Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MPVER others(344): Show |
chr4 | 184382729 | 184479550 |
| a0002 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | MPVER others(344): Show |
chr4 | 184382729 | 184479550 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1047 | 219 | 49 | 38 | 104 | 7 | 19 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0002 | 0/0 | 1047 | 137 | 29 | 35 | 47 | 7 | 19 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0003 | 0/0 | 1047 | 7 | 5 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0004 | 0/0 | 1047 | 6 | 6 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0005 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0006 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0007 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0009 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0010 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0001c0011 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
chr4 | 184382729 | 184479550 | ||
| a0002c0008 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | ATGCC others(1042): Show |
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 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0002 | 0/0 | 2251 | 100 | 20 | 13 | 55 | 3 | 9 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2246): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0003 | 0/0 | 2253 | 78 | 8 | 17 | 46 | 3 | 4 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2248): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0004 | 0/1 | 2257 | 13 | 2 | 7 | 0 | 1 | 2 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2252): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0006 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0007 | 0/0 | 2251 | 3 | 3 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2246): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0010 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2248): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0012 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2232): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0013 | 0/0 | 2251 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2246): Show |
chr4 | 184382729 | 184479550 |
| a0001c0001t0014 | 1/0 | 2257 | 1 | 0 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2252): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0001 | 0/0 | 2252 | 112 | 23 | 29 | 37 | 6 | 17 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0002 | 0/0 | 2251 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2246): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0003 | 0/0 | 2253 | 2 | 0 | 1 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2248): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0004 | 0/0 | 2257 | 4 | 1 | 2 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2252): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0005 | 0/0 | 2242 | 13 | 0 | 3 | 9 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2237): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0006 | 0/0 | 2252 | 3 | 3 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0009 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0002t0011 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2232): Show |
chr4 | 184382729 | 184479550 |
| a0001c0003t0004 | 0/0 | 2257 | 5 | 3 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2252): Show |
chr4 | 184382729 | 184479550 |
| a0001c0003t0008 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2251): Show |
chr4 | 184382729 | 184479550 |
| a0001c0004t0004 | 0/0 | 2257 | 6 | 6 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2252): Show |
chr4 | 184382729 | 184479550 |
| a0001c0005t0001 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0006t0005 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2237): Show |
chr4 | 184382729 | 184479550 |
| a0001c0007t0001 | 0/0 | 2252 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0009t0001 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0001c0010t0003 | 0/0 | 2253 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2248): Show |
chr4 | 184382729 | 184479550 |
| a0001c0011t0001 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2247): Show |
chr4 | 184382729 | 184479550 |
| a0002c0008t0002 | 0/0 | 2251 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | CTCTC others(2246): Show |
chr4 | 184382729 | 184479550 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 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 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0246 | 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 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0006 | 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 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0097 | 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 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0103 | 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 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0130 | 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 |
| a0001c0001t0002g0133 | 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 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0173 | 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 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0245 | 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 |
| a0001c0001t0002g0262 | 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 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0277 | 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 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0002g0354 | 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 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0028 | 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 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0067 | 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 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0132 | 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 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0261 | 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 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0307 | 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 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0004g0206 | 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 |
| a0001c0001t0004g0236 | 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 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0006g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0007g0361 | 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 |
| a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0001t0014g0359 | 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 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0040 | 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 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0105 | 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 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0129 | 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 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0157 | 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 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0228 | 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 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0001g0355 | 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 |
| a0001c0002t0002g0346 | 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 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0124 | 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 |
| a0001c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0006g0364 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0002t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0004g0247 | 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 |
| a0001c0003t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0003t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0192 | 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 |
| a0001c0004t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0004t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0005t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0006t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0009t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0010t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0001c0011t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| a0002c0008t0002g0091 | 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 | g0172 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0123 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0050 | EUR | FIN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0121 | 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 | g0311 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0131 | 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 | g0015 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0108 | 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 | g0054 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0334 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0056 | 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 | g0302 | 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 | g0058 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0235 | 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 | g0152 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01081 | hp2 | a0001 | c0003 | t0004 | g0242 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0338 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01192 | hp2 | a0001 | c0007 | t0001 | g0158 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0111 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0322 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0159 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0118 | 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 | g0010 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0349 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0027 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0032 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0232 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0233 | EUR | IBS | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0038 | 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 | g0366 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0041 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0039 | 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 | g0312 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0350 | 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 | g0321 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01981 | hp2 | a0001 | c0002 | t0005 | g0308 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02004 | hp2 | a0001 | c0002 | t0005 | g0025 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02040 | hp1 | a0001 | c0010 | t0003 | g0049 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02074 | hp2 | a0001 | c0002 | t0005 | g0353 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0319 | 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 | g0345 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02145 | hp2 | a0001 | c0004 | t0004 | g0282 | 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 | g0340 | EAS | CDX | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | CDX | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | CDX | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0363 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02258 | hp2 | a0001 | c0004 | t0004 | g0343 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0243 | 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 | g0089 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | PEL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0193 | 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 | g0331 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0284 | 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 | g0119 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02615 | hp1 | a0001 | c0004 | t0004 | g0326 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0215 | 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 | g0018 | 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 | g0116 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02809 | hp1 | a0001 | c0003 | t0008 | g0182 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02818 | hp1 | a0001 | c0002 | t0006 | g0364 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0346 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0191 | 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 | g0327 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0201 | 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 | g0192 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03098 | hp1 | a0001 | c0002 | t0011 | g0178 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03130 | hp2 | a0001 | c0004 | t0004 | g0342 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0247 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0183 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03209 | hp2 | a0001 | c0003 | t0008 | g0325 | 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 | g0348 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0082 | 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 | g0362 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0323 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0180 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0360 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | 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 | g0007 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | ESN | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0361 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0288 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0169 | 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 | g0167 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0336 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03927 | hp1 | a0001 | c0001 | t0010 | g0094 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0335 | SAS | BEB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0125 | 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 | g0337 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | STU | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0113 | 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 | g0195 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | CHB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | CHB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | YRI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18941 | hp2 | a0001 | c0001 | t0013 | g0072 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0002 | 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 | g0110 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18949 | hp2 | a0001 | c0002 | t0009 | g0011 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0066 | 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 | g0036 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0356 | 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 | g0291 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18965 | hp2 | a0001 | c0002 | t0005 | g0043 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18969 | hp1 | a0001 | c0009 | t0001 | g0014 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0220 | 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 | g0004 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18974 | hp1 | a0001 | c0002 | t0005 | g0106 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18979 | hp1 | a0001 | c0002 | t0005 | g0104 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18983 | hp2 | a0002 | c0008 | t0002 | g0091 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0114 | 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 | g0262 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18991 | hp2 | a0001 | c0002 | t0005 | g0328 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0044 | 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 | g0102 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0270 | 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 | g0045 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0004 | 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 | g0057 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0216 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0358 | 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 | g0355 | 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 | g0042 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19063 | hp1 | a0001 | c0006 | t0005 | g0029 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0304 | 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 | g0081 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0318 | 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 | g0034 | 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 | g0083 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0122 | 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 | g0028 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0306 | 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 | g0280 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0344 | AFR | ASW | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | ASW | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | TSI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0173 | 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 | g0024 | EUR | TSI | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0124 | SAS | GIH | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0287 | SAS | GIH | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0351 | AMR | CLM | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0059 | 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 | g0194 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0303 | 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 | g0189 | AFR | MSL | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA18955 | hp2 | a0001 | c0002 | t0005 | g0274 | EAS | JPT | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0317 | AFR | USA | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0299 | AFR | LWK | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0120 | REF | REF | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0359 | REF | REF | IRF2_chr4_184382729_184479550 | IRF2 | chr4 | 184382729 | 184479550 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0002 a0001c0006 a0001c0007 others(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 | a0001c0009 a0001c0010 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184387821 | T | TA | 4 | a0001c0001t0003 a0001c0001t0010 a0001c0002t0003 others(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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(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 | a0001c0002t0005 a0001c0006t0005 |
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 | a0001c0001t0012 a0001c0002t0011 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
5_prime_UTR_variant | MODIFIER | c.-69T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/9 | 45377 | chr4 | 184474441 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184389340 | C | T | 1 | a0001c0001t0003g0327 | 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 | a0001c0002t0001g0225 | 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 | a0001c0001t0002g0240 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0006g0360 others(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 | a0001c0001t0003g0215 | 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 | a0001c0001t0002g0054 a0001c0001t0002g0063 |
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 | a0001c0001t0001g0181 a0001c0001t0001g0217 a0001c0001t0001g0246 others(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 | 161 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0303 others(158): 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 | a0001c0002t0001g0155 | 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 | a0001c0001t0002g0199 | 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 | a0001c0002t0001g0299 | 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 | a0001c0001t0002g0201 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0024 a0001c0001t0003g0084 others(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 | a0001c0001t0003g0232 a0001c0001t0003g0233 |
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 | a0001c0002t0001g0177 | 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 | 268 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(265): Show |
276 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(273): 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0289 a0001c0001t0002g0099 a0001c0002t0001g0003 others(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 | a0001c0001t0001g0289 a0001c0001t0002g0099 a0001c0002t0001g0003 others(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 | a0001c0002t0001g0185 a0001c0002t0001g0218 a0001c0002t0001g0248 others(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 | a0001c0001t0002g0329 | 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 | a0001c0002t0001g0100 a0001c0002t0001g0109 a0001c0002t0001g0204 |
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 | a0001c0001t0001g0181 | 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 | a0001c0002t0001g0020 a0001c0002t0001g0027 a0001c0002t0001g0100 others(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 | a0001c0001t0002g0099 a0001c0002t0001g0003 a0001c0002t0001g0010 others(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 | a0001c0001t0001g0289 | 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 | a0002c0008t0002g0091 | 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 | a0001c0005t0001g0180 | 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 | 108 | a0001c0001t0001g0184 a0001c0001t0001g0193 a0001c0001t0001g0194 others(105): 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 | a0001c0002t0001g0089 | 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 | a0001c0002t0001g0134 a0001c0002t0001g0290 a0001c0009t0001g0014 others(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 | 207 | a0001c0001t0001g0007 a0001c0001t0001g0181 a0001c0001t0001g0184 others(204): Show |
212 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(209): 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 | a0001c0002t0001g0189 | 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 | a0001c0002t0001g0020 a0001c0002t0001g0027 a0001c0002t0001g0100 others(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 | 100 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0193 others(97): 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 | a0001c0002t0001g0100 a0001c0002t0001g0109 a0001c0002t0001g0204 |
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 | 344 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(341): Show |
354 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(351): 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 | a0001c0002t0001g0235 | 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 | a0001c0003t0008g0325 | 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 | a0001c0002t0001g0198 a0001c0002t0001g0299 a0001c0002t0006g0365 |
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 | 12 | a0001c0001t0001g0007 a0001c0001t0001g0333 a0001c0001t0004g0039 others(9): Show |
13 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(10): 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 | a0001c0001t0002g0293 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0080 others(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 | a0001c0002t0001g0269 | 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 | a0001c0002t0001g0189 | 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 | a0001c0002t0005g0308 | 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 | a0001c0002t0001g0032 a0001c0002t0001g0038 a0001c0002t0001g0040 others(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 | a0001c0001t0002g0345 | 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 | 119 | a0001c0001t0001g0007 a0001c0001t0001g0181 a0001c0001t0001g0193 others(116): Show |
122 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(119): 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 | a0001c0002t0001g0157 a0001c0002t0001g0174 a0001c0002t0003g0139 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0303 others(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 | a0001c0001t0003g0024 a0001c0001t0003g0300 |
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 | a0001c0001t0002g0306 | 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 | a0001c0001t0002g0345 | 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 | a0001c0002t0001g0284 | 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 | a0001c0001t0002g0277 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0194 | 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 | a0001c0002t0005g0043 | 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 | a0001c0001t0002g0006 a0001c0002t0001g0196 a0001c0002t0001g0198 others(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 | a0001c0002t0001g0284 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0303 a0001c0001t0002g0004 others(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 | 10 | a0001c0001t0001g0007 a0001c0001t0003g0300 a0001c0001t0004g0039 others(7): Show |
11 | HG00642.hp2 HG01099.hp2 HG01106.hp1 others(8): 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 | a0001c0001t0004g0205 a0001c0001t0004g0206 |
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 | a0001c0002t0001g0255 a0001c0002t0001g0323 |
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 | a0001c0002t0001g0119 | 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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0002g0057 others(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 | a0001c0002t0001g0218 a0001c0002t0001g0248 a0001c0002t0001g0255 others(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 | a0001c0001t0001g0289 | 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 | a0001c0002t0001g0101 | 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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0012g0216 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0181 a0001c0001t0001g0303 others(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 | a0001c0002t0001g0164 | 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0244 others(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 | a0001c0002t0001g0116 | 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 | a0001c0001t0003g0056 a0001c0001t0003g0118 |
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 | a0001c0002t0001g0010 a0001c0002t0001g0229 |
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 | a0001c0002t0001g0177 | 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 | 50 | a0001c0001t0001g0007 a0001c0001t0001g0217 a0001c0001t0001g0303 others(47): Show |
53 | HG00323.hp1 HG01070.hp2 HG01099.hp2 others(50): 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 | 206 | a0001c0001t0001g0079 a0001c0001t0001g0181 a0001c0001t0001g0289 others(203): 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 | a0001c0001t0001g0143 a0001c0001t0001g0184 a0001c0001t0001g0209 others(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 | a0001c0001t0002g0315 a0001c0001t0003g0132 a0001c0001t0007g0361 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0244 others(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 | a0001c0002t0001g0177 | 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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0002g0057 others(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 | 33 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0002g0208 others(30): 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 | 344 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(341): Show |
354 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(351): 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 | a0001c0001t0003g0019 a0001c0001t0003g0093 a0001c0001t0003g0148 |
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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0054 others(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 | a0001c0002t0001g0284 | 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 | a0001c0001t0002g0006 a0001c0002t0001g0196 a0001c0002t0001g0198 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0345 a0001c0001t0003g0092 others(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 | a0001c0001t0001g0181 a0001c0001t0002g0005 a0001c0001t0002g0026 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0203 a0001c0002t0001g0196 others(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 | a0001c0001t0002g0245 a0001c0001t0003g0066 a0001c0001t0003g0073 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0181 a0001c0001t0001g0303 others(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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0012g0216 others(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 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0063 others(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 | a0001c0004t0004g0192 | 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 | a0001c0001t0002g0006 a0001c0002t0001g0196 a0001c0002t0001g0198 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0283 others(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 | a0001c0002t0001g0038 a0001c0002t0001g0040 |
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 | a0001c0001t0002g0320 | 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 | a0001c0001t0003g0202 a0001c0001t0003g0339 |
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 | a0001c0001t0002g0167 | 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 | a0001c0002t0005g0043 | 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 | a0001c0003t0004g0183 a0001c0003t0004g0242 a0001c0003t0004g0247 others(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 | a0001c0002t0001g0188 | 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 | a0001c0003t0004g0183 a0001c0003t0004g0242 a0001c0003t0004g0247 others(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 | a0001c0002t0001g0299 | 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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): 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 | a0001c0001t0001g0181 a0001c0001t0001g0193 a0001c0001t0001g0217 others(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 | a0001c0002t0005g0034 | 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 | a0001c0002t0001g0284 | 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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): 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 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0061 others(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 | a0001c0001t0001g0194 a0001c0002t0001g0185 |
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 | a0001c0001t0001g0194 a0001c0002t0001g0185 |
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 | a0001c0002t0001g0138 a0001c0002t0001g0168 |
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 | a0001c0001t0001g0181 a0001c0001t0001g0193 a0001c0001t0001g0244 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0071 a0001c0001t0003g0266 |
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 | a0001c0002t0001g0177 | 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 | a0001c0001t0002g0179 a0001c0001t0002g0199 a0001c0001t0002g0223 others(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 | 16 | a0001c0001t0001g0181 a0001c0001t0002g0006 a0001c0001t0004g0039 others(13): Show |
17 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+259dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 7/8 | chr4 | 184398655 | |||||||
| chr4:184398655 | CA | C | 6 | a0001c0003t0004g0183 a0001c0003t0004g0242 a0001c0003t0004g0247 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0333 a0001c0002t0001g0196 others(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 | 284 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0184 others(281): 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 | a0001c0002t0001g0218 a0001c0002t0001g0248 a0001c0002t0001g0344 |
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 | a0001c0001t0002g0163 a0001c0001t0003g0092 a0001c0002t0001g0027 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0002g0208 a0001c0001t0003g0165 |
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 | a0001c0002t0001g0284 | 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 | a0001c0002t0001g0129 | 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 | a0001c0002t0001g0115 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0080 others(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 | 12 | a0001c0001t0001g0007 a0001c0001t0001g0333 a0001c0001t0004g0039 others(9): Show |
13 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(10): 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 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0012g0216 others(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 | a0001c0002t0001g0058 a0001c0002t0001g0089 a0001c0002t0001g0112 others(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 | 94 | a0001c0001t0001g0184 a0001c0001t0001g0193 a0001c0001t0001g0194 others(91): 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 | a0001c0002t0011g0178 | 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 | 139 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0193 others(136): Show |
145 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(142): 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 | a0001c0002t0001g0220 | 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 | a0001c0002t0001g0225 | 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 | 124 | a0001c0001t0001g0184 a0001c0001t0001g0193 a0001c0001t0001g0194 others(121): 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 | a0001c0001t0001g0194 a0001c0002t0001g0185 |
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 | a0001c0001t0002g0358 | 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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0012g0216 others(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 | a0001c0001t0012g0216 | 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 | a0001c0001t0002g0055 a0001c0001t0002g0210 |
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 | 362 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(359): Show |
372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): 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 | a0001c0001t0001g0194 a0001c0001t0002g0191 a0001c0001t0002g0207 others(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 | a0001c0001t0002g0018 | 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0303 | 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 | a0001c0002t0001g0003 a0001c0002t0001g0228 |
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 | a0001c0002t0001g0255 a0001c0002t0001g0323 a0001c0002t0001g0344 |
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 | a0001c0001t0003g0108 | 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 | a0001c0002t0005g0041 | 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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0012g0216 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0303 a0001c0001t0002g0004 others(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 | a0001c0005t0001g0180 | 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 | a0001c0001t0003g0044 | 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 | a0001c0001t0002g0070 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0080 others(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 | a0001c0002t0001g0196 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0003g0118 | 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 | a0001c0002t0001g0226 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0303 a0001c0001t0002g0004 others(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 | a0001c0002t0001g0185 | 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 | a0001c0001t0002g0006 a0001c0002t0001g0196 a0001c0002t0001g0198 others(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 | a0001c0002t0001g0102 | 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 | 215 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(212): 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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0002g0057 others(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 | a0001c0004t0004g0192 a0001c0004t0004g0254 a0001c0004t0004g0282 others(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 | a0001c0001t0012g0216 | 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 | 97 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0002g0035 others(94): 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 | a0001c0001t0001g0217 a0001c0001t0001g0347 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0277 | 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 | a0001c0001t0003g0081 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0289 a0001c0001t0001g0333 others(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 | a0001c0002t0001g0284 | 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 | 106 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0181 others(103): Show |
108 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(105): 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 | a0001c0001t0002g0005 a0001c0001t0002g0018 a0001c0001t0002g0026 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0080 others(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 | a0001c0001t0002g0098 a0001c0001t0002g0320 |
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 | 362 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(359): Show |
372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): 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 | a0001c0002t0001g0125 | 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 | 88 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0001g0217 others(85): 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 | a0001c0005t0001g0180 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0007 | 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 | a0001c0001t0003g0211 | 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 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0003g0017 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0217 a0001c0001t0001g0347 |
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 | 130 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0209 others(127): Show |
137 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(134): Show |
intron_variant | MODIFIER | c.529+2182delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 6/8 | chr4 | 184405975 | |||||||
| chr4:184406043 | A | G | 2 | a0001c0002t0003g0139 a0001c0002t0003g0159 |
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 | a0001c0002t0001g0278 a0001c0002t0006g0366 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0289 a0001c0001t0001g0333 others(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 | a0001c0001t0001g0007 | 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 | a0001c0002t0001g0105 a0001c0002t0001g0357 |
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 | a0001c0002t0005g0025 | 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 | a0001c0001t0001g0194 | 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 | a0001c0002t0001g0185 a0001c0002t0001g0189 a0001c0002t0001g0255 others(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 | a0001c0001t0003g0071 | 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 | a0001c0002t0001g0284 | 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 | a0001c0001t0002g0179 a0001c0001t0002g0199 a0001c0001t0002g0286 others(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 | a0001c0002t0001g0198 a0001c0002t0001g0299 |
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 | a0001c0003t0008g0182 a0001c0003t0008g0325 |
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 | a0001c0001t0001g0007 | 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 | 184 | a0001c0001t0001g0143 a0001c0001t0001g0184 a0001c0001t0001g0209 others(181): 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 | 2 | a0001c0002t0001g0001 a0001c0002t0001g0151 |
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 | 10 | a0001c0001t0002g0062 a0001c0001t0004g0039 a0001c0001t0004g0113 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(7): 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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0002t0006g0366 others(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 | 168 | a0001c0001t0001g0143 a0001c0001t0001g0184 a0001c0001t0001g0209 others(165): 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 | a0001c0002t0003g0159 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0001t0002g0208 a0001c0001t0003g0165 a0001c0001t0012g0216 |
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 | a0001c0001t0002g0035 a0001c0001t0002g0054 a0001c0001t0002g0055 others(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 | a0001c0002t0004g0111 | 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 | a0001c0001t0002g0191 a0001c0001t0002g0207 a0001c0001t0002g0245 others(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 | a0001c0001t0002g0201 a0001c0001t0002g0286 a0001c0002t0001g0185 others(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 | a0001c0001t0003g0074 | 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 | a0001c0001t0002g0197 a0001c0001t0003g0202 a0001c0002t0001g0175 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0193 a0001c0001t0001g0221 others(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 | a0001c0002t0001g0185 a0001c0002t0001g0344 a0001c0002t0006g0364 others(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 | a0001c0001t0003g0118 | 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 | a0001c0002t0001g0255 a0001c0002t0001g0323 |
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 | 67 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0193 others(64): 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 | a0001c0001t0001g0181 a0001c0004t0004g0326 |
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 | a0001c0003t0004g0242 | 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 | a0001c0001t0003g0084 a0001c0001t0003g0085 |
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 | a0001c0001t0006g0360 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0075 a0001c0001t0002g0110 others(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 | a0001c0001t0001g0194 a0001c0001t0002g0264 a0001c0001t0002g0272 others(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 | 103 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0181 others(100): 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 | a0001c0001t0001g0193 a0001c0001t0001g0221 a0001c0001t0001g0222 |
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 | 57 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0097 others(54): Show |
59 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(56): 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 | a0001c0001t0002g0264 a0001c0001t0002g0272 a0001c0002t0001g0265 |
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 | a0001c0002t0001g0032 a0001c0002t0001g0228 a0001c0002t0001g0235 |
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 | 26 | a0001c0001t0001g0181 a0001c0001t0002g0004 a0001c0001t0002g0062 others(23): 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 | a0001c0001t0003g0086 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0193 others(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 | a0001c0001t0002g0080 a0001c0001t0002g0099 a0001c0001t0002g0241 others(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 | 182 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0193 others(179): Show |
189 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(186): 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 | a0001c0001t0004g0187 | 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 | 360 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(357): Show |
370 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(367): Show |
intron_variant | MODIFIER | c.412-2171T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410446 | |||||||
| chr4:184410493 | T | C | 348 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(345): Show |
357 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(354): Show |
intron_variant | MODIFIER | c.412-2218A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410493 | |||||||
| chr4:184410676 | GC | G | 48 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0097 others(45): Show |
50 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.412-2402delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410676 | |||||||
| chr4:184410740 | C | T | 16 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0201 others(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 | 28 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0297 others(25): Show |
29 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.412-2533G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184410808 | |||||||
| chr4:184410823 | A | G | 95 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0193 others(92): 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 | a0001c0001t0001g0143 a0001c0001t0001g0217 a0001c0001t0001g0244 others(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 | 40 | a0001c0001t0001g0181 a0001c0001t0002g0012 a0001c0001t0002g0130 others(37): Show |
41 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.412-2785delA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411059 | |||||||
| chr4:184411081 | G | T | 28 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0297 others(25): Show |
29 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(26): 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 | a0001c0001t0002g0264 a0001c0001t0002g0272 a0001c0001t0002g0306 others(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 | 94 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0193 others(91): 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 | a0001c0001t0001g0181 a0001c0001t0002g0186 a0001c0002t0001g0175 others(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 | a0001c0001t0003g0309 a0001c0001t0003g0319 a0001c0002t0001g0226 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0209 a0001c0001t0002g0004 others(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 | a0001c0001t0003g0073 | 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 | 33 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(30): Show |
34 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(31): 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 | a0001c0001t0001g0007 a0001c0001t0003g0231 a0001c0001t0003g0232 others(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 | a0001c0001t0001g0347 a0001c0001t0002g0345 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | 79 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0012 others(76): Show |
82 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.412-3601G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184411876 | |||||||
| chr4:184411938 | A | G | 221 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0193 others(218): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): 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 | a0001c0001t0001g0181 a0001c0002t0001g0175 a0001c0002t0001g0239 others(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 | a0001c0001t0001g0194 a0001c0001t0002g0099 a0001c0001t0002g0142 others(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 | a0001c0001t0001g0244 a0001c0001t0002g0201 a0001c0001t0002g0207 others(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 | 104 | a0001c0001t0001g0184 a0001c0001t0001g0217 a0001c0001t0001g0289 others(101): Show |
106 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.412-3731delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412005 | |||||||
| chr4:184412005 | TAA | T | 6 | a0001c0001t0002g0012 a0001c0001t0002g0293 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0003g0231 a0001c0001t0003g0232 others(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 | a0001c0001t0002g0131 a0001c0001t0002g0203 a0001c0001t0002g0208 others(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 | a0001c0001t0001g0347 a0001c0001t0002g0277 a0001c0001t0002g0345 others(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 | a0001c0002t0001g0332 | 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 | a0001c0001t0001g0194 a0001c0001t0002g0197 a0001c0001t0002g0223 others(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 | 33 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(30): Show |
34 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.412-4269dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184412543 | |||||||
| chr4:184412589 | A | T | 47 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(44): 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 | a0001c0001t0002g0195 a0001c0001t0003g0215 a0001c0001t0007g0361 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | 28 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(25): Show |
29 | HG00438.hp2 HG00733.hp1 HG01070.hp2 others(26): 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 | a0001c0001t0002g0349 | 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 | a0001c0001t0002g0179 a0001c0001t0003g0017 a0001c0002t0001g0243 others(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 | a0001c0001t0001g0217 a0001c0002t0001g0196 a0001c0002t0001g0249 others(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 | a0001c0001t0001g0217 a0001c0002t0001g0196 a0001c0002t0001g0249 others(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 | a0001c0001t0001g0143 a0001c0001t0002g0004 a0001c0001t0002g0015 others(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 | 28 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(25): Show |
29 | HG00438.hp2 HG00733.hp1 HG01070.hp2 others(26): 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 | a0001c0002t0001g0154 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0004t0004g0282 a0001c0004t0004g0342 a0001c0004t0004g0343 |
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 | 94 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0209 others(91): 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 | 51 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(48): 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 | a0001c0001t0003g0165 | 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 | a0001c0001t0003g0086 | 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 | a0001c0001t0003g0148 a0001c0002t0001g0058 a0001c0002t0001g0089 others(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 | 47 | a0001c0001t0001g0079 a0001c0001t0002g0005 a0001c0001t0002g0097 others(44): 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 | 39 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(36): Show |
40 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(37): 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 | a0001c0001t0002g0208 | 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 | 47 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(44): 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 | a0001c0001t0001g0194 a0001c0001t0002g0197 a0001c0001t0002g0223 others(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 | a0001c0001t0002g0207 a0001c0002t0001g0185 a0001c0002t0001g0344 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0181 a0001c0001t0002g0186 a0001c0002t0001g0175 others(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 | a0001c0002t0001g0122 | 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 | 111 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0303 others(108): 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 | 117 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0289 others(114): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): 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 | a0001c0001t0002g0195 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0286 a0001c0002t0001g0189 a0001c0003t0004g0247 |
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 | a0001c0001t0002g0097 | 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 | a0001c0001t0001g0194 a0001c0001t0002g0197 a0001c0001t0002g0223 others(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 | a0001c0001t0003g0275 | 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 | a0001c0001t0002g0054 a0001c0001t0002g0059 a0001c0001t0002g0061 others(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 | 47 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(44): 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 | a0001c0001t0002g0195 a0001c0001t0003g0215 a0001c0001t0007g0361 others(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 | a0001c0001t0003g0350 a0001c0003t0004g0242 |
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 | 77 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0289 others(74): 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 | a0001c0001t0002g0195 a0001c0001t0003g0215 a0001c0001t0007g0361 others(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 | a0001c0001t0012g0216 | 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 | a0001c0002t0001g0239 a0001c0002t0001g0323 |
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 | a0001c0002t0009g0011 | 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 | 184 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0244 others(181): 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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0209 others(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 | 40 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(37): Show |
41 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(38): 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 | a0001c0001t0001g0217 a0001c0001t0002g0285 a0001c0002t0001g0196 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0011t0001g0083 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0217 a0001c0001t0002g0285 a0001c0002t0001g0196 others(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 | a0001c0001t0002g0201 a0001c0004t0004g0192 |
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 | a0001c0002t0001g0051 | 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 | a0001c0001t0012g0216 | 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 | 46 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(43): 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 | a0001c0001t0012g0216 | 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 | 46 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(43): 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 | a0001c0003t0008g0325 | 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 | a0001c0001t0003g0287 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | 51 | a0001c0001t0001g0079 a0001c0001t0002g0005 a0001c0001t0002g0097 others(48): 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 | 39 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(36): Show |
40 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.411+815T>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417352 | |||||||
| chr4:184417364 | C | G | 48 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(45): 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 | a0001c0002t0001g0301 a0001c0002t0002g0346 |
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 | a0001c0001t0001g0347 a0001c0001t0002g0345 |
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 | 247 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0194 others(244): Show |
255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.411+482A>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417685 | |||||||
| chr4:184417724 | A | G | 237 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0194 others(234): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.411+443T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417724 | |||||||
| chr4:184417767 | T | C | 86 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0012 others(83): Show |
89 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.411+400A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 5/8 | chr4 | 184417767 | |||||||
| chr4:184417841 | A | AC | 48 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(45): 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 | a0001c0001t0001g0347 a0001c0001t0002g0345 a0001c0002t0001g0224 |
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 | a0001c0001t0002g0054 a0001c0001t0002g0059 a0001c0001t0002g0061 others(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 | 161 | a0001c0001t0001g0007 a0001c0001t0001g0209 a0001c0001t0001g0289 others(158): Show |
166 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0060 others(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 | a0001c0002t0001g0126 | 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 | a0001c0001t0001g0347 a0001c0001t0002g0179 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0075 a0001c0001t0002g0163 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0015 a0001c0001t0002g0068 a0001c0001t0002g0310 others(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 | 251 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0194 others(248): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.188-304A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 3/8 | chr4 | 184419012 | |||||||
| chr4:184419132 | A | T | 33 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(30): Show |
34 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(31): 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 | a0001c0001t0003g0350 a0001c0003t0004g0242 |
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 | a0001c0002t0001g0172 | 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 | a0001c0001t0001g0181 a0001c0001t0002g0186 a0001c0002t0001g0175 others(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 | a0001c0001t0002g0195 a0001c0001t0002g0286 a0001c0001t0003g0215 others(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 | a0001c0001t0003g0056 a0001c0002t0001g0229 |
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 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
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 | 45 | a0001c0001t0002g0012 a0001c0001t0002g0098 a0001c0001t0002g0130 others(42): Show |
46 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(43): 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 | 65 | a0001c0001t0001g0194 a0001c0001t0001g0244 a0001c0001t0001g0251 others(62): 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 | 51 | a0001c0001t0001g0079 a0001c0001t0002g0005 a0001c0001t0002g0097 others(48): 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 | a0001c0001t0001g0007 a0001c0001t0001g0303 a0001c0001t0002g0008 others(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 | a0001c0001t0002g0054 | 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 | a0001c0002t0001g0323 | 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 | a0001c0001t0002g0292 a0001c0001t0003g0279 a0001c0002t0001g0280 |
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 | a0001c0001t0001g0347 a0001c0001t0002g0179 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0173 | 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 | a0001c0001t0002g0018 | 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 | a0001c0001t0002g0195 a0001c0001t0002g0286 a0001c0001t0003g0215 others(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 | a0001c0001t0012g0216 | 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 | a0001c0001t0012g0216 | 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 | a0001c0002t0001g0016 a0001c0002t0001g0042 a0001c0002t0001g0048 |
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 | a0001c0001t0001g0194 a0001c0001t0002g0197 a0001c0001t0002g0223 others(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 | a0001c0005t0001g0180 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0347 a0001c0001t0002g0179 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0110 a0001c0001t0003g0076 |
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 | a0001c0001t0001g0194 a0001c0001t0002g0197 a0001c0001t0002g0223 others(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 | a0001c0002t0001g0330 | 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 | 87 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0001g0347 others(84): Show |
90 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(87): 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 | a0001c0001t0003g0053 | 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 | a0001c0001t0002g0212 | 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 | a0001c0001t0002g0213 | 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 | a0001c0001t0002g0195 | 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 | a0001c0001t0002g0186 | 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 | 47 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0057 others(44): 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 | 246 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0209 others(243): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): 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 | a0001c0001t0001g0007 a0001c0001t0001g0209 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0347 a0001c0001t0002g0345 |
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 | a0001c0001t0003g0165 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0005t0001g0180 | 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 | a0001c0001t0002g0054 a0001c0001t0002g0059 a0001c0001t0002g0061 others(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 | a0001c0002t0001g0129 | 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 | a0001c0001t0002g0018 | 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 | 33 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(30): Show |
34 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(31): 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 | a0001c0001t0003g0294 a0001c0002t0005g0043 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0209 a0001c0001t0001g0303 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0002g0191 others(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 | a0001c0002t0001g0112 | 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 | a0001c0002t0001g0154 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0209 others(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 | a0001c0001t0007g0363 a0001c0002t0001g0284 |
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 | 86 | a0001c0001t0001g0289 a0001c0001t0001g0333 a0001c0001t0002g0012 others(83): Show |
89 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.88-4488T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424056 | |||||||
| chr4:184424063 | TAC | T | 202 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0217 others(199): 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 | 59 | a0001c0001t0001g0079 a0001c0001t0001g0244 a0001c0001t0001g0251 others(56): 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 | a0001c0002t0001g0038 a0001c0002t0001g0040 |
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 | a0001c0001t0002g0349 | 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 | a0001c0001t0002g0179 a0001c0001t0002g0277 a0001c0002t0001g0243 others(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 | a0001c0002t0001g0330 | 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 | 59 | a0001c0001t0001g0079 a0001c0001t0001g0244 a0001c0001t0001g0251 others(56): 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 | 59 | a0001c0001t0001g0079 a0001c0001t0001g0244 a0001c0001t0001g0251 others(56): 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 | a0001c0001t0002g0179 a0001c0001t0002g0277 a0001c0002t0001g0243 others(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 | 59 | a0001c0001t0001g0079 a0001c0001t0001g0244 a0001c0001t0001g0251 others(56): 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 | a0001c0001t0003g0165 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0217 a0001c0001t0001g0303 others(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 | 59 | a0001c0001t0001g0079 a0001c0001t0001g0244 a0001c0001t0001g0251 others(56): 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0002g0117 a0001c0001t0003g0066 a0001c0001t0003g0087 others(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 | a0001c0001t0001g0347 a0001c0001t0002g0345 |
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 | 232 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0217 others(229): Show |
239 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.87+4042T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 2/8 | chr4 | 184424936 | |||||||
| chr4:184425049 | T | C | 235 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0217 others(232): Show |
242 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(239): 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 | a0001c0001t0002g0186 | 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 | a0001c0001t0001g0347 a0001c0001t0002g0179 a0001c0001t0002g0277 others(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 | 58 | a0001c0001t0001g0079 a0001c0001t0001g0244 a0001c0001t0001g0251 others(55): 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 | 56 | a0001c0001t0001g0079 a0001c0001t0001g0244 a0001c0001t0001g0251 others(53): 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 | a0001c0001t0002g0054 a0001c0001t0002g0059 a0001c0001t0002g0061 others(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 | a0001c0001t0002g0179 a0001c0001t0002g0277 a0001c0002t0001g0243 others(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 | a0001c0001t0003g0045 a0001c0001t0003g0266 |
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 | a0001c0001t0002g0068 | 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 | a0001c0001t0002g0179 a0001c0001t0002g0277 a0001c0002t0001g0243 others(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 | 30 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(27): Show |
31 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(28): 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 | 241 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(238): 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 | 64 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0244 others(61): 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 | a0001c0002t0005g0106 | 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 | a0001c0001t0002g0068 a0001c0001t0002g0310 a0001c0001t0002g0311 |
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 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0002g0262 others(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 | 126 | a0001c0001t0001g0217 a0001c0001t0001g0289 a0001c0001t0001g0303 others(123): 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 | a0001c0001t0001g0217 a0001c0001t0001g0303 a0001c0001t0001g0348 others(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 | 78 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0244 others(75): 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 | a0001c0001t0002g0026 | 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 | a0001c0001t0002g0306 | 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 | 224 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0217 others(221): Show |
231 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(228): 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 | a0001c0001t0002g0179 a0001c0001t0002g0277 a0001c0002t0001g0243 others(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 | 74 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0244 others(71): 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 | 74 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0244 others(71): 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 | 75 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0244 others(72): 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 | a0001c0001t0002g0197 a0001c0001t0002g0223 a0001c0001t0003g0339 others(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 | a0001c0001t0003g0300 | 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 | a0001c0001t0003g0318 | 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 | a0001c0001t0003g0066 | 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 | a0001c0001t0003g0073 | 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 | 95 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0244 others(92): 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 | a0001c0002t0005g0353 | 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 | 51 | a0001c0001t0001g0079 a0001c0001t0002g0005 a0001c0001t0002g0097 others(48): 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 | a0001c0001t0001g0007 a0001c0001t0003g0231 a0001c0001t0003g0232 others(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 | a0001c0002t0001g0323 | 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 | a0001c0001t0002g0054 a0001c0001t0002g0059 a0001c0001t0002g0061 others(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 | a0001c0001t0002g0179 a0001c0001t0002g0277 a0001c0002t0001g0243 others(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 | 25 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(22): Show |
26 | HG00438.hp2 HG00733.hp1 HG01070.hp2 others(23): 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 | a0001c0001t0001g0217 a0001c0001t0001g0303 a0001c0001t0001g0348 others(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 | a0001c0001t0002g0054 a0001c0001t0002g0059 a0001c0001t0002g0061 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0223 a0001c0001t0003g0339 others(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 | 118 | a0001c0001t0001g0181 a0001c0001t0001g0217 a0001c0001t0001g0289 others(115): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0347 a0001c0001t0002g0195 a0001c0001t0002g0286 others(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 | a0001c0002t0001g0330 | 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 | a0001c0001t0002g0097 | 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 | 32 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0135 others(29): Show |
33 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(30): 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 | a0001c0002t0001g0284 | 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 | a0001c0002t0001g0052 | 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 | a0001c0001t0001g0181 a0001c0001t0002g0186 a0001c0002t0001g0175 others(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 | a0001c0001t0002g0062 a0001c0001t0004g0205 a0001c0001t0004g0206 |
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 | a0001c0001t0002g0163 a0001c0001t0003g0238 a0001c0002t0001g0164 others(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 | a0001c0001t0002g0179 a0001c0002t0001g0243 |
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 | a0001c0001t0001g0181 a0001c0002t0001g0175 a0001c0002t0001g0239 |
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 | a0001c0001t0001g0181 a0001c0002t0001g0175 a0001c0002t0001g0239 others(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 | a0001c0001t0003g0056 a0001c0002t0001g0229 |
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 | a0001c0001t0001g0303 a0001c0001t0001g0348 a0001c0001t0002g0054 others(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 | a0001c0001t0001g0007 a0001c0001t0003g0231 a0001c0001t0003g0232 others(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 | a0001c0001t0001g0303 a0001c0001t0001g0348 a0001c0001t0002g0054 others(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 | 246 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0194 others(243): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.-6-198T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429268 | |||||||
| chr4:184429423 | C | T | 132 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(129): Show |
137 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(134): 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 | a0001c0001t0003g0350 a0001c0003t0004g0242 a0001c0003t0004g0256 |
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 | a0001c0002t0001g0016 a0001c0002t0001g0042 a0001c0002t0001g0048 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0223 a0001c0001t0002g0277 others(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 | 43 | a0001c0001t0001g0333 a0001c0001t0002g0035 a0001c0001t0002g0062 others(40): 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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0221 others(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 | 265 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(262): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-6-580C>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184429650 | |||||||
| chr4:184429780 | A | G | 248 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(245): Show |
255 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(252): 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 | a0001c0001t0002g0195 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0303 a0001c0001t0010g0094 |
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 | a0001c0001t0003g0084 a0001c0001t0003g0085 |
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 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0234 others(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 | a0001c0001t0007g0363 a0001c0002t0001g0250 a0001c0002t0001g0284 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0209 a0001c0001t0003g0023 others(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 | a0001c0001t0001g0303 a0001c0001t0007g0363 a0001c0002t0001g0154 others(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 | a0001c0001t0003g0215 | 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 | a0001c0001t0003g0071 a0001c0002t0001g0033 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0002g0144 a0001c0002t0001g0128 a0001c0002t0001g0321 |
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 | 100 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0035 others(97): Show |
103 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(100): 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 | a0001c0001t0003g0084 a0001c0001t0003g0085 |
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 | a0001c0004t0004g0282 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0002t0001g0175 others(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 | a0001c0001t0001g0217 a0001c0001t0002g0285 a0001c0001t0007g0361 others(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 | 176 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(173): Show |
181 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(178): 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 | a0001c0001t0001g0079 a0001c0001t0002g0026 a0001c0001t0002g0059 others(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 | a0001c0002t0001g0323 | 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 | a0001c0001t0001g0303 a0001c0001t0002g0070 |
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 | 164 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(161): Show |
169 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-6-2723delG | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431792 | |||||||
| chr4:184431863 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0002g0062 a0001c0001t0002g0103 others(28): 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 | 180 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(177): Show |
185 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.-6-2794delT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431863 | |||||||
| chr4:184431941 | C | T | 1 | a0001c0001t0004g0336 | 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 | 166 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(163): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-6-2923A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184431993 | |||||||
| chr4:184432197 | T | C | 362 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(359): Show |
372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): 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 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0234 others(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 | 362 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(359): Show |
372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): 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 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0234 others(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 | 166 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(163): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-6-3242A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432312 | |||||||
| chr4:184432368 | A | G | 166 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(163): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): 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 | a0001c0001t0002g0197 a0001c0001t0002g0201 a0001c0001t0002g0223 others(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 | 99 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0035 others(96): Show |
102 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.-6-3490G>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432560 | |||||||
| chr4:184432645 | T | C | 166 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(163): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): 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 | a0001c0001t0003g0327 | 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 | a0001c0001t0012g0216 | 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 | a0001c0004t0004g0326 | 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 | 166 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(163): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): 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 | a0001c0001t0002g0068 a0001c0001t0002g0310 a0001c0001t0002g0311 |
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 | 166 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(163): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-6-3746G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184432816 | |||||||
| chr4:184432973 | C | T | 342 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(339): Show |
352 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(349): 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 | a0001c0001t0002g0144 a0001c0002t0001g0128 a0001c0002t0001g0321 |
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 | a0001c0001t0001g0303 | 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 | 114 | a0001c0001t0001g0079 a0001c0001t0001g0194 a0001c0001t0001g0217 others(111): 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 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(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 | 100 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0035 others(97): Show |
103 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-6-4130G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184433200 | |||||||
| chr4:184433273 | T | A | 97 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0035 others(94): Show |
100 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(97): 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0223 a0001c0001t0003g0339 others(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 | 186 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(183): Show |
191 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(188): 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 | 107 | a0001c0001t0001g0079 a0001c0001t0001g0194 a0001c0001t0001g0217 others(104): 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 | 28 | a0001c0001t0001g0007 a0001c0001t0002g0103 a0001c0001t0002g0349 others(25): 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 | 190 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0184 others(187): Show |
195 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(192): 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 | a0001c0002t0001g0126 | 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 | 304 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0181 others(301): Show |
311 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(308): 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 | a0001c0001t0002g0063 | 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 | a0001c0004t0004g0342 a0001c0004t0004g0343 |
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 | 362 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(359): Show |
372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): 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 | a0001c0001t0001g0007 a0001c0001t0003g0024 a0001c0001t0003g0118 others(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 | a0001c0001t0002g0306 a0001c0001t0003g0324 a0001c0002t0001g0268 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0221 others(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 | a0001c0001t0003g0017 | 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 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0234 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0221 others(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 | a0002c0008t0002g0091 | 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 | 106 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0062 others(103): Show |
109 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(106): 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 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0234 others(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 | 138 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0244 others(135): Show |
141 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(138): 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 | 144 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0194 others(141): 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 | a0001c0001t0003g0118 | 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 | a0001c0002t0001g0224 | 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 | a0001c0002t0001g0185 | 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 | a0001c0001t0002g0144 a0001c0002t0001g0128 a0001c0002t0001g0321 |
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 | 142 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0244 others(139): Show |
145 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(142): 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 | a0001c0001t0003g0215 | 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 | a0001c0001t0002g0208 | 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 | 342 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(339): Show |
352 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(349): Show |
intron_variant | MODIFIER | c.-6-6672A>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184435742 | |||||||
| chr4:184435757 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0002g0103 a0001c0001t0002g0349 others(24): 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 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0181 others(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 | a0001c0002t0001g0188 | 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 | 144 | a0001c0001t0001g0007 a0001c0001t0001g0194 a0001c0001t0001g0209 others(141): 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 | 362 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(359): Show |
372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): 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 | a0001c0002t0001g0082 | 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 | a0001c0001t0002g0223 | 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 | 105 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0075 others(102): Show |
108 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(105): 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 | a0001c0002t0001g0151 | 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 | a0001c0002t0001g0323 | 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 | a0001c0002t0001g0189 | 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 | a0001c0001t0002g0117 | 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 | a0001c0001t0001g0217 a0001c0001t0002g0285 a0001c0001t0007g0361 others(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 | a0001c0001t0002g0035 | 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 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0234 others(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 | a0001c0002t0001g0189 | 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 | a0001c0002t0001g0189 | 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 | 29 | a0001c0001t0001g0007 a0001c0001t0002g0035 a0001c0001t0002g0103 others(26): 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 | a0001c0001t0002g0297 a0001c0001t0002g0354 a0001c0001t0002g0356 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0209 a0001c0002t0001g0255 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0002g0059 a0001c0001t0002g0171 a0001c0001t0002g0210 others(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 | 111 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0035 others(108): Show |
114 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-6-8295dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184437364 | |||||||
| chr4:184437489 | G | A | 1 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0002g0208 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0137 a0001c0001t0002g0146 others(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 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0234 others(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 | 115 | a0001c0001t0001g0079 a0001c0001t0001g0194 a0001c0001t0001g0217 others(112): 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 | 119 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0062 others(116): Show |
122 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(119): 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0001g0209 a0001c0002t0001g0255 |
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 | a0001c0001t0002g0173 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0001g0194 | 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 | 29 | a0001c0001t0001g0007 a0001c0001t0001g0209 a0001c0001t0002g0103 others(26): 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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0221 others(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 | a0001c0001t0002g0110 a0001c0001t0003g0076 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0347 others(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 | a0001c0001t0002g0135 a0001c0001t0002g0219 a0001c0001t0002g0264 others(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 | a0001c0001t0001g0194 a0001c0001t0002g0186 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0201 a0001c0001t0002g0223 others(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 | a0001c0001t0003g0275 a0001c0002t0001g0166 a0001c0002t0001g0273 |
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 | 362 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(359): Show |
372 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(369): 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 | a0001c0002t0001g0115 | 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 | a0001c0002t0001g0154 | 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 | a0001c0001t0002g0358 | 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 | a0001c0001t0002g0358 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0143 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0222 a0001c0001t0001g0333 a0001c0001t0002g0197 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0181 a0001c0001t0001g0193 others(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 | a0001c0001t0003g0077 a0001c0001t0003g0095 |
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 | 88 | a0001c0001t0001g0194 a0001c0001t0001g0221 a0001c0001t0001g0222 others(85): 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 | a0001c0001t0001g0217 a0001c0001t0001g0246 a0001c0001t0002g0277 others(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 | 3 | a0001c0001t0002g0057 a0001c0001t0003g0002 a0001c0001t0003g0114 |
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 | 360 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(357): Show |
370 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(367): 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 | a0001c0001t0001g0181 a0001c0001t0001g0244 a0001c0001t0004g0257 others(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 | a0001c0002t0001g0175 a0001c0002t0001g0189 a0001c0002t0001g0258 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0001t0003g0076 | 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 | 38 | a0001c0001t0001g0079 a0001c0001t0002g0080 a0001c0001t0002g0098 others(35): 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 | a0001c0001t0002g0358 | 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 | a0001c0001t0002g0358 | 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 | 45 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0080 others(42): 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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0197 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0289 a0001c0001t0001g0347 others(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 | a0001c0001t0001g0209 a0001c0003t0008g0325 |
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 | a0001c0001t0002g0285 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0003g0202 | 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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0197 others(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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0173 others(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 | a0001c0001t0002g0276 | 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 | a0001c0002t0001g0101 | 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 | a0001c0001t0002g0358 | 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 | a0001c0001t0002g0358 | 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 | a0001c0001t0002g0358 | 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 | a0001c0001t0003g0215 a0001c0001t0004g0257 a0001c0002t0001g0338 |
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 | a0001c0001t0003g0202 | 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 | a0001c0001t0001g0347 a0001c0001t0002g0191 a0001c0001t0002g0207 others(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 | a0001c0001t0003g0309 a0001c0001t0003g0319 a0001c0001t0004g0230 others(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 | a0001c0001t0003g0324 | 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 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0201 others(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 | a0001c0001t0002g0203 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0251 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0201 others(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 | a0001c0002t0001g0299 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0289 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0171 others(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 | a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | 354 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(351): Show |
364 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(361): 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 | a0001c0002t0001g0126 | 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 | 350 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(347): Show |
360 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(357): 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 | a0001c0001t0001g0184 a0001c0001t0001g0289 a0001c0001t0001g0347 others(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 | 257 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0193 others(254): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(261): 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 | a0001c0001t0001g0246 a0001c0001t0002g0286 a0001c0001t0004g0190 others(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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0171 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0289 a0001c0001t0001g0347 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0201 others(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 | a0001c0001t0003g0093 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0201 others(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 | a0001c0001t0001g0209 a0001c0003t0008g0325 |
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 | a0001c0002t0001g0338 | 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 | a0001c0001t0003g0064 | 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 | a0001c0001t0012g0216 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0348 a0001c0001t0002g0171 others(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 | a0001c0001t0003g0073 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0289 a0001c0001t0001g0347 others(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 | a0001c0001t0002g0285 | 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 | a0001c0002t0001g0352 | 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 | a0001c0001t0002g0171 | 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 | a0001c0002t0001g0129 | 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 | a0001c0002t0001g0188 | 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 | a0001c0001t0003g0261 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0002g0169 a0001c0001t0003g0023 a0001c0002t0005g0124 |
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 | a0001c0001t0001g0181 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0002t0001g0189 | 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 | 82 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0333 others(79): 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0002g0358 | 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 | 141 | a0001c0001t0001g0079 a0001c0001t0001g0181 a0001c0001t0001g0193 others(138): Show |
146 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(143): 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 | a0001c0001t0001g0246 a0001c0001t0002g0285 a0001c0001t0002g0286 others(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 | a0001c0002t0001g0189 | 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 | a0001c0003t0004g0183 | 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 | a0001c0001t0002g0292 a0001c0001t0002g0293 |
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 | a0001c0001t0001g0246 a0001c0001t0002g0285 a0001c0001t0002g0286 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0004t0004g0342 | 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 | a0001c0001t0004g0187 | 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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0175 others(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 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0003g0064 |
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 | a0001c0001t0003g0318 | 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 | 139 | a0001c0001t0001g0079 a0001c0001t0001g0181 a0001c0001t0001g0193 others(136): Show |
144 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(141): 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 | a0001c0002t0001g0268 a0001c0002t0005g0267 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0175 others(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 | 6 | a0001c0001t0002g0031 a0001c0001t0002g0212 a0001c0001t0002g0358 others(3): Show |
6 | HG01069.hp2 HG01081.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-16585dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184445654 | |||||||
| chr4:184445654 | C | CAA | 70 | a0001c0001t0001g0289 a0001c0001t0002g0006 a0001c0001t0002g0018 others(67): 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 | 43 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0080 others(40): 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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0175 others(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 | 117 | a0001c0001t0001g0079 a0001c0001t0001g0289 a0001c0001t0002g0004 others(114): Show |
122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0209 others(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 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0002t0001g0105 others(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 | a0001c0003t0008g0325 | 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 | a0001c0001t0001g0209 a0001c0001t0002g0207 |
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 | a0001c0002t0001g0338 | 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 | a0001c0002t0001g0288 | 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 | a0001c0001t0002g0169 a0001c0002t0005g0124 |
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 | 335 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(332): Show |
345 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(342): 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 | a0001c0001t0001g0209 a0001c0001t0002g0179 a0001c0001t0002g0191 others(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 | a0001c0001t0003g0176 a0001c0003t0008g0182 |
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 | a0001c0001t0001g0184 a0001c0001t0002g0068 a0001c0001t0002g0070 others(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 | a0001c0001t0001g0246 a0001c0001t0002g0285 a0001c0001t0002g0286 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 |
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 | a0001c0001t0004g0230 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0003g0013 a0001c0001t0003g0066 a0001c0002t0001g0100 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0289 a0001c0001t0002g0035 others(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 | a0001c0001t0001g0209 a0001c0001t0002g0179 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0306 a0001c0001t0003g0044 others(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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): 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 | a0001c0001t0002g0097 | 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 | a0001c0001t0004g0336 a0001c0002t0001g0337 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0217 others(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 | 88 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(85): Show |
91 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(88): 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 | a0001c0001t0001g0303 a0001c0001t0002g0186 a0001c0002t0001g0185 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0002g0059 a0001c0002t0001g0058 a0001c0002t0001g0237 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0195 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0195 |
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 | a0001c0003t0004g0183 | 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 | a0001c0002t0001g0239 | 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 | a0001c0001t0001g0209 a0001c0001t0002g0179 a0001c0001t0002g0207 others(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 | a0001c0002t0001g0119 | 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 | a0001c0002t0001g0338 | 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 | 262 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(259): Show |
271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): 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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0195 |
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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0184 a0001c0001t0002g0068 a0001c0001t0002g0070 others(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 | 113 | a0001c0001t0001g0079 a0001c0001t0001g0289 a0001c0001t0002g0004 others(110): Show |
117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): 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 | a0001c0001t0001g0303 a0001c0001t0002g0186 a0001c0002t0001g0185 others(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 | a0001c0001t0002g0179 a0001c0001t0003g0017 |
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 | a0001c0001t0001g0303 a0001c0001t0002g0186 a0001c0002t0001g0185 |
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 | a0001c0001t0003g0215 | 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 | 114 | a0001c0001t0001g0079 a0001c0001t0001g0289 a0001c0001t0002g0004 others(111): Show |
118 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(115): 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 | a0001c0001t0001g0184 a0001c0001t0002g0006 a0001c0001t0002g0035 others(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 | a0001c0001t0001g0289 a0001c0001t0002g0210 a0001c0001t0002g0212 others(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 | a0001c0003t0004g0183 | 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 | a0001c0002t0001g0214 | 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 | a0001c0002t0001g0299 | 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 | a0001c0002t0001g0112 a0001c0002t0005g0041 |
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 | 273 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(270): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(278): 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 | a0001c0001t0001g0181 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0007g0363 | 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 | a0001c0002t0001g0175 a0001c0002t0001g0177 a0001c0002t0011g0178 |
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 | a0001c0002t0001g0032 | 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 | a0001c0001t0002g0167 | 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 | a0001c0001t0002g0283 | 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 | 90 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(87): Show |
93 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(90): 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 | a0001c0002t0001g0338 | 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 | a0001c0002t0001g0129 | 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 | a0001c0002t0001g0243 | 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 | 107 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(104): Show |
110 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(107): 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 | 110 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0006 others(107): Show |
114 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(111): 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 | a0001c0001t0002g0240 | 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 | a0001c0002t0001g0189 | 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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): 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 | a0001c0001t0002g0006 a0001c0001t0003g0176 a0001c0003t0008g0182 |
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 | a0001c0001t0007g0363 | 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 | a0001c0001t0002g0252 a0001c0002t0001g0269 |
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 | a0001c0002t0001g0301 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0003g0023 | 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 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0001g0289 others(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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): 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 | a0001c0002t0001g0226 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0217 others(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 | a0001c0001t0002g0285 | 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 | a0001c0001t0001g0181 | 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 | a0001c0002t0001g0226 | 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 | a0001c0001t0003g0270 | 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 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0179 a0001c0001t0002g0191 others(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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): 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 | a0001c0001t0004g0156 | 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 | a0001c0001t0001g0333 a0001c0001t0002g0005 a0001c0001t0002g0026 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0347 a0001c0001t0002g0015 a0001c0001t0002g0127 others(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 | a0001c0001t0002g0035 a0001c0001t0002g0068 a0001c0001t0002g0240 others(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 | a0001c0001t0001g0184 a0001c0001t0002g0070 a0001c0001t0002g0203 others(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 | a0001c0001t0002g0252 a0001c0001t0003g0275 a0001c0001t0003g0279 others(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 | a0001c0001t0002g0169 a0001c0001t0002g0276 a0001c0001t0003g0200 others(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 | a0001c0001t0002g0186 a0001c0001t0012g0216 a0001c0002t0001g0185 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0194 a0001c0001t0002g0195 |
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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0244 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0289 a0001c0001t0002g0060 a0001c0001t0002g0061 others(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 | 89 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0006 others(86): Show |
93 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(90): 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 | a0001c0001t0001g0246 a0001c0001t0002g0171 a0001c0001t0002g0173 others(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 | a0001c0001t0002g0201 a0001c0001t0002g0286 a0001c0001t0003g0202 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | a0001c0002t0001g0121 | 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 | a0001c0002t0001g0175 a0001c0002t0001g0177 a0001c0002t0011g0178 |
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 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0296 others(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 | 363 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(360): Show |
373 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(370): 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 | a0001c0001t0002g0012 | 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 | 120 | a0001c0001t0001g0079 a0001c0001t0001g0289 a0001c0001t0002g0004 others(117): Show |
125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): 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 | a0001c0002t0001g0175 a0001c0002t0001g0177 a0001c0002t0011g0178 |
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 | a0001c0002t0001g0037 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | 90 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(87): Show |
93 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-7+20237A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184454142 | |||||||
| chr4:184454215 | G | A | 90 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(87): Show |
93 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(90): 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 | a0001c0001t0003g0279 a0001c0002t0001g0280 |
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 | a0001c0001t0001g0246 a0001c0001t0002g0286 a0001c0001t0004g0190 others(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 | a0001c0001t0001g0246 a0001c0001t0002g0286 a0001c0001t0004g0190 others(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 | 120 | a0001c0001t0001g0079 a0001c0001t0001g0289 a0001c0001t0002g0004 others(117): Show |
125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0193 others(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 | a0001c0001t0002g0006 a0001c0001t0003g0176 a0001c0003t0008g0182 |
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 | a0001c0001t0002g0006 a0001c0003t0008g0182 |
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 | a0001c0001t0003g0066 | 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 | a0001c0002t0001g0280 | 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 | a0001c0002t0001g0168 a0001c0002t0009g0011 |
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 |
318 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(315): Show |
327 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(324): 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 | a0001c0002t0001g0105 | 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 | a0001c0002t0005g0106 | 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 | a0001c0002t0001g0299 | 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 | 102 | a0001c0001t0001g0079 a0001c0001t0001g0194 a0001c0001t0001g0303 others(99): Show |
105 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-7+19077dupA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184455301 | |||||||
| chr4:184455301 | C | CTT | 8 | a0001c0001t0002g0031 a0001c0001t0002g0171 a0001c0001t0002g0173 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0181 others(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 | a0001c0002t0001g0189 | 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 | a0001c0002t0001g0239 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0209 a0001c0001t0001g0244 others(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 | a0001c0001t0003g0065 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0173 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0195 others(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 | a0001c0001t0002g0063 | 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 | a0001c0001t0003g0324 | 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 | 308 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(313): 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 | a0001c0002t0001g0175 a0001c0002t0001g0177 a0001c0002t0001g0239 others(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 | a0001c0001t0006g0360 | 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 | a0001c0001t0001g0303 | 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 | a0001c0002t0001g0227 | 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 | a0001c0002t0001g0338 | 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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
365 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(362): 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 | a0001c0001t0001g0347 a0001c0001t0002g0345 a0001c0002t0001g0344 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0175 a0001c0002t0001g0177 a0001c0002t0011g0178 others(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 | a0001c0001t0007g0363 a0001c0002t0001g0299 a0001c0003t0004g0183 |
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 | a0001c0001t0002g0031 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0001t0003g0231 others(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 | 224 | a0001c0001t0001g0079 a0001c0001t0001g0184 a0001c0001t0001g0193 others(221): Show |
229 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.-7+17373T>G | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457006 | |||||||
| chr4:184457069 | T | G | 228 | a0001c0001t0001g0079 a0001c0001t0001g0184 a0001c0001t0001g0193 others(225): Show |
233 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(230): 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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 |
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 | a0001c0002t0001g0112 | 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 | 102 | a0001c0001t0001g0193 a0001c0001t0001g0244 a0001c0001t0001g0251 others(99): Show |
104 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(101): 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 | a0001c0001t0002g0179 a0001c0001t0003g0017 |
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 | a0001c0001t0001g0194 a0001c0001t0001g0303 a0001c0001t0002g0195 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 others(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 | 113 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(110): Show |
117 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(114): 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 | a0001c0001t0002g0285 | 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 | a0001c0001t0001g0194 | 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 | 108 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(105): Show |
111 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.-7+16529dupT | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184457849 | |||||||
| chr4:184457849 | C | CAA | 6 | a0001c0001t0001g0194 a0001c0001t0001g0303 a0001c0001t0002g0110 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0303 a0001c0001t0002g0195 |
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 | a0001c0002t0005g0025 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0303 a0001c0001t0002g0195 |
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 | a0001c0001t0001g0181 a0001c0001t0002g0006 a0001c0001t0002g0179 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0193 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0001t0003g0200 others(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 | 114 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(111): Show |
118 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(115): 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 | a0001c0002t0001g0351 | 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 | a0001c0001t0001g0194 a0001c0001t0002g0195 |
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 | a0001c0001t0012g0216 | 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 | a0001c0001t0002g0110 | 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 | a0001c0001t0001g0217 a0001c0001t0003g0215 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0002g0285 | 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 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0221 others(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 | a0001c0001t0003g0165 a0001c0001t0004g0156 a0001c0002t0001g0123 others(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 | a0001c0001t0007g0363 a0001c0002t0006g0364 a0001c0002t0006g0365 others(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 | a0001c0001t0001g0209 a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0251 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0333 a0001c0001t0001g0347 others(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 | a0001c0001t0001g0181 a0001c0001t0002g0006 a0001c0001t0002g0296 others(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 | a0001c0001t0001g0303 a0001c0001t0002g0186 a0001c0001t0003g0081 others(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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0002t0001g0172 |
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 | a0001c0001t0002g0291 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0209 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0333 a0001c0001t0001g0347 others(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 | a0001c0001t0002g0291 | 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 | a0001c0001t0002g0169 a0001c0001t0003g0238 a0001c0002t0005g0124 |
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 | 115 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(112): Show |
119 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.-7+13713G>A | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460666 | |||||||
| chr4:184460667 | A | G | 116 | a0001c0001t0001g0079 a0001c0001t0001g0194 a0001c0001t0002g0004 others(113): Show |
120 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.-7+13712T>C | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184460667 | |||||||
| chr4:184460681 | G | GCA | 155 | a0001c0001t0001g0079 a0001c0001t0001g0194 a0001c0001t0001g0209 others(152): Show |
159 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(156): 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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 |
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 | a0001c0002t0004g0111 | 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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0002g0012 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0209 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0193 others(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 | a0001c0002t0001g0112 | 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 | 358 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(355): Show |
368 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(365): 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0002t0001g0239 | 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 | a0001c0001t0004g0113 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0194 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0006g0360 | 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 | a0001c0001t0004g0230 a0001c0002t0001g0229 |
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 | 356 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(353): Show |
366 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(363): 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 | a0001c0003t0004g0183 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0007 a0001c0001t0003g0300 a0001c0002t0001g0302 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0001t0002g0197 others(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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0003g0327 a0001c0004t0004g0326 |
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 | 114 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(111): Show |
118 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(115): 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 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0001g0217 others(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 | a0001c0001t0002g0171 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0303 a0001c0001t0002g0005 others(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 | 234 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0181 others(231): Show |
243 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-7+10719A>T | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184463660 | |||||||
| chr4:184463662 | T | A | 114 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(111): Show |
118 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(115): 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 | a0001c0001t0001g0184 a0001c0001t0003g0017 a0001c0001t0004g0187 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0333 a0001c0001t0001g0347 others(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 | a0001c0001t0006g0360 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0002t0001g0172 |
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 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0002t0001g0172 |
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 | a0001c0001t0002g0203 a0001c0002t0001g0250 |
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 | a0001c0002t0001g0227 | 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 | a0001c0001t0004g0190 | 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 | a0001c0002t0001g0116 | 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 | a0001c0002t0001g0227 | 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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0127 others(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 | a0001c0001t0002g0191 a0001c0002t0001g0189 a0001c0004t0004g0192 |
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 | a0001c0002t0001g0125 | 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 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0002g0345 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0007 a0001c0001t0003g0300 a0001c0002t0001g0302 |
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 | a0001c0001t0002g0292 | 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 | a0001c0001t0002g0117 | 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 | a0001c0001t0001g0184 a0001c0001t0002g0012 a0001c0001t0003g0017 others(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 | a0001c0001t0001g0193 a0001c0001t0002g0191 a0001c0001t0002g0201 others(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 | a0001c0001t0001g0251 a0001c0001t0002g0252 a0001c0001t0003g0253 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0223 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | 134 | a0001c0001t0001g0079 a0001c0001t0001g0181 a0001c0001t0001g0194 others(131): Show |
139 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.-7+8311delA | IRF2 | ENSG00000168310.12 | transcript | ENST00000393593.8 | protein_coding | 1/8 | chr4 | 184466067 | |||||||
| chr4:184466069 | T | G | 2 | a0001c0001t0001g0194 a0001c0001t0002g0195 |
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 | a0001c0001t0002g0012 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(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 | a0001c0001t0002g0240 a0001c0002t0001g0225 a0001c0002t0001g0226 |
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 | a0001c0001t0001g0181 a0001c0001t0001g0194 a0001c0001t0002g0006 others(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 | a0001c0002t0001g0299 | 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 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0002t0001g0020 others(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 | a0001c0001t0002g0283 a0001c0004t0004g0282 |
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 | a0001c0002t0001g0196 | 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 | a0001c0001t0003g0019 | 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 | a0001c0001t0002g0223 a0001c0002t0001g0224 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0303 a0001c0001t0001g0333 others(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 | a0001c0001t0002g0191 a0001c0002t0001g0189 a0001c0004t0004g0192 |
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 | a0001c0001t0003g0176 | 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 | a0001c0001t0003g0350 | 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 | a0001c0002t0001g0249 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0002t0001g0172 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0303 a0001c0001t0001g0333 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0194 a0001c0001t0002g0006 others(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 | 113 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0018 others(110): Show |
117 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(114): 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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0251 a0001c0001t0002g0012 others(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 | a0001c0002t0001g0239 | 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 | a0001c0001t0006g0360 | 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 | a0001c0002t0001g0174 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0002t0001g0172 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0184 others(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 | a0001c0001t0004g0187 | 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 | a0001c0002t0001g0189 | 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 | a0001c0002t0001g0189 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0181 a0001c0001t0001g0184 others(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 | a0001c0001t0002g0018 | 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 | a0001c0001t0002g0298 | 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 | a0001c0001t0002g0117 | 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 | a0001c0001t0002g0203 a0001c0002t0001g0250 |
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 | 246 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0181 others(243): Show |
255 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(252): 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 | a0001c0001t0003g0350 | 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 | a0001c0001t0002g0349 | 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 | a0001c0001t0001g0193 | 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 | a0001c0002t0001g0214 | 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 | a0001c0001t0003g0176 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0003g0118 | 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 | a0001c0001t0002g0191 a0001c0001t0004g0190 a0001c0002t0001g0189 others(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 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0193 | 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 | a0001c0002t0001g0164 | 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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0127 others(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 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0213 others(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 | a0001c0001t0002g0286 | 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 | a0001c0001t0001g0209 a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | a0001c0002t0001g0119 | 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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0127 others(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 | a0001c0002t0001g0016 | 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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0127 others(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 | a0001c0001t0007g0361 a0001c0001t0007g0362 a0001c0001t0007g0363 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0184 a0001c0001t0002g0197 a0001c0001t0002g0199 others(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 | 299 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0143 others(296): Show |
308 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(305): 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 | a0001c0001t0001g0209 a0001c0001t0001g0246 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0012 others(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 | a0001c0002t0005g0353 | 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 | a0001c0002t0001g0123 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0303 a0001c0001t0001g0333 others(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 | a0001c0001t0003g0165 | 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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0002t0001g0198 |
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 | a0001c0001t0002g0197 a0001c0001t0002g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0127 others(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 | a0001c0002t0001g0166 | 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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0251 a0001c0001t0002g0012 a0001c0001t0002g0203 others(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 | a0001c0002t0001g0175 | 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 | a0001c0001t0003g0350 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0303 a0001c0001t0001g0333 others(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 | a0001c0002t0001g0239 | 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 | a0001c0001t0002g0240 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0002t0001g0172 |
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 | a0001c0001t0002g0167 | 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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0127 others(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 | a0001c0001t0002g0291 | 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 | a0001c0001t0003g0013 | 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 | a0001c0001t0003g0170 | 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 | a0001c0002t0001g0122 | 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 | a0001c0002t0005g0353 | 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 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0221 others(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 | a0001c0002t0001g0290 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0246 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0127 others(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 | a0001c0001t0003g0287 | 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 | 115 | a0001c0001t0001g0079 a0001c0001t0002g0004 a0001c0001t0002g0015 others(112): Show |
119 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(116): 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 | a0001c0002t0001g0288 | 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 | a0001c0001t0001g0184 a0001c0001t0004g0187 a0001c0002t0001g0188 |
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 | a0001c0001t0001g0289 | 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 | a0001c0001t0002g0012 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0303 a0001c0001t0001g0333 others(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 | a0001c0001t0002g0354 a0001c0001t0002g0356 a0001c0001t0002g0358 others(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 |