Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3394 |
| ensemblid | ENSG00000140968.12 |
| hgncid | 5358 |
| symbol | IRF8 |
| name | interferon regulatory factor 8 |
| refseq_nuc | NM_002163.4 |
| refseq_prot | NP_002154.1 |
| ensembl_nuc | ENST00000268638.10 |
| ensembl_prot | ENSP00000268638.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 85899162 |
| end | 85922606 |
| strand | + |
| ver | v1.2 |
| region | chr16:85899162-85922606 |
| region5000 | chr16:85894162-85927606 |
| regionname0 | IRF8_chr16_85899162_85922606 |
| regionname5000 | IRF8_chr16_85894162_85927606 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 426 | 429 | 98 | 66 | 210 | 16 | 37 | 164 | IRF8_chr16_85894162_85927606 | IRF8 | MCDRN others(421): Show |
chr16 | 85894162 | 85927606 |
| a0002 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | MCDRN others(421): Show |
chr16 | 85894162 | 85927606 |
| a0003 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | MCDRN others(421): Show |
chr16 | 85894162 | 85927606 |
| a0004 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | MCDRN others(421): Show |
chr16 | 85894162 | 85927606 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1278 | 331 | 67 | 39 | 184 | 10 | 29 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0002 | 0/0 | 1278 | 29 | 12 | 7 | 0 | 4 | 6 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0003 | 0/0 | 1278 | 21 | 1 | 6 | 12 | 0 | 2 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0004 | 0/0 | 1278 | 10 | 0 | 2 | 8 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0005 | 0/0 | 1278 | 9 | 0 | 7 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0006 | 0/0 | 1278 | 6 | 4 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0007 | 0/0 | 1278 | 6 | 3 | 1 | 0 | 2 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0008 | 0/0 | 1278 | 5 | 5 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0009 | 0/0 | 1278 | 5 | 3 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0010 | 0/0 | 1278 | 4 | 0 | 0 | 4 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0001c0011 | 0/0 | 1278 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0002c0013 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0003c0014 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 | ||
| a0004c0012 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | ATGTG others(1273): Show |
chr16 | 85894162 | 85927606 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2666 | 90 | 2 | 11 | 71 | 0 | 6 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0002 | 0/0 | 2666 | 67 | 11 | 3 | 51 | 1 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0003 | 1/1 | 2667 | 54 | 5 | 9 | 17 | 6 | 15 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2662): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0004 | 0/0 | 2666 | 54 | 14 | 7 | 28 | 0 | 5 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0005 | 0/0 | 2666 | 24 | 8 | 6 | 10 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0006 | 0/0 | 2666 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0007 | 0/0 | 2666 | 16 | 12 | 1 | 1 | 2 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0008 | 0/0 | 2666 | 8 | 3 | 0 | 4 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0010 | 0/0 | 2666 | 6 | 6 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0013 | 0/0 | 2666 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0014 | 0/0 | 2667 | 2 | 0 | 1 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2662): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0015 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0016 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2662): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0017 | 0/0 | 2667 | 1 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2662): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0020 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0021 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0001t0022 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0002t0001 | 0/0 | 2666 | 2 | 0 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0002t0002 | 0/0 | 2666 | 15 | 1 | 4 | 0 | 4 | 6 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0002t0005 | 0/0 | 2666 | 5 | 5 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0002t0007 | 0/0 | 2666 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0002t0011 | 0/0 | 2666 | 2 | 2 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0002t0018 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0002t0023 | 0/0 | 2667 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2662): Show |
chr16 | 85894162 | 85927606 |
| a0001c0003t0002 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0003t0004 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0003t0005 | 0/0 | 2666 | 12 | 1 | 5 | 4 | 0 | 2 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0003t0006 | 0/0 | 2666 | 7 | 0 | 1 | 6 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0004t0006 | 0/0 | 2666 | 9 | 0 | 2 | 7 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0004t0019 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0005t0001 | 0/0 | 2666 | 9 | 0 | 7 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0006t0012 | 0/0 | 2666 | 6 | 4 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0007t0005 | 0/0 | 2666 | 6 | 3 | 1 | 0 | 2 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0008t0009 | 0/0 | 2666 | 5 | 5 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0009t0007 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0009t0011 | 0/0 | 2666 | 4 | 2 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0010t0006 | 0/0 | 2666 | 4 | 0 | 0 | 4 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0001c0011t0009 | 0/0 | 2666 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0002c0013t0003 | 0/0 | 2667 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2662): Show |
chr16 | 85894162 | 85927606 |
| a0003c0014t0001 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| a0004c0012t0001 | 0/0 | 2666 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | GCCTG others(2661): Show |
chr16 | 85894162 | 85927606 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0002 | 0/0 | 15 | 1 | 5 | 8 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0003 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0004 | 0/0 | 9 | 2 | 2 | 1 | 1 | 3 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0006 | 1/0 | 8 | 1 | 4 | 0 | 2 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0005 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0008 | 0/0 | 9 | 1 | 3 | 3 | 0 | 2 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0059 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0030 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0008g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0008g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0008g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0013g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0014g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0014g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0015g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0016g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0017g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0020g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0021g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0001t0022g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0002g0007 | 0/0 | 8 | 0 | 2 | 0 | 3 | 3 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0002g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0002g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0018g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0002t0023g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0006g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0003t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0004t0019g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0005t0001g0001 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0005t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0006t0012g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0006t0012g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0006t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0006t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0007t0005g0057 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0007t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0007t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0007t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0007t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0008t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0008t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0008t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0008t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0008t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0009t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0009t0011g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0009t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0009t0011g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0010t0006g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0010t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0001c0011t0009g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0002c0013t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0003c0014t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| a0004c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0017 | g0047 | EUR | GBR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0084 | EUR | GBR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0081 | EUR | FIN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | FIN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | FIN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00408 | hp2 | a0001 | c0003 | t0005 | g0229 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00639 | hp1 | a0001 | c0003 | t0005 | g0138 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00639 | hp2 | a0001 | c0006 | t0012 | g0174 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01081 | hp1 | a0001 | c0006 | t0012 | g0028 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01081 | hp2 | a0001 | c0009 | t0011 | g0055 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01099 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01106 | hp1 | a0001 | c0005 | t0001 | g0108 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01175 | hp1 | a0001 | c0003 | t0005 | g0095 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01243 | hp1 | a0001 | c0009 | t0011 | g0173 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | PUR | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0211 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01256 | hp1 | a0001 | c0003 | t0005 | g0137 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01358 | hp1 | a0001 | c0003 | t0005 | g0187 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01433 | hp2 | a0001 | c0001 | t0014 | g0006 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0017 | EUR | IBS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0052 | EUR | IBS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01516 | hp1 | a0001 | c0007 | t0005 | g0057 | EUR | IBS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0017 | EUR | IBS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01884 | hp2 | a0001 | c0003 | t0005 | g0201 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01891 | hp1 | a0001 | c0008 | t0009 | g0177 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01934 | hp1 | a0001 | c0004 | t0006 | g0234 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01934 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01943 | hp1 | a0001 | c0004 | t0006 | g0232 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01943 | hp2 | a0001 | c0005 | t0001 | g0105 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01952 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01952 | hp2 | a0001 | c0003 | t0006 | g0135 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01978 | hp1 | a0001 | c0007 | t0005 | g0057 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01993 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02015 | hp1 | a0001 | c0003 | t0005 | g0203 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02040 | hp1 | a0001 | c0001 | t0016 | g0016 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02040 | hp2 | a0001 | c0004 | t0019 | g0218 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0193 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02071 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CDX | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | CDX | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CDX | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | CDX | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02257 | hp1 | a0001 | c0011 | t0009 | g0021 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0247 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02258 | hp2 | a0001 | c0011 | t0009 | g0021 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02280 | hp1 | a0001 | c0008 | t0009 | g0165 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0148 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0239 | AMR | PEL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02451 | hp2 | a0001 | c0007 | t0005 | g0179 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02572 | hp1 | a0001 | c0008 | t0009 | g0245 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02615 | hp1 | a0001 | c0002 | t0007 | g0067 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0216 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0070 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0195 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02647 | hp2 | a0001 | c0002 | t0011 | g0080 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02698 | hp1 | a0001 | c0001 | t0014 | g0004 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0183 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02723 | hp2 | a0001 | c0002 | t0005 | g0102 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0056 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02818 | hp2 | a0001 | c0002 | t0018 | g0194 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02886 | hp2 | a0001 | c0002 | t0007 | g0068 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02895 | hp1 | a0001 | c0007 | t0005 | g0178 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02896 | hp2 | a0001 | c0008 | t0009 | g0163 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02897 | hp1 | a0001 | c0008 | t0009 | g0162 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02922 | hp2 | a0001 | c0009 | t0011 | g0157 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02970 | hp1 | a0001 | c0011 | t0009 | g0021 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0065 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03017 | hp1 | a0002 | c0013 | t0003 | g0041 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0189 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0063 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0192 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0181 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0064 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0184 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03209 | hp1 | a0001 | c0006 | t0012 | g0028 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03225 | hp2 | a0001 | c0009 | t0007 | g0090 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0197 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03453 | hp2 | a0001 | c0009 | t0011 | g0055 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0092 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0132 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0246 | AFR | ESN | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03688 | hp1 | a0001 | c0003 | t0005 | g0215 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03831 | hp2 | a0001 | c0003 | t0005 | g0214 | SAS | BEB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | BEB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | BEB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0017 | SAS | BEB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | STU | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | YRI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18522 | hp2 | a0001 | c0006 | t0012 | g0175 | AFR | YRI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18747 | hp2 | a0001 | c0004 | t0006 | g0230 | EAS | CHB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | YRI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18906 | hp2 | a0001 | c0002 | t0011 | g0164 | AFR | YRI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18941 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18942 | hp1 | a0001 | c0003 | t0004 | g0242 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18946 | hp1 | a0001 | c0004 | t0006 | g0058 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18947 | hp1 | a0001 | c0001 | t0008 | g0048 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18948 | hp1 | a0001 | c0003 | t0006 | g0013 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18952 | hp1 | a0001 | c0004 | t0006 | g0147 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18954 | hp1 | a0001 | c0003 | t0005 | g0204 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18954 | hp2 | a0001 | c0001 | t0020 | g0237 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18961 | hp1 | a0001 | c0004 | t0006 | g0231 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18965 | hp1 | a0001 | c0003 | t0006 | g0013 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18967 | hp1 | a0001 | c0003 | t0005 | g0075 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0119 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18971 | hp1 | a0001 | c0010 | t0006 | g0032 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18972 | hp1 | a0001 | c0003 | t0006 | g0013 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18979 | hp2 | a0004 | c0012 | t0001 | g0001 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0129 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18992 | hp2 | a0001 | c0010 | t0006 | g0032 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0025 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19003 | hp1 | a0001 | c0003 | t0006 | g0013 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19006 | hp2 | a0001 | c0003 | t0006 | g0091 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19011 | hp2 | a0001 | c0003 | t0006 | g0136 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19030 | hp1 | a0001 | c0006 | t0012 | g0176 | AFR | LWK | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | LWK | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19043 | hp2 | a0001 | c0007 | t0005 | g0180 | AFR | LWK | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19055 | hp1 | a0001 | c0010 | t0006 | g0205 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19055 | hp2 | a0001 | c0004 | t0006 | g0058 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19056 | hp1 | a0001 | c0004 | t0006 | g0210 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0048 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19074 | hp1 | a0001 | c0004 | t0006 | g0206 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19080 | hp2 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19082 | hp1 | a0001 | c0010 | t0006 | g0032 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | YRI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA19240 | hp2 | a0001 | c0006 | t0012 | g0028 | AFR | YRI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | ASW | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | ASW | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0159 | EUR | TSI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20805 | hp2 | a0001 | c0007 | t0005 | g0209 | EUR | TSI | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0236 | SAS | GIH | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01123 | hp1 | a0001 | c0003 | t0005 | g0202 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG01123 | hp2 | a0001 | c0002 | t0023 | g0007 | AMR | CLM | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0182 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0099 | AFR | ACB | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0217 | AFR | MSL | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | USA | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18955 | hp1 | a0003 | c0014 | t0001 | g0133 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | USA | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | LWK | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | LWK | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0082 | REF | REF | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0006 | REF | REF | IRF8_chr16_85894162_85927606 | IRF8 | chr16 | 85894162 | 85927606 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85903034 | G | A | 1 | a0004 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.19G>A | p.Gly7Ser | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/9 | 82/2668 | 19/1281 | 7/426 | chr16 | 85903034 | |||
| chr16:85903117 | C | G | 1 | a0003 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.102C>G | p.Ser34Arg | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/9 | 165/2668 | 102/1281 | 34/426 | chr16 | 85903117 | |||
| chr16:85921161 | C | G | 1 | a0002 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1160C>G | p.Ala387Gly | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 1223/2668 | 1160/1281 | 387/426 | chr16 | 85921161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85909115 | A | G | 1 | a0001c0005 | 9 | HG01099.hp2 HG01106.hp1 HG01243.hp2 others(6): Show |
synonymous_variant | LOW | c.300A>G | p.Gln100Gln | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/9 | 363/2668 | 300/1281 | 100/426 | chr16 | 85909115 | |||
| chr16:85911598 | C | T | 2 | a0001c0009 a0001c0011 |
8 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(5): Show |
synonymous_variant | LOW | c.387C>T | p.Cys129Cys | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/9 | 450/2668 | 387/1281 | 129/426 | chr16 | 85911598 | |||
| chr16:85911625 | C | T | 1 | a0001c0002 | 29 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(26): Show |
synonymous_variant | LOW | c.414C>T | p.Cys138Cys | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/9 | 477/2668 | 414/1281 | 138/426 | chr16 | 85911625 | |||
| chr16:85911643 | C | T | 1 | a0001c0007 | 6 | HG01516.hp1 HG01978.hp1 HG02451.hp2 others(3): Show |
synonymous_variant | LOW | c.432C>T | p.Asp144Asp | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/9 | 495/2668 | 432/1281 | 144/426 | chr16 | 85911643 | |||
| chr16:85914492 | G | A | 2 | a0001c0003 a0001c0010 |
25 | HG00408.hp2 HG00639.hp1 HG01123.hp1 others(22): Show |
synonymous_variant | LOW | c.573G>A | p.Gly191Gly | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/9 | 636/2668 | 573/1281 | 191/426 | chr16 | 85914492 | |||
| chr16:85918487 | C | T | 1 | a0001c0006 | 6 | HG00639.hp2 HG01081.hp1 HG03209.hp1 others(3): Show |
synonymous_variant | LOW | c.672C>T | p.Pro224Pro | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/9 | 735/2668 | 672/1281 | 224/426 | chr16 | 85918487 | |||
| chr16:85921195 | G | A | 2 | a0001c0004 a0001c0010 |
14 | HG01934.hp1 HG01943.hp1 HG02040.hp2 others(11): Show |
synonymous_variant | LOW | c.1194G>A | p.Pro398Pro | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 1257/2668 | 1194/1281 | 398/426 | chr16 | 85921195 | |||
| chr16:85921237 | A | G | 2 | a0001c0008 a0001c0011 |
8 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
synonymous_variant | LOW | c.1236A>G | p.Ser412Ser | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 1299/2668 | 1236/1281 | 412/426 | chr16 | 85921237 | |||
| chr16:85921276 | C | T | 2 | a0001c0008 a0001c0011 |
8 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
synonymous_variant | LOW | c.1275C>T | p.Thr425Thr | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 1338/2668 | 1275/1281 | 425/426 | chr16 | 85921276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85921446 | C | T | 1 | a0001c0001t0014 | 2 | HG01433.hp2 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*164C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 164 | chr16 | 85921446 | ||||||
| chr16:85921636 | C | T | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0023 others(2): Show |
90 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*354C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 354 | chr16 | 85921636 | ||||||
| chr16:85921698 | G | T | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
337 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 416 | chr16 | 85921698 | ||||||
| chr16:85921701 | T | G | 2 | a0001c0002t0011 a0001c0009t0011 |
6 | HG01081.hp2 HG01243.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*419T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 419 | chr16 | 85921701 | ||||||
| chr16:85921901 | G | A | 1 | a0001c0004t0019 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 619 | chr16 | 85921901 | ||||||
| chr16:85921939 | C | T | 2 | a0001c0008t0009 a0001c0011t0009 |
8 | HG01891.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*657C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 657 | chr16 | 85921939 | ||||||
| chr16:85921944 | G | C | 1 | a0001c0001t0020 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 662 | chr16 | 85921944 | ||||||
| chr16:85921949 | G | T | 1 | a0001c0006t0012 | 6 | HG00639.hp2 HG01081.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*667G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 667 | chr16 | 85921949 | ||||||
| chr16:85921996 | G | A | 1 | a0001c0001t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 714 | chr16 | 85921996 | ||||||
| chr16:85922042 | A | G | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 760 | chr16 | 85922042 | ||||||
| chr16:85922057 | T | C | 9 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(6): Show |
121 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*775T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 775 | chr16 | 85922057 | ||||||
| chr16:85922061 | A | G | 1 | a0001c0001t0022 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*779A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 779 | chr16 | 85922061 | ||||||
| chr16:85922065 | C | T | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0015 others(11): Show |
162 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*783C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 783 | chr16 | 85922065 | ||||||
| chr16:85922123 | CA | C | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(32): Show |
372 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(369): Show |
3_prime_UTR_variant | MODIFIER | c.*843delA | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 843 | INFO_REALIGN_3_PRIME | chr16 | 85922123 | |||||
| chr16:85922303 | A | G | 5 | a0001c0001t0006 a0001c0003t0006 a0001c0004t0006 others(2): Show |
22 | HG01934.hp1 HG01943.hp1 HG01952.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1021A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 1021 | chr16 | 85922303 | ||||||
| chr16:85922342 | C | T | 1 | a0001c0001t0017 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1060C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 1060 | chr16 | 85922342 | ||||||
| chr16:85922438 | A | T | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
342 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*1156A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 9/9 | 1156 | chr16 | 85922438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:85899269 | G | T | 3 | a0001c0001t0007g0246 a0001c0001t0007g0247 a0001c0008t0009g0245 |
3 | HG02258.hp1 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-2+46G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899269 | |||||||
| chr16:85899382 | C | T | 32 | a0001c0001t0001g0060 a0001c0001t0001g0222 a0001c0001t0001g0223 others(29): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-2+159C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899382 | |||||||
| chr16:85899432 | C | T | 29 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0002g0011 others(26): Show |
48 | HG01123.hp1 HG01255.hp2 HG01516.hp1 others(45): Show |
intron_variant | MODIFIER | c.-2+209C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899432 | |||||||
| chr16:85899460 | C | T | 1 | a0001c0002t0007g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2+237C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899460 | |||||||
| chr16:85899504 | A | G | 3 | a0001c0001t0013g0192 a0001c0001t0013g0193 a0001c0002t0018g0194 |
3 | HG02055.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-2+281A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899504 | |||||||
| chr16:85899516 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-2+293G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899516 | |||||||
| chr16:85899587 | A | T | 1 | a0001c0001t0005g0033 | 3 | NA18946.hp2 NA18962.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-2+364A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899587 | |||||||
| chr16:85899622 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-2+399A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899622 | |||||||
| chr16:85899637 | G | A | 3 | a0001c0001t0010g0063 a0001c0001t0010g0064 a0001c0001t0010g0065 |
3 | HG02976.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+414G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899637 | |||||||
| chr16:85899927 | C | G | 1 | a0001c0001t0002g0191 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-2+704C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899927 | |||||||
| chr16:85899942 | T | G | 8 | a0001c0001t0002g0069 a0001c0001t0005g0066 a0001c0001t0013g0192 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+719T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899942 | |||||||
| chr16:85899975 | C | A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(13): Show |
33 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+752C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85899975 | |||||||
| chr16:85900009 | A | T | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-2+786A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900009 | |||||||
| chr16:85900033 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-2+810A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900033 | |||||||
| chr16:85900033 | A | T | 3 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0022g0189 |
3 | HG02280.hp2 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-2+810A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900033 | |||||||
| chr16:85900096 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-2+873T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900096 | |||||||
| chr16:85900112 | C | A | 2 | a0001c0001t0003g0037 a0001c0001t0003g0079 |
3 | HG02698.hp2 HG04228.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-2+889C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900112 | |||||||
| chr16:85900114 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-2+891A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900114 | |||||||
| chr16:85900123 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-2+900A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900123 | |||||||
| chr16:85900136 | C | G | 1 | a0001c0001t0003g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-2+913C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900136 | |||||||
| chr16:85900142 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2+919G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900142 | |||||||
| chr16:85900145 | C | G | 1 | a0001c0001t0005g0030 | 3 | HG01109.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+922C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900145 | |||||||
| chr16:85900197 | G | C | 1 | a0001c0002t0011g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-2+974G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900197 | |||||||
| chr16:85900209 | G | T | 1 | a0001c0003t0005g0187 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-2+986G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900209 | |||||||
| chr16:85900246 | C | G | 2 | a0001c0002t0005g0216 a0001c0002t0005g0217 |
2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+1023C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900246 | |||||||
| chr16:85900250 | A | C | 1 | a0001c0001t0004g0243 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-2+1027A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900250 | |||||||
| chr16:85900279 | A | G | 1 | a0001c0001t0003g0186 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-2+1056A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900279 | |||||||
| chr16:85900280 | C | G | 1 | a0001c0001t0001g0185 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-2+1057C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900280 | |||||||
| chr16:85900321 | G | T | 2 | a0001c0001t0007g0246 a0001c0001t0007g0247 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-2+1098G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900321 | |||||||
| chr16:85900429 | G | A | 1 | a0001c0002t0011g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-2+1206G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900429 | |||||||
| chr16:85900562 | C | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(256): Show |
422 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(419): Show |
intron_variant | MODIFIER | c.-2+1339C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900562 | |||||||
| chr16:85900572 | G | A | 3 | a0001c0001t0013g0192 a0001c0001t0013g0193 a0001c0002t0018g0194 |
3 | HG02055.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-2+1349G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900572 | |||||||
| chr16:85900618 | G | A | 3 | a0001c0001t0003g0081 a0001c0001t0003g0083 a0001c0001t0003g0084 |
3 | HG00099.hp2 HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.-2+1395G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900618 | |||||||
| chr16:85900838 | T | G | 1 | a0001c0001t0003g0085 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-2+1615T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900838 | |||||||
| chr16:85900868 | A | C | 1 | a0001c0001t0003g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-2+1645A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900868 | |||||||
| chr16:85900909 | A | AT | 52 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0002g0011 others(49): Show |
74 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.-2+1690dupT | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 85900909 | ||||||
| chr16:85900960 | A | G | 1 | a0001c0003t0005g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-2+1737A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900960 | |||||||
| chr16:85900977 | T | G | 2 | a0001c0001t0002g0199 a0001c0001t0004g0200 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+1754T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85900977 | |||||||
| chr16:85901011 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-2+1788A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901011 | |||||||
| chr16:85901157 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-1-1858C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901157 | |||||||
| chr16:85901226 | A | T | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-1-1789A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901226 | |||||||
| chr16:85901246 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-1-1769G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901246 | |||||||
| chr16:85901514 | G | A | 7 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(4): Show |
9 | HG02055.hp2 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-1501G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901514 | |||||||
| chr16:85901531 | T | C | 7 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(4): Show |
9 | HG02055.hp2 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-1484T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901531 | |||||||
| chr16:85901536 | T | G | 16 | a0001c0001t0002g0069 a0001c0001t0004g0029 a0001c0001t0004g0172 others(13): Show |
21 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-1-1479T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901536 | |||||||
| chr16:85901589 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-1-1426G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901589 | |||||||
| chr16:85901605 | A | T | 35 | a0001c0001t0001g0161 a0001c0001t0002g0003 a0001c0001t0002g0019 others(32): Show |
64 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-1-1410A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901605 | |||||||
| chr16:85901772 | G | A | 5 | a0001c0001t0002g0069 a0001c0001t0005g0066 a0001c0002t0005g0070 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1243G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901772 | |||||||
| chr16:85901777 | C | G | 1 | a0001c0009t0011g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-1-1238C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901777 | |||||||
| chr16:85901814 | T | G | 5 | a0001c0001t0002g0069 a0001c0001t0005g0066 a0001c0002t0005g0070 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1201T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901814 | |||||||
| chr16:85901900 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-1115C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901900 | |||||||
| chr16:85901927 | A | AT | 8 | a0001c0001t0002g0077 a0001c0001t0002g0191 a0001c0001t0003g0084 others(5): Show |
10 | HG00099.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-1073dupT | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 85901927 | ||||||
| chr16:85901927 | A | T | 1 | a0001c0001t0002g0155 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-1-1088A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901927 | |||||||
| chr16:85901927 | AT | A | 7 | a0001c0001t0003g0038 a0001c0001t0003g0088 a0001c0001t0013g0192 others(4): Show |
8 | HG01255.hp1 HG01358.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-1073delT | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 85901927 | ||||||
| chr16:85901927 | ATT | A | 10 | a0001c0001t0004g0029 a0001c0001t0004g0172 a0001c0001t0007g0171 others(7): Show |
15 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1-1074_-1-1073del others(2): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 85901927 | ||||||
| chr16:85901928 | T | A | 1 | a0001c0001t0002g0155 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-1-1087T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901928 | |||||||
| chr16:85901967 | T | C | 43 | a0001c0001t0001g0161 a0001c0001t0002g0003 a0001c0001t0002g0019 others(40): Show |
74 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1-1048T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85901967 | |||||||
| chr16:85902191 | T | C | 42 | a0001c0001t0001g0161 a0001c0001t0002g0003 a0001c0001t0002g0019 others(39): Show |
73 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-1-824T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902191 | |||||||
| chr16:85902208 | A | G | 1 | a0001c0001t0004g0151 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-1-807A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902208 | |||||||
| chr16:85902272 | A | G | 65 | a0001c0001t0001g0161 a0001c0001t0002g0003 a0001c0001t0002g0019 others(62): Show |
100 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-1-743A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902272 | |||||||
| chr16:85902462 | C | T | 1 | a0001c0002t0002g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-1-553C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902462 | |||||||
| chr16:85902521 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-1-494C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902521 | |||||||
| chr16:85902534 | G | A | 1 | a0001c0001t0005g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-481G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902534 | |||||||
| chr16:85902536 | C | A | 1 | a0001c0001t0005g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-479C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902536 | |||||||
| chr16:85902536 | C | T | 1 | a0001c0008t0009g0177 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1-479C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902536 | |||||||
| chr16:85902542 | G | A | 1 | a0001c0009t0007g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-1-473G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902542 | |||||||
| chr16:85902657 | C | T | 39 | a0001c0001t0001g0060 a0001c0001t0001g0222 a0001c0001t0001g0223 others(36): Show |
60 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-1-358C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902657 | |||||||
| chr16:85902690 | G | C | 2 | a0001c0003t0006g0013 a0001c0003t0006g0091 |
5 | NA18948.hp1 NA18965.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-325G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902690 | |||||||
| chr16:85902783 | T | TGGTGGCT others(3): Show |
217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(214): Show |
356 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(353): Show |
intron_variant | MODIFIER | c.-1-228_-1-219dupGG others(8): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 85902783 | ||||||
| chr16:85902859 | T | G | 4 | a0001c0001t0002g0158 a0001c0001t0007g0246 a0001c0001t0007g0247 others(1): Show |
4 | HG02258.hp1 HG02572.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-156T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 1/8 | chr16 | 85902859 | |||||||
| chr16:85903220 | G | T | 1 | a0003c0014t0001g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.174+31G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903220 | |||||||
| chr16:85903372 | T | C | 75 | a0001c0001t0001g0161 a0001c0001t0002g0003 a0001c0001t0002g0019 others(72): Show |
112 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.174+183T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903372 | |||||||
| chr16:85903383 | G | T | 1 | a0001c0001t0004g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.174+194G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903383 | |||||||
| chr16:85903399 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.174+210C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903399 | |||||||
| chr16:85903427 | G | C | 3 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0022g0189 |
3 | HG02280.hp2 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.174+238G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903427 | |||||||
| chr16:85903495 | C | T | 4 | a0001c0001t0002g0199 a0001c0001t0004g0200 a0001c0001t0007g0211 others(1): Show |
4 | HG01255.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+306C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903495 | |||||||
| chr16:85903696 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.174+507G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903696 | |||||||
| chr16:85903725 | C | T | 2 | a0001c0001t0010g0064 a0001c0001t0010g0065 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.174+536C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903725 | |||||||
| chr16:85903756 | G | C | 17 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(14): Show |
34 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+567G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903756 | |||||||
| chr16:85903880 | T | C | 2 | a0001c0001t0004g0219 a0001c0001t0004g0220 |
2 | HG02056.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.174+691T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903880 | |||||||
| chr16:85903927 | A | T | 6 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(3): Show |
8 | HG02055.hp2 HG02622.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+738A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903927 | |||||||
| chr16:85903976 | A | G | 7 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(4): Show |
9 | HG02055.hp2 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+787A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85903976 | |||||||
| chr16:85904028 | C | A | 1 | a0001c0001t0003g0034 | 2 | HG01109.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.174+839C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904028 | |||||||
| chr16:85904045 | C | T | 11 | a0001c0001t0001g0131 a0001c0001t0002g0188 a0001c0001t0002g0190 others(8): Show |
13 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+856C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904045 | |||||||
| chr16:85904050 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(72): Show |
134 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.174+861C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904050 | |||||||
| chr16:85904247 | G | T | 3 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0022g0189 |
3 | HG02280.hp2 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.174+1058G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904247 | |||||||
| chr16:85904323 | T | G | 1 | a0001c0001t0004g0221 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.174+1134T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904323 | |||||||
| chr16:85904451 | C | G | 3 | a0001c0001t0004g0061 a0001c0001t0004g0240 a0001c0001t0004g0241 |
4 | NA18957.hp1 NA18967.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+1262C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904451 | |||||||
| chr16:85904456 | T | G | 2 | a0001c0001t0021g0092 a0001c0009t0007g0090 |
2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.174+1267T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904456 | |||||||
| chr16:85904614 | C | T | 1 | a0001c0004t0006g0210 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.174+1425C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904614 | |||||||
| chr16:85904810 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0004g0239 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.174+1622_174+1623i others(21): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904810 | ||||||
| chr16:85904812 | C | CT | 15 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(12): Show |
26 | HG00423.hp2 HG00741.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.174+1643dupT | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTT | 21 | a0001c0001t0001g0161 a0001c0001t0001g0222 a0001c0001t0004g0029 others(18): Show |
33 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.174+1642_174+1643d others(4): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTT | 7 | a0001c0001t0004g0031 a0001c0001t0004g0198 a0001c0001t0005g0087 others(4): Show |
9 | HG02040.hp2 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+1640_174+1643d others(6): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(1): Show |
36 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0027 others(33): Show |
55 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.174+1636_174+1643d others(10): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0013g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.174+1633_174+1643d others(13): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(7): Show |
4 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0244 others(1): Show |
5 | HG02559.hp2 NA18939.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+1630_174+1643d others(16): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.174+1629_174+1643d others(17): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(13): Show |
3 | a0001c0001t0004g0226 a0001c0002t0011g0164 a0001c0008t0009g0165 |
3 | HG02280.hp1 NA18906.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.174+1624_174+1643d others(22): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(14): Show |
15 | a0001c0001t0002g0166 a0001c0001t0003g0228 a0001c0001t0003g0233 others(12): Show |
24 | HG00408.hp2 HG01071.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.174+1643_174+1644i others(23): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(15): Show |
15 | a0001c0001t0001g0130 a0001c0001t0001g0235 a0001c0001t0004g0005 others(12): Show |
25 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+1643_174+1644i others(24): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0062 a0001c0001t0020g0237 a0001c0002t0007g0068 |
3 | HG02886.hp2 NA18945.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.174+1643_174+1644i others(25): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0002g0069 a0001c0001t0004g0220 a0001c0001t0004g0238 |
3 | HG02071.hp2 HG02145.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.174+1643_174+1644i others(26): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(21): Show |
1 | a0001c0002t0005g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.174+1643_174+1644i others(30): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0013g0192 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.174+1643_174+1644i others(32): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0013g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.174+1643_174+1644i others(33): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85904812 | ||||||
| chr16:85904812 | C | T | 1 | a0001c0001t0004g0239 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.174+1623C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904812 | |||||||
| chr16:85904870 | T | C | 2 | a0001c0001t0003g0047 a0001c0001t0017g0047 |
2 | HG00099.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.174+1681T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904870 | |||||||
| chr16:85904989 | T | G | 27 | a0001c0001t0001g0161 a0001c0001t0002g0069 a0001c0001t0002g0213 others(24): Show |
42 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.174+1800T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85904989 | |||||||
| chr16:85905075 | C | T | 34 | a0001c0001t0001g0161 a0001c0001t0002g0069 a0001c0001t0002g0213 others(31): Show |
51 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.174+1886C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905075 | |||||||
| chr16:85905149 | A | G | 34 | a0001c0001t0001g0161 a0001c0001t0002g0069 a0001c0001t0002g0213 others(31): Show |
51 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.174+1960A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905149 | |||||||
| chr16:85905211 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.174+2022C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905211 | |||||||
| chr16:85905226 | C | T | 7 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(4): Show |
9 | HG02055.hp2 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+2037C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905226 | |||||||
| chr16:85905229 | G | A | 31 | a0001c0001t0001g0161 a0001c0001t0002g0069 a0001c0001t0002g0199 others(28): Show |
46 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.174+2040G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905229 | |||||||
| chr16:85905316 | C | T | 1 | a0001c0001t0007g0099 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.174+2127C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905316 | |||||||
| chr16:85905362 | G | T | 1 | a0001c0001t0005g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+2173G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905362 | |||||||
| chr16:85905464 | T | C | 1 | a0001c0004t0006g0234 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.174+2275T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905464 | |||||||
| chr16:85905614 | C | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0123 others(2): Show |
6 | HG00438.hp1 HG00673.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+2425C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905614 | |||||||
| chr16:85905658 | TGAGAGGC others(13): Show |
T | 1 | a0001c0001t0004g0221 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.174+2471_174+2490d others(22): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85905658 | ||||||
| chr16:85905702 | G | C | 1 | a0001c0002t0011g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.174+2513G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905702 | |||||||
| chr16:85905830 | G | C | 3 | a0001c0001t0002g0213 a0001c0002t0002g0184 a0001c0004t0006g0058 |
4 | HG02165.hp1 HG03195.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+2641G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905830 | |||||||
| chr16:85905844 | G | C | 2 | a0001c0001t0003g0024 a0001c0001t0008g0048 |
5 | NA18947.hp1 NA18999.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+2655G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905844 | |||||||
| chr16:85905855 | A | T | 1 | a0001c0001t0010g0183 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.174+2666A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905855 | |||||||
| chr16:85905881 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.174+2692A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905881 | |||||||
| chr16:85905918 | G | T | 2 | a0001c0001t0002g0199 a0001c0001t0004g0200 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.174+2729G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905918 | |||||||
| chr16:85905929 | A | C | 3 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0022g0189 |
3 | HG02280.hp2 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.174+2740A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905929 | |||||||
| chr16:85905948 | T | C | 1 | a0001c0001t0007g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.174+2759T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905948 | |||||||
| chr16:85905976 | C | G | 1 | a0001c0001t0002g0020 | 3 | NA18948.hp2 NA18981.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.174+2787C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85905976 | |||||||
| chr16:85906044 | T | A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(14): Show |
34 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+2855T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906044 | |||||||
| chr16:85906052 | C | T | 1 | a0001c0001t0005g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+2863C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906052 | |||||||
| chr16:85906060 | G | A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(14): Show |
34 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+2871G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906060 | |||||||
| chr16:85906111 | G | C | 1 | a0001c0001t0007g0051 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.175-2879G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906111 | |||||||
| chr16:85906257 | G | A | 7 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(4): Show |
9 | HG02055.hp2 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-2733G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906257 | |||||||
| chr16:85906300 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0130 a0001c0001t0007g0129 |
3 | NA18945.hp2 NA18983.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.175-2690T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906300 | |||||||
| chr16:85906347 | G | A | 1 | a0001c0001t0007g0129 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.175-2643G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906347 | |||||||
| chr16:85906347 | G | C | 1 | a0001c0003t0005g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.175-2643G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906347 | |||||||
| chr16:85906347 | G | T | 7 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(4): Show |
9 | HG02055.hp2 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-2643G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906347 | |||||||
| chr16:85906404 | C | T | 7 | a0001c0001t0001g0161 a0001c0002t0002g0007 a0001c0002t0002g0052 others(4): Show |
16 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-2586C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906404 | |||||||
| chr16:85906405 | G | T | 2 | a0001c0002t0005g0216 a0001c0002t0005g0217 |
2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175-2585G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906405 | |||||||
| chr16:85906661 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.175-2329C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906661 | |||||||
| chr16:85906670 | A | G | 1 | a0001c0002t0005g0217 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.175-2320A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906670 | |||||||
| chr16:85906702 | C | T | 8 | a0001c0001t0002g0069 a0001c0001t0005g0066 a0001c0001t0013g0192 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-2288C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906702 | |||||||
| chr16:85906787 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.175-2203A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906787 | |||||||
| chr16:85906807 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.175-2183A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906807 | |||||||
| chr16:85906826 | T | G | 2 | a0001c0001t0021g0092 a0001c0009t0007g0090 |
2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.175-2164T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85906826 | |||||||
| chr16:85907406 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.175-1584G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907406 | |||||||
| chr16:85907407 | C | T | 52 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0130 others(49): Show |
80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.175-1583C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907407 | |||||||
| chr16:85907444 | C | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0128 |
2 | NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.175-1546C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907444 | |||||||
| chr16:85907524 | A | G | 1 | a0001c0001t0005g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.175-1466A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907524 | |||||||
| chr16:85907550 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1440C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907550 | |||||||
| chr16:85907570 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1420T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907570 | |||||||
| chr16:85907571 | G | GAGCTGTG others(3): Show |
1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1419_175-1418i others(12): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907571 | |||||||
| chr16:85907586 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1404G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907586 | |||||||
| chr16:85907589 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1401G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907589 | |||||||
| chr16:85907600 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1390A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907600 | |||||||
| chr16:85907601 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1389C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907601 | |||||||
| chr16:85907605 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1385G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907605 | |||||||
| chr16:85907609 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1381G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907609 | |||||||
| chr16:85907612 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1378G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907612 | |||||||
| chr16:85907623 | G | A | 5 | a0001c0001t0004g0156 a0001c0001t0005g0040 a0001c0001t0005g0096 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-1367G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907623 | |||||||
| chr16:85907635 | G | A | 9 | a0001c0001t0004g0031 a0001c0001t0004g0196 a0001c0001t0004g0198 others(6): Show |
11 | HG02055.hp1 HG02055.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-1355G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907635 | |||||||
| chr16:85907678 | A | G | 1 | a0001c0001t0007g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.175-1312A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907678 | |||||||
| chr16:85907684 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1306T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907684 | |||||||
| chr16:85907724 | A | C | 10 | a0001c0001t0008g0182 a0001c0001t0010g0056 a0001c0001t0010g0063 others(7): Show |
10 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-1266A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907724 | |||||||
| chr16:85907750 | C | A | 1 | a0001c0001t0005g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.175-1240C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907750 | |||||||
| chr16:85907874 | GGAAGTGG others(72): Show |
G | 7 | a0001c0001t0001g0161 a0001c0002t0002g0007 a0001c0002t0002g0052 others(4): Show |
16 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-998_175-920del others(79): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85907874 | ||||||
| chr16:85907884 | A | G | 1 | a0001c0001t0008g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175-1106A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85907884 | |||||||
| chr16:85907998 | G | GGAAAGTT others(72): Show |
1 | a0001c0002t0002g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.175-954_175-876dup others(79): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 85907998 | ||||||
| chr16:85908032 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.175-958T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908032 | |||||||
| chr16:85908145 | T | A | 2 | a0001c0001t0021g0092 a0001c0009t0007g0090 |
2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.175-845T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908145 | |||||||
| chr16:85908168 | C | T | 115 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0130 others(112): Show |
173 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.175-822C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908168 | |||||||
| chr16:85908569 | G | C | 39 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(36): Show |
62 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.175-421G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908569 | |||||||
| chr16:85908814 | T | A | 43 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(40): Show |
65 | HG00438.hp2 HG00544.hp2 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.175-176T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908814 | |||||||
| chr16:85908848 | T | C | 1 | a0001c0001t0003g0085 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.175-142T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908848 | |||||||
| chr16:85908875 | G | A | 1 | a0001c0001t0004g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175-115G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908875 | |||||||
| chr16:85908890 | T | C | 56 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(53): Show |
78 | HG00438.hp2 HG00544.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.175-100T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 2/8 | chr16 | 85908890 | |||||||
| chr16:85909456 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0123 |
3 | HG00673.hp2 NA19058.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.358+283T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85909456 | |||||||
| chr16:85909537 | A | G | 18 | a0001c0001t0004g0029 a0001c0001t0004g0172 a0001c0001t0005g0098 others(15): Show |
20 | HG01167.hp1 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.358+364A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85909537 | |||||||
| chr16:85909562 | G | C | 13 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(10): Show |
29 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.358+389G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85909562 | |||||||
| chr16:85909818 | A | G | 11 | a0001c0001t0008g0182 a0001c0001t0010g0056 a0001c0001t0010g0063 others(8): Show |
11 | HG02451.hp2 HG02559.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+645A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85909818 | |||||||
| chr16:85909860 | T | C | 106 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(103): Show |
163 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.358+687T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85909860 | |||||||
| chr16:85910303 | C | T | 1 | a0001c0003t0002g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.358+1130C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910303 | |||||||
| chr16:85910417 | A | G | 7 | a0001c0001t0007g0026 a0001c0001t0007g0152 a0001c0001t0007g0153 others(4): Show |
12 | HG01081.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.359-1153A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910417 | |||||||
| chr16:85910493 | T | A | 4 | a0001c0009t0007g0090 a0001c0009t0011g0055 a0001c0009t0011g0157 others(1): Show |
7 | HG01081.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-1077T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910493 | |||||||
| chr16:85910634 | T | G | 1 | a0001c0001t0002g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.359-936T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910634 | |||||||
| chr16:85910646 | A | C | 1 | a0001c0001t0002g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.359-924A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910646 | |||||||
| chr16:85910714 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.359-856C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910714 | |||||||
| chr16:85910733 | T | C | 1 | a0001c0005t0001g0105 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.359-837T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910733 | |||||||
| chr16:85910777 | A | G | 1 | a0001c0001t0001g0023 | 3 | NA18956.hp1 NA18983.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.359-793A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910777 | |||||||
| chr16:85910779 | C | T | 1 | a0001c0002t0002g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.359-791C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910779 | |||||||
| chr16:85910780 | A | G | 1 | a0001c0001t0007g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.359-790A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910780 | |||||||
| chr16:85910810 | C | T | 18 | a0001c0001t0005g0066 a0001c0001t0007g0026 a0001c0001t0007g0152 others(15): Show |
20 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.359-760C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910810 | |||||||
| chr16:85910826 | T | C | 1 | a0001c0005t0001g0105 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.359-744T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910826 | |||||||
| chr16:85910833 | A | G | 83 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(80): Show |
135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.359-737A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910833 | |||||||
| chr16:85910951 | G | T | 10 | a0001c0001t0001g0044 a0001c0001t0003g0016 a0001c0001t0003g0018 others(7): Show |
18 | HG02027.hp2 HG02040.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.359-619G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910951 | |||||||
| chr16:85910976 | C | G | 1 | a0001c0003t0005g0187 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.359-594C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910976 | |||||||
| chr16:85910986 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.359-584G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85910986 | |||||||
| chr16:85911074 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.359-496G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911074 | |||||||
| chr16:85911083 | G | A | 1 | a0001c0003t0005g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.359-487G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911083 | |||||||
| chr16:85911194 | G | T | 16 | a0001c0001t0008g0182 a0001c0001t0010g0056 a0001c0001t0010g0063 others(13): Show |
16 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.359-376G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911194 | |||||||
| chr16:85911217 | T | G | 110 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(107): Show |
168 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.359-353T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911217 | |||||||
| chr16:85911414 | C | T | 5 | a0001c0001t0010g0056 a0001c0001t0010g0063 a0001c0001t0010g0064 others(2): Show |
5 | HG02809.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-156C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911414 | |||||||
| chr16:85911428 | T | G | 1 | a0001c0001t0002g0199 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.359-142T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911428 | |||||||
| chr16:85911470 | T | C | 105 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(102): Show |
177 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.359-100T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911470 | |||||||
| chr16:85911500 | G | T | 1 | a0001c0002t0018g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.359-70G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 3/8 | chr16 | 85911500 | |||||||
| chr16:85911763 | C | T | 8 | a0001c0001t0002g0213 a0001c0001t0006g0148 a0001c0004t0006g0058 others(5): Show |
9 | HG01934.hp1 HG01943.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+105C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85911763 | |||||||
| chr16:85911781 | G | C | 8 | a0001c0001t0002g0213 a0001c0001t0006g0148 a0001c0004t0006g0058 others(5): Show |
9 | HG01934.hp1 HG01943.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+123G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85911781 | |||||||
| chr16:85911867 | C | G | 1 | a0001c0001t0005g0066 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.447+209C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85911867 | |||||||
| chr16:85911879 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.447+221C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85911879 | |||||||
| chr16:85911947 | C | G | 5 | a0001c0001t0010g0056 a0001c0001t0010g0063 a0001c0001t0010g0064 others(2): Show |
5 | HG02809.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+289C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85911947 | |||||||
| chr16:85911976 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.447+318T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85911976 | |||||||
| chr16:85912069 | T | G | 130 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(127): Show |
214 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.447+411T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912069 | |||||||
| chr16:85912083 | C | G | 4 | a0001c0001t0005g0087 a0001c0001t0007g0026 a0001c0001t0007g0152 others(1): Show |
6 | HG02109.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+425C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912083 | |||||||
| chr16:85912122 | T | G | 130 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(127): Show |
214 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.447+464T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912122 | |||||||
| chr16:85912137 | G | T | 1 | a0001c0001t0022g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.447+479G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912137 | |||||||
| chr16:85912194 | T | C | 1 | a0001c0001t0022g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.447+536T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912194 | |||||||
| chr16:85912233 | T | C | 153 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(150): Show |
238 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.447+575T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912233 | |||||||
| chr16:85912266 | G | GGATGCCC others(44): Show |
1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.447+619_447+620ins others(51): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 85912266 | ||||||
| chr16:85912411 | C | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(27): Show |
63 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.448-720C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912411 | |||||||
| chr16:85912718 | T | C | 68 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(65): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.448-413T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912718 | |||||||
| chr16:85912844 | T | C | 154 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(151): Show |
234 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.448-287T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912844 | |||||||
| chr16:85912875 | G | C | 108 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(105): Show |
183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.448-256G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912875 | |||||||
| chr16:85912888 | A | G | 68 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(65): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.448-243A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85912888 | |||||||
| chr16:85913045 | T | C | 1 | a0001c0001t0010g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.448-86T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85913045 | |||||||
| chr16:85913078 | A | G | 1 | a0001c0001t0010g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.448-53A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 4/8 | chr16 | 85913078 | |||||||
| chr16:85913258 | T | C | 1 | a0001c0005t0001g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.553+22T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913258 | |||||||
| chr16:85913288 | G | A | 4 | a0001c0001t0005g0087 a0001c0001t0007g0026 a0001c0001t0007g0152 others(1): Show |
6 | HG02109.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.553+52G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913288 | |||||||
| chr16:85913308 | C | T | 1 | a0001c0001t0004g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.553+72C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913308 | |||||||
| chr16:85913330 | A | T | 1 | a0001c0001t0005g0039 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.553+94A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913330 | |||||||
| chr16:85913380 | C | G | 1 | a0001c0001t0022g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.553+144C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913380 | |||||||
| chr16:85913450 | C | T | 3 | a0001c0001t0007g0026 a0001c0001t0007g0152 a0001c0001t0007g0153 |
5 | HG02109.hp2 HG02622.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.553+214C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913450 | |||||||
| chr16:85913498 | T | TCC | 37 | a0001c0001t0004g0200 a0001c0001t0005g0066 a0001c0001t0007g0051 others(34): Show |
44 | HG00408.hp2 HG00639.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.553+265_553+266dup others(2): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 85913498 | ||||||
| chr16:85913501 | C | T | 8 | a0001c0001t0002g0213 a0001c0004t0006g0058 a0001c0004t0006g0147 others(5): Show |
9 | HG01934.hp1 HG01943.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.553+265C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913501 | |||||||
| chr16:85913606 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.553+370C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913606 | |||||||
| chr16:85913721 | A | G | 123 | a0001c0001t0001g0060 a0001c0001t0001g0118 a0001c0001t0001g0223 others(120): Show |
202 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.553+485A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913721 | |||||||
| chr16:85913869 | C | T | 6 | a0001c0002t0002g0007 a0001c0002t0002g0052 a0001c0002t0002g0053 others(3): Show |
15 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.554-604C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913869 | |||||||
| chr16:85913921 | G | C | 117 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(114): Show |
195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.554-552G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913921 | |||||||
| chr16:85913922 | G | A | 4 | a0001c0001t0005g0087 a0001c0001t0007g0026 a0001c0001t0007g0152 others(1): Show |
6 | HG02109.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.554-551G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913922 | |||||||
| chr16:85913954 | C | A | 1 | a0001c0001t0004g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.554-519C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85913954 | |||||||
| chr16:85914173 | T | C | 118 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(115): Show |
196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.554-300T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85914173 | |||||||
| chr16:85914279 | T | C | 2 | a0001c0002t0011g0080 a0001c0002t0011g0164 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.554-194T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85914279 | |||||||
| chr16:85914306 | G | A | 4 | a0001c0001t0002g0069 a0001c0001t0004g0031 a0001c0001t0004g0196 others(1): Show |
6 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.554-167G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85914306 | |||||||
| chr16:85914372 | G | A | 8 | a0001c0001t0005g0039 a0001c0002t0005g0102 a0001c0002t0005g0197 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.554-101G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85914372 | |||||||
| chr16:85914407 | A | G | 2 | a0001c0002t0007g0067 a0001c0002t0007g0068 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.554-66A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 5/8 | chr16 | 85914407 | |||||||
| chr16:85914603 | C | CGAGGATG others(203): Show |
4 | a0001c0001t0004g0094 a0001c0001t0004g0156 a0001c0001t0004g0198 others(1): Show |
4 | HG02630.hp1 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+113_601+322dup others(210): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 85914603 | ||||||
| chr16:85914645 | C | CGAGGATG others(35): Show |
2 | a0001c0001t0002g0213 a0001c0004t0006g0058 |
3 | HG02165.hp1 NA18946.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.601+125_601+126ins others(42): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914645 | |||||||
| chr16:85914646 | A | G | 9 | a0001c0001t0002g0213 a0001c0001t0006g0148 a0001c0004t0006g0058 others(6): Show |
10 | HG01934.hp1 HG01943.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+126A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914646 | |||||||
| chr16:85914659 | A | C | 1 | a0001c0001t0004g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+139A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914659 | |||||||
| chr16:85914695 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.601+175A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914695 | |||||||
| chr16:85914702 | C | T | 1 | a0001c0001t0021g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.601+182C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914702 | |||||||
| chr16:85914723 | T | C | 15 | a0001c0001t0004g0089 a0001c0001t0005g0039 a0001c0002t0002g0007 others(12): Show |
25 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.601+203T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914723 | |||||||
| chr16:85914766 | C | T | 4 | a0001c0001t0005g0087 a0001c0001t0007g0026 a0001c0001t0007g0152 others(1): Show |
6 | HG02109.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+246C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914766 | |||||||
| chr16:85914808 | G | C | 1 | a0001c0001t0004g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+288G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914808 | |||||||
| chr16:85914836 | G | A | 7 | a0001c0002t0005g0102 a0001c0002t0005g0197 a0001c0002t0005g0216 others(4): Show |
7 | HG02451.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+316G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914836 | |||||||
| chr16:85914836 | G | GGAAGTCG others(77): Show |
1 | a0001c0001t0005g0039 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.601+327_601+328ins others(84): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 85914836 | ||||||
| chr16:85914863 | T | A | 1 | a0001c0001t0003g0142 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.601+343T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914863 | |||||||
| chr16:85914871 | TG | T | 18 | a0001c0001t0004g0200 a0001c0001t0007g0051 a0001c0001t0007g0171 others(15): Show |
19 | HG01255.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.601+353delG | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 85914871 | ||||||
| chr16:85914874 | T | A | 18 | a0001c0001t0004g0200 a0001c0001t0007g0051 a0001c0001t0007g0171 others(15): Show |
19 | HG01255.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.601+354T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85914874 | |||||||
| chr16:85915035 | G | A | 113 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(110): Show |
181 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.601+515G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915035 | |||||||
| chr16:85915117 | G | GGAGCCCT others(6): Show |
109 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(106): Show |
175 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.601+598_601+599ins others(13): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 85915117 | ||||||
| chr16:85915117 | G | GGAGCCTT others(6): Show |
4 | a0001c0001t0005g0087 a0001c0001t0007g0026 a0001c0001t0007g0152 others(1): Show |
6 | HG02109.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+598_601+599ins others(13): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 85915117 | ||||||
| chr16:85915175 | G | C | 1 | a0001c0004t0006g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.601+655G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915175 | |||||||
| chr16:85915212 | T | G | 1 | a0001c0001t0002g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.601+692T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915212 | |||||||
| chr16:85915310 | C | T | 4 | a0001c0001t0006g0148 a0001c0004t0006g0206 a0001c0004t0006g0232 others(1): Show |
4 | HG01934.hp1 HG01943.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+790C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915310 | |||||||
| chr16:85915408 | C | G | 7 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0006t0012g0028 others(4): Show |
9 | HG00639.hp2 HG01081.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.601+888C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915408 | |||||||
| chr16:85915465 | G | A | 29 | a0001c0001t0002g0213 a0001c0001t0004g0094 a0001c0001t0004g0156 others(26): Show |
39 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.601+945G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915465 | |||||||
| chr16:85915468 | G | A | 1 | a0001c0003t0006g0135 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.601+948G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915468 | |||||||
| chr16:85915468 | G | C | 8 | a0001c0001t0008g0182 a0001c0001t0010g0056 a0001c0001t0010g0063 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+948G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915468 | |||||||
| chr16:85915501 | C | G | 6 | a0001c0002t0002g0007 a0001c0002t0002g0052 a0001c0002t0002g0053 others(3): Show |
15 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.601+981C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915501 | |||||||
| chr16:85915583 | G | T | 15 | a0001c0001t0004g0200 a0001c0001t0005g0039 a0001c0001t0007g0051 others(12): Show |
17 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.601+1063G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915583 | |||||||
| chr16:85915665 | G | A | 45 | a0001c0001t0002g0027 a0001c0001t0002g0054 a0001c0001t0002g0213 others(42): Show |
59 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.601+1145G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915665 | |||||||
| chr16:85915698 | A | T | 17 | a0001c0001t0002g0027 a0001c0001t0002g0054 a0001c0001t0004g0200 others(14): Show |
22 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.601+1178A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915698 | |||||||
| chr16:85915703 | T | A | 1 | a0001c0001t0004g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.601+1183T>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915703 | |||||||
| chr16:85915705 | C | T | 1 | a0001c0002t0011g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.601+1185C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915705 | |||||||
| chr16:85915773 | A | C | 1 | a0001c0001t0008g0050 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.601+1253A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915773 | |||||||
| chr16:85915818 | A | G | 31 | a0001c0001t0002g0166 a0001c0001t0002g0213 a0001c0001t0004g0094 others(28): Show |
42 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.601+1298A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915818 | |||||||
| chr16:85915853 | G | T | 17 | a0001c0001t0002g0027 a0001c0001t0002g0054 a0001c0001t0004g0200 others(14): Show |
22 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.601+1333G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915853 | |||||||
| chr16:85915867 | G | T | 33 | a0001c0001t0001g0060 a0001c0001t0001g0123 a0001c0001t0001g0223 others(30): Show |
55 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.601+1347G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915867 | |||||||
| chr16:85915888 | T | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0207 |
2 | NA18977.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.601+1368T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915888 | |||||||
| chr16:85915952 | T | C | 166 | a0001c0001t0001g0060 a0001c0001t0001g0123 a0001c0001t0001g0223 others(163): Show |
255 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.601+1432T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85915952 | |||||||
| chr16:85916290 | A | G | 40 | a0001c0001t0002g0213 a0001c0001t0004g0029 a0001c0001t0004g0094 others(37): Show |
53 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.601+1770A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916290 | |||||||
| chr16:85916320 | G | C | 1 | a0001c0002t0002g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.601+1800G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916320 | |||||||
| chr16:85916430 | C | T | 1 | a0001c0001t0004g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.601+1910C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916430 | |||||||
| chr16:85916454 | A | G | 2 | a0001c0010t0006g0032 a0001c0010t0006g0205 |
4 | NA18971.hp1 NA18992.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+1934A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916454 | |||||||
| chr16:85916538 | T | C | 19 | a0001c0001t0002g0027 a0001c0001t0002g0054 a0001c0001t0004g0200 others(16): Show |
24 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.602-1879T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916538 | |||||||
| chr16:85916582 | C | A | 1 | a0001c0001t0020g0237 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.602-1835C>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916582 | |||||||
| chr16:85916841 | C | T | 18 | a0001c0001t0002g0027 a0001c0001t0002g0054 a0001c0001t0004g0200 others(15): Show |
23 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.602-1576C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916841 | |||||||
| chr16:85916850 | C | T | 18 | a0001c0001t0002g0027 a0001c0001t0002g0054 a0001c0001t0004g0200 others(15): Show |
23 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.602-1567C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916850 | |||||||
| chr16:85916902 | G | C | 1 | a0001c0002t0018g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.602-1515G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85916902 | |||||||
| chr16:85917080 | A | G | 58 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(55): Show |
97 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.602-1337A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917080 | |||||||
| chr16:85917258 | G | T | 1 | a0001c0001t0002g0036 | 2 | NA18977.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.602-1159G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917258 | |||||||
| chr16:85917292 | A | G | 5 | a0001c0008t0009g0162 a0001c0008t0009g0163 a0001c0008t0009g0165 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-1125A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917292 | |||||||
| chr16:85917315 | A | G | 62 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(59): Show |
97 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.602-1102A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917315 | |||||||
| chr16:85917370 | A | T | 81 | a0001c0001t0001g0060 a0001c0001t0001g0123 a0001c0001t0001g0223 others(78): Show |
121 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.602-1047A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917370 | |||||||
| chr16:85917408 | G | A | 1 | a0001c0001t0022g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.602-1009G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917408 | |||||||
| chr16:85917589 | A | G | 18 | a0001c0001t0002g0027 a0001c0001t0002g0054 a0001c0001t0004g0200 others(15): Show |
23 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.602-828A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917589 | |||||||
| chr16:85917600 | A | G | 7 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0006t0012g0028 others(4): Show |
9 | HG00639.hp2 HG01081.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-817A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917600 | |||||||
| chr16:85917652 | A | G | 63 | a0001c0001t0001g0060 a0001c0001t0001g0123 a0001c0001t0001g0223 others(60): Show |
98 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.602-765A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917652 | |||||||
| chr16:85917748 | A | G | 128 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(125): Show |
211 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.602-669A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917748 | |||||||
| chr16:85917795 | C | T | 1 | a0001c0002t0005g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.602-622C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917795 | |||||||
| chr16:85917903 | T | C | 1 | a0001c0003t0006g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.602-514T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85917903 | |||||||
| chr16:85918029 | C | T | 7 | a0001c0001t0002g0141 a0001c0002t0002g0007 a0001c0002t0002g0052 others(4): Show |
16 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.602-388C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918029 | |||||||
| chr16:85918030 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(126): Show |
220 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.602-387G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918030 | |||||||
| chr16:85918041 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(127): Show |
222 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.602-376G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918041 | |||||||
| chr16:85918051 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(80): Show |
140 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.602-366A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918051 | |||||||
| chr16:85918076 | A | G | 7 | a0001c0001t0002g0141 a0001c0002t0002g0007 a0001c0002t0002g0052 others(4): Show |
16 | HG00280.hp2 HG00741.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.602-341A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918076 | |||||||
| chr16:85918077 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.602-340T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918077 | |||||||
| chr16:85918131 | C | T | 1 | a0001c0001t0004g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.602-286C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918131 | |||||||
| chr16:85918132 | C | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(125): Show |
220 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.602-285C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918132 | |||||||
| chr16:85918142 | C | G | 79 | a0001c0001t0001g0060 a0001c0001t0001g0123 a0001c0001t0001g0223 others(76): Show |
117 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.602-275C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918142 | |||||||
| chr16:85918190 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(132): Show |
236 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.602-227T>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918190 | |||||||
| chr16:85918383 | C | T | 1 | a0001c0003t0004g0242 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.602-34C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918383 | |||||||
| chr16:85918391 | C | T | 1 | a0001c0004t0006g0231 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.602-26C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 6/8 | chr16 | 85918391 | |||||||
| chr16:85918813 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.988+10G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85918813 | |||||||
| chr16:85918897 | A | G | 5 | a0001c0001t0005g0040 a0001c0001t0005g0096 a0001c0001t0005g0097 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+94A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85918897 | |||||||
| chr16:85919003 | C | T | 1 | a0001c0003t0005g0204 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.988+200C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919003 | |||||||
| chr16:85919137 | A | T | 1 | a0001c0003t0005g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.988+334A>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919137 | |||||||
| chr16:85919139 | A | G | 144 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(141): Show |
233 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.988+336A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919139 | |||||||
| chr16:85919226 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0235 |
3 | HG00408.hp1 HG00621.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.988+423C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919226 | |||||||
| chr16:85919227 | G | A | 5 | a0001c0002t0011g0080 a0001c0002t0011g0164 a0001c0009t0011g0055 others(2): Show |
6 | HG01081.hp2 HG01243.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.988+424G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919227 | |||||||
| chr16:85919276 | GTGCTGCC others(3): Show |
G | 2 | a0001c0001t0004g0031 a0001c0001t0004g0196 |
4 | HG02055.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+475_988+484del others(10): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 85919276 | ||||||
| chr16:85919323 | A | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
349 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(346): Show |
intron_variant | MODIFIER | c.988+520A>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919323 | |||||||
| chr16:85919345 | G | T | 36 | a0001c0001t0002g0107 a0001c0001t0005g0012 a0001c0001t0005g0030 others(33): Show |
50 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.988+542G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919345 | |||||||
| chr16:85919384 | C | G | 1 | a0001c0001t0007g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.988+581C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919384 | |||||||
| chr16:85919404 | C | T | 29 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(26): Show |
49 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.988+601C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919404 | |||||||
| chr16:85919504 | G | A | 5 | a0001c0001t0005g0040 a0001c0001t0005g0096 a0001c0001t0005g0097 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.989-605G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919504 | |||||||
| chr16:85919506 | G | T | 12 | a0001c0001t0004g0029 a0001c0001t0004g0094 a0001c0001t0004g0156 others(9): Show |
16 | HG00639.hp2 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.989-603G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919506 | |||||||
| chr16:85919562 | C | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(37): Show |
71 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.989-547C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919562 | |||||||
| chr16:85919590 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(133): Show |
252 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.989-519C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919590 | |||||||
| chr16:85919607 | T | C | 6 | a0001c0001t0002g0107 a0001c0003t0005g0075 a0001c0003t0005g0202 others(3): Show |
6 | HG00408.hp2 HG00609.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.989-502T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919607 | |||||||
| chr16:85919833 | C | T | 1 | a0001c0003t0005g0203 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.989-276C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919833 | |||||||
| chr16:85919840 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0043 others(19): Show |
41 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.989-269C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919840 | |||||||
| chr16:85919887 | G | T | 18 | a0001c0001t0004g0029 a0001c0001t0004g0094 a0001c0001t0004g0156 others(15): Show |
23 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.989-222G>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919887 | |||||||
| chr16:85919994 | G | A | 1 | a0001c0001t0004g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.989-115G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85919994 | |||||||
| chr16:85920034 | C | G | 1 | a0001c0001t0007g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.989-75C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85920034 | |||||||
| chr16:85920076 | G | C | 29 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(26): Show |
49 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.989-33G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 7/8 | chr16 | 85920076 | |||||||
| chr16:85920239 | C | CT | 17 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0110 others(14): Show |
23 | HG00621.hp1 HG01175.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1104+40dupT | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 85920239 | ||||||
| chr16:85920239 | CT | C | 65 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0101 others(62): Show |
90 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.1104+40delT | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 85920239 | ||||||
| chr16:85920239 | CTT | C | 51 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(48): Show |
98 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1104+39_1104+40del others(2): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 85920239 | ||||||
| chr16:85920239 | CTTT | C | 6 | a0001c0001t0004g0029 a0001c0001t0004g0094 a0001c0001t0004g0156 others(3): Show |
8 | HG01167.hp1 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104+38_1104+40del others(3): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 85920239 | ||||||
| chr16:85920303 | A | G | 30 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(27): Show |
50 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1104+79A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920303 | |||||||
| chr16:85920349 | T | C | 109 | a0001c0001t0001g0060 a0001c0001t0001g0114 a0001c0001t0001g0123 others(106): Show |
184 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1104+125T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920349 | |||||||
| chr16:85920460 | A | G | 5 | a0001c0001t0005g0040 a0001c0001t0005g0096 a0001c0001t0005g0098 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1104+236A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920460 | |||||||
| chr16:85920470 | T | C | 107 | a0001c0001t0001g0060 a0001c0001t0001g0223 a0001c0001t0001g0224 others(104): Show |
182 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.1104+246T>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920470 | |||||||
| chr16:85920542 | G | A | 3 | a0001c0009t0011g0055 a0001c0009t0011g0157 a0001c0009t0011g0173 |
4 | HG01081.hp2 HG01243.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104+318G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920542 | |||||||
| chr16:85920613 | A | G | 3 | a0001c0002t0007g0067 a0001c0002t0007g0068 a0001c0002t0007g0195 |
3 | HG02615.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1104+389A>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920613 | |||||||
| chr16:85920676 | G | A | 3 | a0001c0009t0011g0055 a0001c0009t0011g0157 a0001c0009t0011g0173 |
4 | HG01081.hp2 HG01243.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-430G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920676 | |||||||
| chr16:85920681 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0054 |
5 | HG01884.hp1 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105-425C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920681 | |||||||
| chr16:85920698 | C | T | 3 | a0001c0001t0013g0132 a0001c0001t0013g0192 a0001c0001t0013g0193 |
3 | HG02055.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1105-408C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920698 | |||||||
| chr16:85920732 | C | CTG | 7 | a0001c0001t0007g0051 a0001c0001t0007g0099 a0001c0001t0007g0171 others(4): Show |
8 | HG01255.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105-362_1105-361d others(4): Show |
IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 85920732 | ||||||
| chr16:85920740 | G | A | 1 | a0001c0001t0010g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1105-366G>A | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920740 | |||||||
| chr16:85920982 | G | C | 11 | a0001c0001t0004g0029 a0001c0001t0004g0094 a0001c0001t0004g0156 others(8): Show |
14 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1105-124G>C | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85920982 | |||||||
| chr16:85921003 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1105-103C>T | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85921003 | |||||||
| chr16:85921028 | C | G | 5 | a0001c0001t0005g0040 a0001c0001t0005g0096 a0001c0001t0005g0098 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-78C>G | IRF8 | ENSG00000140968.12 | transcript | ENST00000268638.10 | protein_coding | 8/8 | chr16 | 85921028 |