |
19 | HG01257.hp1 HG01928.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1582+209dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 18/24 | chr2 | 190982173 | |||||||
| chr2:190982776 | G | T | 2 | a0001c0001t0001g0295 a0001c0011t0001g0262 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1447-258C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982776 | |||||||
| chr2:190982780 | ACACACAG others(3): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1447-272_1447-263d others(12): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982780 | |||||||
| chr2:190982935 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1447-417G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982935 | |||||||
| chr2:190982968 | C | T | 1 | a0001c0010t0001g0162 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1447-450G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190982968 | |||||||
| chr2:190983314 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0213 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1446+328G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983314 | |||||||
| chr2:190983409 | A | G | 10 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(7): Show |
14 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1446+233T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983409 | |||||||
| chr2:190983419 | T | C | 2 | a0001c0001t0001g0295 a0001c0011t0001g0262 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1446+223A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983419 | |||||||
| chr2:190983480 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1446+162T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983480 | |||||||
| chr2:190983560 | T | C | 27 | a0001c0001t0001g0316 a0001c0001t0002g0031 a0001c0001t0002g0041 others(24): Show |
32 | HG01261.hp2 HG02258.hp1 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.1446+82A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 17/24 | chr2 | 190983560 | |||||||
| chr2:190983877 | G | T | 1 | a0001c0001t0004g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1348-137C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190983877 | |||||||
| chr2:190983893 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1348-153G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190983893 | |||||||
| chr2:190984002 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1348-262A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190984002 | |||||||
| chr2:190984067 | T | TA | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(68): Show |
89 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1347+242dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 16/24 | chr2 | 190984067 | |||||||
| chr2:190984545 | A | G | 1 | a0001c0008t0001g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1264-152T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984545 | |||||||
| chr2:190984550 | T | C | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-157A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984550 | |||||||
| chr2:190984596 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1264-203C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984596 | |||||||
| chr2:190984603 | G | A | 1 | a0001c0006t0001g0277 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1264-210C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984603 | |||||||
| chr2:190984954 | G | A | 2 | a0001c0001t0006g0086 a0001c0001t0006g0123 |
2 | HG00642.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1264-561C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984954 | |||||||
| chr2:190984963 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1264-570C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190984963 | |||||||
| chr2:190985120 | T | A | 1 | a0001c0001t0001g0301 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1263+499A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985120 | |||||||
| chr2:190985127 | T | C | 1 | a0001c0003t0001g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1263+492A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985127 | |||||||
| chr2:190985240 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1263+379T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985240 | |||||||
| chr2:190985373 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(97): Show |
121 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1263+246T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985373 | |||||||
| chr2:190985374 | C | T | 2 | a0001c0001t0001g0295 a0001c0011t0001g0262 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1263+245G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985374 | |||||||
| chr2:190985503 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1263+116G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 15/24 | chr2 | 190985503 | |||||||
| chr2:190985669 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1222-9G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985669 | |||||||
| chr2:190985840 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(74): Show |
95 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1222-180A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985840 | |||||||
| chr2:190985895 | C | A | 5 | a0001c0001t0001g0295 a0001c0001t0002g0129 a0001c0001t0002g0136 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1222-235G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985895 | |||||||
| chr2:190985974 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1222-314C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190985974 | |||||||
| chr2:190986040 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
321 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.1222-380G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986040 | |||||||
| chr2:190986056 | C | T | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-396G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986056 | |||||||
| chr2:190986119 | C | T | 20 | a0001c0001t0001g0152 a0001c0001t0001g0316 a0001c0001t0002g0031 others(17): Show |
25 | HG01261.hp2 HG02109.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1222-459G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986119 | |||||||
| chr2:190986224 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1222-564T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986224 | |||||||
| chr2:190986267 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1221+587C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986267 | |||||||
| chr2:190986351 | C | A | 1 | a0001c0011t0001g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1221+503G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986351 | |||||||
| chr2:190986375 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1221+479C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986375 | |||||||
| chr2:190986474 | A | G | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0038 others(31): Show |
39 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1221+380T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986474 | |||||||
| chr2:190986496 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1221+358C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986496 | |||||||
| chr2:190986536 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1221+318G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986536 | |||||||
| chr2:190986555 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1221+299C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986555 | |||||||
| chr2:190986569 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1221+285C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986569 | |||||||
| chr2:190986712 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1221+142G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986712 | |||||||
| chr2:190986759 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0155 others(31): Show |
44 | HG00323.hp1 HG00438.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1221+95G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 14/24 | chr2 | 190986759 | |||||||
| chr2:190986980 | C | A | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1128-33G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 13/24 | chr2 | 190986980 | |||||||
| chr2:190987013 | A | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1127+26T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 13/24 | chr2 | 190987013 | |||||||
| chr2:190987079 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0287 |
2 | HG02074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1098-11T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987079 | |||||||
| chr2:190987085 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1098-17A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987085 | |||||||
| chr2:190987171 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0051 others(76): Show |
94 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1098-103C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987171 | |||||||
| chr2:190987271 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(85): Show |
106 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.1098-203A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987271 | |||||||
| chr2:190987274 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0133 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1098-206G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987274 | |||||||
| chr2:190987720 | T | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098-652A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987720 | |||||||
| chr2:190987737 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1098-669C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987737 | |||||||
| chr2:190987899 | T | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
29 | HG01496.hp2 HG02004.hp1 HG02135.hp1 others(26): Show |
intron_variant | MODIFIER | c.1098-831A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987899 | |||||||
| chr2:190987952 | C | T | 2 | a0001c0001t0001g0295 a0001c0011t0001g0262 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1098-884G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987952 | |||||||
| chr2:190987996 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1098-928C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190987996 | |||||||
| chr2:190988218 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1098-1150A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988218 | |||||||
| chr2:190988310 | T | C | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1098-1242A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988310 | |||||||
| chr2:190988426 | T | C | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1097+1189A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988426 | |||||||
| chr2:190988444 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1097+1171A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988444 | |||||||
| chr2:190988496 | G | A | 2 | a0001c0001t0002g0129 a0001c0002t0001g0252 |
2 | HG02486.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1097+1119C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988496 | |||||||
| chr2:190988541 | G | T | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1097+1074C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988541 | |||||||
| chr2:190988561 | G | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(129): Show |
159 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1097+1054C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988561 | |||||||
| chr2:190988569 | G | A | 4 | a0001c0001t0001g0023 a0001c0002t0001g0226 a0001c0007t0005g0137 others(1): Show |
5 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097+1046C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988569 | |||||||
| chr2:190988598 | T | C | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1097+1017A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988598 | |||||||
| chr2:190988599 | C | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0272 others(4): Show |
13 | HG02004.hp1 HG02135.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1097+1016G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988599 | |||||||
| chr2:190988693 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0050 others(9): Show |
18 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1097+922A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988693 | |||||||
| chr2:190988836 | A | C | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1097+779T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988836 | |||||||
| chr2:190988865 | A | G | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1097+750T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988865 | |||||||
| chr2:190988891 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1097+724T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988891 | |||||||
| chr2:190988966 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0304 |
4 | HG02155.hp1 NA19004.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097+649C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190988966 | |||||||
| chr2:190989050 | A | C | 1 | a0001c0001t0001g0023 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1097+565T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989050 | |||||||
| chr2:190989118 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1097+497T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989118 | |||||||
| chr2:190989118 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1097+497T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989118 | |||||||
| chr2:190989159 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1097+456G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989159 | |||||||
| chr2:190989165 | G | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0050 others(16): Show |
29 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1097+450C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989165 | |||||||
| chr2:190989172 | G | T | 1 | a0001c0001t0002g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1097+443C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989172 | |||||||
| chr2:190989213 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(131): Show |
161 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1097+402C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989213 | |||||||
| chr2:190989516 | G | A | 1 | a0001c0011t0001g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1097+99C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989516 | |||||||
| chr2:190989551 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1097+64G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989551 | |||||||
| chr2:190989605 | G | C | 2 | a0001c0001t0001g0288 a0001c0002t0001g0225 |
2 | HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1097+10C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 12/24 | chr2 | 190989605 | |||||||
| chr2:190989697 | T | C | 59 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0072 others(56): Show |
73 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1038-23A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190989697 | |||||||
| chr2:190989876 | C | G | 1 | a0001c0001t0002g0296 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1038-202G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190989876 | |||||||
| chr2:190989913 | C | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(94): Show |
122 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1038-239G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190989913 | |||||||
| chr2:190990000 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1038-326G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990000 | |||||||
| chr2:190990143 | G | C | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1038-469C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990143 | |||||||
| chr2:190990148 | A | G | 134 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(131): Show |
161 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1038-474T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990148 | |||||||
| chr2:190990168 | T | C | 2 | a0001c0001t0002g0308 a0001c0008t0001g0256 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1038-494A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990168 | |||||||
| chr2:190990391 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1038-717G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990391 | |||||||
| chr2:190990795 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(100): Show |
121 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1037+433A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 11/24 | chr2 | 190990795 | |||||||
| chr2:190991419 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0271 others(2): Show |
8 | HG01496.hp2 NA18940.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.945-99G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991419 | |||||||
| chr2:190991516 | C | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG01192.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.945-196G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991516 | |||||||
| chr2:190991586 | C | T | 1 | a0001c0002t0007g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.945-266G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991586 | |||||||
| chr2:190991685 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0072 others(54): Show |
71 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.945-365G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991685 | |||||||
| chr2:190991698 | T | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(94): Show |
122 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.945-378A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991698 | |||||||
| chr2:190991700 | TG | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(80): Show |
99 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.945-381delC | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991700 | |||||||
| chr2:190991701 | G | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0023 others(46): Show |
60 | HG00597.hp1 HG00735.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.945-381C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991701 | |||||||
| chr2:190991705 | T | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
12 | HG04184.hp1 NA18747.hp2 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.945-385A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991705 | |||||||
| chr2:190991869 | T | TA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0155 a0001c0001t0001g0157 others(5): Show |
12 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.945-550dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991869 | |||||||
| chr2:190991886 | G | A | 10 | a0001c0001t0001g0316 a0001c0001t0002g0115 a0001c0001t0002g0119 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.945-566C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991886 | |||||||
| chr2:190991946 | A | G | 12 | a0001c0001t0001g0295 a0001c0001t0001g0316 a0001c0001t0002g0115 others(9): Show |
12 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.945-626T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190991946 | |||||||
| chr2:190992018 | G | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0065 a0001c0001t0001g0066 others(14): Show |
18 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.945-698C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992018 | |||||||
| chr2:190992022 | AT | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG01943.hp1 HG01981.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.945-703delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992022 | |||||||
| chr2:190992029 | T | A | 23 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0156 others(20): Show |
25 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.945-709A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992029 | |||||||
| chr2:190992160 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0051 others(71): Show |
89 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.945-840G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992160 | |||||||
| chr2:190992229 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.945-909T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992229 | |||||||
| chr2:190992474 | TA | T | 10 | a0001c0001t0001g0316 a0001c0001t0002g0115 a0001c0001t0002g0119 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.945-1155delT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992474 | |||||||
| chr2:190992625 | G | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0050 others(12): Show |
21 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.945-1305C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992625 | |||||||
| chr2:190992772 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.945-1452A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992772 | |||||||
| chr2:190992793 | C | CT | 12 | a0001c0001t0001g0295 a0001c0001t0001g0316 a0001c0001t0002g0115 others(9): Show |
12 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.945-1474dupA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992793 | |||||||
| chr2:190992793 | CT | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0071 others(3): Show |
7 | HG00639.hp1 HG01069.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.945-1474delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992793 | |||||||
| chr2:190992820 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0108 |
5 | HG02129.hp1 NA18942.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.945-1500A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992820 | |||||||
| chr2:190992875 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.945-1555G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992875 | |||||||
| chr2:190992978 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(68): Show |
106 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.945-1658A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190992978 | |||||||
| chr2:190993079 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.945-1759G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993079 | |||||||
| chr2:190993085 | G | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.945-1765C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993085 | |||||||
| chr2:190993116 | A | C | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.945-1796T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993116 | |||||||
| chr2:190993120 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.945-1800T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993120 | |||||||
| chr2:190993220 | G | A | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+1841C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993220 | |||||||
| chr2:190993240 | C | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | NA18998.hp2 NA19006.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+1821G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993240 | |||||||
| chr2:190993298 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.944+1763G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993298 | |||||||
| chr2:190993395 | T | C | 5 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(2): Show |
9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.944+1666A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993395 | |||||||
| chr2:190993439 | T | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0260 |
3 | HG02145.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.944+1622A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993439 | |||||||
| chr2:190993449 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.944+1612A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993449 | |||||||
| chr2:190993790 | T | TA | 5 | a0001c0001t0001g0023 a0001c0002t0001g0226 a0001c0007t0005g0137 others(2): Show |
6 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.944+1270dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993790 | |||||||
| chr2:190993910 | A | C | 20 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0065 others(17): Show |
21 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.944+1151T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190993910 | |||||||
| chr2:190994016 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.944+1045G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994016 | |||||||
| chr2:190994104 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(69): Show |
108 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.944+957C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994104 | |||||||
| chr2:190994188 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.944+873T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994188 | |||||||
| chr2:190994263 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+798G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994263 | |||||||
| chr2:190994264 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0072 others(52): Show |
69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.944+797C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994264 | |||||||
| chr2:190994620 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0214 a0001c0001t0016g0321 |
3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.944+441A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994620 | |||||||
| chr2:190994635 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.944+426A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994635 | |||||||
| chr2:190994695 | C | G | 1 | a0001c0001t0001g0292 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.944+366G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994695 | |||||||
| chr2:190994781 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.944+280A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994781 | |||||||
| chr2:190994914 | C | CA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
15 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.944+146dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994914 | |||||||
| chr2:190994914 | C | CAA | 16 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(13): Show |
27 | HG00408.hp2 HG00597.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.944+145_944+146dup others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994914 | |||||||
| chr2:190994925 | A | T | 9 | a0001c0001t0001g0085 a0001c0001t0001g0266 a0001c0001t0002g0115 others(6): Show |
9 | HG01981.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.944+136T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994925 | |||||||
| chr2:190994927 | A | AAT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(10): Show |
16 | HG01433.hp1 HG02155.hp2 HG03130.hp2 others(13): Show |
intron_variant | MODIFIER | c.944+132_944+133dup others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | |||||||
| chr2:190994927 | A | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0085 a0001c0001t0001g0087 others(12): Show |
15 | HG01981.hp2 HG02109.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.944+134T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | |||||||
| chr2:190994927 | AAT | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0001c0001t0001g0167 others(5): Show |
9 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.944+132_944+133del others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | |||||||
| chr2:190994927 | AATAT | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(51): Show |
68 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.944+130_944+133del others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | |||||||
| chr2:190994927 | AATATATA others(5): Show |
A | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+122_944+133del others(12): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994927 | |||||||
| chr2:190994928 | ATAT | A | 5 | a0001c0001t0001g0194 a0001c0001t0001g0212 a0001c0002t0001g0231 others(2): Show |
5 | HG01943.hp2 HG02300.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+130_944+132del others(3): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | |||||||
| chr2:190994928 | ATATAT | A | 12 | a0001c0001t0001g0034 a0001c0001t0001g0063 a0001c0001t0001g0130 others(9): Show |
13 | HG00323.hp1 HG00733.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.944+128_944+132del others(5): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | |||||||
| chr2:190994928 | ATATATAT others(2): Show |
A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0050 others(9): Show |
18 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.944+124_944+132del others(9): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | |||||||
| chr2:190994928 | ATATATAT others(8): Show |
A | 5 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(2): Show |
9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.944+118_944+132del others(15): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994928 | |||||||
| chr2:190994929 | T | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.944+132A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994929 | |||||||
| chr2:190994929 | T | TAC | 3 | a0001c0001t0001g0021 a0001c0001t0001g0071 a0001c0001t0001g0095 |
4 | NA18952.hp1 NA18962.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+131_944+132ins others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994929 | |||||||
| chr2:190994931 | T | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0032 others(53): Show |
70 | HG00438.hp2 HG00642.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.944+130A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994931 | |||||||
| chr2:190994933 | T | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(66): Show |
86 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.944+128A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994933 | |||||||
| chr2:190994935 | T | A | 17 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0194 others(14): Show |
17 | HG00323.hp1 HG00733.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.944+126A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994935 | |||||||
| chr2:190994937 | T | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0293 a0001c0001t0016g0321 others(1): Show |
4 | HG02135.hp2 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+124A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994937 | |||||||
| chr2:190994939 | T | A | 2 | a0001c0001t0001g0214 a0001c0001t0016g0321 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.944+122A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994939 | |||||||
| chr2:190994941 | T | A | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+120A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994941 | |||||||
| chr2:190994943 | T | A | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.944+118A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994943 | |||||||
| chr2:190994945 | T | A | 1 | a0003c0012t0001g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.944+116A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994945 | |||||||
| chr2:190994949 | TATATATA others(3): Show |
T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0286 a0001c0001t0001g0319 others(5): Show |
8 | HG00408.hp1 HG00438.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.944+102_944+111del others(10): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994949 | |||||||
| chr2:190994951 | TATATATA others(1): Show |
T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0044 others(14): Show |
20 | HG01257.hp1 HG01884.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.944+102_944+109del others(8): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994951 | |||||||
| chr2:190994955 | TATAA | T | 35 | a0001c0001t0001g0051 a0001c0001t0001g0072 a0001c0001t0001g0075 others(32): Show |
45 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.944+102_944+105del others(4): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994955 | |||||||
| chr2:190994957 | TAA | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0048 others(24): Show |
34 | HG00280.hp1 HG00438.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.944+102_944+103del others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994957 | |||||||
| chr2:190994959 | A | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(62): Show |
81 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.944+102T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 10/24 | chr2 | 190994959 | |||||||
| chr2:190995286 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.786-67T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995286 | |||||||
| chr2:190995294 | A | G | 1 | a0001c0002t0007g0146 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.786-75T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995294 | |||||||
| chr2:190995327 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0214 a0001c0001t0016g0321 |
3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.786-108T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995327 | |||||||
| chr2:190995327 | A | T | 1 | a0001c0002t0001g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.786-108T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995327 | |||||||
| chr2:190995341 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0214 a0001c0001t0016g0321 |
3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.786-122T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995341 | |||||||
| chr2:190995504 | C | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0072 others(52): Show |
69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.786-285G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995504 | |||||||
| chr2:190995633 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.786-414G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995633 | |||||||
| chr2:190995655 | A | G | 2 | a0001c0001t0002g0308 a0001c0008t0001g0256 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.786-436T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995655 | |||||||
| chr2:190995667 | G | A | 3 | a0001c0001t0002g0129 a0001c0001t0002g0308 a0001c0008t0001g0256 |
3 | HG02486.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.786-448C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995667 | |||||||
| chr2:190995684 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0292 a0001c0001t0001g0293 |
3 | HG02630.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.786-465T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995684 | |||||||
| chr2:190995719 | A | T | 23 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0156 others(20): Show |
25 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.786-500T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995719 | |||||||
| chr2:190995776 | C | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0039 others(114): Show |
138 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.786-557G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995776 | |||||||
| chr2:190995803 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(68): Show |
106 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.786-584G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995803 | |||||||
| chr2:190995851 | T | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0155 a0001c0001t0001g0157 others(5): Show |
12 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.786-632A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190995851 | |||||||
| chr2:190996029 | AT | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0065 a0001c0001t0001g0066 others(14): Show |
18 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.786-811delA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996029 | |||||||
| chr2:190996033 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.786-814C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996033 | |||||||
| chr2:190996043 | G | A | 1 | a0001c0002t0001g0250 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.786-824C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996043 | |||||||
| chr2:190996111 | G | T | 5 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(2): Show |
9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.786-892C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996111 | |||||||
| chr2:190996265 | GCAGTAAT others(6): Show |
G | 3 | a0001c0001t0002g0129 a0001c0001t0002g0308 a0001c0008t0001g0256 |
3 | HG02486.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.786-1059_786-1047d others(15): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996265 | |||||||
| chr2:190996308 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0050 others(10): Show |
19 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.786-1089A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996308 | |||||||
| chr2:190996453 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(1): Show |
8 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.786-1234G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996453 | |||||||
| chr2:190996651 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(12): Show |
24 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+1205G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996651 | |||||||
| chr2:190996726 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.785+1130A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996726 | |||||||
| chr2:190996755 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.785+1101C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190996755 | |||||||
| chr2:190997025 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(12): Show |
24 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+831G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997025 | |||||||
| chr2:190997080 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.785+776G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997080 | |||||||
| chr2:190997099 | G | A | 1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.785+757C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997099 | |||||||
| chr2:190997165 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0005g0307 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.785+691C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997165 | |||||||
| chr2:190997357 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
5 | HG02615.hp2 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+499G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997357 | |||||||
| chr2:190997365 | C | A | 23 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0156 others(20): Show |
25 | HG00438.hp1 HG01257.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.785+491G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997365 | |||||||
| chr2:190997430 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG00639.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.785+426A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997430 | |||||||
| chr2:190997459 | A | G | 58 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0072 others(55): Show |
69 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.785+397T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997459 | |||||||
| chr2:190997502 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.785+354T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997502 | |||||||
| chr2:190997609 | C | G | 5 | a0001c0001t0001g0214 a0001c0001t0002g0129 a0001c0001t0002g0308 others(2): Show |
5 | HG02486.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+247G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997609 | |||||||
| chr2:190997672 | G | A | 47 | a0001c0001t0001g0051 a0001c0001t0001g0072 a0001c0001t0001g0075 others(44): Show |
57 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.785+184C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997672 | |||||||
| chr2:190997722 | C | T | 5 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(2): Show |
9 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+134G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 9/24 | chr2 | 190997722 | |||||||
| chr2:190998023 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01099.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.634-16C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998023 | |||||||
| chr2:190998044 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.634-37T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998044 | |||||||
| chr2:190998050 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.634-43T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998050 | |||||||
| chr2:190998060 | T | C | 22 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0156 others(19): Show |
24 | HG00408.hp1 HG00438.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.634-53A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998060 | |||||||
| chr2:190998175 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(9): Show |
21 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.633+42A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 8/24 | chr2 | 190998175 | |||||||
| chr2:190998464 | C | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0234 |
3 | NA18971.hp1 NA19084.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.542-156G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998464 | |||||||
| chr2:190998522 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0214 a0001c0001t0002g0129 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-214G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998522 | |||||||
| chr2:190998618 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | NA18965.hp2 NA18973.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.542-310G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998618 | |||||||
| chr2:190998672 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.542-364G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998672 | |||||||
| chr2:190998672 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.542-375_542-365del others(11): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998672 | |||||||
| chr2:190998683 | A | G | 12 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
12 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-375T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998683 | |||||||
| chr2:190998833 | A | G | 5 | a0001c0001t0001g0023 a0001c0002t0001g0225 a0001c0002t0001g0226 others(2): Show |
6 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-525T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998833 | |||||||
| chr2:190998914 | T | C | 11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.542-606A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998914 | |||||||
| chr2:190998969 | A | G | 1 | a0001c0008t0001g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.541+657T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190998969 | |||||||
| chr2:190999064 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.541+562A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999064 | |||||||
| chr2:190999179 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.541+447C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999179 | |||||||
| chr2:190999227 | C | T | 1 | a0001c0011t0001g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.541+399G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999227 | |||||||
| chr2:190999472 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.541+154T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999472 | |||||||
| chr2:190999558 | T | A | 2 | a0001c0007t0005g0137 a0001c0007t0005g0138 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.541+68A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999558 | |||||||
| chr2:190999568 | C | A | 1 | a0001c0002t0001g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.541+58G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999568 | |||||||
| chr2:190999576 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0163 |
3 | HG01167.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.541+50T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 7/24 | chr2 | 190999576 | |||||||
| chr2:190999712 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.463-8G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999712 | |||||||
| chr2:190999841 | C | A | 1 | a0001c0002t0001g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.463-137G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999841 | |||||||
| chr2:190999858 | A | G | 3 | a0001c0001t0001g0023 a0001c0002t0001g0225 a0001c0002t0001g0226 |
4 | HG02257.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-154T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999858 | |||||||
| chr2:190999914 | C | A | 1 | a0001c0001t0002g0218 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463-210G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 190999914 | |||||||
| chr2:191000047 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.463-343G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000047 | |||||||
| chr2:191000048 | G | A | 10 | a0001c0001t0001g0316 a0001c0001t0002g0115 a0001c0001t0002g0119 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.463-344C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000048 | |||||||
| chr2:191000160 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.463-456A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000160 | |||||||
| chr2:191000217 | T | C | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.463-513A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000217 | |||||||
| chr2:191000231 | A | C | 62 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0072 others(59): Show |
74 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.463-527T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000231 | |||||||
| chr2:191000278 | C | T | 3 | a0001c0001t0001g0023 a0001c0002t0001g0225 a0001c0002t0001g0226 |
4 | HG02257.hp1 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-574G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000278 | |||||||
| chr2:191000448 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0298 others(1): Show |
8 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.462+626G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000448 | |||||||
| chr2:191000481 | G | GGCCTCT | 30 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(27): Show |
36 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.462+587_462+592dup others(6): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000481 | |||||||
| chr2:191000495 | A | G | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.462+579T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000495 | |||||||
| chr2:191000548 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.462+526G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000548 | |||||||
| chr2:191000548 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0163 |
3 | HG01167.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.462+526G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000548 | |||||||
| chr2:191000723 | C | T | 1 | a0001c0001t0003g0007 | 4 | HG02258.hp2 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+351G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000723 | |||||||
| chr2:191000802 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.462+272C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000802 | |||||||
| chr2:191000999 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0130 |
3 | HG03490.hp2 HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.462+75G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191000999 | |||||||
| chr2:191001010 | A | G | 1 | a0001c0003t0001g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.462+64T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191001010 | |||||||
| chr2:191001051 | G | T | 5 | a0001c0001t0001g0023 a0001c0002t0001g0225 a0001c0002t0001g0226 others(2): Show |
6 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.462+23C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191001051 | |||||||
| chr2:191001066 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.462+8T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 6/24 | chr2 | 191001066 | |||||||
| chr2:191001187 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.373-24A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001187 | |||||||
| chr2:191001445 | T | C | 6 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(3): Show |
10 | HG01261.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-282A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001445 | |||||||
| chr2:191001684 | A | G | 1 | a0001c0002t0007g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.373-521T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001684 | |||||||
| chr2:191001717 | T | C | 1 | a0001c0001t0014g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.373-554A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001717 | |||||||
| chr2:191001751 | T | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0214 a0001c0001t0004g0311 others(3): Show |
6 | HG02486.hp1 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-588A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001751 | |||||||
| chr2:191001804 | C | G | 1 | a0001c0001t0002g0308 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-641G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001804 | |||||||
| chr2:191001821 | A | C | 1 | a0001c0002t0001g0232 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.373-658T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001821 | |||||||
| chr2:191001889 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0160 others(33): Show |
46 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.373-726G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001889 | |||||||
| chr2:191001932 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(80): Show |
117 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.373-769A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001932 | |||||||
| chr2:191001952 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-789G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001952 | |||||||
| chr2:191001995 | T | C | 2 | a0001c0007t0005g0137 a0001c0007t0005g0138 |
2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.373-832A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001995 | |||||||
| chr2:191001997 | C | T | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.373-834G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191001997 | |||||||
| chr2:191002012 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.373-849C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002012 | |||||||
| chr2:191002119 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0154 |
3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.373-956A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002119 | |||||||
| chr2:191002140 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-977A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002140 | |||||||
| chr2:191002268 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.373-1105T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002268 | |||||||
| chr2:191002329 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.373-1166C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002329 | |||||||
| chr2:191002426 | T | C | 2 | a0001c0001t0001g0290 a0001c0002t0001g0253 |
2 | HG00597.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.373-1263A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002426 | |||||||
| chr2:191002558 | T | G | 1 | a0001c0001t0001g0318 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.373-1395A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002558 | |||||||
| chr2:191002606 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(144): Show |
201 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.373-1443G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002606 | |||||||
| chr2:191002627 | A | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(34): Show |
43 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.373-1464T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002627 | |||||||
| chr2:191002635 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.373-1472A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002635 | |||||||
| chr2:191002703 | G | A | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1540C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002703 | |||||||
| chr2:191002790 | T | G | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.373-1627A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002790 | |||||||
| chr2:191002809 | T | C | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1646A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002809 | |||||||
| chr2:191002811 | C | G | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG01943.hp1 HG01981.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1648G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002811 | |||||||
| chr2:191002820 | T | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(27): Show |
36 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.373-1657A>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002820 | |||||||
| chr2:191002988 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.373-1825T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191002988 | |||||||
| chr2:191003060 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.373-1897A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003060 | |||||||
| chr2:191003068 | A | G | 1 | a0001c0007t0005g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.373-1905T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003068 | |||||||
| chr2:191003105 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01346.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.373-1942A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003105 | |||||||
| chr2:191003141 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.373-1978A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003141 | |||||||
| chr2:191003143 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.373-1980C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003143 | |||||||
| chr2:191003305 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.373-2142G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003305 | |||||||
| chr2:191003379 | T | C | 5 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-2216A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003379 | |||||||
| chr2:191003410 | A | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(13): Show |
29 | HG01257.hp2 HG01258.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.373-2247T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003410 | |||||||
| chr2:191003418 | C | G | 1 | a0001c0002t0001g0233 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.373-2255G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003418 | |||||||
| chr2:191003473 | T | A | 2 | a0001c0001t0001g0295 a0001c0011t0001g0262 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.373-2310A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003473 | |||||||
| chr2:191003510 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.373-2347G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003510 | |||||||
| chr2:191003632 | A | G | 1 | a0001c0004t0001g0009 | 4 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2469T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003632 | |||||||
| chr2:191003694 | TA | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(143): Show |
200 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.373-2532delT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003694 | |||||||
| chr2:191003764 | T | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(28): Show |
37 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.373-2601A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003764 | |||||||
| chr2:191003802 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(8): Show |
20 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.373-2639G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003802 | |||||||
| chr2:191003857 | C | A | 50 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0072 others(47): Show |
62 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.373-2694G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003857 | |||||||
| chr2:191003868 | G | C | 1 | a0001c0002t0001g0254 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.373-2705C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003868 | |||||||
| chr2:191003973 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.373-2810A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191003973 | |||||||
| chr2:191004197 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.373-3034G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004197 | |||||||
| chr2:191004216 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(27): Show |
36 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.373-3053A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004216 | |||||||
| chr2:191004248 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0214 a0001c0001t0016g0321 |
3 | HG02970.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.373-3085T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004248 | |||||||
| chr2:191004268 | A | G | 1 | a0001c0001t0002g0308 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-3105T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004268 | |||||||
| chr2:191004437 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(143): Show |
200 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.372+3126C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004437 | |||||||
| chr2:191004527 | A | G | 1 | a0001c0002t0001g0228 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.372+3036T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004527 | |||||||
| chr2:191004754 | G | A | 1 | a0001c0002t0010g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.372+2809C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004754 | |||||||
| chr2:191004896 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.372+2667A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191004896 | |||||||
| chr2:191005185 | A | G | 74 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(71): Show |
95 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.372+2378T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005185 | |||||||
| chr2:191005223 | T | C | 10 | a0001c0001t0001g0316 a0001c0001t0002g0115 a0001c0001t0002g0136 others(7): Show |
10 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.372+2340A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005223 | |||||||
| chr2:191005251 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(1): Show |
8 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+2312G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005251 | |||||||
| chr2:191005252 | T | A | 49 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0072 others(46): Show |
61 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.372+2311A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005252 | |||||||
| chr2:191005259 | G | C | 2 | a0001c0001t0001g0295 a0001c0011t0001g0262 |
2 | HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.372+2304C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005259 | |||||||
| chr2:191005284 | A | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0214 others(12): Show |
16 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.372+2279T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005284 | |||||||
| chr2:191005437 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(31): Show |
44 | HG00408.hp1 HG00438.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.372+2126G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005437 | |||||||
| chr2:191005594 | G | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(122): Show |
156 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.372+1969C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005594 | |||||||
| chr2:191005786 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.372+1777C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005786 | |||||||
| chr2:191005898 | C | T | 58 | a0001c0001t0001g0051 a0001c0001t0001g0072 a0001c0001t0001g0075 others(55): Show |
69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.372+1665G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191005898 | |||||||
| chr2:191006010 | G | C | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.372+1553C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006010 | |||||||
| chr2:191006082 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.372+1481C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006082 | |||||||
| chr2:191006138 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.372+1425A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006138 | |||||||
| chr2:191006224 | C | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(26): Show |
35 | HG00438.hp1 HG01167.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.372+1339G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006224 | |||||||
| chr2:191006225 | G | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0044 others(26): Show |
35 | HG00438.hp1 HG01167.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.372+1338C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006225 | |||||||
| chr2:191006231 | A | G | 5 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0001c0002t0001g0230 others(2): Show |
5 | NA18947.hp2 NA18966.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1332T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006231 | |||||||
| chr2:191006317 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.372+1246A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006317 | |||||||
| chr2:191006416 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.372+1147A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006416 | |||||||
| chr2:191006561 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0020 others(8): Show |
20 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.372+1002G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006561 | |||||||
| chr2:191006812 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.372+751G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006812 | |||||||
| chr2:191006862 | G | A | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+701C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006862 | |||||||
| chr2:191006913 | T | C | 2 | a0001c0003t0001g0193 a0001c0003t0001g0209 |
2 | NA18949.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.372+650A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191006913 | |||||||
| chr2:191007160 | G | A | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+403C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007160 | |||||||
| chr2:191007343 | G | C | 4 | a0001c0001t0002g0031 a0001c0001t0003g0007 a0001c0001t0003g0070 others(1): Show |
8 | HG01261.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+220C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007343 | |||||||
| chr2:191007450 | C | T | 5 | a0001c0001t0002g0115 a0001c0001t0002g0136 a0001c0001t0002g0216 others(2): Show |
5 | HG02622.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+113G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007450 | |||||||
| chr2:191007459 | TAG | T | 49 | a0001c0001t0001g0051 a0001c0001t0001g0072 a0001c0001t0001g0075 others(46): Show |
60 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.372+102_372+103del others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 5/24 | chr2 | 191007459 | |||||||
| chr2:191007716 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.274-55A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007716 | |||||||
| chr2:191007756 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-95C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007756 | |||||||
| chr2:191007826 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.274-165G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007826 | |||||||
| chr2:191007852 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.274-191A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007852 | |||||||
| chr2:191007860 | T | C | 7 | a0001c0001t0002g0115 a0001c0001t0002g0136 a0001c0001t0002g0139 others(4): Show |
7 | HG02622.hp1 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-199A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007860 | |||||||
| chr2:191007873 | C | T | 1 | a0001c0001t0005g0307 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-212G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191007873 | |||||||
| chr2:191008240 | G | GA | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(198): Show |
267 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.274-580dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008240 | |||||||
| chr2:191008240 | G | GAA | 6 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0158 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-581_274-580dup others(2): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008240 | |||||||
| chr2:191008353 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.273+610T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008353 | |||||||
| chr2:191008827 | A | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(169): Show |
232 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.273+136T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008827 | |||||||
| chr2:191008900 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.273+63C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 4/24 | chr2 | 191008900 | |||||||
| chr2:191009395 | A | G | 8 | a0001c0001t0001g0319 a0001c0002t0001g0054 a0001c0002t0001g0055 others(5): Show |
8 | HG00438.hp1 NA18990.hp1 NA19004.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-288T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009395 | |||||||
| chr2:191009414 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.129-307G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009414 | |||||||
| chr2:191009429 | AAAT | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(75): Show |
95 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.129-325_129-323del others(3): Show |
STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009429 | |||||||
| chr2:191009463 | T | TA | 46 | a0001c0001t0001g0210 a0001c0001t0001g0297 a0001c0002t0001g0004 others(43): Show |
58 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.129-357dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009463 | |||||||
| chr2:191009521 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.128+355A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009521 | |||||||
| chr2:191009591 | G | T | 48 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0297 others(45): Show |
61 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.128+285C>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009591 | |||||||
| chr2:191009682 | T | A | 4 | a0001c0001t0004g0310 a0001c0001t0004g0311 a0001c0001t0004g0312 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+194A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 3/24 | chr2 | 191009682 | |||||||
| chr2:191010027 | T | C | 11 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0133 others(8): Show |
12 | HG01192.hp2 HG02145.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-23A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010027 | |||||||
| chr2:191010094 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0012g0148 |
2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-1-90T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010094 | |||||||
| chr2:191010309 | C | T | 71 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0064 others(68): Show |
83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-1-305G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010309 | |||||||
| chr2:191010416 | A | C | 1 | a0001c0001t0004g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-1-412T>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010416 | |||||||
| chr2:191010581 | C | T | 1 | a0001c0002t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1-577G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010581 | |||||||
| chr2:191010642 | TTC | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(96): Show |
137 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.-1-640_-1-639delGA | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010642 | |||||||
| chr2:191010744 | G | C | 1 | a0001c0001t0004g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-1-740C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191010744 | |||||||
| chr2:191011175 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
356 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.-1-1171G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011175 | |||||||
| chr2:191011342 | C | T | 1 | a0001c0011t0001g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-1-1338G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011342 | |||||||
| chr2:191011343 | G | A | 30 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0050 others(27): Show |
37 | HG01192.hp2 HG01257.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.-1-1339C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011343 | |||||||
| chr2:191011383 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-1-1379C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011383 | |||||||
| chr2:191011422 | T | C | 6 | a0001c0001t0002g0136 a0001c0001t0002g0139 a0001c0002t0001g0134 others(3): Show |
6 | HG02109.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-1418A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011422 | |||||||
| chr2:191011689 | G | A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0316 a0001c0001t0001g0317 others(4): Show |
8 | HG01192.hp2 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1685C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011689 | |||||||
| chr2:191011773 | G | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0036 others(5): Show |
14 | HG00621.hp1 HG02015.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+1752C>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191011773 | |||||||
| chr2:191012138 | C | T | 7 | a0001c0002t0001g0054 a0001c0002t0001g0055 a0001c0002t0001g0056 others(4): Show |
7 | HG00438.hp1 NA18990.hp1 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+1387G>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012138 | |||||||
| chr2:191012158 | A | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0071 |
3 | NA18952.hp1 NA18962.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-2+1367T>A | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012158 | |||||||
| chr2:191012347 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0143 |
4 | HG00621.hp1 NA18972.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+1178G>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012347 | |||||||
| chr2:191012416 | T | TA | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(102): Show |
144 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.-2+1108dupT | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012416 | |||||||
| chr2:191012440 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2+1085A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012440 | |||||||
| chr2:191012626 | T | C | 1 | a0001c0002t0010g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-2+899A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191012626 | |||||||
| chr2:191013164 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0053 |
4 | NA18970.hp1 NA18986.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+361T>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191013164 | |||||||
| chr2:191013368 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-2+157A>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191013368 | |||||||
| chr2:191013389 | TG | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(77): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-2+135delC | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 2/24 | chr2 | 191013389 | |||||||
| chr2:191013683 | G | A | 1 | a0001c0011t0001g0262 | 1 | HG02976.hp2 | splice_region_variant&intron_variant | LOW | c.-155-5C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013683 | |||||||
| chr2:191013761 | T | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(65): Show |
87 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-155-83A>G | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013761 | |||||||
| chr2:191013928 | C | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(113): Show |
157 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(154): Show |
intron_variant | MODIFIER | c.-156+90G>C | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013928 | |||||||
| chr2:191013964 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-156+54C>T | STAT1 | ENSG00000115415.21 | transcript | ENST00000361099.8 | protein_coding | 1/24 | chr2 | 191013964 |