| geneid | 3660 |
|---|---|
| ensemblid | ENSG00000168310.12 |
| hgncid | 6117 |
| symbol | IRF2 |
| name | interferon regulatory factor 2 |
| refseq_nuc | NM_002199.4 |
| refseq_prot | NP_002190.2 |
| ensembl_nuc | ENST00000393593.8 |
| ensembl_prot | ENSP00000377218.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 184387729 |
| end | 184474550 |
| strand | - |
| ver | v1.2 |
| region | chr4:184387729-184474550 |
| region5000 | chr4:184382729-184479550 |
| regionname0 | IRF2_chr4_184387729_184474550 |
| regionname5000 | IRF2_chr4_184382729_184479550 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 349 | 375 | 90 | 76 | 155 | 14 | 38 | 119 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0002 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1050 | 219 | 49 | 38 | 104 | 7 | 19 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0002 | 0/0 | 1050 | 137 | 29 | 35 | 47 | 7 | 19 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0003 | 0/0 | 1050 | 7 | 5 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0004 | 0/0 | 1050 | 6 | 6 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0005 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0006 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0007 | 0/0 | 1050 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0008 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0009 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0010 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| c0011 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1203 | 136 | 38 | 31 | 41 | 6 | 20 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0002 | 0/0 | 1202 | 102 | 21 | 13 | 56 | 3 | 9 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0003 | 0/0 | 1204 | 81 | 8 | 18 | 47 | 3 | 5 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0004 | 0/1 | 1208 | 28 | 12 | 11 | 0 | 2 | 2 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0005 | 0/0 | 1193 | 14 | 0 | 3 | 10 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0006 | 0/0 | 1203 | 4 | 4 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0007 | 0/0 | 1202 | 3 | 3 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0008 | 0/0 | 1207 | 2 | 2 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0009 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0010 | 0/0 | 1204 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0011 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0012 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0013 | 0/0 | 1202 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| t0014 | 1/0 | 1208 | 1 | 0 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 219 | 49 | 38 | 104 | 7 | 19 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002 | 0/0 | 1050 | 137 | 29 | 35 | 47 | 7 | 19 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0003 | 0/0 | 1050 | 7 | 5 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0004 | 0/0 | 1050 | 6 | 6 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0005 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0006 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0007 | 0/0 | 1050 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0009 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0010 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0011 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0002c0008 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2252 | 20 | 14 | 1 | 2 | 0 | 3 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0002 | 0/0 | 2251 | 100 | 20 | 13 | 55 | 3 | 9 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0003 | 0/0 | 2253 | 78 | 8 | 17 | 46 | 3 | 4 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0004 | 0/1 | 2257 | 13 | 2 | 7 | 0 | 1 | 2 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0006 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0007 | 0/0 | 2251 | 3 | 3 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0010 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0012 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0013 | 0/0 | 2251 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0001t0014 | 1/0 | 2257 | 1 | 0 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0001 | 0/0 | 2252 | 112 | 23 | 29 | 37 | 6 | 17 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0002 | 0/0 | 2251 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0003 | 0/0 | 2253 | 2 | 0 | 1 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0004 | 0/0 | 2257 | 4 | 1 | 2 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0005 | 0/0 | 2242 | 13 | 0 | 3 | 9 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0006 | 0/0 | 2252 | 3 | 3 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0009 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0002t0011 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0003t0004 | 0/0 | 2257 | 5 | 3 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0003t0008 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0004t0004 | 0/0 | 2257 | 6 | 6 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0005t0001 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0006t0005 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0007t0001 | 0/0 | 2252 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0009t0001 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0010t0003 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0001c0011t0001 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| a0002c0008t0002 | 0/0 | 2251 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | copy fasta | chr4 | 184382729 | 184479550 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0006g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0007g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0007g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0007g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0013g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0014g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0005t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0006t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0007t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0009t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0010t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0011t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0002c0008t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0174 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0125 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0054 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0351 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0204 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01074 | hp2 | a0001 | c0003 | t0004 | g0256 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01081 | hp2 | a0001 | c0003 | t0004 | g0241 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0288 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0289 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0327 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01192 | hp2 | a0001 | c0007 | t0001 | g0151 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0014 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0349 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0152 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0224 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0029 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0045 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0036 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0226 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0227 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0043 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01884 | hp1 | a0001 | c0003 | t0004 | g0259 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0367 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0046 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0342 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0352 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0348 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01981 | hp2 | a0001 | c0002 | t0005 | g0341 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02004 | hp2 | a0001 | c0002 | t0005 | g0027 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02040 | hp1 | a0001 | c0010 | t0003 | g0052 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02074 | hp2 | a0001 | c0002 | t0005 | g0355 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02145 | hp2 | a0001 | c0004 | t0004 | g0285 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | CDX | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | CDX | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CDX | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0364 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02258 | hp2 | a0001 | c0004 | t0004 | g0332 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02280 | hp2 | a0001 | c0002 | t0006 | g0365 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0305 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0282 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02615 | hp1 | a0001 | c0004 | t0004 | g0318 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0157 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02717 | hp2 | a0001 | c0004 | t0004 | g0254 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0118 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02809 | hp1 | a0001 | c0003 | t0008 | g0184 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02818 | hp1 | a0001 | c0002 | t0006 | g0366 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0334 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0317 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02976 | hp2 | a0001 | c0004 | t0004 | g0188 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03098 | hp1 | a0001 | c0002 | t0011 | g0181 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03130 | hp2 | a0001 | c0004 | t0004 | g0331 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0245 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0193 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03209 | hp2 | a0001 | c0003 | t0008 | g0316 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0139 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0363 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0182 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0368 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0362 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0290 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0231 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0326 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03927 | hp1 | a0001 | c0001 | t0010 | g0091 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0126 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0323 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0116 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0138 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0350 | EAS | CHB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | CHB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18941 | hp2 | a0001 | c0001 | t0013 | g0100 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18949 | hp2 | a0001 | c0002 | t0009 | g0009 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18959 | hp2 | a0001 | c0002 | t0005 | g0041 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18965 | hp2 | a0001 | c0002 | t0005 | g0048 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18969 | hp1 | a0001 | c0009 | t0001 | g0012 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18974 | hp1 | a0001 | c0002 | t0005 | g0016 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18979 | hp1 | a0001 | c0002 | t0005 | g0093 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18983 | hp2 | a0002 | c0008 | t0002 | g0089 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18991 | hp2 | a0001 | c0002 | t0005 | g0319 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0210 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19063 | hp1 | a0001 | c0006 | t0005 | g0034 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19066 | hp1 | a0001 | c0002 | t0005 | g0069 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19068 | hp1 | a0001 | c0011 | t0001 | g0074 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19082 | hp1 | a0001 | c0002 | t0005 | g0267 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0333 | AFR | ASW | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | ASW | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | TSI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0175 | EUR | TSI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0136 | EUR | TSI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0025 | EUR | TSI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0166 | SAS | GIH | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | GIH | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0353 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0160 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18955 | hp2 | a0001 | c0002 | t0005 | g0273 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0346 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0303 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0053 | REF | REF | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0014 | g0361 | REF | REF | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184388834
|
C | T | 1 | a0002 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.974G>A | p.Arg325Gln | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 1152/2257 | 974/1050 | 325/349 | chr4 | 184388834 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184388773
|
G | A | 1 | a0001c0007 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.1035C>T | p.Arg345Arg | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 1213/2257 | 1035/1050 | 345/349 | chr4 | 184388773 | ||
| chr4:184388899
|
G | A | 1 | a0001c0003 | 7 | HG01074.hp2 HG01081.hp2 HG01884.hp1 others(4): Show |
synonymous_variant | LOW | c.909C>T | p.Ser303Ser | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 1087/2257 | 909/1050 | 303/349 | chr4 | 184388899 | ||
| chr4:184389043
|
C | T | 1 | a0001c0006 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.765G>A | p.Arg255Arg | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 943/2257 | 765/1050 | 255/349 | chr4 | 184389043 | ||
| chr4:184389064
|
C | T | 5 | a0001c0002a0001c0006a0001c0007others(2): Show | 141 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
splice_region_variant&synonymous_variant | LOW | c.744G>A | p.Gly248Gly | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 922/2257 | 744/1050 | 248/349 | chr4 | 184389064 | ||
| chr4:184390739
|
C | T | 1 | a0001c0004 | 6 | HG02145.hp2 HG02258.hp2 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.705G>A | p.Thr235Thr | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/9 | 883/2257 | 705/1050 | 235/349 | chr4 | 184390739 | ||
| chr4:184398955
|
C | T | 1 | a0001c0005 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.654G>A | p.Glu218Glu | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/9 | 832/2257 | 654/1050 | 218/349 | chr4 | 184398955 | ||
| chr4:184398958
|
G | A | 2 | a0001c0009a0001c0010 | 2 | HG02040.hp1 NA18969.hp1 |
synonymous_variant | LOW | c.651C>T | p.Ser217Ser | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/9 | 829/2257 | 651/1050 | 217/349 | chr4 | 184398958 | ||
| chr4:184399075
|
T | C | 1 | a0001c0011 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.534A>G | p.Val178Val | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/9 | 712/2257 | 534/1050 | 178/349 | chr4 | 184399075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184387821
|
T | TA | 4 | a0001c0001t0003a0001c0001t0010a0001c0002t0003others(1): Show | 82 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*936dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 936 | chr4 | 184387821 | |||||
| chr4:184387821
|
TA | T | 6 | a0001c0001t0002a0001c0001t0007a0001c0001t0013others(3): Show | 108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*936delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 936 | chr4 | 184387821 | |||||
| chr4:184388206
|
CGGGAT | C | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | 329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*547_*551delATCCC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 547 | chr4 | 184388206 | |||||
| chr4:184388206
|
CGGGATGG others(8): Show |
C | 2 | a0001c0002t0005a0001c0006t0005 | 14 | HG01928.hp2 HG01981.hp2 HG02004.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*537_*551delATCCCA others(9): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 537 | chr4 | 184388206 | |||||
| chr4:184388206
|
CGGGATGG others(13): Show |
C | 2 | a0001c0001t0012a0001c0002t0011 | 2 | HG03098.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*532_*551delATCCCA others(14): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 532 | chr4 | 184388206 | |||||
| chr4:184388293
|
C | T | 1 | a0001c0002t0011 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 465 | chr4 | 184388293 | |||||
| chr4:184388451
|
A | G | 1 | a0001c0002t0011 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*307T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 307 | chr4 | 184388451 | |||||
| chr4:184388481
|
A | C | 1 | a0001c0001t0010 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 277 | chr4 | 184388481 | |||||
| chr4:184388616
|
G | A | 1 | a0001c0001t0013 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*142C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 9/9 | 142 | chr4 | 184388616 | |||||
| chr4:184474424
|
A | G | 1 | a0001c0002t0009 | 1 | NA18949.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/9 | 45360 | chr4 | 184474424 | |||||
| chr4:184474441
|
A | G | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | 368 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(365): Show |
5_prime_UTR_variant | MODIFIER | c.-69T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/9 | 45377 | chr4 | 184474441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184389340
|
C | T | 1 | a0001c0001t0003g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.742-274G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389340 | ||||||
| chr4:184389380
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.742-314A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389380 | ||||||
| chr4:184389507
|
A | G | 1 | a0001c0001t0002g0239 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.742-441T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389507 | ||||||
| chr4:184389609
|
A | T | 5 | a0001c0001t0001g0233a0001c0001t0001g0287a0001c0001t0006g0368others(2): Show | 5 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.742-543T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389609 | ||||||
| chr4:184389725
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742-659C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389725 | ||||||
| chr4:184389775
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0070 | 2 | HG00639.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.742-709C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389775 | ||||||
| chr4:184389822
|
G | C | 22 | a0001c0001t0001g0183a0001c0001t0001g0211a0001c0001t0001g0248others(19): Show | 22 | HG00423.hp2 HG01361.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.742-756C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389822 | ||||||
| chr4:184389843
|
T | C | 162 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0307others(159): Show | 166 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.742-777A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389843 | ||||||
| chr4:184389845
|
G | C | 1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.742-779C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389845 | ||||||
| chr4:184389887
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.741+816G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389887 | ||||||
| chr4:184389899
|
C | G | 1 | a0001c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.741+804G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184389899 | ||||||
| chr4:184390207
|
C | A | 1 | a0001c0001t0002g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.741+496G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390207 | ||||||
| chr4:184390253
|
C | T | 19 | a0001c0001t0003g0006a0001c0001t0003g0025a0001c0001t0003g0082others(16): Show | 20 | HG00642.hp2 HG00741.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.741+450G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390253 | ||||||
| chr4:184390259
|
A | G | 2 | a0001c0001t0003g0226a0001c0001t0003g0227 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.741+444T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390259 | ||||||
| chr4:184390280
|
C | G | 1 | a0001c0002t0001g0180 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.741+423G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390280 | ||||||
| chr4:184390283
|
C | G | 271 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(268): Show | 277 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.741+420G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390283 | ||||||
| chr4:184390349
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.741+354A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390349 | ||||||
| chr4:184390354
|
T | C | 87 | a0001c0001t0001g0291a0001c0001t0002g0106a0001c0002t0001g0001others(84): Show | 89 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.741+349A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390354 | ||||||
| chr4:184390416
|
G | A | 80 | a0001c0001t0001g0291a0001c0001t0002g0106a0001c0002t0001g0001others(77): Show | 82 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.741+287C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390416 | ||||||
| chr4:184390461
|
G | C | 6 | a0001c0002t0001g0194a0001c0002t0001g0212a0001c0002t0001g0246others(3): Show | 6 | HG02976.hp1 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.741+242C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390461 | ||||||
| chr4:184390543
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.741+160A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390543 | ||||||
| chr4:184390577
|
C | A | 3 | a0001c0002t0001g0107a0001c0002t0001g0113a0001c0002t0001g0203 | 3 | NA18944.hp2 NA18981.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.741+126G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 8/8 | chr4 | 184390577 | ||||||
| chr4:184390789
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.695-40G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184390789 | ||||||
| chr4:184390824
|
A | G | 15 | a0001c0002t0001g0021a0001c0002t0001g0029a0001c0002t0001g0107others(12): Show | 15 | HG01361.hp1 HG01515.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-75T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184390824 | ||||||
| chr4:184390873
|
C | T | 85 | a0001c0001t0002g0106a0001c0002t0001g0001a0001c0002t0001g0007others(82): Show | 87 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.695-124G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184390873 | ||||||
| chr4:184390874
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.695-125C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184390874 | ||||||
| chr4:184390896
|
C | T | 1 | a0002c0008t0002g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.695-147G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184390896 | ||||||
| chr4:184390983
|
T | G | 1 | a0001c0005t0001g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.695-234A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184390983 | ||||||
| chr4:184391012
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.695-263G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391012 | ||||||
| chr4:184391027
|
C | T | 109 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0215others(106): Show | 110 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.695-278G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391027 | ||||||
| chr4:184391031
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.695-282G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391031 | ||||||
| chr4:184391185
|
C | T | 4 | a0001c0002t0001g0134a0001c0002t0001g0292a0001c0009t0001g0012others(1): Show | 4 | NA18952.hp1 NA18969.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-436G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391185 | ||||||
| chr4:184391201
|
C | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0189others(206): Show | 213 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.695-452G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391201 | ||||||
| chr4:184391302
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.695-553A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391302 | ||||||
| chr4:184391418
|
C | T | 15 | a0001c0002t0001g0021a0001c0002t0001g0029a0001c0002t0001g0107others(12): Show | 15 | HG01361.hp1 HG01515.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-669G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391418 | ||||||
| chr4:184391530
|
C | T | 101 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0001g0192others(98): Show | 102 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.695-781G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391530 | ||||||
| chr4:184391570
|
TG | T | 3 | a0001c0002t0001g0107a0001c0002t0001g0113a0001c0002t0001g0203 | 3 | NA18944.hp2 NA18981.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.695-822delC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391570 | ||||||
| chr4:184391706
|
G | C | 347 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(344): Show | 355 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.695-957C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391706 | ||||||
| chr4:184391742
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.695-993C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184391742 | ||||||
| chr4:184392027
|
G | A | 1 | a0001c0003t0008g0316 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.695-1278C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392027 | ||||||
| chr4:184392209
|
G | T | 3 | a0001c0002t0001g0197a0001c0002t0001g0303a0001c0002t0006g0365 | 3 | HG02280.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.695-1460C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392209 | ||||||
| chr4:184392244
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0324a0001c0001t0004g0044others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.695-1495T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392244 | ||||||
| chr4:184392274
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.695-1525G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392274 | ||||||
| chr4:184392841
|
C | A | 10 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0080others(7): Show | 11 | HG00323.hp1 HG02083.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.695-2092G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392841 | ||||||
| chr4:184392917
|
G | A | 1 | a0001c0002t0001g0249 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.695-2168C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392917 | ||||||
| chr4:184392984
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.695-2235A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392984 | ||||||
| chr4:184392993
|
G | A | 1 | a0001c0002t0005g0341 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.695-2244C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184392993 | ||||||
| chr4:184393076
|
G | A | 4 | a0001c0002t0001g0036a0001c0002t0001g0043a0001c0002t0001g0045others(1): Show | 4 | HG00639.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-2327C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393076 | ||||||
| chr4:184393234
|
T | A | 1 | a0001c0001t0002g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.695-2485A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393234 | ||||||
| chr4:184393259
|
G | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0189others(118): Show | 123 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.695-2510C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393259 | ||||||
| chr4:184393444
|
C | T | 4 | a0001c0002t0001g0159a0001c0002t0001g0176a0001c0002t0003g0139others(1): Show | 4 | HG01257.hp1 HG01496.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-2695G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393444 | ||||||
| chr4:184393565
|
C | T | 82 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0307others(79): Show | 85 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.695-2816G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393565 | ||||||
| chr4:184393570
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.695-2821A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393570 | ||||||
| chr4:184393846
|
C | T | 2 | a0001c0001t0003g0025a0001c0001t0003g0304 | 2 | HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.695-3097G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393846 | ||||||
| chr4:184393879
|
G | A | 1 | a0001c0001t0002g0339 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.695-3130C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393879 | ||||||
| chr4:184393883
|
C | T | 1 | a0001c0001t0002g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.695-3134G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184393883 | ||||||
| chr4:184394064
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.695-3315G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394064 | ||||||
| chr4:184394230
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.695-3481C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394230 | ||||||
| chr4:184394316
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.695-3567G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394316 | ||||||
| chr4:184394364
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.695-3615C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394364 | ||||||
| chr4:184394515
|
C | T | 1 | a0001c0002t0005g0048 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.695-3766G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394515 | ||||||
| chr4:184394578
|
G | A | 8 | a0001c0001t0002g0004a0001c0002t0001g0191a0001c0002t0001g0197others(5): Show | 9 | HG01109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.695-3829C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394578 | ||||||
| chr4:184394588
|
G | A | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.695-3839C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394588 | ||||||
| chr4:184394638
|
C | T | 77 | a0001c0001t0001g0079a0001c0001t0001g0307a0001c0001t0002g0002others(74): Show | 79 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.695-3889G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394638 | ||||||
| chr4:184394666
|
AGAT | A | 11 | a0001c0001t0001g0005a0001c0001t0003g0304a0001c0001t0004g0044others(8): Show | 12 | HG00642.hp2 HG01099.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-3920_695-3918d others(5): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394666 | ||||||
| chr4:184394745
|
C | T | 2 | a0001c0001t0004g0204a0001c0001t0004g0205 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.695-3996G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394745 | ||||||
| chr4:184394815
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0315 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.695-4066C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394815 | ||||||
| chr4:184394939
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.694+3976C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394939 | ||||||
| chr4:184394997
|
A | C | 20 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0002g0061others(17): Show | 20 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.694+3918T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184394997 | ||||||
| chr4:184395049
|
C | T | 5 | a0001c0002t0001g0212a0001c0002t0001g0246a0001c0002t0001g0255others(2): Show | 5 | HG02976.hp1 HG03130.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+3866G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395049 | ||||||
| chr4:184395138
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.694+3777C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395138 | ||||||
| chr4:184395140
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.694+3775C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395140 | ||||||
| chr4:184395177
|
C | T | 17 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0012g0210others(14): Show | 17 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.694+3738G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395177 | ||||||
| chr4:184395211
|
A | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0183a0001c0001t0001g0307others(84): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.694+3704T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395211 | ||||||
| chr4:184395227
|
C | T | 1 | a0001c0002t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.694+3688G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395227 | ||||||
| chr4:184395239
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.694+3676C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395239 | ||||||
| chr4:184395279
|
T | G | 9 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0243others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+3636A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395279 | ||||||
| chr4:184395344
|
T | C | 1 | a0001c0002t0001g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.694+3571A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395344 | ||||||
| chr4:184395368
|
G | T | 2 | a0001c0001t0003g0060a0001c0001t0003g0120 | 2 | HG00738.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.694+3547C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395368 | ||||||
| chr4:184395399
|
C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0223 | 3 | HG01106.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.694+3516G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395399 | ||||||
| chr4:184395410
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.694+3505G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395410 | ||||||
| chr4:184395412
|
C | CAA | 51 | a0001c0001t0001g0005a0001c0001t0001g0211a0001c0001t0001g0307others(48): Show | 54 | HG00323.hp1 HG01070.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.694+3501_694+3502d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395412 | ||||||
| chr4:184395412
|
C | CAAA | 208 | a0001c0001t0001g0079a0001c0001t0001g0183a0001c0001t0001g0291others(205): Show | 213 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.694+3500_694+3502d others(5): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395412 | ||||||
| chr4:184395412
|
C | CAAAA | 72 | a0001c0001t0001g0143a0001c0001t0001g0233a0001c0001t0001g0287others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.694+3499_694+3502d others(6): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395412 | ||||||
| chr4:184395412
|
C | CAAAAA | 7 | a0001c0001t0002g0344a0001c0001t0003g0133a0001c0001t0007g0362others(4): Show | 7 | HG01255.hp2 HG02280.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+3498_694+3502d others(7): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395412 | ||||||
| chr4:184395412
|
CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0243others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+3492_694+3502d others(13): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395412 | ||||||
| chr4:184395486
|
C | A | 1 | a0001c0002t0001g0180 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.694+3429G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395486 | ||||||
| chr4:184395492
|
T | C | 20 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0002g0061others(17): Show | 20 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.694+3423A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395492 | ||||||
| chr4:184395559
|
G | C | 34 | a0001c0001t0001g0233a0001c0001t0001g0287a0001c0001t0002g0207others(31): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.694+3356C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395559 | ||||||
| chr4:184395643
|
C | T | 347 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(344): Show | 355 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.694+3272G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395643 | ||||||
| chr4:184395716
|
T | C | 3 | a0001c0001t0003g0020a0001c0001t0003g0090a0001c0001t0003g0148 | 3 | HG01346.hp2 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.694+3199A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395716 | ||||||
| chr4:184395743
|
C | T | 12 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0058others(9): Show | 12 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.694+3172G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184395743 | ||||||
| chr4:184396310
|
G | A | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.694+2605C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396310 | ||||||
| chr4:184396345
|
A | G | 7 | a0001c0001t0002g0004a0001c0002t0001g0191a0001c0002t0001g0197others(4): Show | 8 | HG01109.hp2 HG02486.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.694+2570T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396345 | ||||||
| chr4:184396386
|
C | T | 18 | a0001c0001t0002g0196a0001c0001t0002g0330a0001c0001t0003g0076others(15): Show | 18 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.694+2529G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396386 | ||||||
| chr4:184396420
|
A | G | 11 | a0001c0001t0001g0183a0001c0001t0002g0003a0001c0001t0002g0028others(8): Show | 12 | HG00323.hp1 HG02083.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.694+2495T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396420 | ||||||
| chr4:184396425
|
TA | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0202a0001c0002t0001g0191others(6): Show | 10 | HG01081.hp2 HG01109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+2489delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396425 | ||||||
| chr4:184396426
|
A | T | 7 | a0001c0001t0002g0244a0001c0001t0003g0102a0001c0001t0003g0122others(4): Show | 7 | HG01884.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+2489T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396426 | ||||||
| chr4:184396426
|
AT | A | 90 | a0001c0001t0001g0079a0001c0001t0001g0183a0001c0001t0001g0307others(87): Show | 93 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.694+2488delA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396426 | ||||||
| chr4:184396426
|
ATT | A | 16 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0012g0210others(13): Show | 16 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.694+2487_694+2488d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396426 | ||||||
| chr4:184396428
|
T | A | 34 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0070others(31): Show | 34 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.694+2487A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396428 | ||||||
| chr4:184396442
|
T | C | 1 | a0001c0004t0004g0188 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.694+2473A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396442 | ||||||
| chr4:184396527
|
G | A | 1 | a0001c0001t0004g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.694+2388C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396527 | ||||||
| chr4:184396568
|
G | A | 7 | a0001c0001t0002g0004a0001c0002t0001g0191a0001c0002t0001g0197others(4): Show | 8 | HG01109.hp2 HG02486.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.694+2347C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396568 | ||||||
| chr4:184396576
|
G | A | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0281others(1): Show | 4 | HG02698.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+2339C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396576 | ||||||
| chr4:184396587
|
A | G | 2 | a0001c0002t0001g0043a0001c0002t0001g0045 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.694+2328T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396587 | ||||||
| chr4:184396619
|
A | G | 1 | a0001c0001t0002g0314 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.694+2296T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396619 | ||||||
| chr4:184396647
|
G | A | 2 | a0001c0001t0003g0201a0001c0001t0003g0328 | 2 | HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.694+2268C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396647 | ||||||
| chr4:184396754
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.694+2161G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396754 | ||||||
| chr4:184396874
|
G | A | 1 | a0001c0002t0005g0048 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.694+2041C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396874 | ||||||
| chr4:184396878
|
A | T | 6 | a0001c0003t0004g0193a0001c0003t0004g0241a0001c0003t0004g0245others(3): Show | 6 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+2037T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396878 | ||||||
| chr4:184396912
|
G | A | 1 | a0001c0002t0001g0289 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.694+2003C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396912 | ||||||
| chr4:184396978
|
T | C | 1 | a0001c0001t0002g0252 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.694+1937A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396978 | ||||||
| chr4:184396984
|
A | G | 6 | a0001c0003t0004g0193a0001c0003t0004g0241a0001c0003t0004g0245others(3): Show | 6 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+1931T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184396984 | ||||||
| chr4:184397072
|
G | A | 1 | a0001c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.694+1843C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397072 | ||||||
| chr4:184397117
|
A | T | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.694+1798T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397117 | ||||||
| chr4:184397139
|
A | C | 54 | a0001c0001t0001g0183a0001c0001t0001g0192a0001c0001t0001g0211others(51): Show | 55 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.694+1776T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397139 | ||||||
| chr4:184397371
|
A | G | 1 | a0001c0002t0005g0069 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.694+1544T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397371 | ||||||
| chr4:184397432
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.694+1483G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397432 | ||||||
| chr4:184397468
|
T | C | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.694+1447A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397468 | ||||||
| chr4:184397531
|
G | GAA | 10 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0066others(7): Show | 10 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+1382_694+1383d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397531 | ||||||
| chr4:184397542
|
G | A | 2 | a0001c0001t0001g0189a0001c0002t0001g0194 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.694+1373C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397542 | ||||||
| chr4:184397685
|
C | T | 2 | a0001c0001t0001g0189a0001c0002t0001g0194 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.694+1230G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397685 | ||||||
| chr4:184397686
|
G | A | 2 | a0001c0002t0001g0138a0001c0002t0001g0170 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.694+1229C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397686 | ||||||
| chr4:184397848
|
G | C | 16 | a0001c0001t0001g0183a0001c0001t0001g0192a0001c0001t0001g0243others(13): Show | 17 | HG00323.hp1 HG02083.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+1067C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184397848 | ||||||
| chr4:184398182
|
G | A | 3 | a0001c0001t0003g0038a0001c0001t0003g0099a0001c0001t0003g0266 | 3 | NA18962.hp1 NA18979.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.694+733C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398182 | ||||||
| chr4:184398443
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.694+472G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398443 | ||||||
| chr4:184398481
|
TC | T | 6 | a0001c0001t0002g0179a0001c0001t0002g0198a0001c0001t0002g0217others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+433delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398481 | ||||||
| chr4:184398486
|
G | A | 1 | a0001c0001t0003g0253 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.694+429C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398486 | ||||||
| chr4:184398655
|
C | CA | 17 | a0001c0001t0001g0183a0001c0001t0002g0004a0001c0001t0004g0044others(14): Show | 18 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.694+259dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398655 | ||||||
| chr4:184398655
|
CA | C | 6 | a0001c0003t0004g0193a0001c0003t0004g0241a0001c0003t0004g0245others(3): Show | 6 | HG01081.hp2 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+259delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398655 | ||||||
| chr4:184398662
|
A | T | 13 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0058others(10): Show | 13 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.694+253T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398662 | ||||||
| chr4:184398666
|
A | AT | 4 | a0001c0001t0001g0005a0001c0001t0001g0324a0001c0002t0001g0191others(1): Show | 5 | HG01256.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+248_694+249ins others(1): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398666 | ||||||
| chr4:184398666
|
A | T | 286 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0189others(283): Show | 292 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.694+249T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398666 | ||||||
| chr4:184398669
|
A | T | 3 | a0001c0002t0001g0212a0001c0002t0001g0246a0001c0002t0001g0333 | 3 | HG03130.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.694+246T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398669 | ||||||
| chr4:184398670
|
T | A | 13 | a0001c0001t0002g0163a0001c0001t0003g0076a0001c0002t0001g0029others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.694+245A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398670 | ||||||
| chr4:184398870
|
C | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0251others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+45G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398870 | ||||||
| chr4:184399102
|
A | G | 2 | a0001c0001t0002g0207a0001c0001t0003g0167 | 2 | HG00733.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.530-23T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399102 | ||||||
| chr4:184399131
|
G | C | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.530-52C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399131 | ||||||
| chr4:184399164
|
G | C | 1 | a0001c0002t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.530-85C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399164 | ||||||
| chr4:184399174
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.530-95C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399174 | ||||||
| chr4:184399317
|
C | T | 9 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0080others(6): Show | 10 | HG00323.hp1 HG02083.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.530-238G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399317 | ||||||
| chr4:184399482
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0324a0001c0001t0004g0044others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.530-403C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399482 | ||||||
| chr4:184399553
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0251others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-474A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399553 | ||||||
| chr4:184399599
|
G | C | 17 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0012g0210others(14): Show | 17 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.530-520C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399599 | ||||||
| chr4:184399866
|
G | A | 13 | a0001c0002t0001g0063a0001c0002t0001g0087a0001c0002t0001g0115others(10): Show | 13 | HG00280.hp1 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.530-787C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399866 | ||||||
| chr4:184399962
|
G | T | 96 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0233others(93): Show | 98 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.530-883C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184399962 | ||||||
| chr4:184400205
|
T | C | 1 | a0001c0002t0011g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.530-1126A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184400205 | ||||||
| chr4:184400361
|
C | T | 142 | a0001c0001t0001g0005a0001c0001t0001g0189a0001c0001t0001g0192others(139): Show | 146 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.530-1282G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184400361 | ||||||
| chr4:184400717
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.530-1638G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184400717 | ||||||
| chr4:184400786
|
C | T | 1 | a0001c0002t0001g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.530-1707G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184400786 | ||||||
| chr4:184400787
|
A | G | 126 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0215others(123): Show | 129 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.530-1708T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184400787 | ||||||
| chr4:184401169
|
C | T | 2 | a0001c0001t0001g0189a0001c0002t0001g0194 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.530-2090G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401169 | ||||||
| chr4:184401283
|
A | C | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.530-2204T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401283 | ||||||
| chr4:184401366
|
G | A | 16 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0012g0210others(13): Show | 16 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.530-2287C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401366 | ||||||
| chr4:184401499
|
T | C | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.530-2420A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401499 | ||||||
| chr4:184401721
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0235 | 2 | HG00642.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.530-2642C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401721 | ||||||
| chr4:184401820
|
A | G | 365 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(362): Show | 373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.530-2741T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401820 | ||||||
| chr4:184401831
|
A | T | 5 | a0001c0001t0001g0189a0001c0001t0002g0187a0001c0001t0002g0206others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.530-2752T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401831 | ||||||
| chr4:184401995
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.530-2916C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184401995 | ||||||
| chr4:184402094
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.530-3015T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402094 | ||||||
| chr4:184402101
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.530-3022G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402101 | ||||||
| chr4:184402332
|
T | C | 2 | a0001c0002t0001g0001a0001c0002t0001g0222 | 3 | HG01168.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.530-3253A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402332 | ||||||
| chr4:184402402
|
G | A | 3 | a0001c0002t0001g0255a0001c0002t0001g0315a0001c0002t0001g0333 | 3 | HG02976.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.530-3323C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402402 | ||||||
| chr4:184402407
|
T | G | 1 | a0001c0001t0003g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.530-3328A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402407 | ||||||
| chr4:184402408
|
C | T | 1 | a0001c0002t0005g0046 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.530-3329G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402408 | ||||||
| chr4:184402450
|
C | G | 1 | a0001c0002t0001g0162 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.530-3371G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402450 | ||||||
| chr4:184402468
|
C | T | 16 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0012g0210others(13): Show | 16 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.530-3389G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402468 | ||||||
| chr4:184402572
|
G | A | 104 | a0001c0001t0001g0079a0001c0001t0001g0307a0001c0001t0002g0002others(101): Show | 106 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.530-3493C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402572 | ||||||
| chr4:184402610
|
A | G | 1 | a0001c0005t0001g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.530-3531T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402610 | ||||||
| chr4:184402701
|
G | A | 1 | a0001c0001t0003g0037 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.530-3622C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402701 | ||||||
| chr4:184402787
|
G | C | 1 | a0001c0001t0002g0098 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.530-3708C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402787 | ||||||
| chr4:184402889
|
G | C | 8 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0080others(5): Show | 9 | HG02083.hp2 HG02132.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-3810C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402889 | ||||||
| chr4:184402893
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.530-3814C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402893 | ||||||
| chr4:184402909
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0251others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-3830T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402909 | ||||||
| chr4:184402917
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.530-3838C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402917 | ||||||
| chr4:184402995
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.530-3916G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184402995 | ||||||
| chr4:184403028
|
C | G | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.530-3949G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403028 | ||||||
| chr4:184403033
|
C | A | 97 | a0001c0001t0001g0079a0001c0001t0001g0307a0001c0001t0002g0002others(94): Show | 99 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.530-3954G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403033 | ||||||
| chr4:184403102
|
T | C | 1 | a0001c0002t0001g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530-4023A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403102 | ||||||
| chr4:184403320
|
G | A | 7 | a0001c0001t0002g0004a0001c0002t0001g0191a0001c0002t0001g0197others(4): Show | 8 | HG01109.hp2 HG02486.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.530-4241C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403320 | ||||||
| chr4:184403430
|
T | C | 1 | a0001c0002t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.530-4351A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403430 | ||||||
| chr4:184403456
|
T | A | 217 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(214): Show | 220 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.530-4377A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403456 | ||||||
| chr4:184403562
|
T | C | 21 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0002g0061others(18): Show | 21 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.530-4483A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403562 | ||||||
| chr4:184403618
|
C | G | 6 | a0001c0004t0004g0188a0001c0004t0004g0254a0001c0004t0004g0285others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.530-4539G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403618 | ||||||
| chr4:184403747
|
C | T | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.529+4411G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403747 | ||||||
| chr4:184403785
|
C | T | 99 | a0001c0001t0001g0233a0001c0001t0001g0287a0001c0001t0002g0040others(96): Show | 101 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.529+4373G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403785 | ||||||
| chr4:184403814
|
T | C | 29 | a0001c0001t0001g0211a0001c0001t0001g0335a0001c0001t0002g0003others(26): Show | 30 | HG01361.hp1 HG01515.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.529+4344A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403814 | ||||||
| chr4:184403968
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.529+4190C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403968 | ||||||
| chr4:184403985
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.529+4173G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184403985 | ||||||
| chr4:184404016
|
T | G | 1 | a0001c0001t0003g0026 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.529+4142A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404016 | ||||||
| chr4:184404088
|
G | A | 93 | a0001c0001t0001g0143a0001c0001t0001g0291a0001c0001t0001g0324others(90): Show | 94 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.529+4070C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404088 | ||||||
| chr4:184404156
|
A | G | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529+4002T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404156 | ||||||
| chr4:184404202
|
G | T | 107 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0183others(104): Show | 109 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.529+3956C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404202 | ||||||
| chr4:184404338
|
T | C | 30 | a0001c0001t0002g0003a0001c0001t0002g0019a0001c0001t0002g0028others(27): Show | 31 | HG01361.hp1 HG01515.hp1 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.529+3820A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404338 | ||||||
| chr4:184404460
|
T | G | 8 | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0080others(5): Show | 9 | HG02083.hp2 HG02132.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+3698A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404460 | ||||||
| chr4:184404654
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0314 | 2 | NA18973.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.529+3504G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404654 | ||||||
| chr4:184404743
|
A | G | 365 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(362): Show | 373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.529+3415T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404743 | ||||||
| chr4:184404942
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.529+3216G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184404942 | ||||||
| chr4:184405009
|
G | A | 90 | a0001c0001t0001g0211a0001c0001t0001g0233a0001c0001t0001g0287others(87): Show | 93 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+3149C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405009 | ||||||
| chr4:184405109
|
T | C | 1 | a0001c0005t0001g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.529+3049A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405109 | ||||||
| chr4:184405141
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0251others(1): Show | 4 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+3017C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405141 | ||||||
| chr4:184405182
|
T | C | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.529+2976A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405182 | ||||||
| chr4:184405210
|
C | T | 1 | a0001c0001t0003g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529+2948G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405210 | ||||||
| chr4:184405481
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.529+2677C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405481 | ||||||
| chr4:184405725
|
G | A | 6 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0251others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+2433C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405725 | ||||||
| chr4:184405772
|
C | T | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.529+2386G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405772 | ||||||
| chr4:184405819
|
C | A | 108 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(105): Show | 110 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.529+2339G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405819 | ||||||
| chr4:184405855
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0335 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.529+2303A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405855 | ||||||
| chr4:184405975
|
CA | C | 133 | a0001c0001t0001g0005a0001c0001t0001g0211a0001c0001t0001g0233others(130): Show | 138 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.529+2182delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405975 | ||||||
| chr4:184406043
|
A | G | 2 | a0001c0002t0003g0139a0001c0002t0003g0152 | 2 | HG01257.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.529+2115T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406043 | ||||||
| chr4:184406145
|
A | G | 2 | a0001c0002t0001g0279a0001c0002t0006g0367 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.529+2013T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406145 | ||||||
| chr4:184406232
|
CT | C | 145 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0192others(142): Show | 148 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.529+1925delA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406232 | ||||||
| chr4:184406278
|
G | A | 10 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0251others(7): Show | 10 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.529+1880C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406278 | ||||||
| chr4:184406298
|
T | A | 108 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0291others(105): Show | 111 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.529+1860A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406298 | ||||||
| chr4:184406519
|
C | T | 92 | a0001c0001t0001g0143a0001c0001t0001g0291a0001c0001t0001g0324others(89): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.529+1639G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406519 | ||||||
| chr4:184406826
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.529+1332C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406826 | ||||||
| chr4:184406957
|
G | A | 2 | a0001c0002t0001g0094a0001c0002t0001g0359 | 2 | HG02165.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.529+1201C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184406957 | ||||||
| chr4:184407007
|
A | C | 1 | a0001c0001t0002g0135 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.529+1151T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407007 | ||||||
| chr4:184407093
|
C | T | 1 | a0001c0002t0005g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.529+1065G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407093 | ||||||
| chr4:184407176
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.529+982T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407176 | ||||||
| chr4:184407195
|
C | T | 5 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0001g0255others(2): Show | 5 | HG02976.hp1 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+963G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407195 | ||||||
| chr4:184407441
|
A | T | 1 | a0001c0001t0003g0099 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.529+717T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407441 | ||||||
| chr4:184407454
|
C | A | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529+704G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407454 | ||||||
| chr4:184407485
|
C | T | 6 | a0001c0001t0002g0179a0001c0001t0002g0198a0001c0001t0002g0284others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+673G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407485 | ||||||
| chr4:184407491
|
A | T | 2 | a0001c0002t0001g0197a0001c0002t0001g0303 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.529+667T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407491 | ||||||
| chr4:184407506
|
C | T | 2 | a0001c0003t0008g0184a0001c0003t0008g0316 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.529+652G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407506 | ||||||
| chr4:184407550
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.529+608G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407550 | ||||||
| chr4:184407663
|
A | G | 186 | a0001c0001t0001g0143a0001c0001t0001g0211a0001c0001t0001g0233others(183): Show | 190 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.529+495T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407663 | ||||||
| chr4:184407738
|
C | T | 3 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0154 | 3 | HG01167.hp2 HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.529+420G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407738 | ||||||
| chr4:184407819
|
C | G | 11 | a0001c0001t0002g0067a0001c0001t0004g0044a0001c0001t0004g0053others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.529+339G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407819 | ||||||
| chr4:184407890
|
C | T | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0002t0006g0367others(3): Show | 6 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+268G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407890 | ||||||
| chr4:184407898
|
G | A | 170 | a0001c0001t0001g0143a0001c0001t0001g0211a0001c0001t0001g0233others(167): Show | 173 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.529+260C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407898 | ||||||
| chr4:184407902
|
C | T | 1 | a0001c0002t0003g0152 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.529+256G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407902 | ||||||
| chr4:184407965
|
T | TCTAA | 31 | a0001c0001t0001g0192a0001c0001t0001g0215a0001c0001t0001g0216others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.529+189_529+192dup others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407965 | ||||||
| chr4:184407967
|
T | TAA | 3 | a0001c0001t0002g0207a0001c0001t0003g0167a0001c0001t0012g0210 | 3 | HG00733.hp2 HG02738.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.529+189_529+190dup others(2): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184407967 | ||||||
| chr4:184408073
|
G | A | 12 | a0001c0001t0002g0040a0001c0001t0002g0058a0001c0001t0002g0059others(9): Show | 12 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.529+85C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184408073 | ||||||
| chr4:184408356
|
A | G | 1 | a0001c0002t0001g0250 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.412-81T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408356 | ||||||
| chr4:184408476
|
C | T | 1 | a0001c0002t0004g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.412-201G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408476 | ||||||
| chr4:184408506
|
G | A | 4 | a0001c0001t0002g0187a0001c0001t0002g0206a0001c0001t0002g0244others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-231C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408506 | ||||||
| chr4:184408550
|
A | G | 9 | a0001c0001t0002g0200a0001c0001t0002g0284a0001c0002t0001g0185others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-275T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408550 | ||||||
| chr4:184408873
|
G | T | 1 | a0001c0001t0003g0073 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.412-598C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408873 | ||||||
| chr4:184408932
|
C | G | 5 | a0001c0001t0002g0196a0001c0001t0003g0201a0001c0002t0001g0177others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-657G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408932 | ||||||
| chr4:184408973
|
T | C | 14 | a0001c0001t0001g0183a0001c0001t0001g0192a0001c0001t0001g0215others(11): Show | 15 | HG01891.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.412-698A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408973 | ||||||
| chr4:184408983
|
C | G | 4 | a0001c0002t0001g0194a0001c0002t0001g0333a0001c0002t0006g0365others(1): Show | 4 | HG02280.hp2 HG02818.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-708G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184408983 | ||||||
| chr4:184409112
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-837C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409112 | ||||||
| chr4:184409167
|
C | T | 2 | a0001c0002t0001g0255a0001c0002t0001g0315 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.412-892G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409167 | ||||||
| chr4:184409246
|
G | C | 68 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0192others(65): Show | 69 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.412-971C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409246 | ||||||
| chr4:184409259
|
G | A | 2 | a0001c0001t0001g0183a0001c0004t0004g0318 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.412-984C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409259 | ||||||
| chr4:184409333
|
A | G | 1 | a0001c0003t0004g0241 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.412-1058T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409333 | ||||||
| chr4:184409345
|
C | G | 2 | a0001c0001t0003g0082a0001c0001t0003g0083 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.412-1070G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409345 | ||||||
| chr4:184409389
|
A | C | 1 | a0001c0001t0006g0368 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.412-1114T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409389 | ||||||
| chr4:184409442
|
G | A | 28 | a0001c0001t0002g0003a0001c0001t0002g0075a0001c0001t0002g0114others(25): Show | 29 | HG00544.hp2 HG01074.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.412-1167C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409442 | ||||||
| chr4:184409444
|
T | C | 30 | a0001c0001t0001g0189a0001c0001t0002g0264a0001c0001t0002g0271others(27): Show | 30 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.412-1169A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409444 | ||||||
| chr4:184409497
|
G | A | 104 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0183others(101): Show | 107 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.412-1222C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409497 | ||||||
| chr4:184409504
|
C | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.412-1229G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409504 | ||||||
| chr4:184409515
|
T | C | 58 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0104others(55): Show | 60 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.412-1240A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409515 | ||||||
| chr4:184409623
|
G | T | 3 | a0001c0001t0002g0264a0001c0001t0002g0271a0001c0002t0001g0265 | 3 | NA18959.hp1 NA19064.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.412-1348C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409623 | ||||||
| chr4:184409651
|
T | C | 1 | a0001c0001t0004g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.412-1376A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409651 | ||||||
| chr4:184409883
|
C | T | 3 | a0001c0002t0001g0036a0001c0002t0001g0222a0001c0002t0001g0229 | 3 | HG01074.hp1 HG01168.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.412-1608G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409883 | ||||||
| chr4:184409904
|
CA | C | 27 | a0001c0001t0001g0183a0001c0001t0002g0002a0001c0001t0002g0067others(24): Show | 28 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.412-1630delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184409904 | ||||||
| chr4:184410020
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.412-1745C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410020 | ||||||
| chr4:184410049
|
C | T | 109 | a0001c0001t0001g0005a0001c0001t0001g0192a0001c0001t0001g0211others(106): Show | 111 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.412-1774G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410049 | ||||||
| chr4:184410171
|
G | C | 6 | a0001c0001t0002g0080a0001c0001t0002g0106a0001c0001t0002g0240others(3): Show | 6 | HG02523.hp2 NA18950.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-1896C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410171 | ||||||
| chr4:184410191
|
T | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0189others(181): Show | 190 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.412-1916A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410191 | ||||||
| chr4:184410279
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.412-2004C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410279 | ||||||
| chr4:184410344
|
A | G | 1 | a0001c0001t0004g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.412-2069T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410344 | ||||||
| chr4:184410446
|
A | G | 363 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(360): Show | 371 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.412-2171T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410446 | ||||||
| chr4:184410493
|
T | C | 351 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(348): Show | 358 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(355): Show |
intron_variant | MODIFIER | c.412-2218A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410493 | ||||||
| chr4:184410676
|
GC | G | 49 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0104others(46): Show | 51 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.412-2402delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410676 | ||||||
| chr4:184410740
|
C | T | 16 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0200others(13): Show | 16 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.412-2465G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410740 | ||||||
| chr4:184410808
|
C | T | 29 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0299others(26): Show | 30 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.412-2533G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410808 | ||||||
| chr4:184410823
|
A | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0192others(93): Show | 98 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.412-2548T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410823 | ||||||
| chr4:184411059
|
C | CT | 24 | a0001c0001t0001g0143a0001c0001t0001g0211a0001c0001t0001g0243others(21): Show | 24 | HG02055.hp1 HG02145.hp1 HG02300.hp2 others(21): Show |
intron_variant | MODIFIER | c.412-2785dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411059 | ||||||
| chr4:184411059
|
CT | C | 41 | a0001c0001t0001g0183a0001c0001t0002g0010a0001c0001t0002g0131others(38): Show | 42 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.412-2785delA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411059 | ||||||
| chr4:184411081
|
G | T | 29 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0299others(26): Show | 30 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.412-2806C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411081 | ||||||
| chr4:184411143
|
C | T | 16 | a0001c0001t0002g0264a0001c0001t0002g0271a0001c0001t0002g0339others(13): Show | 16 | HG00558.hp2 HG01928.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.412-2868G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411143 | ||||||
| chr4:184411271
|
C | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0192others(92): Show | 97 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.412-2996G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411271 | ||||||
| chr4:184411306
|
A | G | 6 | a0001c0001t0001g0183a0001c0001t0002g0195a0001c0002t0001g0177others(3): Show | 6 | HG01099.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-3031T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411306 | ||||||
| chr4:184411310
|
C | T | 3 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0002t0001g0220 | 3 | HG02132.hp1 HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.412-3035G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411310 | ||||||
| chr4:184411417
|
T | C | 86 | a0001c0001t0001g0143a0001c0001t0001g0233a0001c0001t0002g0002others(83): Show | 89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.412-3142A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411417 | ||||||
| chr4:184411542
|
T | C | 1 | a0001c0001t0003g0122 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.412-3267A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411542 | ||||||
| chr4:184411576
|
ACGGAGCC others(9): Show |
A | 34 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(31): Show | 35 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.412-3317_412-3302d others(18): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411576 | ||||||
| chr4:184411688
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0003g0225a0001c0001t0003g0226others(6): Show | 10 | HG00642.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.412-3413A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411688 | ||||||
| chr4:184411691
|
A | G | 1 | a0001c0001t0004g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.412-3416T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411691 | ||||||
| chr4:184411796
|
C | T | 2 | a0001c0001t0001g0335a0001c0001t0002g0330 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.412-3521G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411796 | ||||||
| chr4:184411801
|
G | A | 17 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(14): Show | 17 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.412-3526C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411801 | ||||||
| chr4:184411876
|
C | T | 81 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0010others(78): Show | 83 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.412-3601G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411876 | ||||||
| chr4:184411938
|
A | G | 224 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0189others(221): Show | 229 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.412-3663T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411938 | ||||||
| chr4:184411991
|
C | T | 5 | a0001c0001t0001g0183a0001c0002t0001g0177a0001c0002t0001g0238others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-3716G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411991 | ||||||
| chr4:184412005
|
T | TA | 31 | a0001c0001t0001g0189a0001c0001t0002g0106a0001c0001t0002g0142others(28): Show | 31 | HG01074.hp2 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.412-3731dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412005 | ||||||
| chr4:184412005
|
T | TAA | 11 | a0001c0001t0001g0243a0001c0001t0002g0200a0001c0001t0002g0206others(8): Show | 11 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.412-3732_412-3731d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412005 | ||||||
| chr4:184412005
|
TA | T | 105 | a0001c0001t0001g0211a0001c0001t0001g0287a0001c0001t0001g0291others(102): Show | 107 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.412-3731delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412005 | ||||||
| chr4:184412005
|
TAA | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0295a0001c0002t0001g0031others(3): Show | 6 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-3732_412-3731d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412005 | ||||||
| chr4:184412005
|
TAAAAAAA others(4): Show |
T | 9 | a0001c0001t0001g0005a0001c0001t0003g0225a0001c0001t0003g0226others(6): Show | 10 | HG00642.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.412-3741_412-3731d others(13): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412005 | ||||||
| chr4:184412025
|
A | G | 23 | a0001c0001t0002g0132a0001c0001t0002g0202a0001c0001t0002g0207others(20): Show | 23 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.412-3750T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412025 | ||||||
| chr4:184412076
|
A | G | 5 | a0001c0001t0001g0335a0001c0001t0002g0278a0001c0001t0002g0330others(2): Show | 5 | HG02145.hp1 HG02615.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-3801T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412076 | ||||||
| chr4:184412131
|
G | A | 1 | a0001c0002t0001g0320 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.412-3856C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412131 | ||||||
| chr4:184412245
|
A | G | 10 | a0001c0001t0001g0189a0001c0001t0002g0196a0001c0001t0002g0217others(7): Show | 10 | HG01074.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.412-3970T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412245 | ||||||
| chr4:184412543
|
C | CT | 34 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(31): Show | 35 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.412-4269dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412543 | ||||||
| chr4:184412589
|
A | T | 48 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(45): Show | 49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.412-4314T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412589 | ||||||
| chr4:184412612
|
T | G | 4 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0007g0362others(1): Show | 4 | HG02717.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-4337A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412612 | ||||||
| chr4:184412694
|
G | A | 17 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(14): Show | 17 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.412-4419C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412694 | ||||||
| chr4:184412742
|
G | A | 29 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(26): Show | 30 | HG00438.hp2 HG00733.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.412-4467C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412742 | ||||||
| chr4:184412820
|
C | T | 1 | a0001c0001t0002g0337 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.412-4545G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412820 | ||||||
| chr4:184412908
|
C | T | 4 | a0001c0001t0002g0179a0001c0001t0003g0015a0001c0002t0001g0242others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-4633G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412908 | ||||||
| chr4:184413023
|
C | T | 4 | a0001c0001t0001g0211a0001c0002t0001g0191a0001c0002t0001g0247others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-4748G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184413023 | ||||||
| chr4:184413030
|
C | T | 4 | a0001c0001t0001g0211a0001c0002t0001g0191a0001c0002t0001g0247others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-4755G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184413030 | ||||||
| chr4:184413231
|
A | G | 48 | a0001c0001t0001g0143a0001c0001t0002g0002a0001c0001t0002g0013others(45): Show | 49 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.411+4936T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184413231 | ||||||
| chr4:184413332
|
G | A | 29 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(26): Show | 30 | HG00438.hp2 HG00733.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.411+4835C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184413332 | ||||||
| chr4:184413603
|
T | C | 1 | a0001c0002t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.411+4564A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184413603 | ||||||
| chr4:184413638
|
T | G | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.411+4529A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184413638 | ||||||
| chr4:184413829
|
G | T | 15 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+4338C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184413829 | ||||||
| chr4:184414119
|
G | T | 3 | a0001c0004t0004g0285a0001c0004t0004g0331a0001c0004t0004g0332 | 3 | HG02145.hp2 HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.411+4048C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414119 | ||||||
| chr4:184414121
|
A | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0233others(92): Show | 97 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.411+4046T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414121 | ||||||
| chr4:184414123
|
T | C | 52 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(49): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.411+4044A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414123 | ||||||
| chr4:184414226
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.411+3941G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414226 | ||||||
| chr4:184414427
|
A | C | 1 | a0001c0001t0003g0084 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.411+3740T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414427 | ||||||
| chr4:184414452
|
C | G | 1 | a0001c0002t0001g0162 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.411+3715G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414452 | ||||||
| chr4:184414665
|
G | T | 10 | a0001c0001t0003g0148a0001c0002t0001g0063a0001c0002t0001g0087others(7): Show | 10 | HG00280.hp1 HG00738.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.411+3502C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414665 | ||||||
| chr4:184414712
|
A | G | 48 | a0001c0001t0001g0079a0001c0001t0002g0003a0001c0001t0002g0104others(45): Show | 49 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.411+3455T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414712 | ||||||
| chr4:184414735
|
A | G | 40 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(37): Show | 41 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.411+3432T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184414735 | ||||||
| chr4:184415023
|
G | C | 1 | a0001c0001t0002g0207 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.411+3144C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415023 | ||||||
| chr4:184415108
|
A | G | 48 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(45): Show | 49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.411+3059T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415108 | ||||||
| chr4:184415239
|
T | C | 10 | a0001c0001t0001g0189a0001c0001t0002g0196a0001c0001t0002g0217others(7): Show | 10 | HG01074.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.411+2928A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415239 | ||||||
| chr4:184415358
|
C | T | 5 | a0001c0001t0002g0206a0001c0002t0001g0194a0001c0002t0001g0333others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+2809G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415358 | ||||||
| chr4:184415585
|
A | G | 16 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(13): Show | 16 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.411+2582T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415585 | ||||||
| chr4:184415656
|
G | A | 6 | a0001c0001t0001g0183a0001c0001t0002g0195a0001c0002t0001g0177others(3): Show | 6 | HG01099.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+2511C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415656 | ||||||
| chr4:184415658
|
C | T | 1 | a0001c0002t0001g0124 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.411+2509G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415658 | ||||||
| chr4:184415663
|
G | A | 112 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0307others(109): Show | 115 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.411+2504C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415663 | ||||||
| chr4:184415698
|
T | C | 119 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0291others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.411+2469A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415698 | ||||||
| chr4:184415771
|
A | G | 1 | a0001c0001t0002g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.411+2396T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415771 | ||||||
| chr4:184415825
|
T | C | 16 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(13): Show | 16 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.411+2342A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415825 | ||||||
| chr4:184415928
|
G | A | 3 | a0001c0001t0002g0284a0001c0002t0001g0185a0001c0003t0004g0245 | 3 | HG03139.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.411+2239C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415928 | ||||||
| chr4:184415977
|
A | G | 1 | a0001c0001t0002g0104 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.411+2190T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184415977 | ||||||
| chr4:184416027
|
A | C | 8 | a0001c0001t0001g0189a0001c0001t0002g0196a0001c0001t0002g0217others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+2140T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416027 | ||||||
| chr4:184416049
|
A | G | 1 | a0001c0001t0003g0274 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.411+2118T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416049 | ||||||
| chr4:184416164
|
A | T | 10 | a0001c0001t0002g0058a0001c0001t0002g0064a0001c0001t0002g0066others(7): Show | 11 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.411+2003T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416164 | ||||||
| chr4:184416223
|
C | T | 48 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(45): Show | 49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.411+1944G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416223 | ||||||
| chr4:184416224
|
G | A | 4 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0007g0362others(1): Show | 4 | HG02717.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1943C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416224 | ||||||
| chr4:184416242
|
C | T | 2 | a0001c0001t0003g0352a0001c0003t0004g0241 | 2 | HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.411+1925G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416242 | ||||||
| chr4:184416266
|
T | C | 78 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0291others(75): Show | 80 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.411+1901A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416266 | ||||||
| chr4:184416275
|
G | A | 4 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0007g0362others(1): Show | 4 | HG02717.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1892C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416275 | ||||||
| chr4:184416323
|
A | C | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+1844T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416323 | ||||||
| chr4:184416324
|
A | C | 2 | a0001c0002t0001g0238a0001c0002t0001g0315 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.411+1843T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416324 | ||||||
| chr4:184416328
|
C | A | 1 | a0001c0002t0009g0009 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.411+1839G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416328 | ||||||
| chr4:184416328
|
CA | C | 186 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0243others(183): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.411+1838delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416328 | ||||||
| chr4:184416332
|
A | C | 63 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0215others(60): Show | 65 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.411+1835T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416332 | ||||||
| chr4:184416333
|
A | C | 41 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(38): Show | 42 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.411+1834T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416333 | ||||||
| chr4:184416334
|
A | C | 5 | a0001c0001t0001g0211a0001c0001t0002g0283a0001c0002t0001g0191others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+1833T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416334 | ||||||
| chr4:184416345
|
G | GA | 18 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(15): Show | 18 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.411+1821dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416345 | ||||||
| chr4:184416382
|
T | C | 1 | a0001c0011t0001g0074 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.411+1785A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416382 | ||||||
| chr4:184416398
|
T | TA | 23 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(20): Show | 23 | HG00408.hp2 HG01496.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.411+1768dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416398 | ||||||
| chr4:184416448
|
T | TA | 5 | a0001c0001t0001g0211a0001c0001t0002g0283a0001c0002t0001g0191others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+1718dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416448 | ||||||
| chr4:184416461
|
A | G | 2 | a0001c0001t0002g0200a0001c0004t0004g0188 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.411+1706T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416461 | ||||||
| chr4:184416540
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.411+1627A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416540 | ||||||
| chr4:184416566
|
G | C | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+1601C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416566 | ||||||
| chr4:184416730
|
C | CA | 47 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(44): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.411+1436dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416730 | ||||||
| chr4:184416775
|
G | A | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+1392C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416775 | ||||||
| chr4:184416978
|
G | A | 47 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(44): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.411+1189C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416978 | ||||||
| chr4:184416990
|
G | A | 1 | a0001c0003t0008g0316 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.411+1177C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184416990 | ||||||
| chr4:184417028
|
T | C | 1 | a0001c0001t0003g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.411+1139A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417028 | ||||||
| chr4:184417047
|
A | G | 15 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+1120T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417047 | ||||||
| chr4:184417156
|
A | T | 52 | a0001c0001t0001g0079a0001c0001t0002g0003a0001c0001t0002g0104others(49): Show | 53 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.411+1011T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417156 | ||||||
| chr4:184417352
|
A | T | 40 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(37): Show | 41 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.411+815T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417352 | ||||||
| chr4:184417364
|
C | G | 49 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(46): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.411+803G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417364 | ||||||
| chr4:184417385
|
T | A | 1 | a0001c0001t0003g0253 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+782A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417385 | ||||||
| chr4:184417443
|
G | A | 2 | a0001c0002t0001g0305a0001c0002t0002g0334 | 2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.411+724C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417443 | ||||||
| chr4:184417494
|
G | A | 2 | a0001c0001t0001g0335a0001c0001t0002g0330 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.411+673C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417494 | ||||||
| chr4:184417685
|
T | G | 250 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0189others(247): Show | 256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.411+482A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417685 | ||||||
| chr4:184417724
|
A | G | 240 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0189others(237): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.411+443T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417724 | ||||||
| chr4:184417767
|
T | C | 88 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0010others(85): Show | 90 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.411+400A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417767 | ||||||
| chr4:184417841
|
A | AC | 49 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(46): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.411+325_411+326ins others(1): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417841 | ||||||
| chr4:184417860
|
T | C | 3 | a0001c0001t0001g0335a0001c0001t0002g0330a0001c0002t0001g0218 | 3 | HG02145.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.411+307A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417860 | ||||||
| chr4:184417889
|
G | T | 10 | a0001c0001t0002g0058a0001c0001t0002g0064a0001c0001t0002g0066others(7): Show | 11 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.411+278C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417889 | ||||||
| chr4:184418363
|
C | T | 163 | a0001c0001t0001g0005a0001c0001t0001g0233a0001c0001t0001g0291others(160): Show | 167 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.365-150G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 4/8 | chr4 | 184418363 | ||||||
| chr4:184418487
|
T | C | 12 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0065others(9): Show | 13 | HG00280.hp2 HG00323.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+45A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 4/8 | chr4 | 184418487 | ||||||
| chr4:184418492
|
C | G | 1 | a0001c0002t0001g0127 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.364+40G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 4/8 | chr4 | 184418492 | ||||||
| chr4:184418737
|
A | T | 6 | a0001c0001t0001g0335a0001c0001t0002g0179a0001c0001t0002g0278others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-29T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184418737 | ||||||
| chr4:184418740
|
G | A | 9 | a0001c0001t0002g0040a0001c0001t0002g0075a0001c0001t0002g0163others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-32C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184418740 | ||||||
| chr4:184418811
|
C | A | 15 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(12): Show | 15 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-103G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184418811 | ||||||
| chr4:184418823
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0096a0001c0001t0002g0311others(1): Show | 4 | HG00438.hp1 HG00609.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-115A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184418823 | ||||||
| chr4:184419012
|
T | C | 254 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0189others(251): Show | 260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.188-304A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419012 | ||||||
| chr4:184419132
|
A | T | 34 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(31): Show | 35 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.187+337T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419132 | ||||||
| chr4:184419156
|
G | C | 2 | a0001c0001t0003g0352a0001c0003t0004g0241 | 2 | HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.187+313C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419156 | ||||||
| chr4:184419235
|
C | T | 1 | a0001c0002t0001g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.187+234G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419235 | ||||||
| chr4:184419253
|
T | C | 5 | a0001c0001t0001g0183a0001c0001t0002g0195a0001c0002t0001g0177others(2): Show | 5 | HG01099.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+216A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419253 | ||||||
| chr4:184419448
|
C | T | 8 | a0001c0001t0002g0190a0001c0001t0002g0284a0001c0001t0003g0209others(5): Show | 8 | HG02717.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+21G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419448 | ||||||
| chr4:184419451
|
C | T | 2 | a0001c0001t0003g0060a0001c0002t0001g0223 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.187+18G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419451 | ||||||
| chr4:184419452
|
G | A | 2 | a0001c0001t0003g0049a0001c0001t0003g0050 | 2 | NA18988.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.187+17C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419452 | ||||||
| chr4:184419571
|
G | GA | 46 | a0001c0001t0002g0010a0001c0001t0002g0105a0001c0001t0002g0131others(43): Show | 47 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(44): Show |
splice_region_variant&intron_variant | LOW | c.88-4dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184419571 | ||||||
| chr4:184419571
|
G | GAA | 66 | a0001c0001t0001g0189a0001c0001t0001g0243a0001c0001t0001g0251others(63): Show | 67 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
splice_region_variant&intron_variant | LOW | c.88-5_88-4dupTT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184419571 | ||||||
| chr4:184419571
|
G | GAAA | 52 | a0001c0001t0001g0079a0001c0001t0002g0003a0001c0001t0002g0104others(49): Show | 53 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(50): Show |
splice_region_variant&intron_variant | LOW | c.88-6_88-4dupTTT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184419571 | ||||||
| chr4:184419571
|
GAA | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0307a0001c0001t0002g0008others(67): Show | 72 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.88-5_88-4delTT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184419571 | ||||||
| chr4:184419667
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.88-99C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184419667 | ||||||
| chr4:184419676
|
G | A | 1 | a0001c0002t0001g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.88-108C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184419676 | ||||||
| chr4:184419678
|
T | C | 3 | a0001c0001t0002g0294a0001c0001t0003g0276a0001c0002t0001g0277 | 3 | NA18971.hp2 NA19002.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.88-110A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184419678 | ||||||
| chr4:184420170
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0002g0179a0001c0001t0002g0278others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-602C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184420170 | ||||||
| chr4:184420204
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.88-636C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184420204 | ||||||
| chr4:184420237
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.88-669A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184420237 | ||||||
| chr4:184420252
|
G | A | 8 | a0001c0001t0002g0190a0001c0001t0002g0284a0001c0001t0003g0209others(5): Show | 8 | HG02717.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-684C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184420252 | ||||||
| chr4:184420283
|
G | A | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88-715C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184420283 | ||||||
| chr4:184420299
|
A | G | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88-731T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184420299 | ||||||
| chr4:184421013
|
A | T | 3 | a0001c0002t0001g0018a0001c0002t0001g0047a0001c0002t0001g0051 | 3 | NA18984.hp1 NA18986.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.88-1445T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421013 | ||||||
| chr4:184421129
|
C | T | 10 | a0001c0001t0001g0189a0001c0001t0002g0196a0001c0001t0002g0217others(7): Show | 10 | HG01074.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.88-1561G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421129 | ||||||
| chr4:184421522
|
C | T | 1 | a0001c0005t0001g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88-1954G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421522 | ||||||
| chr4:184421564
|
T | C | 68 | a0001c0001t0001g0143a0001c0001t0001g0189a0001c0001t0001g0192others(65): Show | 70 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.88-1996A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421564 | ||||||
| chr4:184421585
|
C | T | 6 | a0001c0001t0001g0335a0001c0001t0002g0179a0001c0001t0002g0278others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-2017G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421585 | ||||||
| chr4:184421613
|
T | C | 2 | a0001c0001t0002g0114a0001c0001t0003g0101 | 2 | NA18944.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.88-2045A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421613 | ||||||
| chr4:184421732
|
T | TACAC | 8 | a0001c0001t0001g0189a0001c0001t0002g0196a0001c0001t0002g0217others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-2168_88-2165dup others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421732 | ||||||
| chr4:184421872
|
G | A | 1 | a0001c0002t0001g0321 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.88-2304C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421872 | ||||||
| chr4:184421904
|
T | G | 89 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0001g0335others(86): Show | 91 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.88-2336A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421904 | ||||||
| chr4:184421991
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.88-2423C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184421991 | ||||||
| chr4:184422042
|
C | CAAAACAG others(339): Show |
1 | a0001c0001t0002g0234 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.88-2475_88-2474ins others(346): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422042 | ||||||
| chr4:184422042
|
C | CAAAACAG others(340): Show |
1 | a0001c0001t0002g0237 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.88-2475_88-2474ins others(347): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422042 | ||||||
| chr4:184422056
|
G | A | 1 | a0001c0001t0002g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.88-2488C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422056 | ||||||
| chr4:184422168
|
C | A | 1 | a0001c0001t0002g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.88-2600G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422168 | ||||||
| chr4:184422405
|
A | G | 48 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0061others(45): Show | 49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.88-2837T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422405 | ||||||
| chr4:184422481
|
C | T | 249 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0211others(246): Show | 255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.88-2913G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422481 | ||||||
| chr4:184422579
|
A | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0211a0001c0001t0001g0233others(85): Show | 91 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.88-3011T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422579 | ||||||
| chr4:184422659
|
G | A | 2 | a0001c0001t0001g0335a0001c0001t0002g0330 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.88-3091C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422659 | ||||||
| chr4:184422901
|
A | T | 1 | a0001c0001t0003g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.88-3333T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184422901 | ||||||
| chr4:184423078
|
G | A | 14 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(11): Show | 14 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.88-3510C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423078 | ||||||
| chr4:184423153
|
C | T | 1 | a0001c0005t0001g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88-3585G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423153 | ||||||
| chr4:184423185
|
G | A | 10 | a0001c0001t0002g0058a0001c0001t0002g0064a0001c0001t0002g0066others(7): Show | 11 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.88-3617C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423185 | ||||||
| chr4:184423210
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.88-3642G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423210 | ||||||
| chr4:184423212
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.88-3644G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423212 | ||||||
| chr4:184423273
|
C | A | 34 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(31): Show | 35 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.88-3705G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423273 | ||||||
| chr4:184423422
|
T | C | 2 | a0001c0001t0003g0297a0001c0002t0005g0048 | 2 | NA18951.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.88-3854A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423422 | ||||||
| chr4:184423452
|
A | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0233a0001c0001t0001g0307others(22): Show | 26 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.88-3884T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423452 | ||||||
| chr4:184423503
|
C | T | 14 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0002g0187others(11): Show | 14 | HG01891.hp2 HG02280.hp2 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.88-3935G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423503 | ||||||
| chr4:184423504
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.88-3936C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423504 | ||||||
| chr4:184423551
|
A | C | 1 | a0001c0002t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.88-3983T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423551 | ||||||
| chr4:184423778
|
C | T | 57 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0215others(54): Show | 59 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.88-4210G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423778 | ||||||
| chr4:184423779
|
G | A | 2 | a0001c0001t0007g0364a0001c0002t0001g0282 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.88-4211C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184423779 | ||||||
| chr4:184424056
|
A | G | 88 | a0001c0001t0001g0291a0001c0001t0001g0324a0001c0001t0002g0010others(85): Show | 90 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.88-4488T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424056 | ||||||
| chr4:184424063
|
TAC | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0211others(201): Show | 209 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.88-4497_88-4496del others(2): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424063 | ||||||
| chr4:184424067
|
C | T | 60 | a0001c0001t0001g0079a0001c0001t0001g0243a0001c0001t0001g0251others(57): Show | 61 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.88-4499G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424067 | ||||||
| chr4:184424238
|
G | A | 2 | a0001c0002t0001g0043a0001c0002t0001g0045 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.88-4670C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424238 | ||||||
| chr4:184424335
|
T | C | 1 | a0001c0001t0002g0337 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.87+4643A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424335 | ||||||
| chr4:184424408
|
A | T | 4 | a0001c0001t0002g0179a0001c0001t0002g0278a0001c0002t0001g0242others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+4570T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424408 | ||||||
| chr4:184424443
|
G | A | 1 | a0001c0002t0001g0321 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.87+4535C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424443 | ||||||
| chr4:184424496
|
G | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0243a0001c0001t0001g0251others(57): Show | 61 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.87+4482C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424496 | ||||||
| chr4:184424505
|
AG | A | 60 | a0001c0001t0001g0079a0001c0001t0001g0243a0001c0001t0001g0251others(57): Show | 61 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.87+4472delC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424505 | ||||||
| chr4:184424535
|
G | C | 4 | a0001c0001t0002g0179a0001c0001t0002g0278a0001c0002t0001g0242others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+4443C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424535 | ||||||
| chr4:184424561
|
T | C | 60 | a0001c0001t0001g0079a0001c0001t0001g0243a0001c0001t0001g0251others(57): Show | 61 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.87+4417A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424561 | ||||||
| chr4:184424667
|
T | C | 1 | a0001c0001t0003g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.87+4311A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424667 | ||||||
| chr4:184424684
|
G | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0211a0001c0001t0001g0307others(72): Show | 77 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.87+4294C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424684 | ||||||
| chr4:184424738
|
G | T | 60 | a0001c0001t0001g0079a0001c0001t0001g0243a0001c0001t0001g0251others(57): Show | 61 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.87+4240C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424738 | ||||||
| chr4:184424840
|
G | C | 1 | a0001c0001t0002g0066 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.87+4138C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424840 | ||||||
| chr4:184424902
|
G | T | 5 | a0001c0001t0002g0119a0001c0001t0003g0085a0001c0001t0003g0102others(2): Show | 5 | NA18747.hp2 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+4076C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424902 | ||||||
| chr4:184424922
|
T | C | 2 | a0001c0001t0001g0335a0001c0001t0002g0330 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.87+4056A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424922 | ||||||
| chr4:184424936
|
A | G | 235 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0211others(232): Show | 240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.87+4042T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424936 | ||||||
| chr4:184425049
|
T | C | 238 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0211others(235): Show | 243 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.87+3929A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425049 | ||||||
| chr4:184425131
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.87+3847G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425131 | ||||||
| chr4:184425141
|
TG | T | 6 | a0001c0001t0001g0335a0001c0001t0002g0179a0001c0001t0002g0278others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+3836delC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425141 | ||||||
| chr4:184425288
|
T | G | 59 | a0001c0001t0001g0079a0001c0001t0001g0243a0001c0001t0001g0251others(56): Show | 60 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.87+3690A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425288 | ||||||
| chr4:184425314
|
C | G | 57 | a0001c0001t0001g0079a0001c0001t0001g0243a0001c0001t0001g0251others(54): Show | 58 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.87+3664G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425314 | ||||||
| chr4:184425372
|
G | C | 10 | a0001c0001t0002g0058a0001c0001t0002g0064a0001c0001t0002g0066others(7): Show | 11 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.87+3606C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425372 | ||||||
| chr4:184425557
|
C | T | 4 | a0001c0001t0002g0179a0001c0001t0002g0278a0001c0002t0001g0242others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+3421G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425557 | ||||||
| chr4:184425609
|
C | G | 2 | a0001c0001t0003g0038a0001c0001t0003g0266 | 2 | NA18962.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.87+3369G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425609 | ||||||
| chr4:184425725
|
G | T | 1 | a0001c0001t0002g0096 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.87+3253C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425725 | ||||||
| chr4:184425777
|
A | T | 4 | a0001c0001t0002g0179a0001c0001t0002g0278a0001c0002t0001g0242others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+3201T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425777 | ||||||
| chr4:184425976
|
G | GTTTT | 31 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(28): Show | 32 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.87+2998_87+3001dup others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425976 | ||||||
| chr4:184425978
|
TTTTG | T | 242 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0189others(239): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.87+2996_87+2999del others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425978 | ||||||
| chr4:184425978
|
TTTTGTTT others(1): Show |
T | 65 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0243others(62): Show | 67 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.87+2992_87+2999del others(8): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425978 | ||||||
| chr4:184425978
|
TTTTGTTT others(5): Show |
T | 1 | a0001c0002t0005g0016 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.87+2988_87+2999del others(12): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425978 | ||||||
| chr4:184425978
|
TTTTGTTT others(9): Show |
T | 3 | a0001c0001t0002g0096a0001c0001t0002g0311a0001c0001t0002g0312 | 3 | HG00438.hp1 NA18965.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.87+2984_87+2999del others(16): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425978 | ||||||
| chr4:184425982
|
G | T | 8 | a0001c0001t0002g0234a0001c0001t0002g0237a0001c0001t0002g0261others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.87+2996C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425982 | ||||||
| chr4:184425986
|
G | T | 127 | a0001c0001t0001g0211a0001c0001t0001g0291a0001c0001t0001g0307others(124): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.87+2992C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425986 | ||||||
| chr4:184425990
|
G | T | 34 | a0001c0001t0001g0211a0001c0001t0001g0307a0001c0001t0001g0336others(31): Show | 34 | HG00735.hp2 HG00741.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.87+2988C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184425990 | ||||||
| chr4:184426086
|
C | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0243others(76): Show | 81 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.87+2892G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426086 | ||||||
| chr4:184426214
|
C | T | 1 | a0001c0001t0002g0028 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.87+2764G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426214 | ||||||
| chr4:184426231
|
G | T | 1 | a0001c0001t0002g0339 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.87+2747C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426231 | ||||||
| chr4:184426383
|
C | T | 227 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0211others(224): Show | 232 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.87+2595G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426383 | ||||||
| chr4:184426604
|
T | C | 4 | a0001c0001t0002g0179a0001c0001t0002g0278a0001c0002t0001g0242others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+2374A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426604 | ||||||
| chr4:184426672
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0243others(72): Show | 77 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.87+2306G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426672 | ||||||
| chr4:184426678
|
C | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0243others(72): Show | 77 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.87+2300G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426678 | ||||||
| chr4:184426729
|
C | G | 76 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0243others(73): Show | 78 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.87+2249G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426729 | ||||||
| chr4:184426892
|
C | G | 6 | a0001c0001t0002g0196a0001c0001t0002g0217a0001c0001t0003g0328others(3): Show | 6 | HG01074.hp2 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+2086G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426892 | ||||||
| chr4:184426963
|
C | T | 1 | a0001c0001t0003g0304 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.87+2015G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426963 | ||||||
| chr4:184426968
|
C | T | 1 | a0001c0001t0003g0347 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.87+2010G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426968 | ||||||
| chr4:184426969
|
G | A | 1 | a0001c0001t0003g0102 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.87+2009C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184426969 | ||||||
| chr4:184427000
|
G | T | 1 | a0001c0001t0003g0122 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.87+1978C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427000 | ||||||
| chr4:184427030
|
A | C | 96 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0243others(93): Show | 99 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.87+1948T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427030 | ||||||
| chr4:184427042
|
T | C | 1 | a0001c0002t0005g0355 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.87+1936A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427042 | ||||||
| chr4:184427145
|
A | G | 52 | a0001c0001t0001g0079a0001c0001t0002g0003a0001c0001t0002g0104others(49): Show | 53 | HG00423.hp1 HG00621.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.87+1833T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427145 | ||||||
| chr4:184427321
|
T | A | 9 | a0001c0001t0001g0005a0001c0001t0003g0225a0001c0001t0003g0226others(6): Show | 10 | HG00642.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.87+1657A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427321 | ||||||
| chr4:184427336
|
C | T | 1 | a0001c0002t0001g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.87+1642G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427336 | ||||||
| chr4:184427341
|
A | T | 21 | a0001c0001t0002g0058a0001c0001t0002g0064a0001c0001t0002g0066others(18): Show | 22 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.87+1637T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427341 | ||||||
| chr4:184427387
|
G | A | 4 | a0001c0001t0002g0179a0001c0001t0002g0278a0001c0002t0001g0242others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+1591C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427387 | ||||||
| chr4:184427426
|
C | T | 26 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(23): Show | 27 | HG00438.hp2 HG00733.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.87+1552G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427426 | ||||||
| chr4:184427451
|
C | T | 68 | a0001c0001t0001g0211a0001c0001t0001g0307a0001c0001t0001g0336others(65): Show | 69 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.87+1527G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427451 | ||||||
| chr4:184427558
|
A | T | 10 | a0001c0001t0002g0058a0001c0001t0002g0064a0001c0001t0002g0066others(7): Show | 11 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.87+1420T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427558 | ||||||
| chr4:184427584
|
A | G | 5 | a0001c0001t0002g0196a0001c0001t0002g0217a0001c0001t0003g0328others(2): Show | 5 | HG01891.hp1 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+1394T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427584 | ||||||
| chr4:184427762
|
A | G | 119 | a0001c0001t0001g0183a0001c0001t0001g0211a0001c0001t0001g0291others(116): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.87+1216T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427762 | ||||||
| chr4:184427840
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.87+1138G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427840 | ||||||
| chr4:184427935
|
C | G | 9 | a0001c0001t0001g0335a0001c0001t0002g0190a0001c0001t0002g0284others(6): Show | 9 | HG02145.hp1 HG02717.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.87+1043G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184427935 | ||||||
| chr4:184428049
|
G | A | 1 | a0001c0002t0001g0321 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.87+929C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428049 | ||||||
| chr4:184428248
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.87+730G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428248 | ||||||
| chr4:184428300
|
A | T | 33 | a0001c0001t0002g0010a0001c0001t0002g0131a0001c0001t0002g0135others(30): Show | 34 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.87+678T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428300 | ||||||
| chr4:184428465
|
T | C | 1 | a0001c0002t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.87+513A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428465 | ||||||
| chr4:184428519
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.87+459G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428519 | ||||||
| chr4:184428585
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.87+393G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428585 | ||||||
| chr4:184428641
|
A | G | 5 | a0001c0001t0001g0183a0001c0001t0002g0195a0001c0002t0001g0177others(2): Show | 5 | HG01099.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+337T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428641 | ||||||
| chr4:184428772
|
G | A | 1 | a0001c0002t0001g0250 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.87+206C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428772 | ||||||
| chr4:184428802
|
A | C | 3 | a0001c0001t0002g0067a0001c0001t0004g0204a0001c0001t0004g0205 | 3 | HG01070.hp1 HG01071.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.87+176T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428802 | ||||||
| chr4:184428824
|
A | G | 5 | a0001c0001t0002g0163a0001c0001t0003g0232a0001c0002t0001g0165others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+154T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184428824 | ||||||
| chr4:184429073
|
T | C | 2 | a0001c0001t0002g0179a0001c0002t0001g0242 | 2 | HG02280.hp1 HG02451.hp2 |
splice_region_variant&intron_variant | LOW | c.-6-3A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429073 | ||||||
| chr4:184429109
|
C | A | 3 | a0001c0001t0001g0183a0001c0002t0001g0177a0001c0002t0001g0238 | 3 | HG02630.hp2 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-6-39G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429109 | ||||||
| chr4:184429112
|
A | G | 4 | a0001c0001t0001g0183a0001c0002t0001g0177a0001c0002t0001g0238others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-42T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429112 | ||||||
| chr4:184429118
|
G | A | 2 | a0001c0001t0003g0060a0001c0002t0001g0223 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-6-48C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429118 | ||||||
| chr4:184429140
|
C | A | 1 | a0001c0004t0004g0254 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-6-70G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429140 | ||||||
| chr4:184429153
|
T | C | 73 | a0001c0001t0001g0307a0001c0001t0001g0336a0001c0001t0002g0058others(70): Show | 74 | HG00323.hp1 HG00621.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.-6-83A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429153 | ||||||
| chr4:184429200
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0003g0225a0001c0001t0003g0226others(6): Show | 10 | HG00642.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6-130C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429200 | ||||||
| chr4:184429202
|
C | T | 26 | a0001c0001t0001g0307a0001c0001t0001g0336a0001c0001t0002g0058others(23): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-6-132G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429202 | ||||||
| chr4:184429212
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-6-142T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429212 | ||||||
| chr4:184429268
|
A | G | 249 | a0001c0001t0001g0005a0001c0001t0001g0189a0001c0001t0001g0211others(246): Show | 255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.-6-198T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429268 | ||||||
| chr4:184429423
|
C | T | 133 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(130): Show | 138 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.-6-353G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429423 | ||||||
| chr4:184429430
|
G | A | 3 | a0001c0001t0003g0352a0001c0003t0004g0241a0001c0003t0004g0256 | 3 | HG01074.hp2 HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-6-360C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429430 | ||||||
| chr4:184429438
|
T | A | 3 | a0001c0002t0001g0018a0001c0002t0001g0047a0001c0002t0001g0051 | 3 | NA18984.hp1 NA18986.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-6-368A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429438 | ||||||
| chr4:184429473
|
A | C | 9 | a0001c0001t0002g0196a0001c0001t0002g0217a0001c0001t0002g0278others(6): Show | 9 | HG01891.hp1 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-403T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429473 | ||||||
| chr4:184429558
|
T | C | 44 | a0001c0001t0001g0324a0001c0001t0002g0040a0001c0001t0002g0067others(41): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.-6-488A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429558 | ||||||
| chr4:184429584
|
T | C | 67 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0215others(64): Show | 69 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-6-514A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429584 | ||||||
| chr4:184429650
|
G | C | 267 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(264): Show | 274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.-6-580C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429650 | ||||||
| chr4:184429780
|
A | G | 250 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(247): Show | 256 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-6-710T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429780 | ||||||
| chr4:184429817
|
A | T | 1 | a0001c0001t0002g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-6-747T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429817 | ||||||
| chr4:184429922
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-6-852T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429922 | ||||||
| chr4:184430268
|
C | CTGTATGC others(28): Show |
2 | a0001c0001t0001g0307a0001c0001t0010g0091 | 2 | HG02559.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-6-1233_-6-1199dup others(35): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430268 | ||||||
| chr4:184430268
|
C | CTGTATGC others(98): Show |
2 | a0001c0001t0003g0082a0001c0001t0003g0083 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-6-1199_-6-1198ins others(105): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430268 | ||||||
| chr4:184430268
|
CTGTATGC others(28): Show |
C | 8 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0228others(5): Show | 8 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-1233_-6-1199del others(35): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430268 | ||||||
| chr4:184430283
|
T | A | 4 | a0001c0001t0007g0364a0001c0002t0001g0250a0001c0002t0001g0282others(1): Show | 4 | HG00423.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-1213A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430283 | ||||||
| chr4:184430283
|
T | TGTCTGGC others(28): Show |
62 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0211others(59): Show | 64 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-6-1248_-6-1214dup others(35): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430283 | ||||||
| chr4:184430283
|
TGTCTGGC others(28): Show |
T | 14 | a0001c0001t0001g0189a0001c0001t0001g0233a0001c0001t0003g0024others(11): Show | 14 | HG00642.hp2 HG01255.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-1248_-6-1214del others(35): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430283 | ||||||
| chr4:184430318
|
A | T | 5 | a0001c0001t0001g0307a0001c0001t0007g0364a0001c0002t0001g0156others(2): Show | 5 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-1248T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430318 | ||||||
| chr4:184430355
|
T | C | 1 | a0001c0001t0003g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6-1285A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430355 | ||||||
| chr4:184430444
|
C | T | 2 | a0001c0001t0003g0099a0001c0002t0001g0068 | 2 | HG02080.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-6-1374G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430444 | ||||||
| chr4:184430714
|
G | A | 1 | a0001c0001t0002g0263 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-6-1644C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184430714 | ||||||
| chr4:184431056
|
C | T | 20 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(17): Show | 20 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-6-1986G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431056 | ||||||
| chr4:184431150
|
C | T | 3 | a0001c0001t0002g0144a0001c0002t0001g0129a0001c0002t0001g0348 | 3 | HG01975.hp2 HG01978.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-6-2080G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431150 | ||||||
| chr4:184431259
|
T | C | 101 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0040others(98): Show | 104 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-6-2189A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431259 | ||||||
| chr4:184431262
|
T | C | 2 | a0001c0001t0003g0082a0001c0001t0003g0083 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-6-2192A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431262 | ||||||
| chr4:184431346
|
C | T | 1 | a0001c0004t0004g0285 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-6-2276G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431346 | ||||||
| chr4:184431441
|
A | C | 8 | a0001c0001t0001g0183a0001c0001t0001g0287a0001c0002t0001g0177others(5): Show | 8 | HG02622.hp1 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-2371T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431441 | ||||||
| chr4:184431570
|
A | G | 5 | a0001c0001t0001g0211a0001c0001t0002g0283a0001c0001t0007g0362others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-2500T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431570 | ||||||
| chr4:184431597
|
A | AGCG | 177 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(174): Show | 182 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-6-2530_-6-2528dup others(3): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431597 | ||||||
| chr4:184431647
|
G | C | 62 | a0001c0001t0001g0079a0001c0001t0002g0028a0001c0001t0002g0064others(59): Show | 62 | HG00621.hp1 HG00733.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.-6-2577C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431647 | ||||||
| chr4:184431685
|
G | A | 1 | a0001c0002t0001g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-6-2615C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431685 | ||||||
| chr4:184431774
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0002g0098 | 2 | HG02559.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-6-2704C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431774 | ||||||
| chr4:184431792
|
GC | G | 165 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(162): Show | 170 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.-6-2723delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431792 | ||||||
| chr4:184431863
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0002g0067a0001c0001t0002g0110others(29): Show | 34 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-6-2793C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431863 | ||||||
| chr4:184431863
|
GA | G | 181 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(178): Show | 186 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-6-2794delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431863 | ||||||
| chr4:184431941
|
C | T | 1 | a0001c0001t0004g0326 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-6-2871G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431941 | ||||||
| chr4:184431993
|
T | A | 167 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(164): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-6-2923A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431993 | ||||||
| chr4:184432197
|
T | C | 365 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(362): Show | 373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-6-3127A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432197 | ||||||
| chr4:184432202
|
C | A | 7 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0228others(4): Show | 7 | HG00323.hp1 HG00639.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-3132G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432202 | ||||||
| chr4:184432251
|
A | G | 365 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(362): Show | 373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-6-3181T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432251 | ||||||
| chr4:184432279
|
C | T | 7 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0228others(4): Show | 7 | HG00323.hp1 HG00639.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-3209G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432279 | ||||||
| chr4:184432312
|
T | C | 167 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(164): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-6-3242A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432312 | ||||||
| chr4:184432368
|
A | G | 167 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(164): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-6-3298T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432368 | ||||||
| chr4:184432389
|
C | T | 12 | a0001c0001t0002g0196a0001c0001t0002g0200a0001c0001t0002g0217others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-3319G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432389 | ||||||
| chr4:184432560
|
C | A | 100 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0040others(97): Show | 103 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-6-3490G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432560 | ||||||
| chr4:184432645
|
T | C | 167 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(164): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-6-3575A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432645 | ||||||
| chr4:184432660
|
C | T | 1 | a0001c0001t0003g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-6-3590G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432660 | ||||||
| chr4:184432670
|
C | T | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-6-3600G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432670 | ||||||
| chr4:184432697
|
T | C | 1 | a0001c0004t0004g0318 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-6-3627A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432697 | ||||||
| chr4:184432711
|
G | C | 167 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(164): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-6-3641C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432711 | ||||||
| chr4:184432758
|
G | A | 3 | a0001c0001t0002g0096a0001c0001t0002g0311a0001c0001t0002g0312 | 3 | HG00438.hp1 NA18965.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-6-3688C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432758 | ||||||
| chr4:184432816
|
C | T | 167 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(164): Show | 172 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-6-3746G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432816 | ||||||
| chr4:184432973
|
C | T | 345 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(342): Show | 353 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(350): Show |
intron_variant | MODIFIER | c.-6-3903G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432973 | ||||||
| chr4:184433022
|
G | C | 3 | a0001c0001t0002g0144a0001c0002t0001g0129a0001c0002t0001g0348 | 3 | HG01975.hp2 HG01978.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-6-3952C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433022 | ||||||
| chr4:184433074
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-6-4004G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433074 | ||||||
| chr4:184433144
|
T | C | 115 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0211others(112): Show | 116 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.-6-4074A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433144 | ||||||
| chr4:184433194
|
T | C | 68 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(65): Show | 70 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.-6-4124A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433194 | ||||||
| chr4:184433200
|
C | T | 101 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0040others(98): Show | 104 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-6-4130G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433200 | ||||||
| chr4:184433273
|
T | A | 98 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0040others(95): Show | 101 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-6-4203A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433273 | ||||||
| chr4:184433338
|
G | T | 21 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-4268C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433338 | ||||||
| chr4:184433442
|
G | T | 6 | a0001c0001t0002g0196a0001c0001t0002g0217a0001c0001t0003g0328others(3): Show | 6 | HG01891.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-4372C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433442 | ||||||
| chr4:184433655
|
GGGTT | G | 187 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(184): Show | 192 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-6-4589_-6-4586del others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433655 | ||||||
| chr4:184433756
|
G | A | 108 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0211others(105): Show | 109 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-6-4686C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433756 | ||||||
| chr4:184433783
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0002g0110a0001c0001t0002g0337others(26): Show | 31 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-6-4713G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433783 | ||||||
| chr4:184433806
|
C | G | 191 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(188): Show | 196 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-6-4736G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433806 | ||||||
| chr4:184433808
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-6-4738T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433808 | ||||||
| chr4:184433820
|
T | A | 306 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0183others(303): Show | 312 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.-6-4750A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433820 | ||||||
| chr4:184433947
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-6-4877C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433947 | ||||||
| chr4:184433956
|
G | T | 2 | a0001c0004t0004g0331a0001c0004t0004g0332 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-6-4886C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433956 | ||||||
| chr4:184433967
|
T | A | 365 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(362): Show | 373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-6-4897A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433967 | ||||||
| chr4:184433973
|
GATTA | G | 5 | a0001c0001t0001g0005a0001c0001t0003g0025a0001c0001t0003g0120others(2): Show | 7 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-4907_-6-4904del others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433973 | ||||||
| chr4:184434025
|
C | T | 7 | a0001c0001t0002g0339a0001c0001t0003g0350a0001c0002t0001g0268others(4): Show | 7 | HG00558.hp2 HG01928.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-4955G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434025 | ||||||
| chr4:184434133
|
A | G | 58 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0215others(55): Show | 60 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.-6-5063T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434133 | ||||||
| chr4:184434264
|
G | A | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-6-5194C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434264 | ||||||
| chr4:184434307
|
C | A | 7 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0228others(4): Show | 7 | HG00323.hp1 HG00639.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-5237G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434307 | ||||||
| chr4:184434402
|
T | C | 58 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0215others(55): Show | 60 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.-6-5332A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434402 | ||||||
| chr4:184434599
|
T | C | 1 | a0002c0008t0002g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-6-5529A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434599 | ||||||
| chr4:184434727
|
G | A | 107 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0067others(104): Show | 110 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-6-5657C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434727 | ||||||
| chr4:184434756
|
GACAGT | G | 8 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0228others(5): Show | 8 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-5691_-6-5687del others(5): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184434756 | ||||||
| chr4:184435018
|
C | T | 139 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0251others(136): Show | 142 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-6-5948G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435018 | ||||||
| chr4:184435045
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-6-5975A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435045 | ||||||
| chr4:184435091
|
G | C | 146 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0189others(143): Show | 149 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-6-6021C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435091 | ||||||
| chr4:184435142
|
A | G | 1 | a0001c0001t0003g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-6-6072T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435142 | ||||||
| chr4:184435195
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-6-6125G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435195 | ||||||
| chr4:184435196
|
G | A | 1 | a0001c0002t0001g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-6-6126C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435196 | ||||||
| chr4:184435431
|
G | C | 3 | a0001c0001t0002g0144a0001c0002t0001g0129a0001c0002t0001g0348 | 3 | HG01975.hp2 HG01978.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-6-6361C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435431 | ||||||
| chr4:184435519
|
T | A | 143 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0251others(140): Show | 146 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-6-6449A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435519 | ||||||
| chr4:184435552
|
A | G | 1 | a0001c0001t0003g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6-6482T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435552 | ||||||
| chr4:184435557
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-6-6487C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435557 | ||||||
| chr4:184435574
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-6-6504G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435574 | ||||||
| chr4:184435742
|
T | C | 345 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(342): Show | 353 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(350): Show |
intron_variant | MODIFIER | c.-6-6672A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435742 | ||||||
| chr4:184435757
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0002g0110a0001c0001t0002g0337others(25): Show | 30 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-6-6687C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435757 | ||||||
| chr4:184435984
|
C | CT | 151 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0183others(148): Show | 153 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-6-6915dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435984 | ||||||
| chr4:184436016
|
C | T | 1 | a0001c0002t0001g0289 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-6-6946G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436016 | ||||||
| chr4:184436071
|
G | C | 146 | a0001c0001t0001g0005a0001c0001t0001g0189a0001c0001t0001g0211others(143): Show | 149 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-6-7001C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436071 | ||||||
| chr4:184436126
|
A | G | 365 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(362): Show | 373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-6-7056T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436126 | ||||||
| chr4:184436128
|
C | G | 1 | a0001c0002t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-6-7058G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436128 | ||||||
| chr4:184436157
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-6-7087T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436157 | ||||||
| chr4:184436251
|
A | T | 106 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0075others(103): Show | 109 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-6-7181T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436251 | ||||||
| chr4:184436277
|
G | A | 1 | a0001c0002t0001g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6-7207C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436277 | ||||||
| chr4:184436281
|
C | T | 1 | a0001c0002t0001g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-6-7211G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436281 | ||||||
| chr4:184436302
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-7232G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436302 | ||||||
| chr4:184436337
|
A | T | 1 | a0001c0001t0002g0119 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-6-7267T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436337 | ||||||
| chr4:184436345
|
A | C | 5 | a0001c0001t0001g0211a0001c0001t0002g0283a0001c0001t0007g0362others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-7275T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436345 | ||||||
| chr4:184436360
|
G | T | 1 | a0001c0001t0002g0040 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-6-7290C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436360 | ||||||
| chr4:184436423
|
C | G | 8 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0228others(5): Show | 8 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-7353G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436423 | ||||||
| chr4:184436582
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-7512A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436582 | ||||||
| chr4:184436615
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-7545A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436615 | ||||||
| chr4:184436637
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0002g0040a0001c0001t0002g0110others(27): Show | 32 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-6-7567T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184436637 | ||||||
| chr4:184437115
|
G | C | 5 | a0001c0001t0002g0299a0001c0001t0002g0356a0001c0001t0002g0358others(2): Show | 5 | HG00609.hp2 HG01255.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-8045C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437115 | ||||||
| chr4:184437212
|
C | T | 1 | a0001c0002t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-6-8142G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437212 | ||||||
| chr4:184437239
|
G | A | 56 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0215others(53): Show | 58 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-6-8169C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437239 | ||||||
| chr4:184437294
|
G | A | 2 | a0001c0001t0001g0233a0001c0002t0001g0255 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-6-8224C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437294 | ||||||
| chr4:184437358
|
A | AT | 31 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(28): Show | 31 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.-6-8289dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437358 | ||||||
| chr4:184437364
|
T | A | 7 | a0001c0001t0002g0064a0001c0001t0002g0173a0001c0001t0002g0234others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-8294A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437364 | ||||||
| chr4:184437364
|
T | TA | 112 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0040others(109): Show | 115 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-6-8295dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437364 | ||||||
| chr4:184437476
|
G | A | 1 | a0001c0001t0004g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-6-8406C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437476 | ||||||
| chr4:184437489
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-6-8419C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437489 | ||||||
| chr4:184437546
|
C | T | 19 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-8476G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437546 | ||||||
| chr4:184437638
|
G | A | 19 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-8568C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437638 | ||||||
| chr4:184437693
|
T | C | 1 | a0001c0001t0002g0207 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-6-8623A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437693 | ||||||
| chr4:184437734
|
T | C | 12 | a0001c0001t0002g0003a0001c0001t0002g0137a0001c0001t0002g0146others(9): Show | 13 | HG00423.hp1 HG01261.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-8664A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437734 | ||||||
| chr4:184437749
|
G | A | 9 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0228others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6-8679C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437749 | ||||||
| chr4:184437831
|
CA | C | 116 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0211others(113): Show | 117 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.-6-8762delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437831 | ||||||
| chr4:184437831
|
CAA | C | 120 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0067others(117): Show | 123 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.-6-8763_-6-8762del others(2): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437831 | ||||||
| chr4:184437831
|
CAAA | C | 20 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(17): Show | 20 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-6-8764_-6-8762del others(3): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437831 | ||||||
| chr4:184437860
|
G | T | 2 | a0001c0001t0001g0233a0001c0002t0001g0255 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-6-8790C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437860 | ||||||
| chr4:184437867
|
C | T | 1 | a0001c0001t0002g0175 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-6-8797G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437867 | ||||||
| chr4:184437868
|
G | A | 19 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-8798C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437868 | ||||||
| chr4:184437965
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-6-8895G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437965 | ||||||
| chr4:184438124
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0233a0001c0001t0002g0110others(27): Show | 32 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-6-9054G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438124 | ||||||
| chr4:184438262
|
G | T | 66 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0215others(63): Show | 68 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-6-9192C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438262 | ||||||
| chr4:184438396
|
T | C | 2 | a0001c0001t0002g0114a0001c0001t0003g0101 | 2 | NA18944.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-6-9326A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438396 | ||||||
| chr4:184438423
|
C | A | 19 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6-9353G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438423 | ||||||
| chr4:184438478
|
A | C | 21 | a0001c0001t0001g0243a0001c0001t0001g0251a0001c0001t0001g0335others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-9408T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438478 | ||||||
| chr4:184438521
|
A | G | 19 | a0001c0001t0002g0135a0001c0001t0002g0213a0001c0001t0002g0264others(16): Show | 19 | HG00558.hp2 HG01928.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-9451T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438521 | ||||||
| chr4:184438606
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0002g0195 | 2 | HG01099.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-6-9536A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438606 | ||||||
| chr4:184438640
|
G | A | 14 | a0001c0001t0002g0196a0001c0001t0002g0200a0001c0001t0002g0217others(11): Show | 14 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-9570C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438640 | ||||||
| chr4:184438644
|
G | C | 3 | a0001c0001t0003g0274a0001c0002t0001g0168a0001c0002t0001g0272 | 3 | NA18986.hp2 NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-6-9574C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438644 | ||||||
| chr4:184438670
|
C | T | 365 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(362): Show | 373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.-6-9600G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438670 | ||||||
| chr4:184438685
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-6-9615G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438685 | ||||||
| chr4:184438750
|
G | C | 1 | a0001c0002t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6-9680C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438750 | ||||||
| chr4:184438800
|
G | T | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-9730C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438800 | ||||||
| chr4:184438801
|
GCATGAAA others(53): Show |
G | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-9791_-6-9732del others(60): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438801 | ||||||
| chr4:184438837
|
A | T | 1 | a0001c0001t0004g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-9767T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438837 | ||||||
| chr4:184438887
|
C | T | 108 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0192others(105): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-6-9817G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438887 | ||||||
| chr4:184438948
|
C | T | 1 | a0001c0001t0002g0313 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-6-9878G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438948 | ||||||
| chr4:184438989
|
G | A | 1 | a0001c0001t0004g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-9919C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184438989 | ||||||
| chr4:184439313
|
T | TA | 13 | a0001c0001t0001g0216a0001c0001t0001g0324a0001c0001t0002g0196others(10): Show | 13 | HG01256.hp1 HG01891.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6-10244dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439313 | ||||||
| chr4:184439313
|
TA | T | 99 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0192others(96): Show | 101 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-6-10244delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439313 | ||||||
| chr4:184439343
|
C | T | 2 | a0001c0001t0003g0077a0001c0001t0003g0092 | 2 | NA18957.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-6-10273G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439343 | ||||||
| chr4:184439353
|
T | TA | 89 | a0001c0001t0001g0189a0001c0001t0001g0215a0001c0001t0001g0216others(86): Show | 90 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.-6-10284dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439353 | ||||||
| chr4:184439353
|
TA | T | 10 | a0001c0001t0001g0211a0001c0001t0001g0248a0001c0001t0002g0278others(7): Show | 10 | HG02055.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-10284delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439353 | ||||||
| chr4:184439580
|
G | A | 4 | a0001c0001t0002g0061a0001c0001t0003g0017a0001c0001t0003g0039others(1): Show | 4 | NA18943.hp1 NA18964.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-10510C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439580 | ||||||
| chr4:184439610
|
C | T | 363 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(360): Show | 371 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.-6-10540G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439610 | ||||||
| chr4:184439616
|
C | G | 6 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0004g0257others(3): Show | 6 | HG01109.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-10546G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439616 | ||||||
| chr4:184439804
|
C | T | 5 | a0001c0002t0001g0177a0001c0002t0001g0185a0001c0002t0001g0258others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-10734G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439804 | ||||||
| chr4:184439805
|
G | A | 9 | a0001c0001t0001g0192a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6-10735C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439805 | ||||||
| chr4:184439928
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-6-10858G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184439928 | ||||||
| chr4:184440088
|
C | T | 39 | a0001c0001t0001g0079a0001c0001t0002g0080a0001c0001t0002g0105others(36): Show | 39 | HG00408.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.-6-11018G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440088 | ||||||
| chr4:184440138
|
T | C | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-11068A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440138 | ||||||
| chr4:184440139
|
G | T | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-11069C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440139 | ||||||
| chr4:184440141
|
C | T | 46 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0080others(43): Show | 47 | HG00408.hp2 HG00738.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.-6-11071G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440141 | ||||||
| chr4:184440276
|
C | T | 5 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0196others(2): Show | 5 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-11206G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440276 | ||||||
| chr4:184440310
|
C | T | 75 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0335others(72): Show | 76 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-6-11240G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440310 | ||||||
| chr4:184440342
|
C | T | 2 | a0001c0001t0001g0233a0001c0003t0008g0316 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-6-11272G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440342 | ||||||
| chr4:184440487
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6-11417A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440487 | ||||||
| chr4:184440520
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-11450A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440520 | ||||||
| chr4:184440529
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-6-11459G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440529 | ||||||
| chr4:184440544
|
C | A | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0196others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-11474G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440544 | ||||||
| chr4:184440598
|
C | T | 14 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0175others(11): Show | 14 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-11528G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440598 | ||||||
| chr4:184440603
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-6-11533G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440603 | ||||||
| chr4:184440605
|
T | C | 1 | a0001c0002t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-6-11535A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440605 | ||||||
| chr4:184440652
|
C | T | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-11582G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440652 | ||||||
| chr4:184440653
|
T | C | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-11583A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440653 | ||||||
| chr4:184440654
|
C | T | 1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-11584G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440654 | ||||||
| chr4:184440763
|
G | T | 3 | a0001c0001t0003g0209a0001c0001t0004g0257a0001c0002t0001g0327 | 3 | HG01109.hp2 HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-6-11693C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440763 | ||||||
| chr4:184440816
|
A | G | 1 | a0001c0001t0003g0201 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-6-11746T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440816 | ||||||
| chr4:184440919
|
A | G | 8 | a0001c0001t0001g0335a0001c0001t0002g0187a0001c0001t0002g0206others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-11849T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184440919 | ||||||
| chr4:184441031
|
A | C | 4 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0004g0224others(1): Show | 4 | HG01106.hp2 HG01361.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-11961T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184441031 | ||||||
| chr4:184441119
|
C | T | 1 | a0001c0001t0003g0350 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-6-12049G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184441119 | ||||||
| chr4:184441181
|
G | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0237 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-6-12111C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184441181 | ||||||
| chr4:184441478
|
A | G | 13 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0200others(10): Show | 13 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6-12408T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184441478 | ||||||
| chr4:184441682
|
T | A | 1 | a0001c0001t0002g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-6-12612A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184441682 | ||||||
| chr4:184441883
|
G | A | 53 | a0001c0001t0001g0251a0001c0001t0001g0287a0001c0001t0001g0291others(50): Show | 54 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.-6-12813C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184441883 | ||||||
| chr4:184442004
|
C | T | 16 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0200others(13): Show | 16 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-6-12934G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442004 | ||||||
| chr4:184442221
|
G | A | 1 | a0001c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-13151C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442221 | ||||||
| chr4:184442485
|
A | C | 26 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0002g0010others(23): Show | 27 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-6-13415T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442485 | ||||||
| chr4:184442507
|
A | T | 14 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0173others(11): Show | 14 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-13437T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442507 | ||||||
| chr4:184442528
|
T | C | 2 | a0001c0001t0002g0173a0001c0001t0002g0175 | 2 | HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-6-13458A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442528 | ||||||
| chr4:184442558
|
A | G | 357 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(354): Show | 365 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(362): Show |
intron_variant | MODIFIER | c.-6-13488T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442558 | ||||||
| chr4:184442565
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-6-13495G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442565 | ||||||
| chr4:184442626
|
C | G | 353 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(350): Show | 361 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.-6-13556G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442626 | ||||||
| chr4:184442652
|
A | G | 82 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0335others(79): Show | 84 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-6-13582T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442652 | ||||||
| chr4:184442675
|
T | C | 259 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0189others(256): Show | 265 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.-6-13605A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442675 | ||||||
| chr4:184442675
|
T | G | 8 | a0001c0001t0001g0248a0001c0001t0002g0284a0001c0001t0004g0186others(5): Show | 8 | HG01106.hp2 HG01361.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-13605A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442675 | ||||||
| chr4:184442758
|
C | T | 14 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0173others(11): Show | 14 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-13688G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442758 | ||||||
| chr4:184442776
|
T | C | 83 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0335others(80): Show | 85 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-6-13706A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442776 | ||||||
| chr4:184442795
|
C | T | 137 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(134): Show | 142 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-6-13725G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442795 | ||||||
| chr4:184442940
|
T | C | 12 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0200others(9): Show | 12 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-13870A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442940 | ||||||
| chr4:184442996
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-6-13926C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442996 | ||||||
| chr4:184442999
|
C | CACT | 12 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0200others(9): Show | 12 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-13932_-6-13930d others(5): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184442999 | ||||||
| chr4:184443003
|
G | A | 2 | a0001c0001t0001g0233a0001c0003t0008g0316 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-6-13933C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443003 | ||||||
| chr4:184443012
|
G | A | 1 | a0001c0002t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6-13942C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443012 | ||||||
| chr4:184443043
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-6-13973T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443043 | ||||||
| chr4:184443162
|
C | A | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-6-14092G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443162 | ||||||
| chr4:184443237
|
A | AG | 14 | a0001c0001t0001g0251a0001c0001t0001g0336a0001c0001t0002g0173others(11): Show | 14 | HG00733.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6-14168dupC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443237 | ||||||
| chr4:184443604
|
C | T | 1 | a0001c0001t0003g0122 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-6-14534G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443604 | ||||||
| chr4:184443607
|
TC | T | 38 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0001g0335others(35): Show | 40 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.-6-14538delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443607 | ||||||
| chr4:184443709
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6-14639A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443709 | ||||||
| chr4:184443810
|
C | T | 1 | a0001c0002t0001g0354 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-6-14740G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443810 | ||||||
| chr4:184443899
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-6-14829A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184443899 | ||||||
| chr4:184444116
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-6-15046C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444116 | ||||||
| chr4:184444213
|
T | C | 1 | a0001c0002t0001g0289 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-6-15143A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444213 | ||||||
| chr4:184444274
|
A | C | 1 | a0001c0001t0003g0262 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-6-15204T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444274 | ||||||
| chr4:184444319
|
T | C | 22 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0251others(19): Show | 22 | HG00733.hp2 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-6-15249A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444319 | ||||||
| chr4:184444343
|
G | A | 3 | a0001c0001t0002g0171a0001c0001t0003g0024a0001c0002t0005g0166 | 3 | HG02074.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-6-15273C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444343 | ||||||
| chr4:184444386
|
C | A | 16 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0251others(13): Show | 16 | HG00733.hp2 HG01109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-6-15316G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444386 | ||||||
| chr4:184444386
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-15316G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444386 | ||||||
| chr4:184444435
|
T | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0324others(80): Show | 86 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-6-15365A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444435 | ||||||
| chr4:184444463
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-6-15393G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444463 | ||||||
| chr4:184444469
|
G | GGATTAAA others(3): Show |
1 | a0001c0001t0002g0360 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-6-15409_-6-15400d others(12): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444469 | ||||||
| chr4:184444495
|
T | C | 144 | a0001c0001t0001g0079a0001c0001t0001g0183a0001c0001t0001g0189others(141): Show | 147 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-6-15425A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444495 | ||||||
| chr4:184444530
|
A | G | 13 | a0001c0001t0001g0248a0001c0001t0002g0283a0001c0001t0002g0284others(10): Show | 13 | HG01884.hp1 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6-15460T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444530 | ||||||
| chr4:184444840
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-15770A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444840 | ||||||
| chr4:184444947
|
G | A | 1 | a0001c0003t0004g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-15877C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444947 | ||||||
| chr4:184444987
|
C | T | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | NA18946.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-6-15917G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184444987 | ||||||
| chr4:184445103
|
G | A | 13 | a0001c0001t0001g0248a0001c0001t0002g0283a0001c0001t0002g0284others(10): Show | 13 | HG01884.hp1 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6-16033C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445103 | ||||||
| chr4:184445135
|
G | T | 16 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0251others(13): Show | 16 | HG00733.hp2 HG01109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-6-16065C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445135 | ||||||
| chr4:184445185
|
C | A | 1 | a0001c0004t0004g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-6-16115G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445185 | ||||||
| chr4:184445197
|
G | A | 1 | a0001c0001t0004g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-6-16127C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445197 | ||||||
| chr4:184445216
|
G | A | 5 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0177others(2): Show | 5 | HG02896.hp2 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-16146C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445216 | ||||||
| chr4:184445242
|
G | A | 3 | a0001c0001t0002g0298a0001c0001t0002g0299a0001c0001t0003g0071 | 3 | HG00609.hp2 NA18946.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-6-16172C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445242 | ||||||
| chr4:184445293
|
C | G | 1 | a0001c0001t0002g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-6-16223G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445293 | ||||||
| chr4:184445418
|
C | T | 1 | a0001c0001t0003g0347 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-6-16348G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445418 | ||||||
| chr4:184445497
|
T | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0183a0001c0001t0001g0189others(139): Show | 145 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-6-16427A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445497 | ||||||
| chr4:184445531
|
T | C | 2 | a0001c0002t0001g0268a0001c0002t0005g0267 | 2 | HG00558.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-6-16461A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445531 | ||||||
| chr4:184445653
|
AC | A | 5 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0177others(2): Show | 5 | HG02896.hp2 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-16584delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445653 | ||||||
| chr4:184445654
|
C | CA | 7 | a0001c0001t0002g0035a0001c0001t0002g0234a0001c0001t0002g0360others(4): Show | 7 | HG01069.hp2 HG01081.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-16585dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445654 | ||||||
| chr4:184445654
|
C | CAA | 71 | a0001c0001t0001g0291a0001c0001t0002g0004a0001c0001t0002g0019others(68): Show | 73 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-6-16586_-6-16585d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445654 | ||||||
| chr4:184445654
|
C | CAAA | 44 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0080others(41): Show | 45 | HG00738.hp2 HG01099.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.-6-16587_-6-16585d others(5): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445654 | ||||||
| chr4:184445655
|
A | T | 5 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0177others(2): Show | 5 | HG02896.hp2 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-16585T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445655 | ||||||
| chr4:184445695
|
T | C | 120 | a0001c0001t0001g0079a0001c0001t0001g0291a0001c0001t0002g0002others(117): Show | 123 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-6-16625A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445695 | ||||||
| chr4:184445734
|
C | A | 190 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(187): Show | 195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.-6-16664G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445734 | ||||||
| chr4:184445948
|
T | C | 1 | a0001c0001t0002g0106 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-6-16878A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445948 | ||||||
| chr4:184445999
|
G | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(155): Show | 163 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.-6-16929C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445999 | ||||||
| chr4:184446038
|
TAG | T | 6 | a0001c0001t0003g0073a0001c0001t0003g0122a0001c0002t0001g0094others(3): Show | 6 | HG00738.hp2 HG02040.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-16970_-6-16969d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446038 | ||||||
| chr4:184446172
|
C | G | 1 | a0001c0003t0008g0316 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-6-17102G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446172 | ||||||
| chr4:184446255
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0002g0206 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-6-17185C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446255 | ||||||
| chr4:184446467
|
G | A | 1 | a0001c0002t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6-17397C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446467 | ||||||
| chr4:184446545
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-6-17475C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446545 | ||||||
| chr4:184446653
|
A | G | 2 | a0001c0001t0002g0171a0001c0002t0005g0166 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-6-17583T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446653 | ||||||
| chr4:184446677
|
A | G | 338 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(335): Show | 346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.-6-17607T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446677 | ||||||
| chr4:184446691
|
T | A | 9 | a0001c0001t0001g0233a0001c0001t0002g0179a0001c0001t0002g0187others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6-17621A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446691 | ||||||
| chr4:184446724
|
C | T | 2 | a0001c0001t0003g0178a0001c0003t0008g0184 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-6-17654G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446724 | ||||||
| chr4:184446769
|
C | G | 40 | a0001c0001t0001g0287a0001c0001t0002g0096a0001c0001t0002g0098others(37): Show | 40 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-6-17699G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446769 | ||||||
| chr4:184446848
|
G | A | 12 | a0001c0001t0001g0248a0001c0001t0002g0283a0001c0001t0002g0284others(9): Show | 12 | HG01167.hp1 HG01884.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-17778C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446848 | ||||||
| chr4:184446869
|
T | C | 3 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-17799A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446869 | ||||||
| chr4:184446911
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-6-17841C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446911 | ||||||
| chr4:184446934
|
C | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(188): Show | 196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.-6-17864G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446934 | ||||||
| chr4:184446976
|
G | T | 4 | a0001c0001t0003g0011a0001c0001t0003g0102a0001c0002t0001g0107others(1): Show | 4 | NA18947.hp2 NA18957.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-17906C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184446976 | ||||||
| chr4:184447081
|
A | C | 221 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(218): Show | 226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.-6-18011T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447081 | ||||||
| chr4:184447120
|
A | C | 60 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0002g0040others(57): Show | 61 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-6-18050T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447120 | ||||||
| chr4:184447162
|
C | T | 9 | a0001c0001t0001g0233a0001c0001t0002g0179a0001c0001t0002g0187others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6-18092G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447162 | ||||||
| chr4:184447347
|
C | T | 12 | a0001c0001t0002g0035a0001c0001t0002g0339a0001c0001t0003g0037others(9): Show | 12 | HG02040.hp1 NA18942.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-18277G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447347 | ||||||
| chr4:184447436
|
A | G | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.-6-18366T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447436 | ||||||
| chr4:184447531
|
A | T | 1 | a0001c0001t0002g0104 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-6-18461T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447531 | ||||||
| chr4:184447616
|
C | A | 2 | a0001c0001t0004g0326a0001c0002t0001g0323 | 2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-6-18546G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447616 | ||||||
| chr4:184447659
|
A | G | 140 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(137): Show | 145 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-6-18589T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447659 | ||||||
| chr4:184447684
|
G | C | 91 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(88): Show | 92 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-6-18614C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447684 | ||||||
| chr4:184447916
|
C | T | 3 | a0001c0001t0001g0307a0001c0001t0002g0195a0001c0002t0001g0194 | 3 | HG01099.hp1 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-6-18846G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447916 | ||||||
| chr4:184447932
|
G | C | 218 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(215): Show | 223 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.-6-18862C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447932 | ||||||
| chr4:184447955
|
G | A | 4 | a0001c0001t0002g0064a0001c0002t0001g0063a0001c0002t0001g0231others(1): Show | 4 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-18885C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447955 | ||||||
| chr4:184447985
|
C | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0002g0190others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-18915G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184447985 | ||||||
| chr4:184448176
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0002g0190 | 3 | HG02109.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-6-19106C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448176 | ||||||
| chr4:184448201
|
G | C | 1 | a0001c0003t0004g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-19131C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448201 | ||||||
| chr4:184448215
|
C | G | 1 | a0001c0002t0001g0238 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-6-19145G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448215 | ||||||
| chr4:184448243
|
AG | A | 4 | a0001c0001t0001g0233a0001c0001t0002g0179a0001c0001t0002g0206others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-19174delC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448243 | ||||||
| chr4:184448282
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-6-19212C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448282 | ||||||
| chr4:184448293
|
C | A | 1 | a0001c0002t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6-19223G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448293 | ||||||
| chr4:184448298
|
G | A | 265 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(262): Show | 272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.-6-19228C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448298 | ||||||
| chr4:184448326
|
TG | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0002g0190 | 3 | HG02109.hp2 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-6-19257delC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448326 | ||||||
| chr4:184448485
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-6-19415G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448485 | ||||||
| chr4:184448811
|
C | T | 40 | a0001c0001t0001g0287a0001c0001t0002g0096a0001c0001t0002g0098others(37): Show | 40 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-6-19741G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448811 | ||||||
| chr4:184448912
|
G | A | 116 | a0001c0001t0001g0079a0001c0001t0001g0291a0001c0001t0002g0002others(113): Show | 118 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-6-19842C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448912 | ||||||
| chr4:184448919
|
C | T | 4 | a0001c0001t0001g0307a0001c0001t0002g0195a0001c0002t0001g0194others(1): Show | 4 | HG01099.hp1 HG02559.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-19849G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448919 | ||||||
| chr4:184448933
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0003g0015 | 2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-6-19863G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448933 | ||||||
| chr4:184448937
|
A | C | 3 | a0001c0001t0001g0307a0001c0001t0002g0195a0001c0002t0001g0194 | 3 | HG01099.hp1 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-6-19867T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448937 | ||||||
| chr4:184448967
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6-19897C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184448967 | ||||||
| chr4:184449029
|
C | T | 117 | a0001c0001t0001g0079a0001c0001t0001g0291a0001c0001t0002g0002others(114): Show | 119 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-6-19959G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449029 | ||||||
| chr4:184449053
|
G | C | 47 | a0001c0001t0001g0287a0001c0001t0002g0004a0001c0001t0002g0040others(44): Show | 48 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-6-19983C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449053 | ||||||
| chr4:184449072
|
A | G | 26 | a0001c0001t0001g0291a0001c0001t0002g0213a0001c0001t0002g0228others(23): Show | 27 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-6-20002T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449072 | ||||||
| chr4:184449116
|
C | T | 1 | a0001c0003t0004g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-20046G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449116 | ||||||
| chr4:184449169
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-6-20099G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449169 | ||||||
| chr4:184449270
|
T | C | 1 | a0001c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-20200A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449270 | ||||||
| chr4:184449277
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-6-20207C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449277 | ||||||
| chr4:184449301
|
G | T | 2 | a0001c0002t0001g0115a0001c0002t0005g0046 | 2 | HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-6-20231C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449301 | ||||||
| chr4:184449313
|
C | A | 276 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(273): Show | 282 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.-6-20243G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449313 | ||||||
| chr4:184449436
|
A | G | 12 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0251others(9): Show | 12 | HG00733.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-20366T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449436 | ||||||
| chr4:184449492
|
C | T | 1 | a0001c0001t0007g0364 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-6-20422G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449492 | ||||||
| chr4:184449653
|
T | A | 3 | a0001c0002t0001g0177a0001c0002t0001g0180a0001c0002t0011g0181 | 3 | HG02895.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-6-20583A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449653 | ||||||
| chr4:184449767
|
T | C | 1 | a0001c0002t0001g0036 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-6-20697A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449767 | ||||||
| chr4:184449864
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-6-20794C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184449864 | ||||||
| chr4:184450017
|
T | G | 1 | a0001c0001t0002g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-6-20947A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450017 | ||||||
| chr4:184450082
|
C | T | 93 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(90): Show | 94 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-6-21012G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450082 | ||||||
| chr4:184450083
|
G | A | 1 | a0001c0002t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6-21013C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450083 | ||||||
| chr4:184450233
|
A | G | 1 | a0001c0002t0001g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-6-21163T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450233 | ||||||
| chr4:184450710
|
T | G | 1 | a0001c0002t0001g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-6-21640A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450710 | ||||||
| chr4:184450795
|
GTTA | G | 110 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(107): Show | 111 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-6-21728_-6-21726d others(5): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450795 | ||||||
| chr4:184450826
|
G | A | 113 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0004others(110): Show | 115 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.-6-21756C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450826 | ||||||
| chr4:184450898
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-6-21828C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450898 | ||||||
| chr4:184450967
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-21897C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450967 | ||||||
| chr4:184450987
|
A | G | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.-6-21917T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450987 | ||||||
| chr4:184450997
|
C | A | 3 | a0001c0001t0002g0004a0001c0001t0003g0178a0001c0003t0008g0184 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-21927G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184450997 | ||||||
| chr4:184451417
|
T | A | 1 | a0001c0001t0007g0364 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-6-22347A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451417 | ||||||
| chr4:184451455
|
C | A | 2 | a0001c0001t0002g0252a0001c0002t0001g0249 | 2 | HG02135.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-6-22385G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451455 | ||||||
| chr4:184451524
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-6-22454G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451524 | ||||||
| chr4:184451669
|
A | G | 2 | a0001c0001t0002g0173a0001c0001t0002g0175 | 2 | HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-6-22599T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451669 | ||||||
| chr4:184451778
|
A | C | 1 | a0001c0002t0001g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7+22601T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451778 | ||||||
| chr4:184451788
|
A | C | 1 | a0001c0001t0003g0024 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-7+22591T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451788 | ||||||
| chr4:184451980
|
T | C | 67 | a0001c0001t0001g0233a0001c0001t0001g0287a0001c0001t0001g0291others(64): Show | 68 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-7+22399A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451980 | ||||||
| chr4:184451986
|
A | G | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.-7+22393T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184451986 | ||||||
| chr4:184452148
|
C | G | 1 | a0001c0002t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+22231G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452148 | ||||||
| chr4:184452152
|
C | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(134): Show | 143 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-7+22227G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452152 | ||||||
| chr4:184452163
|
G | C | 1 | a0001c0001t0002g0283 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-7+22216C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452163 | ||||||
| chr4:184452363
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-7+22016G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452363 | ||||||
| chr4:184452453
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+21926C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452453 | ||||||
| chr4:184452477
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-7+21902C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452477 | ||||||
| chr4:184452478
|
C | T | 1 | a0001c0001t0003g0269 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-7+21901G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452478 | ||||||
| chr4:184452508
|
C | T | 11 | a0001c0001t0002g0213a0001c0001t0002g0234a0001c0001t0002g0235others(8): Show | 11 | HG01069.hp2 HG01071.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+21871G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452508 | ||||||
| chr4:184452633
|
C | T | 11 | a0001c0001t0002g0004a0001c0001t0002g0179a0001c0001t0002g0187others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7+21746G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452633 | ||||||
| chr4:184452738
|
C | T | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.-7+21641G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452738 | ||||||
| chr4:184452765
|
T | C | 1 | a0001c0001t0004g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-7+21614A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452765 | ||||||
| chr4:184452770
|
C | CAAAAAAA | 72 | a0001c0001t0001g0324a0001c0001t0002g0003a0001c0001t0002g0028others(69): Show | 74 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-7+21602_-7+21608d others(9): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(1): Show |
44 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(41): Show | 46 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.-7+21601_-7+21608d others(10): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(2): Show |
17 | a0001c0001t0001g0335a0001c0001t0002g0013a0001c0001t0002g0128others(14): Show | 18 | HG00609.hp1 HG00642.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-7+21600_-7+21608d others(11): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(3): Show |
20 | a0001c0001t0002g0040a0001c0001t0002g0096a0001c0001t0002g0239others(17): Show | 20 | HG00558.hp2 HG03098.hp1 HG03453.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7+21599_-7+21608d others(12): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(4): Show |
19 | a0001c0001t0001g0287a0001c0001t0002g0098a0001c0001t0002g0202others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7+21598_-7+21608d others(13): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0252a0001c0001t0003g0274a0001c0001t0003g0276others(3): Show | 6 | HG02135.hp2 NA18971.hp2 NA19054.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+21597_-7+21608d others(14): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0002g0171a0001c0001t0002g0275a0001c0001t0003g0199others(1): Show | 4 | HG02083.hp1 HG02922.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+21596_-7+21608d others(15): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0002g0195a0001c0001t0012g0210a0001c0002t0001g0194others(1): Show | 4 | HG01099.hp1 HG02523.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+21595_-7+21608d others(16): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0192 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7+21591_-7+21608d others(20): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0189a0001c0001t0002g0190 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-7+21590_-7+21608d others(21): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0002g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-7+21588_-7+21608d others(23): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-7+21608_-7+21609i others(32): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0233 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7+21608_-7+21609i others(34): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
CAA | C | 10 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0251others(7): Show | 10 | HG00733.hp2 HG02165.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+21607_-7+21608d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
CAAA | C | 34 | a0001c0001t0001g0291a0001c0001t0002g0065a0001c0001t0002g0066others(31): Show | 35 | HG00280.hp1 HG00323.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-7+21606_-7+21608d others(5): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
CAAAA | C | 92 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 94 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.-7+21605_-7+21608d others(6): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
CAAAAA | C | 6 | a0001c0001t0001g0248a0001c0001t0002g0173a0001c0001t0002g0175others(3): Show | 6 | HG02451.hp2 HG03098.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+21604_-7+21608d others(7): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452770
|
CAAAAAA | C | 11 | a0001c0001t0002g0200a0001c0001t0002g0284a0001c0001t0003g0201others(8): Show | 11 | HG01167.hp1 HG01884.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7+21603_-7+21608d others(8): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452770 | ||||||
| chr4:184452798
|
G | A | 137 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(134): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-7+21581C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452798 | ||||||
| chr4:184452817
|
TAGAG | T | 46 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0287others(43): Show | 46 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-7+21558_-7+21561d others(6): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452817 | ||||||
| chr4:184452892
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-7+21487T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184452892 | ||||||
| chr4:184453242
|
A | C | 3 | a0001c0002t0001g0177a0001c0002t0001g0180a0001c0002t0011g0181 | 3 | HG02895.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-7+21137T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184453242 | ||||||
| chr4:184453331
|
C | T | 7 | a0001c0001t0002g0294a0001c0001t0002g0295a0001c0001t0002g0298others(4): Show | 7 | HG00609.hp2 NA18946.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+21048G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184453331 | ||||||
| chr4:184453450
|
C | T | 366 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(363): Show | 374 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.-7+20929G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184453450 | ||||||
| chr4:184453673
|
T | C | 1 | a0001c0001t0002g0010 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-7+20706A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184453673 | ||||||
| chr4:184453751
|
C | T | 123 | a0001c0001t0001g0079a0001c0001t0001g0291a0001c0001t0002g0002others(120): Show | 126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-7+20628G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184453751 | ||||||
| chr4:184453941
|
T | C | 3 | a0001c0002t0001g0177a0001c0002t0001g0180a0001c0002t0011g0181 | 3 | HG02895.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-7+20438A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184453941 | ||||||
| chr4:184454049
|
A | G | 1 | a0001c0002t0001g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-7+20330T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454049 | ||||||
| chr4:184454124
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7+20255G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454124 | ||||||
| chr4:184454137
|
G | A | 220 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0189others(217): Show | 225 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.-7+20242C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454137 | ||||||
| chr4:184454142
|
T | A | 93 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(90): Show | 94 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-7+20237A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454142 | ||||||
| chr4:184454215
|
G | A | 93 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(90): Show | 94 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-7+20164C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454215 | ||||||
| chr4:184454314
|
T | G | 2 | a0001c0001t0003g0276a0001c0002t0001g0277 | 2 | NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-7+20065A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454314 | ||||||
| chr4:184454336
|
G | C | 1 | a0001c0001t0003g0253 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-7+20043C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454336 | ||||||
| chr4:184454426
|
T | A | 10 | a0001c0001t0001g0248a0001c0001t0002g0284a0001c0001t0004g0186others(7): Show | 10 | HG01884.hp1 HG02717.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+19953A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454426 | ||||||
| chr4:184454495
|
T | G | 10 | a0001c0001t0001g0248a0001c0001t0002g0284a0001c0001t0004g0186others(7): Show | 10 | HG01884.hp1 HG02717.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+19884A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454495 | ||||||
| chr4:184454723
|
G | A | 123 | a0001c0001t0001g0079a0001c0001t0001g0291a0001c0001t0002g0002others(120): Show | 126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-7+19656C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454723 | ||||||
| chr4:184454784
|
T | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0189others(140): Show | 148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-7+19595A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454784 | ||||||
| chr4:184454912
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0003g0178a0001c0003t0008g0184 | 4 | HG02809.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+19467G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454912 | ||||||
| chr4:184454938
|
C | A | 2 | a0001c0001t0002g0004a0001c0003t0008g0184 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-7+19441G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454938 | ||||||
| chr4:184455067
|
A | C | 1 | a0001c0001t0003g0102 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-7+19312T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455067 | ||||||
| chr4:184455116
|
T | A | 1 | a0001c0002t0001g0277 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-7+19263A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455116 | ||||||
| chr4:184455249
|
C | CCCCTCCC others(5): Show |
2 | a0001c0002t0001g0170a0001c0002t0009g0009 | 2 | HG03710.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-7+19129_-7+19130i others(14): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455249 | ||||||
| chr4:184455249
|
C | CCCCTCCC others(4): Show |
321 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(318): Show | 328 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.-7+19119_-7+19129d others(13): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455249 | ||||||
| chr4:184455249
|
C | CCCCTCCC others(25): Show |
1 | a0001c0002t0001g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-7+19129_-7+19130i others(34): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455249 | ||||||
| chr4:184455253
|
T | TCCCCCTT others(5): Show |
1 | a0001c0002t0005g0016 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-7+19114_-7+19125d others(14): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455253 | ||||||
| chr4:184455258
|
C | CTTCCCTC others(4): Show |
1 | a0001c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-7+19120_-7+19121i others(13): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455258 | ||||||
| chr4:184455301
|
C | CT | 104 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0307others(101): Show | 106 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-7+19077dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455301 | ||||||
| chr4:184455301
|
C | CTT | 8 | a0001c0001t0002g0035a0001c0001t0002g0173a0001c0001t0002g0175others(5): Show | 8 | HG03540.hp2 HG03654.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+19076_-7+19077d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455301 | ||||||
| chr4:184455301
|
CT | C | 155 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0183others(152): Show | 160 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.-7+19077delA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455301 | ||||||
| chr4:184455334
|
G | T | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7+19045C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455334 | ||||||
| chr4:184455435
|
G | A | 1 | a0001c0002t0001g0238 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-7+18944C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455435 | ||||||
| chr4:184455573
|
C | T | 39 | a0001c0001t0001g0183a0001c0001t0001g0233a0001c0001t0001g0243others(36): Show | 39 | HG00733.hp2 HG01070.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.-7+18806G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455573 | ||||||
| chr4:184455574
|
A | T | 1 | a0001c0001t0003g0072 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-7+18805T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455574 | ||||||
| chr4:184455620
|
T | A | 2 | a0001c0001t0002g0173a0001c0001t0002g0175 | 2 | HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+18759A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455620 | ||||||
| chr4:184455666
|
C | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+18713G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455666 | ||||||
| chr4:184455722
|
A | G | 3 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+18657T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455722 | ||||||
| chr4:184455731
|
A | G | 4 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0002g0190others(1): Show | 4 | HG02109.hp2 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+18648T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455731 | ||||||
| chr4:184455732
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-7+18647T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455732 | ||||||
| chr4:184455886
|
G | C | 1 | a0001c0001t0003g0350 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-7+18493C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455886 | ||||||
| chr4:184456068
|
G | C | 311 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(308): Show | 317 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.-7+18311C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456068 | ||||||
| chr4:184456072
|
T | C | 5 | a0001c0002t0001g0177a0001c0002t0001g0180a0001c0002t0001g0238others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+18307A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456072 | ||||||
| chr4:184456084
|
C | T | 1 | a0001c0001t0006g0368 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7+18295G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456084 | ||||||
| chr4:184456110
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-7+18269T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456110 | ||||||
| chr4:184456242
|
T | C | 1 | a0001c0002t0001g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7+18137A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456242 | ||||||
| chr4:184456265
|
T | C | 1 | a0001c0002t0001g0327 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-7+18114A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456265 | ||||||
| chr4:184456337
|
A | G | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.-7+18042T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456337 | ||||||
| chr4:184456542
|
A | G | 6 | a0001c0001t0001g0335a0001c0001t0002g0330a0001c0002t0001g0333others(3): Show | 6 | HG02145.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+17837T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456542 | ||||||
| chr4:184456581
|
C | A | 3 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+17798G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456581 | ||||||
| chr4:184456635
|
C | T | 4 | a0001c0002t0001g0177a0001c0002t0001g0180a0001c0002t0011g0181others(1): Show | 4 | HG01081.hp2 HG02895.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+17744G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456635 | ||||||
| chr4:184456682
|
GTCCTGCA others(8): Show |
G | 3 | a0001c0001t0007g0364a0001c0002t0001g0303a0001c0003t0004g0193 | 3 | HG02258.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-7+17682_-7+17696d others(17): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456682 | ||||||
| chr4:184456732
|
A | G | 1 | a0001c0001t0002g0035 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-7+17647T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456732 | ||||||
| chr4:184456756
|
G | T | 1 | a0001c0001t0002g0128 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-7+17623C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456756 | ||||||
| chr4:184456769
|
G | A | 4 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0003g0225others(1): Show | 4 | HG00280.hp1 HG03540.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+17610C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184456769 | ||||||
| chr4:184457006
|
A | C | 227 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0192others(224): Show | 230 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.-7+17373T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457006 | ||||||
| chr4:184457069
|
T | G | 231 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0192others(228): Show | 234 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.-7+17310A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457069 | ||||||
| chr4:184457115
|
C | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+17264G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457115 | ||||||
| chr4:184457129
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-7+17250G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457129 | ||||||
| chr4:184457209
|
A | G | 104 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0251others(101): Show | 105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-7+17170T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457209 | ||||||
| chr4:184457361
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0003g0015 | 2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-7+17018C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457361 | ||||||
| chr4:184457501
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0307a0001c0001t0002g0190 | 3 | HG02109.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-7+16878G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457501 | ||||||
| chr4:184457666
|
G | A | 4 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197others(1): Show | 4 | HG03540.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+16713C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457666 | ||||||
| chr4:184457726
|
C | A | 116 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(113): Show | 118 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.-7+16653G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457726 | ||||||
| chr4:184457727
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-7+16652C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457727 | ||||||
| chr4:184457847
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7+16532A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457847 | ||||||
| chr4:184457849
|
C | CA | 110 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(107): Show | 112 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.-7+16529dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457849 | ||||||
| chr4:184457849
|
C | CAA | 6 | a0001c0001t0001g0189a0001c0001t0001g0307a0001c0001t0002g0114others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+16528_-7+16529d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457849 | ||||||
| chr4:184457849
|
CA | C | 7 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0001t0003g0199others(4): Show | 7 | HG02809.hp2 HG02922.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+16529delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457849 | ||||||
| chr4:184457902
|
T | G | 3 | a0001c0001t0001g0189a0001c0001t0001g0307a0001c0001t0002g0190 | 3 | HG02109.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-7+16477A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457902 | ||||||
| chr4:184457921
|
C | T | 1 | a0001c0002t0005g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-7+16458G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457921 | ||||||
| chr4:184458348
|
A | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0307a0001c0001t0002g0190 | 3 | HG02109.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-7+16031T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184458348 | ||||||
| chr4:184458730
|
G | C | 9 | a0001c0001t0001g0183a0001c0001t0002g0004a0001c0001t0002g0179others(6): Show | 10 | HG01081.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+15649C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184458730 | ||||||
| chr4:184458763
|
C | G | 167 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0001g0192others(164): Show | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-7+15616G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184458763 | ||||||
| chr4:184458784
|
C | G | 4 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0001t0003g0199others(1): Show | 4 | HG02922.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+15595G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184458784 | ||||||
| chr4:184458964
|
AAT | A | 5 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0001t0003g0199others(2): Show | 5 | HG02922.hp2 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+15413_-7+15414d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184458964 | ||||||
| chr4:184459126
|
A | G | 117 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(114): Show | 119 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.-7+15253T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459126 | ||||||
| chr4:184459288
|
A | C | 1 | a0001c0002t0001g0353 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-7+15091T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459288 | ||||||
| chr4:184459289
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0002g0190 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-7+15090T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459289 | ||||||
| chr4:184459301
|
C | T | 1 | a0001c0001t0012g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7+15078G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459301 | ||||||
| chr4:184459407
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-7+14972C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459407 | ||||||
| chr4:184459542
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0003g0209 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-7+14837T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459542 | ||||||
| chr4:184459582
|
T | C | 4 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0001t0003g0199others(1): Show | 4 | HG02922.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+14797A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459582 | ||||||
| chr4:184459596
|
G | C | 1 | a0001c0001t0002g0283 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-7+14783C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459596 | ||||||
| chr4:184459901
|
T | C | 43 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(40): Show | 43 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-7+14478A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459901 | ||||||
| chr4:184459978
|
G | A | 15 | a0001c0001t0003g0167a0001c0001t0004g0150a0001c0002t0001g0125others(12): Show | 15 | HG00280.hp2 HG00639.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7+14401C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459978 | ||||||
| chr4:184459991
|
A | G | 4 | a0001c0001t0007g0364a0001c0002t0006g0365a0001c0002t0006g0366others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+14388T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184459991 | ||||||
| chr4:184460030
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0002g0206a0001c0001t0002g0207 | 3 | HG00733.hp2 HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-7+14349G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460030 | ||||||
| chr4:184460279
|
C | A | 14 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7+14100G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460279 | ||||||
| chr4:184460323
|
G | C | 47 | a0001c0001t0001g0192a0001c0001t0001g0251a0001c0001t0002g0010others(44): Show | 47 | HG00423.hp2 HG00558.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.-7+14056C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460323 | ||||||
| chr4:184460362
|
C | G | 1 | a0001c0003t0004g0256 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-7+14017G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460362 | ||||||
| chr4:184460429
|
C | T | 158 | a0001c0001t0001g0143a0001c0001t0001g0192a0001c0001t0001g0211others(155): Show | 159 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.-7+13950G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460429 | ||||||
| chr4:184460434
|
C | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0324a0001c0001t0001g0335others(63): Show | 70 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-7+13945G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460434 | ||||||
| chr4:184460620
|
AACACACA others(17): Show |
A | 1 | a0001c0002t0001g0162 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-7+13735_-7+13758d others(26): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460620 | ||||||
| chr4:184460641
|
G | GCA | 11 | a0001c0001t0001g0183a0001c0001t0002g0004a0001c0001t0002g0298others(8): Show | 12 | HG00609.hp2 HG02630.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7+13736_-7+13737d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460641 | ||||||
| chr4:184460641
|
GCA | G | 9 | a0001c0001t0001g0307a0001c0001t0002g0195a0001c0001t0003g0026others(6): Show | 9 | HG01099.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+13736_-7+13737d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460641 | ||||||
| chr4:184460643
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0002t0001g0174 | 3 | HG00280.hp1 HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+13736T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460643 | ||||||
| chr4:184460649
|
ACACACAC others(3): Show |
A | 1 | a0001c0001t0002g0293 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-7+13720_-7+13729d others(12): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460649 | ||||||
| chr4:184460655
|
A | G | 44 | a0001c0001t0001g0189a0001c0001t0001g0211a0001c0001t0001g0215others(41): Show | 44 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7+13724T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460655 | ||||||
| chr4:184460658
|
TGCAC | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0324a0001c0001t0001g0335others(62): Show | 69 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-7+13717_-7+13720d others(6): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460658 | ||||||
| chr4:184460662
|
C | T | 1 | a0001c0001t0002g0293 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-7+13717G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460662 | ||||||
| chr4:184460665
|
G | GCA | 3 | a0001c0001t0002g0171a0001c0001t0003g0232a0001c0002t0005g0166 | 3 | HG03688.hp1 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-7+13712_-7+13713d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460665 | ||||||
| chr4:184460666
|
C | T | 118 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(115): Show | 120 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.-7+13713G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460666 | ||||||
| chr4:184460667
|
A | G | 119 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0002g0002others(116): Show | 121 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.-7+13712T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460667 | ||||||
| chr4:184460681
|
G | GCA | 158 | a0001c0001t0001g0079a0001c0001t0001g0189a0001c0001t0001g0211others(155): Show | 160 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.-7+13696_-7+13697d others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460681 | ||||||
| chr4:184460681
|
G | GCACA | 3 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+13697_-7+13698i others(6): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460681 | ||||||
| chr4:184460681
|
G | GCACACGC others(15): Show |
1 | a0001c0002t0004g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7+13697_-7+13698i others(24): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460681 | ||||||
| chr4:184460685
|
G | A | 4 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0001t0003g0199others(1): Show | 4 | HG02922.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+13694C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460685 | ||||||
| chr4:184460690
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-7+13689G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460690 | ||||||
| chr4:184460707
|
A | G | 44 | a0001c0001t0001g0189a0001c0001t0001g0211a0001c0001t0001g0215others(41): Show | 44 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7+13672T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460707 | ||||||
| chr4:184460828
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7+13551A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460828 | ||||||
| chr4:184460907
|
C | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0189others(187): Show | 195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.-7+13472G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460907 | ||||||
| chr4:184461078
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-7+13301C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461078 | ||||||
| chr4:184461137
|
T | G | 361 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(358): Show | 369 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-7+13242A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461137 | ||||||
| chr4:184461358
|
C | T | 224 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(221): Show | 229 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-7+13021G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461358 | ||||||
| chr4:184461362
|
G | A | 1 | a0001c0002t0001g0238 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-7+13017C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461362 | ||||||
| chr4:184461452
|
T | G | 1 | a0001c0001t0004g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-7+12927A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461452 | ||||||
| chr4:184461684
|
G | GC | 19 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0002g0004others(16): Show | 20 | HG01081.hp2 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7+12694dupG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461684 | ||||||
| chr4:184461685
|
C | CT | 223 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(220): Show | 228 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-7+12693_-7+12694i others(3): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461685 | ||||||
| chr4:184461756
|
G | A | 1 | a0001c0001t0006g0368 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7+12623C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461756 | ||||||
| chr4:184461762
|
C | T | 2 | a0001c0001t0004g0224a0001c0002t0001g0223 | 2 | HG01106.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-7+12617G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461762 | ||||||
| chr4:184461865
|
T | C | 359 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(356): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.-7+12514A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461865 | ||||||
| chr4:184461984
|
T | C | 1 | a0001c0003t0004g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+12395A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184461984 | ||||||
| chr4:184462303
|
C | T | 224 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(221): Show | 229 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-7+12076G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184462303 | ||||||
| chr4:184462442
|
C | G | 3 | a0001c0001t0001g0005a0001c0001t0003g0304a0001c0002t0001g0306 | 4 | HG00642.hp2 HG00741.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+11937G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184462442 | ||||||
| chr4:184462592
|
T | C | 232 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(229): Show | 237 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-7+11787A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184462592 | ||||||
| chr4:184462673
|
A | G | 8 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0002g0196others(5): Show | 8 | HG00280.hp1 HG02922.hp2 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+11706T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184462673 | ||||||
| chr4:184463033
|
A | G | 5 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0001t0003g0199others(2): Show | 5 | HG02922.hp2 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+11346T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463033 | ||||||
| chr4:184463039
|
T | C | 2 | a0001c0001t0003g0317a0001c0004t0004g0318 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-7+11340A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463039 | ||||||
| chr4:184463316
|
G | C | 117 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(114): Show | 119 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.-7+11063C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463316 | ||||||
| chr4:184463470
|
A | G | 47 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(44): Show | 47 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-7+10909T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463470 | ||||||
| chr4:184463643
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-7+10736G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463643 | ||||||
| chr4:184463658
|
A | T | 64 | a0001c0001t0001g0143a0001c0001t0001g0307a0001c0001t0002g0003others(61): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-7+10721T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463658 | ||||||
| chr4:184463660
|
T | A | 237 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0183others(234): Show | 244 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.-7+10719A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463660 | ||||||
| chr4:184463662
|
T | A | 117 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(114): Show | 119 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.-7+10717A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463662 | ||||||
| chr4:184463707
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0003g0015a0001c0001t0004g0288 | 3 | HG01099.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-7+10672T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463707 | ||||||
| chr4:184463760
|
T | C | 224 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(221): Show | 229 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-7+10619A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463760 | ||||||
| chr4:184464238
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0324a0001c0001t0001g0335others(28): Show | 33 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-7+10141C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464238 | ||||||
| chr4:184464263
|
A | T | 1 | a0001c0001t0006g0368 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7+10116T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464263 | ||||||
| chr4:184464288
|
C | CT | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0002t0001g0174 | 3 | HG00280.hp1 HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+10090dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464288 | ||||||
| chr4:184464320
|
G | A | 16 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7+10059C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464320 | ||||||
| chr4:184464496
|
T | C | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0002t0001g0174 | 3 | HG00280.hp1 HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+9883A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464496 | ||||||
| chr4:184464550
|
T | C | 2 | a0001c0001t0002g0202a0001c0002t0001g0250 | 2 | HG00423.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-7+9829A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464550 | ||||||
| chr4:184464695
|
C | A | 1 | a0001c0002t0001g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7+9684G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464695 | ||||||
| chr4:184464771
|
T | G | 1 | a0001c0001t0004g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-7+9608A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464771 | ||||||
| chr4:184464939
|
T | C | 1 | a0001c0002t0001g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-7+9440A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184464939 | ||||||
| chr4:184465092
|
A | G | 1 | a0001c0002t0001g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7+9287T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465092 | ||||||
| chr4:184465181
|
AC | A | 61 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0128others(58): Show | 62 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-7+9197delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465181 | ||||||
| chr4:184465201
|
G | A | 3 | a0001c0001t0002g0187a0001c0002t0001g0185a0001c0004t0004g0188 | 3 | HG02965.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-7+9178C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465201 | ||||||
| chr4:184465381
|
A | T | 1 | a0001c0002t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-7+8998T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465381 | ||||||
| chr4:184465402
|
T | C | 7 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0002g0330others(4): Show | 7 | HG02145.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+8977A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465402 | ||||||
| chr4:184465489
|
G | GA | 220 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(217): Show | 225 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-7+8889dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465489 | ||||||
| chr4:184465517
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0003g0304a0001c0002t0001g0306 | 4 | HG00642.hp2 HG00741.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+8862G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465517 | ||||||
| chr4:184465757
|
C | T | 1 | a0001c0001t0002g0294 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-7+8622G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184465757 | ||||||
| chr4:184466034
|
T | C | 1 | a0001c0001t0002g0119 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-7+8345A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466034 | ||||||
| chr4:184466060
|
G | GT | 7 | a0001c0001t0001g0287a0001c0001t0002g0010a0001c0001t0003g0015others(4): Show | 7 | HG00642.hp2 HG01070.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+8318dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466060 | ||||||
| chr4:184466060
|
G | GTT | 41 | a0001c0001t0001g0192a0001c0001t0002g0187a0001c0001t0002g0200others(38): Show | 41 | HG00423.hp2 HG00558.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.-7+8317_-7+8318dup others(2): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466060 | ||||||
| chr4:184466060
|
G | GTTT | 5 | a0001c0001t0001g0251a0001c0001t0002g0252a0001c0001t0003g0253others(2): Show | 5 | HG02135.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+8316_-7+8318dup others(3): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466060 | ||||||
| chr4:184466066
|
T | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0217others(1): Show | 4 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+8313A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466066 | ||||||
| chr4:184466067
|
G | T | 228 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0192others(225): Show | 233 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-7+8312C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466067 | ||||||
| chr4:184466067
|
GT | G | 137 | a0001c0001t0001g0079a0001c0001t0001g0183a0001c0001t0001g0189others(134): Show | 140 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.-7+8311delA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466067 | ||||||
| chr4:184466069
|
T | G | 2 | a0001c0001t0001g0189a0001c0001t0002g0190 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-7+8310A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466069 | ||||||
| chr4:184466239
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-7+8140G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466239 | ||||||
| chr4:184466240
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7+8139C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466240 | ||||||
| chr4:184466263
|
C | A | 4 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0237others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+8116G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466263 | ||||||
| chr4:184466340
|
C | T | 3 | a0001c0001t0002g0239a0001c0002t0001g0219a0001c0002t0001g0220 | 3 | HG02040.hp2 HG02165.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-7+8039G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466340 | ||||||
| chr4:184466557
|
T | C | 12 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0002g0004others(9): Show | 13 | HG01081.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+7822A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466557 | ||||||
| chr4:184466665
|
A | C | 1 | a0001c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-7+7714T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466665 | ||||||
| chr4:184466682
|
C | T | 4 | a0001c0001t0003g0022a0001c0001t0003g0024a0001c0002t0001g0021others(1): Show | 4 | HG02074.hp1 NA18951.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+7697G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466682 | ||||||
| chr4:184466700
|
C | G | 2 | a0001c0001t0002g0281a0001c0004t0004g0285 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-7+7679G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466700 | ||||||
| chr4:184466998
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-7+7381C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466998 | ||||||
| chr4:184467117
|
A | T | 1 | a0001c0001t0003g0020 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-7+7262T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467117 | ||||||
| chr4:184467213
|
T | C | 2 | a0001c0001t0002g0217a0001c0002t0001g0218 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-7+7166A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467213 | ||||||
| chr4:184467333
|
G | A | 67 | a0001c0001t0001g0005a0001c0001t0001g0307a0001c0001t0001g0324others(64): Show | 71 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-7+7046C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467333 | ||||||
| chr4:184467343
|
T | C | 3 | a0001c0001t0002g0187a0001c0002t0001g0185a0001c0004t0004g0188 | 3 | HG02965.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-7+7036A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467343 | ||||||
| chr4:184467439
|
G | A | 1 | a0001c0001t0003g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-7+6940C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467439 | ||||||
| chr4:184467442
|
T | G | 1 | a0001c0001t0003g0352 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-7+6937A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467442 | ||||||
| chr4:184467776
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-7+6603C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467776 | ||||||
| chr4:184467881
|
A | G | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0002t0001g0174 | 3 | HG00280.hp1 HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+6498T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184467881 | ||||||
| chr4:184468161
|
T | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0307a0001c0001t0001g0324others(64): Show | 71 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-7+6218A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468161 | ||||||
| chr4:184468184
|
G | T | 13 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0002g0004others(10): Show | 14 | HG01081.hp2 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+6195C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468184 | ||||||
| chr4:184468223
|
C | T | 116 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0019others(113): Show | 118 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.-7+6156G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468223 | ||||||
| chr4:184468253
|
T | C | 185 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0211others(182): Show | 190 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.-7+6126A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468253 | ||||||
| chr4:184468276
|
TCAGGAGT others(7): Show |
T | 44 | a0001c0001t0001g0192a0001c0001t0001g0251a0001c0001t0002g0010others(41): Show | 44 | HG00423.hp2 HG00558.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7+6089_-7+6102del others(14): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468276 | ||||||
| chr4:184468286
|
G | A | 1 | a0001c0002t0001g0238 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-7+6093C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468286 | ||||||
| chr4:184468329
|
A | C | 1 | a0001c0001t0006g0368 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7+6050T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468329 | ||||||
| chr4:184468379
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-7+6000G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468379 | ||||||
| chr4:184468406
|
T | G | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0002t0001g0174 | 3 | HG00280.hp1 HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+5973A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468406 | ||||||
| chr4:184468494
|
G | GA | 168 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0233others(165): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-7+5884dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468494 | ||||||
| chr4:184468691
|
G | C | 1 | a0001c0001t0004g0288 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-7+5688C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468691 | ||||||
| chr4:184468752
|
G | T | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7+5627C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468752 | ||||||
| chr4:184468753
|
G | T | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7+5626C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468753 | ||||||
| chr4:184468922
|
A | T | 132 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0211others(129): Show | 137 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.-7+5457T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184468922 | ||||||
| chr4:184469006
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-7+5373G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469006 | ||||||
| chr4:184469222
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-7+5157G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469222 | ||||||
| chr4:184469246
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-7+5133C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469246 | ||||||
| chr4:184469251
|
C | T | 2 | a0001c0001t0002g0202a0001c0002t0001g0250 | 2 | HG00423.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-7+5128G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469251 | ||||||
| chr4:184469301
|
T | A | 249 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0183others(246): Show | 256 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-7+5078A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469301 | ||||||
| chr4:184469301
|
T | G | 1 | a0001c0001t0003g0352 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-7+5078A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469301 | ||||||
| chr4:184469365
|
G | C | 1 | a0001c0001t0002g0337 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+5014C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469365 | ||||||
| chr4:184469414
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7+4965G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469414 | ||||||
| chr4:184469479
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7+4900G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469479 | ||||||
| chr4:184469497
|
C | T | 1 | a0001c0001t0003g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-7+4882G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469497 | ||||||
| chr4:184469796
|
A | G | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-7+4583T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469796 | ||||||
| chr4:184469932
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7+4447A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184469932 | ||||||
| chr4:184470037
|
C | T | 4 | a0001c0001t0002g0187a0001c0001t0004g0186a0001c0002t0001g0185others(1): Show | 4 | HG02965.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+4342G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470037 | ||||||
| chr4:184470067
|
G | C | 46 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(43): Show | 46 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.-7+4312C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470067 | ||||||
| chr4:184470131
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7+4248C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470131 | ||||||
| chr4:184470189
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-7+4190C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470189 | ||||||
| chr4:184470254
|
G | A | 61 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0128others(58): Show | 62 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-7+4125C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470254 | ||||||
| chr4:184470275
|
A | G | 4 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0237others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+4104T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470275 | ||||||
| chr4:184470423
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-7+3956C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470423 | ||||||
| chr4:184470478
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0002g0206a0001c0001t0002g0207 | 3 | HG00733.hp2 HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-7+3901G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470478 | ||||||
| chr4:184470554
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-7+3825C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470554 | ||||||
| chr4:184470599
|
A | G | 63 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0128others(60): Show | 64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-7+3780T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470599 | ||||||
| chr4:184470601
|
G | T | 1 | a0001c0002t0001g0018 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7+3778C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470601 | ||||||
| chr4:184470606
|
G | T | 63 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0128others(60): Show | 64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-7+3773C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470606 | ||||||
| chr4:184470689
|
C | CA | 7 | a0001c0001t0007g0362a0001c0001t0007g0363a0001c0001t0007g0364others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+3689dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470689 | ||||||
| chr4:184470701
|
AAAAG | A | 8 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0002g0187others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+3674_-7+3677del others(4): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470701 | ||||||
| chr4:184470702
|
AAAG | A | 12 | a0001c0001t0001g0287a0001c0001t0002g0196a0001c0001t0002g0198others(9): Show | 12 | HG01099.hp2 HG02922.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+3674_-7+3676del others(3): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470702 | ||||||
| chr4:184470703
|
AAG | A | 302 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0143others(299): Show | 309 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.-7+3674_-7+3675del others(2): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470703 | ||||||
| chr4:184470704
|
AG | A | 34 | a0001c0001t0001g0233a0001c0001t0001g0248a0001c0001t0002g0008others(31): Show | 35 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-7+3674delC | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470704 | ||||||
| chr4:184470714
|
A | G | 64 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0010others(61): Show | 65 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-7+3665T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470714 | ||||||
| chr4:184470756
|
C | T | 1 | a0001c0002t0005g0355 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-7+3623G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470756 | ||||||
| chr4:184470789
|
C | T | 1 | a0001c0002t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-7+3590G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470789 | ||||||
| chr4:184470996
|
A | AAC | 76 | a0001c0001t0001g0143a0001c0001t0001g0183a0001c0001t0002g0003others(73): Show | 78 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.-7+3382_-7+3383ins others(2): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184470996 | ||||||
| chr4:184471246
|
G | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0307a0001c0001t0001g0324others(65): Show | 72 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-7+3133C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471246 | ||||||
| chr4:184471292
|
T | C | 1 | a0001c0001t0003g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7+3087A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471292 | ||||||
| chr4:184471365
|
C | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0002t0001g0197 | 3 | HG03540.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+3014G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471365 | ||||||
| chr4:184471528
|
T | C | 4 | a0001c0001t0002g0196a0001c0001t0002g0198a0001c0001t0003g0199others(1): Show | 4 | HG02922.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+2851A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471528 | ||||||
| chr4:184471593
|
G | C | 63 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0128others(60): Show | 64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-7+2786C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471593 | ||||||
| chr4:184471624
|
G | A | 1 | a0001c0002t0001g0168 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-7+2755C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471624 | ||||||
| chr4:184471726
|
T | A | 64 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0010others(61): Show | 65 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-7+2653A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471726 | ||||||
| chr4:184471800
|
T | C | 64 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0010others(61): Show | 65 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-7+2579A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184471800 | ||||||
| chr4:184472141
|
T | C | 40 | a0001c0001t0001g0251a0001c0001t0002g0010a0001c0001t0002g0202others(37): Show | 40 | HG00423.hp2 HG00558.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.-7+2238A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472141 | ||||||
| chr4:184472254
|
A | G | 1 | a0001c0002t0001g0177 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-7+2125T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472254 | ||||||
| chr4:184472352
|
G | A | 1 | a0001c0001t0003g0352 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-7+2027C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472352 | ||||||
| chr4:184472467
|
C | G | 67 | a0001c0001t0001g0005a0001c0001t0001g0307a0001c0001t0001g0324others(64): Show | 71 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-7+1912G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472467 | ||||||
| chr4:184472474
|
G | C | 1 | a0001c0002t0001g0238 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-7+1905C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472474 | ||||||
| chr4:184472571
|
G | C | 1 | a0001c0001t0002g0239 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-7+1808C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472571 | ||||||
| chr4:184472653
|
A | C | 3 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0002t0001g0174 | 3 | HG00280.hp1 HG03540.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+1726T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472653 | ||||||
| chr4:184472855
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-7+1524C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472855 | ||||||
| chr4:184472872
|
C | T | 58 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0128others(55): Show | 59 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+1507G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184472872 | ||||||
| chr4:184473134
|
A | C | 1 | a0001c0001t0002g0293 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-7+1245T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473134 | ||||||
| chr4:184473170
|
A | C | 1 | a0001c0001t0003g0011 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-7+1209T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473170 | ||||||
| chr4:184473216
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-7+1163C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473216 | ||||||
| chr4:184473233
|
C | A | 1 | a0001c0002t0001g0124 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-7+1146G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473233 | ||||||
| chr4:184473344
|
G | A | 1 | a0001c0002t0005g0355 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-7+1035C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473344 | ||||||
| chr4:184473347
|
G | C | 37 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(34): Show | 37 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7+1032C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473347 | ||||||
| chr4:184473707
|
C | G | 1 | a0001c0002t0001g0292 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-7+672G>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473707 | ||||||
| chr4:184473775
|
T | TCC | 46 | a0001c0001t0001g0243a0001c0001t0001g0248a0001c0001t0001g0251others(43): Show | 46 | HG00423.hp2 HG00558.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.-7+602_-7+603dupGG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473775 | ||||||
| chr4:184473858
|
C | T | 50 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0128others(47): Show | 51 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-7+521G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473858 | ||||||
| chr4:184473867
|
C | A | 1 | a0001c0001t0003g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-7+512G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473867 | ||||||
| chr4:184473956
|
G | T | 118 | a0001c0001t0001g0079a0001c0001t0002g0002a0001c0001t0002g0013others(115): Show | 120 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.-7+423C>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184473956 | ||||||
| chr4:184474079
|
AACCTCCT others(17): Show |
A | 1 | a0001c0002t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-7+276_-7+299delAG others(22): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184474079 | ||||||
| chr4:184474080
|
ACCT | A | 3 | a0001c0001t0001g0287a0001c0001t0004g0288a0001c0002t0001g0289 | 3 | HG01099.hp2 HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-7+296_-7+298delAG others(1): Show |
IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184474080 | ||||||
| chr4:184474169
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7+210G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184474169 | ||||||
| chr4:184474182
|
A | C | 1 | a0001c0001t0002g0010 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-7+197T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184474182 | ||||||
| chr4:184474231
|
T | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0307a0001c0001t0001g0324others(70): Show | 77 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-7+148A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184474231 | ||||||
| chr4:184474258
|
G | A | 5 | a0001c0001t0002g0356a0001c0001t0002g0358a0001c0001t0002g0360others(2): Show | 5 | NA18955.hp1 NA18960.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+121C>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184474258 |