Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55656 |
| ensemblid | ENSG00000164941.14 |
| hgncid | 26048 |
| symbol | INTS8 |
| name | integrator complex subunit 8 |
| refseq_nuc | NM_017864.4 |
| refseq_prot | NP_060334.2 |
| ensembl_nuc | ENST00000523731.6 |
| ensembl_prot | ENSP00000430338.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 94823287 |
| end | 94881746 |
| strand | + |
| ver | v1.2 |
| region | chr8:94823287-94881746 |
| region5000 | chr8:94818287-94886746 |
| regionname0 | INTS8_chr8_94823287_94881746 |
| regionname5000 | INTS8_chr8_94818287_94886746 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 995 | 304 | 92 | 51 | 118 | 10 | 31 | 82 | INTS8_chr8_94818287_94886746 | INTS8 | MSAEA others(990): Show |
chr8 | 94818287 | 94886746 |
| a0002 | 0/0 | 995 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | MSAEA others(990): Show |
chr8 | 94818287 | 94886746 |
| a0003 | 0/0 | 995 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | MSAEA others(990): Show |
chr8 | 94818287 | 94886746 |
| a0004 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | MSAEA others(990): Show |
chr8 | 94818287 | 94886746 |
| a0005 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | MSAEA others(990): Show |
chr8 | 94818287 | 94886746 |
| a0006 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | MSAEA others(990): Show |
chr8 | 94818287 | 94886746 |
| a0007 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | MSAEA others(990): Show |
chr8 | 94818287 | 94886746 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2985 | 145 | 45 | 16 | 65 | 5 | 12 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0001c0002 | 0/0 | 2985 | 125 | 26 | 24 | 53 | 5 | 17 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0001c0003 | 0/0 | 2985 | 32 | 19 | 11 | 0 | 0 | 2 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0001c0004 | 0/0 | 2985 | 2 | 2 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0002c0007 | 0/0 | 2985 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0003c0008 | 0/0 | 2985 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0004c0005 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0005c0010 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0006c0009 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 | ||
| a0007c0006 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | ATGAG others(2980): Show |
chr8 | 94818287 | 94886746 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4645 | 138 | 42 | 15 | 65 | 5 | 9 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0001t0003 | 0/0 | 4645 | 3 | 2 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0001t0006 | 0/0 | 4645 | 3 | 0 | 0 | 0 | 0 | 3 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0001t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0002t0001 | 0/0 | 4645 | 115 | 25 | 21 | 48 | 5 | 16 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0002t0004 | 0/0 | 4645 | 3 | 0 | 3 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0002t0005 | 0/0 | 4645 | 3 | 0 | 0 | 3 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0002t0008 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0002t0009 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0002t0010 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0002t0011 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0003t0001 | 0/0 | 4645 | 28 | 15 | 11 | 0 | 0 | 2 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0003t0002 | 0/0 | 4645 | 4 | 4 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0001c0004t0001 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0002c0007t0001 | 0/0 | 4645 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0003c0008t0001 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0004c0005t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0005c0010t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0006c0009t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| a0007c0006t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | GCCAT others(4640): Show |
chr8 | 94818287 | 94886746 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 1/0 | 4 | 0 | 1 | 2 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0002 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0009g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0010g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0002c0007t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0003c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0004c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0005c0010t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0006c0009t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0007c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0122 | EUR | GBR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0169 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01069 | hp2 | a0002 | c0007 | t0001 | g0009 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0275 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0170 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0119 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0178 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0182 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0251 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0180 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0133 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0181 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | IBS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0101 | EUR | IBS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0183 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0261 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0277 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0131 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0276 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02698 | hp1 | a0003 | c0008 | t0001 | g0219 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0259 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0256 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0079 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0279 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0250 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0253 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0254 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0280 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0036 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04184 | hp1 | a0001 | c0002 | t0010 | g0160 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0179 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0252 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18942 | hp1 | a0001 | c0002 | t0011 | g0110 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18954 | hp2 | a0004 | c0005 | t0001 | g0204 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18956 | hp1 | a0005 | c0010 | t0001 | g0025 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18959 | hp2 | a0006 | c0009 | t0001 | g0242 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18965 | hp1 | a0001 | c0002 | t0005 | g0092 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18994 | hp2 | a0007 | c0006 | t0001 | g0153 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0278 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0260 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19066 | hp2 | a0001 | c0002 | t0005 | g0006 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19070 | hp2 | a0001 | c0002 | t0005 | g0090 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19087 | hp2 | a0001 | c0002 | t0009 | g0136 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0258 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ASW | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20129 | hp2 | a0001 | c0002 | t0008 | g0132 | AFR | ASW | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | GIH | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0035 | SAS | GIH | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | USA | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0257 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0049 | REF | REF | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94841498 | T | C | 1 | a0004 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1025T>C | p.Ile342Thr | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/27 | 1170/4645 | 1025/2988 | 342/995 | chr8 | 94841498 | |||
| chr8:94841557 | G | T | 1 | a0005 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.1084G>T | p.Val362Phe | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/27 | 1229/4645 | 1084/2988 | 362/995 | chr8 | 94841557 | |||
| chr8:94866159 | A | C | 1 | a0002 | 1 | HG01069.hp2 | missense_variant&splice_region_variant | MODERATE | c.2263A>C | p.Ser755Arg | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/27 | 2408/4645 | 2263/2988 | 755/995 | chr8 | 94866159 | |||
| chr8:94873386 | A | G | 1 | a0007 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.2546A>G | p.Tyr849Cys | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/27 | 2691/4645 | 2546/2988 | 849/995 | chr8 | 94873386 | |||
| chr8:94873463 | G | A | 1 | a0003 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2623G>A | p.Val875Ile | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/27 | 2768/4645 | 2623/2988 | 875/995 | chr8 | 94873463 | |||
| chr8:94874571 | A | T | 1 | a0006 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.2657A>T | p.Lys886Ile | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/27 | 2802/4645 | 2657/2988 | 886/995 | chr8 | 94874571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94825062 | G | A | 1 | a0001c0004 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.300G>A | p.Glu100Glu | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/27 | 445/4645 | 300/2988 | 100/995 | chr8 | 94825062 | |||
| chr8:94865559 | T | C | 5 | a0001c0002 a0001c0003 a0001c0004 others(2): Show |
161 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
synonymous_variant | LOW | c.2130T>C | p.Ser710Ser | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 17/27 | 2275/4645 | 2130/2988 | 710/995 | chr8 | 94865559 | |||
| chr8:94874569 | A | T | 1 | a0006c0009 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.2655A>T | p.Ile885Ile | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/27 | 2800/4645 | 2655/2988 | 885/995 | chr8 | 94874569 | |||
| chr8:94876079 | C | T | 3 | a0001c0002 a0001c0004 a0007c0006 |
128 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
synonymous_variant | LOW | c.2694C>T | p.Ala898Ala | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 24/27 | 2839/4645 | 2694/2988 | 898/995 | chr8 | 94876079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94823314 | G | T | 1 | a0001c0002t0011 | 1 | NA18942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-118G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/27 | 118 | chr8 | 94823314 | ||||||
| chr8:94823329 | G | A | 2 | a0001c0001t0003 a0001c0001t0007 |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-103G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/27 | 103 | chr8 | 94823329 | ||||||
| chr8:94880572 | T | C | 1 | a0001c0001t0007 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*338T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 338 | chr8 | 94880572 | ||||||
| chr8:94880754 | C | T | 1 | a0001c0001t0006 | 3 | HG02738.hp1 HG03831.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*520C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 520 | chr8 | 94880754 | ||||||
| chr8:94880786 | A | G | 1 | a0001c0002t0010 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 552 | chr8 | 94880786 | ||||||
| chr8:94880899 | A | T | 1 | a0001c0002t0005 | 3 | NA18965.hp1 NA19066.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*665A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 665 | chr8 | 94880899 | ||||||
| chr8:94881028 | C | A | 1 | a0001c0003t0002 | 4 | HG03130.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*794C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 794 | chr8 | 94881028 | ||||||
| chr8:94881219 | C | G | 2 | a0001c0001t0003 a0001c0001t0007 |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*985C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 985 | chr8 | 94881219 | ||||||
| chr8:94881272 | C | A | 1 | a0001c0002t0008 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1038C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 1038 | chr8 | 94881272 | ||||||
| chr8:94881362 | A | G | 2 | a0001c0001t0003 a0001c0001t0007 |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1128A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 1128 | chr8 | 94881362 | ||||||
| chr8:94881481 | T | C | 1 | a0001c0002t0009 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1247T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 1247 | chr8 | 94881481 | ||||||
| chr8:94881687 | T | C | 1 | a0001c0002t0004 | 3 | HG01109.hp2 HG01358.hp1 HG02273.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1453T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 27/27 | 1453 | chr8 | 94881687 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94823626 | T | G | 5 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+65T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823626 | |||||||
| chr8:94823634 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.130+73C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823634 | |||||||
| chr8:94823683 | C | CCCCTCCC others(53): Show |
1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+123_130+124ins others(60): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94823683 | ||||||
| chr8:94823688 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+127T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823688 | |||||||
| chr8:94823708 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130+147C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823708 | |||||||
| chr8:94823716 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+155C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823716 | |||||||
| chr8:94823717 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+156A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823717 | |||||||
| chr8:94823732 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+171G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823732 | |||||||
| chr8:94823733 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+172T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823733 | |||||||
| chr8:94823734 | CAAAGAAA others(13): Show |
C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+174_130+193del others(20): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823734 | |||||||
| chr8:94823755 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+194G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823755 | |||||||
| chr8:94823758 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+197T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823758 | |||||||
| chr8:94823772 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+211A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823772 | |||||||
| chr8:94823776 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+215G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823776 | |||||||
| chr8:94823785 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+224G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823785 | |||||||
| chr8:94823786 | T | A | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+225T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823786 | |||||||
| chr8:94823788 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+227C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823788 | |||||||
| chr8:94823792 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+231C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823792 | |||||||
| chr8:94823793 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+232A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823793 | |||||||
| chr8:94823803 | C | G | 1 | a0001c0001t0001g0285 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.130+242C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823803 | |||||||
| chr8:94823805 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+244T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823805 | |||||||
| chr8:94823806 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+245T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823806 | |||||||
| chr8:94823807 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+246G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823807 | |||||||
| chr8:94823808 | GTCCTTTT others(29): Show |
G | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+249_130+284del others(36): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94823808 | ||||||
| chr8:94823845 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+284T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823845 | |||||||
| chr8:94823899 | G | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(40): Show |
43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.130+338G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823899 | |||||||
| chr8:94823900 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.130+339C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823900 | |||||||
| chr8:94823912 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.130+351C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823912 | |||||||
| chr8:94824001 | AT | A | 125 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(122): Show |
134 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.130+447delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824001 | ||||||
| chr8:94824079 | T | C | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.130+518T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824079 | |||||||
| chr8:94824410 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.131-483A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824410 | |||||||
| chr8:94824431 | C | T | 1 | a0001c0002t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.131-462C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824431 | |||||||
| chr8:94824456 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.131-437C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824456 | |||||||
| chr8:94824584 | A | T | 129 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(126): Show |
138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.131-309A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824584 | |||||||
| chr8:94824638 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-255C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824638 | |||||||
| chr8:94824673 | C | G | 2 | a0001c0003t0001g0275 a0001c0003t0001g0276 |
2 | HG01070.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.131-220C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824673 | |||||||
| chr8:94824708 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-185C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824708 | |||||||
| chr8:94824766 | C | CA | 29 | a0001c0001t0001g0013 a0001c0001t0001g0172 a0001c0001t0001g0173 others(26): Show |
30 | HG01069.hp2 HG01070.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.131-117dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824766 | ||||||
| chr8:94824777 | CCCAAACT others(31): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.131-109_131-72delT others(37): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824777 | ||||||
| chr8:94824784 | T | TC | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(38): Show |
42 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.131-97dupC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824784 | ||||||
| chr8:94824784 | T | TCC | 21 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0187 others(18): Show |
21 | HG00438.hp1 HG01517.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.131-98_131-97dupCC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824784 | ||||||
| chr8:94824784 | TC | T | 82 | a0001c0001t0001g0159 a0001c0001t0001g0199 a0001c0001t0001g0223 others(79): Show |
87 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.131-97delC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824784 | ||||||
| chr8:94824784 | TCC | T | 19 | a0001c0002t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0009 others(16): Show |
20 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.131-98_131-97delCC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824784 | ||||||
| chr8:94824791 | CCCCCCAC others(3): Show |
C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0043 others(3): Show |
6 | HG00558.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-96_131-87delAC others(8): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824791 | ||||||
| chr8:94824793 | CCCCACCC others(1): Show |
C | 13 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0026 others(10): Show |
13 | HG00544.hp2 HG01243.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-96_131-89delAC others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824793 | ||||||
| chr8:94824801 | A | AC | 9 | a0001c0001t0001g0222 a0001c0001t0001g0240 a0001c0001t0001g0244 others(6): Show |
9 | HG01243.hp2 HG02080.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-85dupC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824801 | ||||||
| chr8:94824808 | C | CA | 5 | a0001c0001t0001g0217 a0001c0002t0001g0123 a0001c0002t0001g0145 others(2): Show |
5 | HG00544.hp1 HG01358.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-78dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr8 | 94824808 | ||||||
| chr8:94824870 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.131-23A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824870 | |||||||
| chr8:94824884 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
16 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.131-9A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94824884 | |||||||
| chr8:94825211 | G | GA | 43 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(40): Show |
43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.305+144_305+145ins others(1): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825211 | |||||||
| chr8:94825283 | C | G | 2 | a0001c0003t0001g0169 a0001c0003t0001g0170 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.305+216C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825283 | |||||||
| chr8:94825373 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.305+306A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825373 | |||||||
| chr8:94825397 | A | AC | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
11 | HG00544.hp2 HG00673.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.305+331dupC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 94825397 | ||||||
| chr8:94825427 | GA | G | 37 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(34): Show |
37 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.305+374delA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 94825427 | ||||||
| chr8:94825435 | A | T | 11 | a0001c0002t0001g0166 a0001c0002t0001g0167 a0001c0002t0001g0168 others(8): Show |
11 | HG00621.hp1 HG01069.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.305+368A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825435 | |||||||
| chr8:94825437 | A | T | 5 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+370A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825437 | |||||||
| chr8:94825439 | A | T | 3 | a0001c0001t0001g0262 a0001c0002t0001g0164 a0001c0002t0001g0165 |
3 | HG03139.hp2 HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.305+372A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825439 | |||||||
| chr8:94825440 | A | T | 156 | a0001c0001t0001g0013 a0001c0001t0001g0159 a0001c0001t0001g0255 others(153): Show |
166 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.305+373A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825440 | |||||||
| chr8:94825441 | AT | A | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.305+375delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825441 | |||||||
| chr8:94825442 | T | A | 157 | a0001c0001t0001g0013 a0001c0001t0001g0159 a0001c0001t0001g0201 others(154): Show |
167 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.305+375T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825442 | |||||||
| chr8:94825504 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.305+437G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825504 | |||||||
| chr8:94825632 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.305+565G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825632 | |||||||
| chr8:94825721 | C | A | 18 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(15): Show |
18 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.305+654C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825721 | |||||||
| chr8:94825761 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.305+694C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825761 | |||||||
| chr8:94825833 | G | GT | 90 | a0001c0001t0001g0159 a0001c0001t0001g0274 a0001c0002t0001g0001 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.305+774dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 94825833 | ||||||
| chr8:94825992 | G | A | 43 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(40): Show |
43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.305+925G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825992 | |||||||
| chr8:94826075 | T | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.305+1008T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826075 | |||||||
| chr8:94826118 | C | G | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.305+1051C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826118 | |||||||
| chr8:94826127 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.305+1060G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826127 | |||||||
| chr8:94826184 | T | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(40): Show |
43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.306-1079T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826184 | |||||||
| chr8:94826210 | T | C | 210 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.306-1053T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826210 | |||||||
| chr8:94826286 | T | A | 9 | a0001c0002t0001g0006 a0001c0002t0001g0088 a0001c0002t0001g0089 others(6): Show |
9 | HG00609.hp2 HG02135.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.306-977T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826286 | |||||||
| chr8:94826304 | C | T | 1 | a0001c0003t0001g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.306-959C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826304 | |||||||
| chr8:94826312 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.306-951C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826312 | |||||||
| chr8:94826315 | T | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.306-948T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826315 | |||||||
| chr8:94826474 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
16 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.306-789C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826474 | |||||||
| chr8:94826499 | A | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-764A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826499 | |||||||
| chr8:94826625 | A | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-638A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826625 | |||||||
| chr8:94826641 | A | G | 210 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.306-622A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826641 | |||||||
| chr8:94826744 | T | TA | 20 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0203 others(17): Show |
20 | HG00438.hp1 HG01516.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.306-518dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr8 | 94826744 | ||||||
| chr8:94826817 | G | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.306-446G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826817 | |||||||
| chr8:94826857 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-406G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826857 | |||||||
| chr8:94826901 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.306-362G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826901 | |||||||
| chr8:94827029 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.306-234C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94827029 | |||||||
| chr8:94827083 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.306-180C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94827083 | |||||||
| chr8:94827124 | T | G | 3 | a0001c0002t0001g0001 a0001c0002t0001g0056 a0001c0002t0001g0095 |
6 | HG00408.hp1 HG00558.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.306-139T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94827124 | |||||||
| chr8:94827137 | A | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-126A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94827137 | |||||||
| chr8:94827223 | C | T | 1 | a0001c0003t0001g0259 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.306-40C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94827223 | |||||||
| chr8:94827246 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.306-17C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94827246 | |||||||
| chr8:94827503 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.446+100G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 3/26 | chr8 | 94827503 | |||||||
| chr8:94827597 | T | C | 2 | a0001c0001t0001g0205 a0004c0005t0001g0204 |
2 | NA18954.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.447-125T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 3/26 | chr8 | 94827597 | |||||||
| chr8:94827906 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.518+113C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94827906 | |||||||
| chr8:94827963 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.518+170A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94827963 | |||||||
| chr8:94828045 | GT | G | 67 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(64): Show |
67 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.518+264delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr8 | 94828045 | ||||||
| chr8:94828045 | GTT | G | 127 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(124): Show |
136 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.518+263_518+264del others(2): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr8 | 94828045 | ||||||
| chr8:94828287 | C | T | 1 | a0001c0003t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.518+494C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828287 | |||||||
| chr8:94828459 | T | A | 1 | a0001c0002t0001g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.519-516T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828459 | |||||||
| chr8:94828513 | G | A | 1 | a0001c0003t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519-462G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828513 | |||||||
| chr8:94828572 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.519-403C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828572 | |||||||
| chr8:94828575 | A | C | 1 | a0003c0008t0001g0219 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.519-400A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828575 | |||||||
| chr8:94828595 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.519-380T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828595 | |||||||
| chr8:94828678 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.519-297G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828678 | |||||||
| chr8:94828730 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.519-245C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828730 | |||||||
| chr8:94828845 | A | G | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.519-130A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828845 | |||||||
| chr8:94828886 | G | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.519-89G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828886 | |||||||
| chr8:94828957 | C | G | 5 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01975.hp1 HG02004.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-18C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 4/26 | chr8 | 94828957 | |||||||
| chr8:94829283 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.570+257G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829283 | |||||||
| chr8:94829399 | G | T | 1 | a0001c0002t0001g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.570+373G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829399 | |||||||
| chr8:94829401 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.570+375G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829401 | |||||||
| chr8:94829417 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+391G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829417 | |||||||
| chr8:94829479 | A | G | 1 | a0001c0002t0001g0087 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+453A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829479 | |||||||
| chr8:94829485 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.570+459C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829485 | |||||||
| chr8:94829539 | G | A | 1 | a0001c0003t0001g0259 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.570+513G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829539 | |||||||
| chr8:94829947 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0097 |
2 | NA18981.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.570+921G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829947 | |||||||
| chr8:94829981 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+955C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94829981 | |||||||
| chr8:94830072 | T | A | 1 | a0001c0003t0001g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.570+1046T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830072 | |||||||
| chr8:94830096 | G | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+1070G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830096 | |||||||
| chr8:94830392 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.570+1366G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830392 | |||||||
| chr8:94830466 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.570+1440C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830466 | |||||||
| chr8:94830478 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.570+1452G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830478 | |||||||
| chr8:94830490 | T | C | 3 | a0001c0002t0001g0054 a0001c0002t0001g0061 a0001c0002t0001g0164 |
3 | HG02109.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.570+1464T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830490 | |||||||
| chr8:94830656 | C | T | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.571-1336C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830656 | |||||||
| chr8:94830659 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.571-1333G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830659 | |||||||
| chr8:94830860 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1132C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830860 | |||||||
| chr8:94830883 | T | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.571-1109T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94830883 | |||||||
| chr8:94831003 | G | A | 2 | a0001c0003t0001g0008 a0001c0003t0001g0178 |
3 | HG01168.hp1 HG01169.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.571-989G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94831003 | |||||||
| chr8:94831086 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.571-906G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94831086 | |||||||
| chr8:94831168 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.571-824C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | chr8 | 94831168 | |||||||
| chr8:94831482 | C | CT | 125 | a0001c0001t0001g0047 a0001c0001t0001g0159 a0001c0001t0001g0176 others(122): Show |
134 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.571-493dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr8 | 94831482 | ||||||
| chr8:94831482 | C | CTT | 6 | a0001c0002t0001g0093 a0001c0002t0001g0094 a0001c0002t0001g0161 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-494_571-493dup others(2): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr8 | 94831482 | ||||||
| chr8:94832189 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.753+15C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832189 | |||||||
| chr8:94832210 | T | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 |
3 | HG00099.hp2 HG00738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.753+36T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832210 | |||||||
| chr8:94832273 | T | A | 1 | a0001c0002t0001g0063 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.753+99T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832273 | |||||||
| chr8:94832516 | A | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+342A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832516 | |||||||
| chr8:94832737 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+563C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832737 | |||||||
| chr8:94832769 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.753+595C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832769 | |||||||
| chr8:94832855 | C | T | 136 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(133): Show |
145 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.753+681C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832855 | |||||||
| chr8:94832867 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+693C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832867 | |||||||
| chr8:94832900 | C | T | 4 | a0001c0003t0002g0250 a0001c0003t0002g0252 a0001c0003t0002g0253 others(1): Show |
4 | HG03130.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+726C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832900 | |||||||
| chr8:94832944 | G | A | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.753+770G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832944 | |||||||
| chr8:94833023 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.753+849T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833023 | |||||||
| chr8:94833042 | T | A | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG00642.hp1 HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.753+868T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833042 | |||||||
| chr8:94833172 | A | G | 1 | a0001c0001t0007g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.753+998A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833172 | |||||||
| chr8:94833562 | A | G | 7 | a0001c0002t0001g0059 a0001c0002t0001g0082 a0001c0002t0001g0083 others(4): Show |
7 | HG01167.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+1388A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833562 | |||||||
| chr8:94833621 | C | A | 8 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0068 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+1447C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833621 | |||||||
| chr8:94833736 | G | A | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.753+1562G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833736 | |||||||
| chr8:94833991 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.753+1817C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833991 | |||||||
| chr8:94833998 | C | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.753+1824C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94833998 | |||||||
| chr8:94834189 | T | G | 1 | a0001c0003t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.753+2015T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834189 | |||||||
| chr8:94834362 | G | GGT | 9 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0175 others(6): Show |
9 | HG00438.hp1 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.754-2127_754-2126d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834362 | ||||||
| chr8:94834362 | G | GGTGT | 32 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(29): Show |
32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.754-2129_754-2126d others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834362 | ||||||
| chr8:94834362 | G | GGTGTGT | 4 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0051 others(1): Show |
4 | HG02258.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-2131_754-2126d others(8): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834362 | ||||||
| chr8:94834362 | G | GGTGTGTG others(1): Show |
3 | a0001c0001t0001g0052 a0001c0001t0003g0014 a0001c0001t0007g0016 |
3 | HG01109.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.754-2133_754-2126d others(10): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834362 | ||||||
| chr8:94834362 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0003g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.754-2135_754-2126d others(12): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834362 | ||||||
| chr8:94834362 | GGT | G | 144 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0159 others(141): Show |
155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.754-2127_754-2126d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834362 | ||||||
| chr8:94834362 | GGTGT | G | 12 | a0001c0001t0001g0186 a0001c0001t0001g0206 a0001c0001t0001g0222 others(9): Show |
12 | HG02257.hp2 HG02976.hp2 HG03130.hp2 others(9): Show |
intron_variant | MODIFIER | c.754-2129_754-2126d others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834362 | ||||||
| chr8:94834419 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.754-2105C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834419 | |||||||
| chr8:94834545 | G | A | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.754-1979G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834545 | |||||||
| chr8:94834565 | G | A | 1 | a0001c0003t0001g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.754-1959G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834565 | |||||||
| chr8:94834603 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-1921C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834603 | |||||||
| chr8:94834703 | C | CA | 7 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0002t0001g0060 others(4): Show |
7 | HG00609.hp1 HG01934.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.754-1804dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834703 | ||||||
| chr8:94834703 | CA | C | 7 | a0001c0001t0001g0191 a0001c0001t0001g0248 a0001c0001t0003g0014 others(4): Show |
7 | HG01109.hp1 HG01975.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.754-1804delA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94834703 | ||||||
| chr8:94834922 | T | C | 210 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.754-1602T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834922 | |||||||
| chr8:94834968 | T | G | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.754-1556T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834968 | |||||||
| chr8:94835024 | G | A | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.754-1500G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835024 | |||||||
| chr8:94835129 | G | A | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG00642.hp1 HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.754-1395G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835129 | |||||||
| chr8:94835282 | T | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 |
3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.754-1242T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835282 | |||||||
| chr8:94835360 | A | G | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.754-1164A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835360 | |||||||
| chr8:94835461 | G | A | 1 | a0001c0003t0001g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.754-1063G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835461 | |||||||
| chr8:94835504 | G | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
16 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.754-1020G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835504 | |||||||
| chr8:94835515 | T | A | 1 | a0001c0002t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.754-1009T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835515 | |||||||
| chr8:94835605 | C | CT | 48 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(45): Show |
48 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.754-907dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr8 | 94835605 | ||||||
| chr8:94835646 | C | G | 153 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0002t0001g0001 others(150): Show |
163 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.754-878C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835646 | |||||||
| chr8:94835664 | A | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.754-860A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835664 | |||||||
| chr8:94835748 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-776C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835748 | |||||||
| chr8:94835991 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.754-533A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835991 | |||||||
| chr8:94836118 | A | T | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.754-406A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94836118 | |||||||
| chr8:94836145 | C | T | 3 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0007g0016 |
3 | HG01109.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.754-379C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94836145 | |||||||
| chr8:94836171 | T | C | 253 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(250): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.754-353T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94836171 | |||||||
| chr8:94836254 | G | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0223 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.754-270G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94836254 | |||||||
| chr8:94836794 | C | T | 4 | a0001c0003t0001g0277 a0001c0003t0001g0278 a0001c0003t0001g0279 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.861+163C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94836794 | |||||||
| chr8:94836805 | G | A | 194 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(191): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.861+174G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94836805 | |||||||
| chr8:94836835 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.861+204C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94836835 | |||||||
| chr8:94836844 | TTC | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.861+219_861+220del others(2): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 94836844 | ||||||
| chr8:94837018 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0229 |
5 | HG00733.hp1 HG00738.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.861+387G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837018 | |||||||
| chr8:94837083 | A | G | 2 | a0001c0002t0001g0080 a0001c0002t0001g0081 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.861+452A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837083 | |||||||
| chr8:94837110 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.861+479C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837110 | |||||||
| chr8:94837263 | A | G | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.861+632A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837263 | |||||||
| chr8:94837557 | CT | C | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(12): Show |
15 | HG02145.hp2 HG02257.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.862-895delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 94837557 | ||||||
| chr8:94837632 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.862-831G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837632 | |||||||
| chr8:94837635 | C | T | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.862-828C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837635 | |||||||
| chr8:94837636 | C | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0179 a0001c0003t0001g0180 others(4): Show |
7 | HG01069.hp2 HG01255.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.862-827C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837636 | |||||||
| chr8:94837695 | A | C | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.862-768A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837695 | |||||||
| chr8:94837777 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.862-686C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94837777 | |||||||
| chr8:94838003 | CT | C | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.862-455delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 94838003 | ||||||
| chr8:94838010 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.862-453T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94838010 | |||||||
| chr8:94838044 | C | CT | 10 | a0001c0001t0001g0283 a0001c0002t0001g0006 a0001c0002t0001g0088 others(7): Show |
10 | HG00609.hp2 HG02135.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.862-402dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 94838044 | ||||||
| chr8:94838044 | CT | C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(33): Show |
36 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.862-402delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr8 | 94838044 | ||||||
| chr8:94838103 | G | T | 2 | a0001c0003t0001g0177 a0001c0003t0001g0256 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.862-360G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94838103 | |||||||
| chr8:94838145 | G | A | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.862-318G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94838145 | |||||||
| chr8:94838292 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.862-171C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94838292 | |||||||
| chr8:94838352 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.862-111G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 7/26 | chr8 | 94838352 | |||||||
| chr8:94838679 | C | G | 1 | a0001c0002t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1017+61C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94838679 | |||||||
| chr8:94838715 | G | A | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1017+97G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94838715 | |||||||
| chr8:94838786 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1017+168T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94838786 | |||||||
| chr8:94839179 | GC | G | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+564delC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr8 | 94839179 | ||||||
| chr8:94839262 | G | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+644G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839262 | |||||||
| chr8:94839474 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1017+856A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839474 | |||||||
| chr8:94839571 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1017+953C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839571 | |||||||
| chr8:94839590 | T | G | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+972T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839590 | |||||||
| chr8:94839600 | T | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+982T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839600 | |||||||
| chr8:94839640 | C | T | 1 | a0001c0003t0001g0259 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1017+1022C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839640 | |||||||
| chr8:94839702 | A | G | 1 | a0007c0006t0001g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1017+1084A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839702 | |||||||
| chr8:94839798 | A | G | 1 | a0001c0002t0001g0152 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1017+1180A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839798 | |||||||
| chr8:94839800 | G | GCCAAGGC others(3): Show |
1 | a0001c0001t0001g0285 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1017+1182_1017+118 others(14): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94839800 | |||||||
| chr8:94840008 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1017+1390A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840008 | |||||||
| chr8:94840053 | G | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+1435G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840053 | |||||||
| chr8:94840210 | G | C | 2 | a0001c0003t0001g0251 a0001c0003t0001g0258 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1018-1281G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840210 | |||||||
| chr8:94840413 | C | T | 1 | a0001c0003t0001g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1018-1078C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840413 | |||||||
| chr8:94840552 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1018-939T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840552 | |||||||
| chr8:94840559 | G | GT | 178 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(175): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1018-916dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr8 | 94840559 | ||||||
| chr8:94840559 | G | GTT | 10 | a0001c0001t0001g0028 a0001c0001t0001g0288 a0001c0001t0001g0289 others(7): Show |
10 | HG00621.hp1 HG00642.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018-917_1018-916d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr8 | 94840559 | ||||||
| chr8:94840594 | G | T | 1 | a0001c0003t0001g0280 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-897G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840594 | |||||||
| chr8:94840632 | A | C | 1 | a0001c0002t0001g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1018-859A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840632 | |||||||
| chr8:94840658 | A | C | 1 | a0001c0003t0002g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1018-833A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840658 | |||||||
| chr8:94840712 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-779C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840712 | |||||||
| chr8:94840715 | G | A | 2 | a0001c0001t0001g0176 a0006c0009t0001g0242 |
2 | NA18959.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1018-776G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840715 | |||||||
| chr8:94840757 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1018-734C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840757 | |||||||
| chr8:94840846 | C | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-645C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840846 | |||||||
| chr8:94840913 | A | AT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0241 a0001c0001t0001g0283 others(3): Show |
6 | HG02738.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-561dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr8 | 94840913 | ||||||
| chr8:94840913 | AT | A | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1018-561delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr8 | 94840913 | ||||||
| chr8:94840952 | A | G | 195 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1018-539A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840952 | |||||||
| chr8:94840966 | G | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-525G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840966 | |||||||
| chr8:94840969 | G | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-522G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840969 | |||||||
| chr8:94840998 | C | T | 1 | a0001c0002t0011g0110 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1018-493C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94840998 | |||||||
| chr8:94841361 | A | G | 2 | a0001c0002t0001g0054 a0001c0002t0001g0061 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1018-130A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94841361 | |||||||
| chr8:94841480 | G | A | 138 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(135): Show |
147 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.1018-11G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 8/26 | chr8 | 94841480 | |||||||
| chr8:94841679 | A | G | 125 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(122): Show |
134 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1118+88A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/26 | chr8 | 94841679 | |||||||
| chr8:94841720 | A | G | 153 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0002t0001g0001 others(150): Show |
163 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1118+129A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/26 | chr8 | 94841720 | |||||||
| chr8:94842061 | TC | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1119-284delC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 94842061 | ||||||
| chr8:94842065 | T | C | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1119-282T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/26 | chr8 | 94842065 | |||||||
| chr8:94842066 | C | T | 1 | a0001c0002t0001g0148 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1119-281C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/26 | chr8 | 94842066 | |||||||
| chr8:94842073 | G | GA | 47 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(44): Show |
47 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1119-259dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr8 | 94842073 | ||||||
| chr8:94842081 | A | AT | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1119-266_1119-265i others(3): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 9/26 | chr8 | 94842081 | |||||||
| chr8:94842592 | G | C | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1260+104G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94842592 | |||||||
| chr8:94842638 | G | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1260+150G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94842638 | |||||||
| chr8:94842658 | T | C | 3 | a0001c0002t0001g0113 a0001c0002t0001g0150 a0001c0002t0001g0165 |
3 | HG02698.hp2 HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1260+170T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94842658 | |||||||
| chr8:94842945 | GAGA | G | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1260+460_1260+462d others(5): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94842945 | ||||||
| chr8:94843222 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1260+734A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843222 | |||||||
| chr8:94843297 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1260+809G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843297 | |||||||
| chr8:94843338 | C | T | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1260+850C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843338 | |||||||
| chr8:94843428 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1260+940G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843428 | |||||||
| chr8:94843537 | A | T | 4 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0146 others(1): Show |
4 | HG00544.hp1 HG02056.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+1049A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843537 | |||||||
| chr8:94843566 | C | CA | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1260+1090dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94843566 | ||||||
| chr8:94843641 | G | T | 194 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(191): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1260+1153G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843641 | |||||||
| chr8:94843667 | A | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+1179A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843667 | |||||||
| chr8:94843706 | C | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1260+1218C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843706 | |||||||
| chr8:94843725 | CAT | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.1260+1242_1260+124 others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94843725 | ||||||
| chr8:94843840 | T | C | 7 | a0001c0002t0001g0059 a0001c0002t0001g0082 a0001c0002t0001g0083 others(4): Show |
7 | HG01167.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+1352T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843840 | |||||||
| chr8:94843864 | A | G | 1 | a0001c0003t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1260+1376A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843864 | |||||||
| chr8:94843995 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+1507T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843995 | |||||||
| chr8:94843998 | C | T | 7 | a0001c0003t0001g0009 a0001c0003t0001g0179 a0001c0003t0001g0180 others(4): Show |
7 | HG01069.hp2 HG01255.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260+1510C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843998 | |||||||
| chr8:94844017 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1260+1529A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844017 | |||||||
| chr8:94844026 | C | CT | 165 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(162): Show |
174 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1260+1550dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94844026 | ||||||
| chr8:94844100 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1260+1612G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844100 | |||||||
| chr8:94844180 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1260+1692G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844180 | |||||||
| chr8:94844428 | G | C | 2 | a0001c0003t0001g0177 a0001c0003t0001g0256 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1260+1940G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844428 | |||||||
| chr8:94844440 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+1952C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844440 | |||||||
| chr8:94844458 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1260+1970A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844458 | |||||||
| chr8:94844614 | A | G | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1260+2126A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844614 | |||||||
| chr8:94844677 | A | G | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+2189A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844677 | |||||||
| chr8:94844683 | A | G | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1260+2195A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844683 | |||||||
| chr8:94844725 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1260+2237C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844725 | |||||||
| chr8:94844752 | C | CT | 14 | a0001c0001t0001g0174 a0001c0001t0001g0223 a0001c0001t0001g0238 others(11): Show |
14 | HG01109.hp1 HG01928.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1260+2280dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94844752 | ||||||
| chr8:94844772 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1260+2284T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844772 | |||||||
| chr8:94844778 | G | A | 2 | a0001c0001t0003g0015 a0001c0001t0007g0016 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1260+2290G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844778 | |||||||
| chr8:94844820 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+2332T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844820 | |||||||
| chr8:94844875 | C | T | 2 | a0001c0002t0001g0080 a0001c0002t0001g0081 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1260+2387C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844875 | |||||||
| chr8:94844910 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+2422G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844910 | |||||||
| chr8:94844912 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1260+2424C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94844912 | |||||||
| chr8:94845185 | AT | A | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1260+2699delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94845185 | ||||||
| chr8:94845325 | G | A | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1260+2837G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94845325 | |||||||
| chr8:94845662 | G | C | 195 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1260+3174G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94845662 | |||||||
| chr8:94845677 | G | A | 1 | a0001c0003t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1260+3189G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94845677 | |||||||
| chr8:94845963 | A | G | 1 | a0001c0003t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1260+3475A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94845963 | |||||||
| chr8:94846138 | T | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-3324T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846138 | |||||||
| chr8:94846210 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1261-3252T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846210 | |||||||
| chr8:94846308 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1261-3154C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846308 | |||||||
| chr8:94846336 | G | A | 1 | a0001c0002t0010g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1261-3126G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846336 | |||||||
| chr8:94846431 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-3031C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846431 | |||||||
| chr8:94846454 | C | A | 227 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(224): Show |
239 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1261-3008C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846454 | |||||||
| chr8:94846493 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1261-2969C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846493 | |||||||
| chr8:94846506 | T | C | 195 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1261-2956T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846506 | |||||||
| chr8:94846678 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-2784G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846678 | |||||||
| chr8:94846679 | C | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-2783C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846679 | |||||||
| chr8:94846739 | T | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-2723T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846739 | |||||||
| chr8:94846787 | G | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1261-2675G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846787 | |||||||
| chr8:94846942 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1261-2520C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846942 | |||||||
| chr8:94846955 | G | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.1261-2507G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94846955 | |||||||
| chr8:94847029 | G | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1261-2433G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94847029 | |||||||
| chr8:94847171 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-2291C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94847171 | |||||||
| chr8:94847214 | G | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-2248G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94847214 | |||||||
| chr8:94847320 | G | A | 1 | a0001c0002t0001g0115 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1261-2142G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94847320 | |||||||
| chr8:94847419 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1261-2043G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94847419 | |||||||
| chr8:94847943 | A | G | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1261-1519A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94847943 | |||||||
| chr8:94848013 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0053 |
3 | HG02723.hp1 HG06807.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1261-1436_1261-143 others(19): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94848013 | ||||||
| chr8:94848013 | C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0288 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-1436_1261-143 others(20): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94848013 | ||||||
| chr8:94848013 | C | CTTTTTTT others(10): Show |
24 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
24 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1261-1436_1261-143 others(21): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94848013 | ||||||
| chr8:94848013 | C | CTTTTTTT others(11): Show |
6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG00544.hp2 HG02027.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1436_1261-143 others(22): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94848013 | ||||||
| chr8:94848013 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0019 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1261-1436_1261-143 others(23): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94848013 | ||||||
| chr8:94848013 | C | T | 2 | a0001c0002t0001g0054 a0001c0002t0001g0061 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1261-1449C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848013 | |||||||
| chr8:94848031 | T | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1431T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848031 | |||||||
| chr8:94848071 | T | C | 1 | a0001c0003t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1261-1391T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848071 | |||||||
| chr8:94848075 | C | A | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1261-1387C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848075 | |||||||
| chr8:94848075 | C | T | 3 | a0001c0003t0001g0251 a0001c0003t0001g0258 a0001c0003t0001g0259 |
3 | HG01261.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1261-1387C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848075 | |||||||
| chr8:94848433 | TC | T | 3 | a0001c0002t0001g0104 a0001c0002t0001g0142 a0001c0002t0001g0143 |
3 | HG01258.hp2 NA18992.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1261-1027delC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr8 | 94848433 | ||||||
| chr8:94848613 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1261-849C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848613 | |||||||
| chr8:94848707 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0223 a0001c0001t0001g0227 others(2): Show |
5 | HG02109.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-755C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848707 | |||||||
| chr8:94848735 | T | C | 1 | a0001c0003t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1261-727T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848735 | |||||||
| chr8:94848834 | T | C | 1 | a0001c0002t0001g0093 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1261-628T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94848834 | |||||||
| chr8:94849057 | A | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1261-405A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94849057 | |||||||
| chr8:94849225 | T | C | 2 | a0001c0001t0003g0015 a0001c0001t0007g0016 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1261-237T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94849225 | |||||||
| chr8:94849557 | CT | C | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1331+36delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr8 | 94849557 | ||||||
| chr8:94849597 | T | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.1331+65T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 11/26 | chr8 | 94849597 | |||||||
| chr8:94849675 | A | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1331+143A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 11/26 | chr8 | 94849675 | |||||||
| chr8:94849736 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1332-180A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 11/26 | chr8 | 94849736 | |||||||
| chr8:94850360 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1507+269C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94850360 | |||||||
| chr8:94850364 | G | T | 1 | a0001c0002t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1507+273G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94850364 | |||||||
| chr8:94850469 | A | G | 128 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0002t0001g0001 others(125): Show |
137 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1507+378A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94850469 | |||||||
| chr8:94850611 | CA | C | 150 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0159 others(147): Show |
160 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1507+540delA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr8 | 94850611 | ||||||
| chr8:94850611 | CAA | C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(27): Show |
30 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1507+539_1507+540d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr8 | 94850611 | ||||||
| chr8:94850611 | CAAA | C | 7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507+538_1507+540d others(5): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr8 | 94850611 | ||||||
| chr8:94850673 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507+582G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94850673 | |||||||
| chr8:94850682 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1507+591T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94850682 | |||||||
| chr8:94850730 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1507+639C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94850730 | |||||||
| chr8:94850800 | T | TG | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507+711dupG | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr8 | 94850800 | ||||||
| chr8:94850806 | T | G | 7 | a0001c0003t0001g0251 a0001c0003t0001g0258 a0001c0003t0001g0259 others(4): Show |
7 | HG01261.hp2 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1507+715T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94850806 | |||||||
| chr8:94851052 | A | G | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1508-501A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851052 | |||||||
| chr8:94851121 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1508-432G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851121 | |||||||
| chr8:94851132 | T | C | 191 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(188): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1508-421T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851132 | |||||||
| chr8:94851235 | TAA | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1508-317_1508-316d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851235 | |||||||
| chr8:94851262 | T | C | 1 | a0001c0002t0001g0284 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1508-291T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851262 | |||||||
| chr8:94851282 | A | G | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1508-271A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851282 | |||||||
| chr8:94851287 | A | G | 1 | a0001c0003t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1508-266A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851287 | |||||||
| chr8:94851692 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1641+6C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94851692 | |||||||
| chr8:94851705 | A | G | 1 | a0001c0002t0011g0110 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1641+19A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94851705 | |||||||
| chr8:94851780 | G | A | 1 | a0001c0002t0004g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1641+94G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94851780 | |||||||
| chr8:94852069 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1641+383G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852069 | |||||||
| chr8:94852189 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
16 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1641+503C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852189 | |||||||
| chr8:94852362 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1641+676T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852362 | |||||||
| chr8:94852399 | T | G | 1 | a0001c0003t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1641+713T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852399 | |||||||
| chr8:94852492 | C | A | 1 | a0001c0002t0001g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1641+806C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852492 | |||||||
| chr8:94852502 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1641+816T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852502 | |||||||
| chr8:94852658 | G | C | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1641+972G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852658 | |||||||
| chr8:94852674 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1641+988C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852674 | |||||||
| chr8:94852692 | A | G | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1641+1006A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852692 | |||||||
| chr8:94852734 | A | G | 1 | a0001c0002t0005g0092 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1641+1048A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852734 | |||||||
| chr8:94852777 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1642-1028C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852777 | |||||||
| chr8:94852778 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1642-1027G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852778 | |||||||
| chr8:94852903 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1642-902C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852903 | |||||||
| chr8:94852964 | C | G | 5 | a0001c0001t0001g0174 a0001c0001t0001g0223 a0001c0001t0001g0227 others(2): Show |
5 | HG02109.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1642-841C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852964 | |||||||
| chr8:94852972 | T | C | 1 | a0001c0003t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1642-833T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94852972 | |||||||
| chr8:94853391 | C | T | 2 | a0001c0001t0003g0015 a0001c0001t0007g0016 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1642-414C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 13/26 | chr8 | 94853391 | |||||||
| chr8:94853922 | A | G | 2 | a0001c0002t0001g0058 a0001c0002t0001g0078 |
2 | HG00438.hp2 NA19054.hp1 |
splice_region_variant&intron_variant | LOW | c.1752+7A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94853922 | |||||||
| chr8:94853990 | A | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1752+75A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94853990 | |||||||
| chr8:94854128 | A | G | 7 | a0001c0002t0001g0116 a0001c0002t0001g0138 a0001c0002t0001g0139 others(4): Show |
7 | HG01928.hp1 HG01975.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+213A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854128 | |||||||
| chr8:94854158 | G | GTGAGCTG others(3): Show |
42 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1752+244_1752+245i others(12): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr8 | 94854158 | ||||||
| chr8:94854276 | CCTTTTCC others(4): Show |
C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0239 |
2 | NA18949.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1752+377_1752+387d others(13): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr8 | 94854276 | ||||||
| chr8:94854373 | A | G | 1 | a0001c0002t0001g0284 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1752+458A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854373 | |||||||
| chr8:94854379 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1752+464A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854379 | |||||||
| chr8:94854489 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1752+574G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854489 | |||||||
| chr8:94854514 | C | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+599C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854514 | |||||||
| chr8:94854610 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+695C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854610 | |||||||
| chr8:94854662 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752+747A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854662 | |||||||
| chr8:94854894 | G | A | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0003t0001g0180 others(2): Show |
5 | HG01255.hp1 HG01346.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1752+979G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854894 | |||||||
| chr8:94854908 | A | AT | 151 | a0001c0001t0001g0013 a0001c0001t0001g0159 a0001c0001t0001g0217 others(148): Show |
161 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.1752+1011dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr8 | 94854908 | ||||||
| chr8:94854948 | T | A | 195 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1752+1033T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854948 | |||||||
| chr8:94855297 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
16 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1752+1382A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94855297 | |||||||
| chr8:94855393 | A | ATC | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1381_1753-138 others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr8 | 94855393 | ||||||
| chr8:94855458 | T | G | 1 | a0001c0002t0001g0087 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1753-1319T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94855458 | |||||||
| chr8:94855459 | T | C | 16 | a0001c0002t0001g0060 a0001c0002t0001g0063 a0001c0002t0001g0072 others(13): Show |
16 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1753-1318T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94855459 | |||||||
| chr8:94855538 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-1239C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94855538 | |||||||
| chr8:94855602 | C | A | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1753-1175C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94855602 | |||||||
| chr8:94855885 | G | T | 2 | a0001c0002t0001g0076 a0001c0002t0001g0077 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1753-892G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94855885 | |||||||
| chr8:94856187 | T | C | 2 | a0001c0002t0001g0058 a0001c0002t0001g0078 |
2 | HG00438.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1753-590T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856187 | |||||||
| chr8:94856227 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1753-550C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856227 | |||||||
| chr8:94856252 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0034 |
2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1753-525G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856252 | |||||||
| chr8:94856270 | A | G | 1 | a0007c0006t0001g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1753-507A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856270 | |||||||
| chr8:94856347 | T | C | 4 | a0001c0003t0001g0277 a0001c0003t0001g0278 a0001c0003t0001g0279 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753-430T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856347 | |||||||
| chr8:94856380 | G | A | 149 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0002t0001g0001 others(146): Show |
159 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.1753-397G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856380 | |||||||
| chr8:94856393 | G | T | 1 | a0001c0002t0001g0147 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1753-384G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856393 | |||||||
| chr8:94856417 | A | G | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1753-360A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856417 | |||||||
| chr8:94856421 | C | G | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1753-356C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856421 | |||||||
| chr8:94856591 | T | G | 195 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1753-186T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856591 | |||||||
| chr8:94856671 | T | G | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1753-106T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856671 | |||||||
| chr8:94856704 | C | G | 20 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0203 others(17): Show |
20 | HG00438.hp1 HG01516.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.1753-73C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856704 | |||||||
| chr8:94857071 | C | CT | 44 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(41): Show |
46 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1954+112dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr8 | 94857071 | ||||||
| chr8:94857071 | CT | C | 6 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0002t0001g0108 others(3): Show |
6 | HG00099.hp1 HG00642.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1954+112delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr8 | 94857071 | ||||||
| chr8:94857151 | C | A | 1 | a0001c0002t0001g0142 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1954+173C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857151 | |||||||
| chr8:94857352 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1954+374A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857352 | |||||||
| chr8:94857423 | G | A | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1954+445G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857423 | |||||||
| chr8:94857520 | A | T | 1 | a0001c0002t0001g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1954+542A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857520 | |||||||
| chr8:94857584 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0286 |
2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1954+606T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857584 | |||||||
| chr8:94857793 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1954+815G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857793 | |||||||
| chr8:94857892 | A | C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(33): Show |
36 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1954+914A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857892 | |||||||
| chr8:94857902 | G | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954+924G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857902 | |||||||
| chr8:94857925 | A | T | 2 | a0001c0002t0001g0059 a0001c0002t0001g0086 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1954+947A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94857925 | |||||||
| chr8:94858073 | A | G | 1 | a0001c0002t0001g0137 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1954+1095A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94858073 | |||||||
| chr8:94858136 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1954+1158G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94858136 | |||||||
| chr8:94858570 | C | T | 2 | a0001c0003t0001g0177 a0001c0003t0001g0256 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1955-941C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94858570 | |||||||
| chr8:94858571 | G | A | 3 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0152 |
3 | HG02080.hp1 NA18942.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1955-940G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94858571 | |||||||
| chr8:94858655 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1955-856C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94858655 | |||||||
| chr8:94858718 | G | C | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1955-793G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94858718 | |||||||
| chr8:94858981 | G | C | 1 | a0001c0002t0001g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1955-530G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94858981 | |||||||
| chr8:94859272 | C | A | 1 | a0001c0002t0001g0083 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1955-239C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94859272 | |||||||
| chr8:94859333 | C | T | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG02145.hp2 HG02257.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1955-178C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94859333 | |||||||
| chr8:94859375 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1955-136A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 15/26 | chr8 | 94859375 | |||||||
| chr8:94859772 | TAG | T | 187 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2076+143_2076+144d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94859772 | ||||||
| chr8:94859908 | G | A | 34 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.2076+276G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94859908 | |||||||
| chr8:94860282 | T | TA | 153 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0002t0001g0001 others(150): Show |
163 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.2076+660dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94860282 | ||||||
| chr8:94860302 | C | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+670C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860302 | |||||||
| chr8:94860307 | C | T | 1 | a0001c0003t0001g0183 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2076+675C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860307 | |||||||
| chr8:94860441 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+809G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860441 | |||||||
| chr8:94860535 | T | C | 253 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(250): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.2076+903T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860535 | |||||||
| chr8:94860567 | G | A | 187 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2076+935G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860567 | |||||||
| chr8:94860579 | C | CA | 99 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0034 others(96): Show |
100 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.2076+972dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94860579 | ||||||
| chr8:94860579 | C | CAA | 9 | a0001c0001t0001g0051 a0001c0001t0001g0245 a0001c0002t0001g0056 others(6): Show |
10 | HG01168.hp1 HG01169.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076+971_2076+972d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94860579 | ||||||
| chr8:94860579 | CA | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0194 others(16): Show |
21 | HG00408.hp2 HG01975.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2076+972delA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94860579 | ||||||
| chr8:94860579 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2076+961_2076+972d others(14): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94860579 | ||||||
| chr8:94860599 | A | C | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2076+967A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860599 | |||||||
| chr8:94860668 | A | G | 1 | a0001c0002t0001g0121 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2076+1036A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860668 | |||||||
| chr8:94860683 | G | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0044 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+1051G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860683 | |||||||
| chr8:94860727 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2076+1095C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860727 | |||||||
| chr8:94860774 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2076+1142G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860774 | |||||||
| chr8:94860821 | C | T | 6 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(3): Show |
6 | HG01109.hp1 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2076+1189C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860821 | |||||||
| chr8:94860895 | A | T | 1 | a0001c0002t0001g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2076+1263A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860895 | |||||||
| chr8:94860914 | G | A | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2076+1282G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860914 | |||||||
| chr8:94860962 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2076+1330C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860962 | |||||||
| chr8:94860974 | A | G | 2 | a0001c0001t0001g0271 a0004c0005t0001g0204 |
2 | HG02165.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.2076+1342A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860974 | |||||||
| chr8:94861020 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2076+1388G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861020 | |||||||
| chr8:94861055 | T | TC | 44 | a0001c0001t0001g0255 a0001c0002t0001g0007 a0001c0002t0001g0054 others(41): Show |
45 | HG00544.hp1 HG00639.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.2076+1424dupC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861055 | ||||||
| chr8:94861056 | C | CA | 62 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(59): Show |
62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2076+1443dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861056 | ||||||
| chr8:94861056 | C | CAA | 7 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0038 others(4): Show |
7 | HG00544.hp2 HG01884.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2076+1442_2076+144 others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861056 | ||||||
| chr8:94861056 | CAAAAAAA others(3): Show |
C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0181 |
2 | HG01358.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2076+1434_2076+144 others(14): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861056 | ||||||
| chr8:94861057 | A | C | 102 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(99): Show |
111 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.2076+1425A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861057 | |||||||
| chr8:94861058 | A | C | 1 | a0001c0003t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2076+1426A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861058 | |||||||
| chr8:94861062 | A | C | 3 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0152 |
3 | HG02080.hp1 NA18942.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.2076+1430A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861062 | |||||||
| chr8:94861067 | A | C | 2 | a0001c0003t0001g0179 a0001c0003t0001g0181 |
2 | HG01358.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2076+1435A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861067 | |||||||
| chr8:94861256 | A | AT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0173 a0001c0001t0001g0174 others(16): Show |
20 | HG00609.hp1 HG01928.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.2076+1647dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATT | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG02145.hp2 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2076+1646_2076+164 others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTT | 28 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(25): Show |
29 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2076+1642_2076+164 others(10): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT | 61 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(58): Show |
64 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2076+1641_2076+164 others(11): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(1): Show |
73 | a0001c0001t0001g0040 a0001c0002t0001g0001 a0001c0002t0001g0004 others(70): Show |
79 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2076+1640_2076+164 others(12): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(2): Show |
17 | a0001c0001t0003g0017 a0001c0002t0001g0057 a0001c0002t0001g0105 others(14): Show |
17 | HG00544.hp1 HG02129.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.2076+1639_2076+164 others(13): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(3): Show |
6 | a0001c0001t0001g0207 a0001c0001t0003g0014 a0001c0002t0001g0068 others(3): Show |
6 | HG01109.hp1 HG02074.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2076+1638_2076+164 others(14): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0255 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+1637_2076+164 others(15): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0052 a0001c0001t0003g0015 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2076+1636_2076+164 others(16): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02040.hp1 HG02165.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+1634_2076+164 others(18): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(8): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0265 others(3): Show |
8 | HG00408.hp2 HG00621.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.2076+1633_2076+164 others(19): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0272 |
2 | HG02074.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2076+1632_2076+164 others(20): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0266 a0001c0001t0001g0273 |
2 | HG01192.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2076+1631_2076+164 others(21): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | A | ATTTTTTT others(24): Show |
1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2076+1647_2076+164 others(35): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861256 | ATTTTTTT others(3): Show |
A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0149 |
2 | NA18962.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2076+1638_2076+164 others(14): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94861256 | ||||||
| chr8:94861284 | C | G | 192 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(189): Show |
202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.2076+1652C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861284 | |||||||
| chr8:94861292 | C | T | 191 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(188): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.2076+1660C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861292 | |||||||
| chr8:94861313 | G | C | 192 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(189): Show |
202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.2076+1681G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861313 | |||||||
| chr8:94861383 | T | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+1751T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861383 | |||||||
| chr8:94861411 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
16 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.2076+1779A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861411 | |||||||
| chr8:94861451 | C | T | 2 | a0001c0002t0001g0064 a0001c0002t0001g0065 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2076+1819C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861451 | |||||||
| chr8:94861533 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2076+1901T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861533 | |||||||
| chr8:94861584 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2076+1952C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861584 | |||||||
| chr8:94861604 | G | A | 4 | a0001c0003t0001g0277 a0001c0003t0001g0278 a0001c0003t0001g0279 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+1972G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861604 | |||||||
| chr8:94861765 | G | C | 153 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0002t0001g0001 others(150): Show |
163 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.2076+2133G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861765 | |||||||
| chr8:94861980 | G | A | 9 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(6): Show |
10 | HG01069.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2076+2348G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861980 | |||||||
| chr8:94862053 | G | A | 1 | a0001c0003t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2076+2421G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862053 | |||||||
| chr8:94862207 | G | A | 2 | a0001c0003t0001g0251 a0001c0003t0001g0258 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2076+2575G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862207 | |||||||
| chr8:94862211 | G | A | 23 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(20): Show |
23 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.2076+2579G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862211 | |||||||
| chr8:94862326 | A | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(203): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.2076+2694A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862326 | |||||||
| chr8:94862352 | T | C | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2076+2720T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862352 | |||||||
| chr8:94862361 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 |
3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2076+2729C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862361 | |||||||
| chr8:94862374 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076+2742G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862374 | |||||||
| chr8:94862437 | C | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 |
3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2076+2805C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862437 | |||||||
| chr8:94862442 | C | G | 1 | a0001c0003t0001g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2076+2810C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862442 | |||||||
| chr8:94862520 | G | T | 1 | a0001c0002t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2076+2888G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862520 | |||||||
| chr8:94862569 | C | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0007g0016 |
3 | HG01109.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2076+2937C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862569 | |||||||
| chr8:94862578 | G | A | 1 | a0001c0002t0001g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2077-2928G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862578 | |||||||
| chr8:94862867 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2077-2639G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862867 | |||||||
| chr8:94862874 | CGT | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2077-2629_2077-262 others(6): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94862874 | ||||||
| chr8:94862994 | G | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2077-2512G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862994 | |||||||
| chr8:94863154 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2077-2352G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863154 | |||||||
| chr8:94863163 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2077-2343G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863163 | |||||||
| chr8:94863164 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2077-2342G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863164 | |||||||
| chr8:94863184 | G | A | 3 | a0001c0002t0001g0054 a0001c0002t0001g0061 a0001c0002t0001g0164 |
3 | HG02109.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2077-2322G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863184 | |||||||
| chr8:94863242 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2077-2264G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863242 | |||||||
| chr8:94863285 | G | A | 23 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(20): Show |
23 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.2077-2221G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863285 | |||||||
| chr8:94863448 | A | G | 127 | a0001c0001t0001g0159 a0001c0002t0001g0001 a0001c0002t0001g0002 others(124): Show |
136 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.2077-2058A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863448 | |||||||
| chr8:94863598 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2077-1908G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863598 | |||||||
| chr8:94863639 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2077-1867T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863639 | |||||||
| chr8:94863679 | G | A | 1 | a0001c0002t0001g0135 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2077-1827G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863679 | |||||||
| chr8:94863794 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2077-1712C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863794 | |||||||
| chr8:94863817 | G | A | 1 | a0001c0002t0001g0124 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2077-1689G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863817 | |||||||
| chr8:94863920 | T | C | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2077-1586T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863920 | |||||||
| chr8:94863927 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0223 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2077-1579G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863927 | |||||||
| chr8:94864018 | A | C | 4 | a0001c0002t0001g0167 a0001c0002t0004g0119 a0001c0002t0004g0131 others(1): Show |
4 | HG01109.hp2 HG01192.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2077-1488A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864018 | |||||||
| chr8:94864168 | C | CT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
16 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.2077-1328dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94864168 | ||||||
| chr8:94864317 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(28): Show |
31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.2077-1189C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864317 | |||||||
| chr8:94864640 | G | A | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2077-866G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864640 | |||||||
| chr8:94864735 | T | G | 137 | a0001c0001t0001g0159 a0001c0001t0001g0255 a0001c0002t0001g0001 others(134): Show |
146 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2077-771T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864735 | |||||||
| chr8:94864753 | A | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2077-753A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864753 | |||||||
| chr8:94864814 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2077-692C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864814 | |||||||
| chr8:94864860 | C | A | 2 | a0001c0003t0001g0251 a0001c0003t0001g0258 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2077-646C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864860 | |||||||
| chr8:94864975 | A | C | 1 | a0001c0002t0001g0138 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2077-531A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864975 | |||||||
| chr8:94865014 | A | AT | 5 | a0001c0002t0001g0004 a0001c0002t0001g0102 a0001c0002t0001g0157 others(2): Show |
7 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.2077-481dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr8 | 94865014 | ||||||
| chr8:94865057 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2077-449C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94865057 | |||||||
| chr8:94865086 | A | G | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2077-420A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94865086 | |||||||
| chr8:94865335 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2077-171C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94865335 | |||||||
| chr8:94865355 | T | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0207 a0001c0001t0001g0213 others(13): Show |
18 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2077-151T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94865355 | |||||||
| chr8:94865376 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2077-130C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94865376 | |||||||
| chr8:94865398 | G | C | 1 | a0001c0002t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2077-108G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94865398 | |||||||
| chr8:94865468 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2077-38C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94865468 | |||||||
| chr8:94865956 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.2262-202G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 17/26 | chr8 | 94865956 | |||||||
| chr8:94866025 | G | A | 204 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(201): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.2262-133G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 17/26 | chr8 | 94866025 | |||||||
| chr8:94866030 | A | G | 1 | a0001c0002t0001g0082 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2262-128A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 17/26 | chr8 | 94866030 | |||||||
| chr8:94866344 | G | A | 1 | a0001c0003t0001g0259 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2295+153G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866344 | |||||||
| chr8:94866346 | G | A | 9 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(6): Show |
10 | HG01069.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2295+155G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866346 | |||||||
| chr8:94866458 | A | G | 1 | a0001c0002t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2295+267A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866458 | |||||||
| chr8:94866475 | A | C | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2295+284A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866475 | |||||||
| chr8:94866500 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2295+309G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866500 | |||||||
| chr8:94866807 | C | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.2296-333C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866807 | |||||||
| chr8:94866817 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2296-323G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866817 | |||||||
| chr8:94866886 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2296-254T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | chr8 | 94866886 | |||||||
| chr8:94867000 | TA | T | 35 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.2296-137delA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr8 | 94867000 | ||||||
| chr8:94867521 | C | CT | 9 | a0001c0001t0001g0159 a0001c0001t0001g0196 a0001c0001t0001g0197 others(6): Show |
9 | HG02074.hp2 HG02257.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.2414+204dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94867521 | ||||||
| chr8:94867521 | CT | C | 141 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0050 others(138): Show |
151 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.2414+204delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94867521 | ||||||
| chr8:94867521 | CTT | C | 44 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
44 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2414+203_2414+204d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94867521 | ||||||
| chr8:94867546 | CAG | C | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2414+212_2414+213d others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94867546 | ||||||
| chr8:94867674 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2414+337C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94867674 | |||||||
| chr8:94867894 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0239 |
2 | NA18949.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2414+557C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94867894 | |||||||
| chr8:94868241 | A | G | 57 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(54): Show |
60 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.2414+904A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868241 | |||||||
| chr8:94868321 | T | C | 1 | a0001c0002t0001g0104 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2414+984T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868321 | |||||||
| chr8:94868518 | G | C | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.2414+1181G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868518 | |||||||
| chr8:94868576 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2414+1239C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868576 | |||||||
| chr8:94868645 | C | T | 2 | a0001c0002t0001g0080 a0001c0002t0001g0081 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2414+1308C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868645 | |||||||
| chr8:94868680 | C | CT | 38 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2414+1352dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94868680 | ||||||
| chr8:94868692 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2414+1355A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868692 | |||||||
| chr8:94868698 | C | T | 3 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0007g0016 |
3 | HG01109.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2414+1361C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868698 | |||||||
| chr8:94868713 | C | T | 1 | a0001c0003t0001g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2414+1376C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868713 | |||||||
| chr8:94868813 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414+1476G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94868813 | |||||||
| chr8:94868980 | A | AT | 53 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(50): Show |
57 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.2414+1662dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94868980 | ||||||
| chr8:94869179 | TCATGTTG others(505): Show |
T | 1 | a0001c0001t0001g0022 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2414+1862_2415-217 others(4): Show |
INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94869179 | ||||||
| chr8:94869395 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(12): Show |
17 | HG00408.hp2 HG00621.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.2414+2058C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869395 | |||||||
| chr8:94869554 | A | G | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2414+2217A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869554 | |||||||
| chr8:94869557 | A | G | 1 | a0006c0009t0001g0242 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2414+2220A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869557 | |||||||
| chr8:94869606 | C | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(30): Show |
33 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.2414+2269C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869606 | |||||||
| chr8:94869638 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2415-2246A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869638 | |||||||
| chr8:94869665 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-2219G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869665 | |||||||
| chr8:94869771 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2415-2113A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869771 | |||||||
| chr8:94869783 | G | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0099 |
2 | HG01993.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2415-2101G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869783 | |||||||
| chr8:94869968 | A | G | 1 | a0001c0002t0001g0135 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2415-1916A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94869968 | |||||||
| chr8:94870053 | A | AT | 3 | a0001c0001t0003g0015 a0001c0001t0003g0017 a0001c0001t0007g0016 |
3 | HG03098.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2415-1828dupT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94870053 | ||||||
| chr8:94870057 | A | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0238 a0001c0001t0003g0015 others(3): Show |
6 | HG00673.hp2 HG01928.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2415-1827A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870057 | |||||||
| chr8:94870061 | T | A | 24 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
24 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2415-1823T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870061 | |||||||
| chr8:94870137 | T | C | 93 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0001t0001g0268 others(90): Show |
102 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.2415-1747T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870137 | |||||||
| chr8:94870184 | T | C | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2415-1700T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870184 | |||||||
| chr8:94870241 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-1643C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870241 | |||||||
| chr8:94870270 | G | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-1614G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870270 | |||||||
| chr8:94870341 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01516.hp2 HG01517.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.2415-1543G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870341 | |||||||
| chr8:94870466 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2415-1418A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870466 | |||||||
| chr8:94870581 | A | G | 5 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01975.hp1 HG02004.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.2415-1303A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870581 | |||||||
| chr8:94870718 | G | T | 4 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0068 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2415-1166G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870718 | |||||||
| chr8:94870741 | T | A | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2415-1143T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870741 | |||||||
| chr8:94870945 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2415-939A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870945 | |||||||
| chr8:94870993 | G | C | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2415-891G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870993 | |||||||
| chr8:94871004 | A | G | 65 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(62): Show |
67 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2415-880A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94871004 | |||||||
| chr8:94871224 | C | T | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2415-660C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94871224 | |||||||
| chr8:94871312 | CA | C | 199 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(196): Show |
211 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.2415-556delA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94871312 | ||||||
| chr8:94871337 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2415-547G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94871337 | |||||||
| chr8:94871472 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 |
3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2415-412C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94871472 | |||||||
| chr8:94871477 | C | CA | 15 | a0001c0001t0001g0173 a0001c0001t0001g0205 a0001c0001t0001g0206 others(12): Show |
15 | HG01516.hp2 HG01517.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.2415-394dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr8 | 94871477 | ||||||
| chr8:94872296 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 |
3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2533+294C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872296 | |||||||
| chr8:94872368 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2533+366G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872368 | |||||||
| chr8:94872377 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2533+375G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872377 | |||||||
| chr8:94872378 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2533+376C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872378 | |||||||
| chr8:94872431 | G | A | 2 | a0001c0003t0001g0275 a0001c0003t0001g0276 |
2 | HG01070.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2533+429G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872431 | |||||||
| chr8:94872481 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2533+479G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872481 | |||||||
| chr8:94872486 | G | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2533+484G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872486 | |||||||
| chr8:94872497 | T | C | 2 | a0001c0003t0001g0257 a0001c0003t0001g0260 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2533+495T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872497 | |||||||
| chr8:94872908 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2534-466G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94872908 | |||||||
| chr8:94873169 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2534-205G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94873169 | |||||||
| chr8:94873236 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2534-138C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94873236 | |||||||
| chr8:94873296 | T | TA | 3 | a0001c0002t0001g0111 a0001c0002t0001g0156 a0001c0002t0001g0284 |
3 | HG00621.hp1 NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2534-77dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr8 | 94873296 | ||||||
| chr8:94873321 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0207 a0001c0001t0001g0213 others(13): Show |
18 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2534-53C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94873321 | |||||||
| chr8:94873333 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2534-41A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 21/26 | chr8 | 94873333 | |||||||
| chr8:94873651 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2637+174G>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94873651 | |||||||
| chr8:94873707 | C | T | 1 | a0001c0003t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2637+230C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94873707 | |||||||
| chr8:94873742 | C | T | 2 | a0001c0002t0001g0116 a0001c0002t0001g0141 |
2 | NA18944.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2637+265C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94873742 | |||||||
| chr8:94873787 | C | G | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.2637+310C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94873787 | |||||||
| chr8:94873825 | A | T | 202 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.2637+348A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94873825 | |||||||
| chr8:94873881 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2637+404G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94873881 | |||||||
| chr8:94874223 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 |
3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2638-329T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94874223 | |||||||
| chr8:94874246 | C | T | 2 | a0001c0002t0001g0096 a0001c0002t0001g0097 |
2 | NA18981.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2638-306C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94874246 | |||||||
| chr8:94874247 | GT | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(202): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.2638-294delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr8 | 94874247 | ||||||
| chr8:94874323 | A | G | 202 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.2638-229A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94874323 | |||||||
| chr8:94874333 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2638-219T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94874333 | |||||||
| chr8:94874396 | G | A | 39 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(36): Show |
39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2638-156G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 22/26 | chr8 | 94874396 | |||||||
| chr8:94874752 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2688+150T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94874752 | |||||||
| chr8:94874819 | A | G | 1 | a0001c0002t0001g0152 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2688+217A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94874819 | |||||||
| chr8:94874832 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2688+230G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94874832 | |||||||
| chr8:94874918 | A | C | 1 | a0001c0002t0001g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2688+316A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94874918 | |||||||
| chr8:94874997 | G | C | 143 | a0001c0001t0001g0034 a0001c0002t0001g0001 a0001c0002t0001g0002 others(140): Show |
153 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.2688+395G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94874997 | |||||||
| chr8:94875067 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG02559.hp2 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2688+465C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94875067 | |||||||
| chr8:94875194 | A | G | 1 | a0001c0002t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2688+592A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94875194 | |||||||
| chr8:94875324 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2688+722C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94875324 | |||||||
| chr8:94875726 | G | A | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2689-348G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94875726 | |||||||
| chr8:94875761 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2689-313C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94875761 | |||||||
| chr8:94875968 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2689-106C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 23/26 | chr8 | 94875968 | |||||||
| chr8:94876164 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2762+17A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 24/26 | chr8 | 94876164 | |||||||
| chr8:94876334 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2827+49A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 25/26 | chr8 | 94876334 | |||||||
| chr8:94876571 | G | C | 11 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0178 others(8): Show |
12 | HG01069.hp2 HG01070.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.2871+82G>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94876571 | |||||||
| chr8:94876698 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2871+209C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94876698 | |||||||
| chr8:94876707 | A | C | 1 | a0001c0003t0002g0250 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2871+218A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94876707 | |||||||
| chr8:94876753 | G | A | 45 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(42): Show |
45 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.2871+264G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94876753 | |||||||
| chr8:94876971 | A | C | 1 | a0001c0003t0001g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2871+482A>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94876971 | |||||||
| chr8:94877291 | T | C | 2 | a0001c0002t0001g0139 a0001c0002t0001g0158 |
2 | HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.2871+802T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877291 | |||||||
| chr8:94877299 | T | A | 1 | a0001c0002t0010g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2871+810T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877299 | |||||||
| chr8:94877407 | A | G | 1 | a0001c0003t0001g0258 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2871+918A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877407 | |||||||
| chr8:94877583 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2871+1094T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877583 | |||||||
| chr8:94877628 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2871+1139C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877628 | |||||||
| chr8:94877711 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2871+1222G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877711 | |||||||
| chr8:94877751 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0207 a0001c0001t0001g0213 others(13): Show |
18 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2871+1262T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877751 | |||||||
| chr8:94877778 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 |
3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2871+1289C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94877778 | |||||||
| chr8:94877978 | T | TC | 7 | a0001c0002t0001g0059 a0001c0002t0001g0082 a0001c0002t0001g0083 others(4): Show |
7 | HG01167.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2871+1491dupC | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr8 | 94877978 | ||||||
| chr8:94878091 | C | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0185 a0001c0001t0001g0186 others(16): Show |
19 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2871+1602C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878091 | |||||||
| chr8:94878348 | A | G | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2872-1770A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878348 | |||||||
| chr8:94878506 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0017 others(1): Show |
4 | HG01109.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2872-1612G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878506 | |||||||
| chr8:94878676 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2872-1442C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878676 | |||||||
| chr8:94878714 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2872-1404C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878714 | |||||||
| chr8:94878755 | A | T | 202 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.2872-1363A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878755 | |||||||
| chr8:94878885 | T | G | 202 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.2872-1233T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878885 | |||||||
| chr8:94878967 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2872-1151G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878967 | |||||||
| chr8:94879097 | G | A | 2 | a0001c0003t0001g0177 a0001c0003t0001g0256 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2872-1021G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879097 | |||||||
| chr8:94879128 | C | A | 160 | a0001c0001t0001g0005 a0001c0001t0001g0207 a0001c0001t0001g0213 others(157): Show |
172 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.2872-990C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879128 | |||||||
| chr8:94879143 | C | G | 6 | a0001c0001t0001g0173 a0001c0001t0001g0205 a0001c0001t0001g0215 others(3): Show |
6 | NA18954.hp2 NA18978.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.2872-975C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879143 | |||||||
| chr8:94879225 | C | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(203): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.2872-893C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879225 | |||||||
| chr8:94879439 | A | G | 2 | a0001c0003t0001g0275 a0001c0003t0001g0276 |
2 | HG01070.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2872-679A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879439 | |||||||
| chr8:94879478 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2872-640C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879478 | |||||||
| chr8:94879615 | C | A | 160 | a0001c0001t0001g0005 a0001c0001t0001g0207 a0001c0001t0001g0213 others(157): Show |
172 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.2872-503C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879615 | |||||||
| chr8:94879615 | C | CA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0175 a0001c0001t0001g0232 others(2): Show |
6 | NA18949.hp2 NA18954.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.2872-494dupA | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr8 | 94879615 | ||||||
| chr8:94879625 | C | A | 12 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(9): Show |
12 | HG00609.hp2 HG01993.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2872-493C>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879625 | |||||||
| chr8:94879626 | CT | C | 201 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(198): Show |
213 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.2872-478delT | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr8 | 94879626 | ||||||
| chr8:94879627 | T | C | 11 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0002t0001g0056 others(8): Show |
11 | HG00609.hp2 HG01993.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2872-491T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879627 | |||||||
| chr8:94879628 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2872-490T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879628 | |||||||
| chr8:94879758 | T | C | 4 | a0001c0003t0001g0277 a0001c0003t0001g0278 a0001c0003t0001g0279 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2872-360T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879758 | |||||||
| chr8:94879961 | T | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0281 |
2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2872-157T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94879961 | |||||||
| chr8:94880031 | T | G | 2 | a0001c0003t0001g0169 a0001c0003t0001g0170 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2872-87T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94880031 |