Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 995 | 304 | 92 | 51 | 118 | 10 | 31 | 82 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0002 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0003 | 0/0 | 995 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0004 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0005 | 0/0 | 995 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0006 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0007 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2988 | 145 | 45 | 16 | 65 | 5 | 12 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0002 | 0/0 | 2988 | 125 | 26 | 24 | 53 | 5 | 17 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0003 | 0/0 | 2988 | 32 | 19 | 11 | 0 | 0 | 2 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0004 | 0/0 | 2988 | 2 | 2 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0005 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0006 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0007 | 0/0 | 2988 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0008 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0009 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| c0010 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1658 | 289 | 84 | 48 | 117 | 10 | 28 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0002 | 0/0 | 1658 | 4 | 4 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0003 | 0/0 | 1658 | 3 | 2 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0004 | 0/0 | 1658 | 3 | 0 | 3 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0005 | 0/0 | 1658 | 3 | 0 | 0 | 3 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0006 | 0/0 | 1658 | 3 | 0 | 0 | 0 | 0 | 3 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0007 | 0/0 | 1658 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0008 | 0/0 | 1658 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0009 | 0/0 | 1658 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0010 | 0/0 | 1658 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| t0011 | 0/0 | 1658 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0003 | 1/0 | 3 | 0 | 1 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2988 | 145 | 45 | 16 | 65 | 5 | 12 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002 | 0/0 | 2988 | 125 | 26 | 24 | 53 | 5 | 17 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0003 | 0/0 | 2988 | 32 | 19 | 11 | 0 | 0 | 2 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0004 | 0/0 | 2988 | 2 | 2 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0002c0010 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0003c0007 | 0/0 | 2988 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0004c0006 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0005c0008 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0006c0009 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0007c0005 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | 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 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0001t0003 | 0/0 | 4645 | 3 | 2 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0001t0006 | 0/0 | 4645 | 3 | 0 | 0 | 0 | 0 | 3 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0001t0007 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002t0001 | 0/0 | 4645 | 115 | 25 | 21 | 48 | 5 | 16 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002t0004 | 0/0 | 4645 | 3 | 0 | 3 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002t0005 | 0/0 | 4645 | 3 | 0 | 0 | 3 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002t0008 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002t0009 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002t0010 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0002t0011 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0003t0001 | 0/0 | 4645 | 28 | 15 | 11 | 0 | 0 | 2 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0003t0002 | 0/0 | 4645 | 4 | 4 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0001c0004t0001 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0002c0010t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0003c0007t0001 | 0/0 | 4645 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0004c0006t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0005c0008t0001 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0006c0009t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| a0007c0005t0001 | 0/0 | 4645 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | copy fasta | chr8 | 94818287 | 94886746 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 1/0 | 3 | 0 | 1 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 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 |
| 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0062 | 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 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0067 | 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 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0110 | 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 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0010g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0002t0011g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0003t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0002c0010t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0003c0007t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0004c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0005c0008t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0006c0009t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| a0007c0005t0001g0238 | 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 | g0092 | EUR | GBR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0022 | 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 | g0258 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0035 | 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 | g0031 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0119 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01069 | hp2 | a0003 | c0007 | t0001 | g0006 | 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 | g0284 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0146 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0179 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0189 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0177 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0056 | AMR | CLM | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0178 | 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 | g0207 | EUR | IBS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | IBS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0081 | EUR | IBS | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0180 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0223 | 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 | g0027 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0226 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0240 | 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 | g0235 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CDX | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0289 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | 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 | g0098 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0285 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02698 | hp1 | a0005 | c0008 | t0001 | g0243 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0194 | 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 | g0006 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0014 | 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 | g0132 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0197 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0059 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0064 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0181 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0287 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0188 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0116 | 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 | g0069 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0191 | 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 | g0039 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0192 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0288 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0161 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04184 | hp1 | a0001 | c0002 | t0010 | g0115 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0176 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0294 | 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 | g0190 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18942 | hp1 | a0001 | c0002 | t0011 | g0086 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18954 | hp2 | a0007 | c0005 | t0001 | g0238 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18956 | hp1 | a0002 | c0010 | t0001 | g0019 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18959 | hp2 | a0006 | c0009 | t0001 | g0222 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18965 | hp1 | a0001 | c0002 | t0005 | g0074 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18994 | hp2 | a0004 | c0006 | t0001 | g0109 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0286 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0199 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0070 | 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 | g0157 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19066 | hp2 | a0001 | c0002 | t0005 | g0073 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19070 | hp2 | a0001 | c0002 | t0005 | g0071 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19087 | hp2 | a0001 | c0002 | t0009 | g0100 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0193 | AFR | YRI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ASW | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20129 | hp2 | a0001 | c0002 | t0008 | g0099 | AFR | ASW | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0085 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | GIH | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0024 | SAS | GIH | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0171 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | USA | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0198 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | INTS8_chr8_94818287_94886746 | INTS8 | chr8 | 94818287 | 94886746 |
| 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 | a0007 | 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 | a0002 | 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 | a0003 | 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 | a0004 | 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 | a0005 | 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 |
| 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 | a0001c0002a0001c0003a0001c0004others(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 | a0001c0002a0001c0004a0004c0006 | 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 |
| 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 | a0001c0001t0003a0001c0001t0007 | 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 | a0001c0001t0003a0001c0001t0007 | 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 | a0001c0001t0003a0001c0001t0007 | 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 |
| 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 | a0001c0001t0001g0012a0001c0001t0003g0009a0001c0001t0003g0011others(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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0296 | 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 | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(41): 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 | a0001c0002t0001g0293 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.130+351C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 1/26 | chr8 | 94823912 | ||||||
| chr8:94824001
|
AT | A | 129 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(126): 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0291a0001c0001t0001g0292 | 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 | a0001c0002t0001g0174 | 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 | a0001c0001t0001g0290 | 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 | 133 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(130): 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 | a0001c0001t0001g0012a0001c0001t0003g0009a0001c0001t0003g0011others(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 | a0001c0003t0001g0284a0001c0003t0001g0285 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0012a0001c0001t0001g0182a0001c0001t0001g0183others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0008a0001c0001t0001g0184a0001c0001t0001g0236others(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 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0266others(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 | a0001c0001t0001g0114a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0002t0001g0055a0001c0003t0001g0005a0001c0003t0001g0006others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(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 | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(11): Show | 14 | HG00544.hp2 HG01243.hp1 HG02071.hp1 others(11): 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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0264others(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 | a0001c0001t0001g0266a0001c0002t0001g0123a0001c0002t0001g0169others(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 | a0001c0001t0001g0029 | 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 | 15 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0228others(12): 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 | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(41): 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 | a0001c0003t0001g0119a0001c0003t0001g0120 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(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 | 38 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 38 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(35): 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 | a0001c0002t0001g0118a0001c0002t0001g0164a0001c0002t0001g0165others(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 | a0001c0001t0001g0012a0001c0001t0003g0009a0001c0001t0003g0011others(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 | a0001c0001t0001g0283a0001c0002t0001g0116a0001c0002t0001g0117 | 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 | 160 | a0001c0001t0001g0012a0001c0001t0001g0114a0001c0001t0001g0257others(157): 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 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(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 | 161 | a0001c0001t0001g0012a0001c0001t0001g0114a0001c0001t0001g0200others(158): 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0201others(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 | a0001c0003t0001g0226 | 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 | 94 | a0001c0001t0001g0114a0001c0001t0001g0263a0001c0002t0001g0001others(91): 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 | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.305+925G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94825992 | ||||||
| chr8:94826075
|
T | G | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.305+1008T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826075 | ||||||
| chr8:94826118
|
C | G | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0276 | 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 | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 44 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.306-1079T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826184 | ||||||
| chr8:94826210
|
T | C | 216 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(213): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): 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 | a0001c0002t0001g0055a0001c0002t0001g0070a0001c0002t0001g0072others(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 | a0001c0003t0001g0199 | 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 | a0001c0001t0001g0012a0001c0001t0003g0009a0001c0001t0003g0011others(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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.306-948T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94826315 | ||||||
| chr8:94826474
|
C | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0228others(12): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 216 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(213): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): 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 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0206others(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 | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0037 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.306-180C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 2/26 | chr8 | 94827083 | ||||||
| chr8:94827124
|
T | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0076others(1): Show | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0003t0001g0194 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0277a0007c0005t0001g0238 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0012 | 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 | 68 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(65): Show | 68 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(65): 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 | 131 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(128): 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 | a0001c0003t0001g0193 | 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 | a0001c0002t0001g0051 | 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 | a0001c0003t0002g0188 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0005c0008t0001g0243 | 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 | a0001c0001t0001g0258 | 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 | a0001c0002t0001g0057 | 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 | a0001c0001t0001g0048 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | a0001c0001t0001g0258 | 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 | a0001c0002t0001g0117 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0002t0001g0069 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0003t0001g0194 | 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 | a0001c0002t0001g0077a0001c0002t0001g0078 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0003t0001g0189 | 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 | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): 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 | a0001c0002t0001g0058 | 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 | a0001c0003t0001g0226 | 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 | a0001c0001t0001g0210 | 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 | a0001c0002t0001g0050a0001c0002t0001g0116a0001c0002t0001g0124 | 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 | a0001c0001t0003g0011 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | 43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): 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 | a0001c0003t0001g0005a0001c0003t0001g0175 | 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 | a0001c0001t0003g0011 | 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | 129 | a0001c0001t0001g0028a0001c0001t0001g0114a0001c0001t0001g0184others(126): 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 | a0001c0002t0001g0075a0001c0002t0001g0138a0001c0002t0001g0162others(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 | a0001c0001t0001g0114 | 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 | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0038others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+36T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832210 | ||||||
| chr8:94832273
|
T | A | 1 | a0001c0002t0001g0060 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.753+595C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94832769 | ||||||
| chr8:94832855
|
C | T | 140 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(137): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0003t0002g0188a0001c0003t0002g0190a0001c0003t0002g0191others(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 | a0001c0003t0001g0226 | 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 | a0001c0001t0001g0201 | 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 | a0001c0002t0001g0085a0001c0002t0001g0142a0001c0002t0001g0143 | 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 | a0001c0001t0007g0010 | 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 | a0001c0002t0001g0057a0001c0002t0001g0066a0001c0002t0001g0067others(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 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0255 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0003t0001g0176 | 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 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0186others(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 | 33 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(30): Show | 33 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(30): 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 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0047others(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 | a0001c0001t0001g0048a0001c0001t0003g0013a0001c0001t0007g0010 | 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 | a0001c0001t0003g0009 | 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 | 149 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0114others(146): 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 | a0001c0001t0001g0202a0001c0001t0001g0234a0001c0001t0001g0239others(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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0003t0001g0189 | 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 | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): 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 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0002t0001g0058others(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 | a0001c0001t0001g0224a0001c0001t0001g0269a0001c0001t0003g0009others(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 | 216 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(213): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.754-1602T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94834922 | ||||||
| chr8:94834968
|
T | G | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0002t0001g0085a0001c0002t0001g0142a0001c0002t0001g0143 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0003t0001g0181 | 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 | 15 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0228others(12): 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 | a0001c0002t0001g0125 | 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 | 49 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(46): Show | 49 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(46): 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 | 157 | a0001c0001t0001g0114a0001c0001t0001g0257a0001c0002t0001g0001others(154): 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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.754-860A>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 6/26 | chr8 | 94835664 | ||||||
| chr8:94835748
|
C | T | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0007g0010 | 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 | 259 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(256): Show | 266 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(263): 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 | a0001c0001t0001g0183a0001c0001t0001g0196 | 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 | a0001c0003t0001g0286a0001c0003t0001g0287a0001c0003t0001g0288others(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 | 199 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): 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 | a0001c0001t0001g0274 | 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 | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): 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 | 4 | a0001c0001t0001g0007a0001c0001t0001g0213a0001c0001t0001g0247others(1): Show | 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 | a0001c0002t0001g0065a0001c0002t0001g0134 | 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 | a0001c0001t0001g0261 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0003t0001g0006a0001c0003t0001g0176a0001c0003t0001g0177others(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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): 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 | a0001c0001t0001g0273 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0292a0001c0002t0001g0055a0001c0002t0001g0070others(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 | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 37 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(34): 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 | a0001c0003t0001g0181a0001c0003t0001g0197 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0262 | 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 | a0001c0002t0001g0161 | 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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0272 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0003t0001g0194 | 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 | a0004c0006t0001g0109 | 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 | a0001c0002t0001g0108 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0270 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0003t0001g0189a0001c0003t0001g0193 | 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 | a0001c0003t0001g0181 | 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 | a0001c0001t0001g0016 | 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 | 183 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(180): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): 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 | a0001c0001t0001g0030a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0003t0001g0288 | 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 | a0001c0002t0001g0118 | 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 | a0001c0003t0002g0192 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0184a0006c0009t0001g0222 | 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 | a0001c0001t0001g0264 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0001t0001g0012a0001c0001t0001g0254a0001c0001t0001g0292others(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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): 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 | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0002t0011g0086 | 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 | a0001c0002t0001g0050a0001c0002t0001g0124 | 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 | 142 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(139): 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 | 129 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(126): 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 | 157 | a0001c0001t0001g0114a0001c0001t0001g0257a0001c0002t0001g0001others(154): 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0002t0001g0122 | 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 | 48 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 48 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(45): 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0002t0001g0117a0001c0002t0001g0159a0001c0002t0001g0167 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0195a0001c0001t0001g0205 | 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 | a0001c0001t0001g0214 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0001t0003g0011 | 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 | a0001c0002t0001g0105a0001c0002t0001g0106a0001c0002t0001g0158others(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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | 199 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(196): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+1218C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 10/26 | chr8 | 94843706 | ||||||
| chr8:94843725
|
CAT | C | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): 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 | a0001c0002t0001g0057a0001c0002t0001g0066a0001c0002t0001g0067others(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 | a0001c0003t0002g0188 | 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 | a0001c0001t0001g0049 | 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 | a0001c0003t0001g0006a0001c0003t0001g0176a0001c0003t0001g0177others(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 | a0001c0002t0001g0141 | 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 | 170 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(167): Show | 175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0278 | 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 | a0001c0003t0001g0181a0001c0003t0001g0197 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0037 | 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 | a0001c0003t0001g0226 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0183a0001c0001t0001g0196a0001c0001t0001g0221others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0003g0009a0001c0001t0007g0010 | 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 | a0001c0001t0001g0049 | 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 | a0001c0002t0001g0065a0001c0002t0001g0134 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0270 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): 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 | a0001c0003t0001g0193 | 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 | a0001c0003t0002g0188 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0205 | 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 | a0001c0002t0010g0115 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 233 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(230): Show | 240 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(237): 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 | a0001c0001t0001g0221 | 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 | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0001t0001g0277 | 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 | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): 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 | a0001c0001t0001g0207a0001c0001t0001g0279 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0002t0001g0089 | 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 | a0001c0002t0001g0164 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0049 | 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 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0297others(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 |
25 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 25 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(22): 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 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0035others(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 | a0001c0001t0001g0015 | 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 | a0001c0002t0001g0050a0001c0002t0001g0124 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0003t0001g0172 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0194 | 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 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0173 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0183a0001c0001t0001g0196a0001c0001t0001g0212others(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 | a0001c0003t0001g0193 | 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 | a0001c0002t0001g0075 | 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 | 43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): 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 | a0001c0001t0003g0009a0001c0001t0007g0010 | 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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): 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 | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1331+65T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 11/26 | chr8 | 94849597 | ||||||
| chr8:94849675
|
A | G | 43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): 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 | a0001c0001t0001g0048 | 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 | a0001c0002t0001g0068 | 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 | a0001c0002t0001g0068 | 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 | 132 | a0001c0001t0001g0114a0001c0001t0001g0257a0001c0002t0001g0001others(129): 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 | 154 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0114others(151): 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 | 31 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(28): Show | 31 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(28): 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0003t0001g0189a0001c0003t0001g0193a0001c0003t0001g0194others(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 | a0001c0003t0001g0226 | 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 | a0001c0001t0001g0012 | 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 | 196 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(193): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1508-421T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 12/26 | chr8 | 94851132 | ||||||
| chr8:94851235
|
TAA | T | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): 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 | a0001c0002t0001g0293 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0003t0002g0188 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0002t0011g0086 | 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 | a0001c0002t0004g0146 | 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 | a0001c0001t0001g0298 | 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 | 15 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0228others(12): 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 | a0001c0001t0001g0020 | 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 | a0001c0003t0001g0178 | 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 | a0001c0002t0001g0079 | 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 | a0001c0001t0001g0031 | 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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0002t0005g0074 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0183a0001c0001t0001g0196a0001c0001t0001g0212others(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 | a0001c0003t0001g0176 | 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 | a0001c0001t0003g0009a0001c0001t0007g0010 | 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 | a0001c0002t0001g0053a0001c0002t0001g0133 | 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 | 43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): 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 | a0001c0002t0001g0090a0001c0002t0001g0102a0001c0002t0001g0103others(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 |
43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): 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 | a0001c0001t0001g0215a0001c0001t0001g0253 | 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 | a0001c0002t0001g0293 | 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 | a0001c0001t0001g0048 | 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 | a0001c0002t0001g0075 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0212a0001c0001t0001g0246a0001c0003t0001g0177others(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 | 155 | a0001c0001t0001g0012a0001c0001t0001g0114a0001c0001t0001g0219others(152): 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 | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1752+1033T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94854948 | ||||||
| chr8:94855297
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0228others(12): 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0002t0001g0069 | 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 | a0001c0002t0001g0058a0001c0002t0001g0060a0001c0002t0001g0061others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0003g0011 | 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 | a0001c0002t0001g0131a0001c0002t0001g0132 | 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 | a0001c0002t0001g0053a0001c0002t0001g0133 | 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 | a0001c0001t0001g0264 | 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 | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0038 | 3 | HG00099.hp2 HG00738.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1753-525G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 14/26 | chr8 | 94856252 | ||||||
| chr8:94856270
|
A | G | 1 | a0004c0006t0001g0109 | 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 | a0001c0003t0001g0286a0001c0003t0001g0287a0001c0003t0001g0288others(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 | 153 | a0001c0001t0001g0114a0001c0001t0001g0257a0001c0002t0001g0001others(150): 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 | a0001c0002t0001g0106 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | 200 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0206others(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 | 46 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(43): Show | 47 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(44): 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 | a0001c0001t0001g0206a0001c0001t0001g0241a0001c0002t0001g0092others(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 | a0001c0002t0001g0173 | 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 | a0001c0001t0001g0212a0001c0001t0001g0246 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0002t0001g0065 | 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 | a0001c0001t0001g0235a0001c0001t0001g0295 | 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 | a0001c0001t0001g0262 | 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 | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 37 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(34): 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0002t0001g0057a0001c0002t0001g0068 | 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 | a0001c0002t0001g0101 | 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 | a0001c0002t0001g0091 | 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 | a0001c0003t0001g0181a0001c0003t0001g0197 | 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 | a0001c0002t0001g0093a0001c0002t0001g0108a0001c0002t0001g0123 | 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 | a0001c0003t0001g0226 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0002t0001g0079 | 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 | a0001c0002t0001g0135 | 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 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(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 | a0001c0001t0001g0027 | 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 | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(189): Show | 198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): 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 | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.2076+276G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94859908 | ||||||
| chr8:94860282
|
T | TA | 157 | a0001c0001t0001g0114a0001c0001t0001g0257a0001c0002t0001g0001others(154): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0003t0001g0180 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 259 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(256): Show | 266 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.2076+903T>C | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860535 | ||||||
| chr8:94860567
|
G | A | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(189): Show | 198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.2076+935G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94860567 | ||||||
| chr8:94860579
|
C | CA | 101 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(98): Show | 101 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(98): 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 | a0001c0001t0001g0047a0001c0001t0001g0256a0001c0002t0001g0051others(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 | 20 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0227others(17): 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 | a0001c0002t0001g0050 | 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 | a0001c0003t0001g0226 | 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 | a0001c0002t0001g0148 | 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 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0001c0002t0001g0063 | 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 | a0001c0001t0003g0011 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0002t0001g0062 | 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 | a0001c0003t0001g0226 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0233a0007c0005t0001g0238 | 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 | a0001c0001t0001g0220 | 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 | 45 | a0001c0001t0001g0257a0001c0002t0001g0050a0001c0002t0001g0051others(42): 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 | 63 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(60): 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 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0003t0001g0176a0001c0003t0001g0178 | 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 | 105 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(102): 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 | a0001c0003t0002g0188 | 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 | a0001c0002t0001g0093a0001c0002t0001g0108a0001c0002t0001g0123 | 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 | a0001c0003t0001g0176a0001c0003t0001g0178 | 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 | 20 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(17): 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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0203others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(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 | 63 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0027others(60): Show | 65 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(62): 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 |
76 | a0001c0001t0001g0042a0001c0002t0001g0001a0001c0002t0001g0004others(73): 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 | a0001c0001t0003g0011a0001c0002t0001g0052a0001c0002t0001g0084others(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 | a0001c0001t0001g0240a0001c0001t0003g0013a0001c0002t0001g0126others(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 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0257others(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 | a0001c0001t0001g0048a0001c0001t0003g0009 | 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 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(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 |
7 | a0001c0001t0001g0008a0001c0001t0001g0231a0001c0001t0001g0232others(4): 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 | a0001c0001t0001g0260a0001c0001t0001g0261 | 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 | a0001c0001t0001g0228a0001c0001t0001g0262 | 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 | a0001c0001t0001g0012 | 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 | a0001c0002t0001g0107a0001c0002t0001g0166 | 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 | 197 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(194): Show | 203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.2076+1652C>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861284 | ||||||
| chr8:94861292
|
C | T | 196 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(193): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.2076+1660C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94861292 | ||||||
| chr8:94861313
|
G | C | 197 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(194): Show | 203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 15 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0228others(12): 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 | a0001c0002t0001g0125a0001c0002t0001g0170 | 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 | a0001c0002t0001g0054 | 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 | a0001c0001t0001g0249 | 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 | a0001c0003t0001g0286a0001c0003t0001g0287a0001c0003t0001g0288others(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 | 157 | a0001c0001t0001g0114a0001c0001t0001g0257a0001c0002t0001g0001others(154): 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0003t0002g0188 | 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 | a0001c0003t0001g0189a0001c0003t0001g0193 | 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 | 24 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.2076+2579G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862211 | ||||||
| chr8:94862326
|
A | T | 212 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(209): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.2076+2694A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94862326 | ||||||
| chr8:94862352
|
T | C | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049 | 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 | a0001c0003t0001g0189 | 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 | a0001c0002t0001g0137 | 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 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0007g0010 | 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 | a0001c0002t0001g0095 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0002t0001g0050a0001c0002t0001g0116a0001c0002t0001g0124 | 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 | a0001c0001t0001g0207a0001c0001t0001g0279 | 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 | 24 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.2077-2221G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94863285 | ||||||
| chr8:94863448
|
A | G | 131 | a0001c0001t0001g0114a0001c0002t0001g0001a0001c0002t0001g0002others(128): 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0262 | 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 | a0001c0002t0001g0121 | 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 | a0001c0002t0001g0080 | 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 | a0001c0002t0001g0093 | 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 | a0001c0003t0001g0226 | 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 | a0001c0001t0001g0183a0001c0001t0001g0196 | 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 | a0001c0002t0001g0164a0001c0002t0004g0056a0001c0002t0004g0098others(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 | 15 | a0001c0001t0001g0008a0001c0001t0001g0227a0001c0001t0001g0228others(12): 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 | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2077-1189C>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864317 | ||||||
| chr8:94864640
|
G | A | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2077-866G>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 16/26 | chr8 | 94864640 | ||||||
| chr8:94864735
|
T | G | 141 | a0001c0001t0001g0114a0001c0001t0001g0257a0001c0002t0001g0001others(138): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0042 | 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 | a0001c0003t0001g0189a0001c0003t0001g0193 | 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 | a0001c0002t0001g0102 | 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 | 6 | a0001c0002t0001g0004a0001c0002t0001g0082a0001c0002t0001g0112others(3): 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0003t0001g0226 | 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | 17 | a0001c0001t0001g0008a0001c0001t0001g0208a0001c0001t0001g0227others(14): 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 | a0001c0001t0001g0195 | 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 | a0001c0002t0001g0068 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0007 | 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 | 210 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(207): Show | 217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): 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 | a0001c0002t0001g0066 | 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 | a0001c0003t0001g0194 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0002t0001g0161 | 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 | a0001c0003t0001g0226 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 43 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(40): 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0274 | 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 | 36 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(33): Show | 36 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(33): 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 | a0001c0001t0001g0114a0001c0001t0001g0216a0001c0001t0001g0218others(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 | 145 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0046others(142): 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 | 45 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(42): Show | 45 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(42): 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0215a0001c0001t0001g0253 | 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 | 58 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(55): 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 | a0001c0002t0001g0141 | 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 | a0001c0001t0001g0291a0001c0001t0001g0292 | 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 | a0001c0001t0001g0275 | 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 | a0001c0002t0001g0065a0001c0002t0001g0134 | 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 | 39 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(36): 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0007g0010 | 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 | a0001c0003t0001g0189 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): 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 | a0001c0001t0001g0017 | 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 | 16 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0047others(13): 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 | a0001c0001t0003g0011 | 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 | a0006c0009t0001g0222 | 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 | 34 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(31): Show | 34 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(31): 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0228a0001c0002t0001g0140 | 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 | a0001c0002t0001g0121 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0007g0010 | 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 | a0001c0001t0001g0018a0001c0001t0001g0221a0001c0001t0003g0009others(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 | 25 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(22): Show | 25 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2415-1823T>A | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 20/26 | chr8 | 94870061 | ||||||
| chr8:94870137
|
T | C | 97 | a0001c0001t0001g0037a0001c0001t0001g0230a0001c0001t0001g0242others(94): 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0207a0001c0001t0001g0240a0001c0001t0001g0279 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(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 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0128others(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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0002t0001g0140 | 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 | a0001c0001t0003g0011 | 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 | 67 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(64): Show | 68 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(65): 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | 205 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(202): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049 | 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 | a0001c0001t0001g0185a0001c0001t0001g0207a0001c0001t0001g0215others(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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049 | 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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0241 | 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 | a0001c0003t0001g0284a0001c0003t0001g0285 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0003t0001g0198a0001c0003t0001g0199 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0035 | 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 | a0001c0002t0001g0161 | 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 | a0001c0002t0001g0087a0001c0002t0001g0111a0001c0002t0001g0293 | 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 | 17 | a0001c0001t0001g0008a0001c0001t0001g0208a0001c0001t0001g0227others(14): 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0210 | 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 | a0001c0003t0001g0129 | 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 | a0001c0002t0001g0090a0001c0002t0001g0156 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | 208 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049 | 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 | a0001c0002t0001g0077a0001c0002t0001g0078 | 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 | 211 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): 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 | 208 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): 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 | a0001c0001t0001g0201 | 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 | 40 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 40 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(37): 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 | a0001c0001t0001g0209 | 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 | a0001c0002t0001g0108 | 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 | a0001c0001t0001g0012 | 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 | a0001c0002t0001g0061 | 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 | 147 | a0001c0001t0001g0023a0001c0002t0001g0001a0001c0002t0001g0002others(144): 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0002t0001g0161 | 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 | a0001c0001t0001g0195a0001c0001t0001g0205 | 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 | a0001c0003t0001g0226 | 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 | a0001c0002t0001g0150 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0259 | 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 | a0001c0003t0001g0005a0001c0003t0001g0006a0001c0003t0001g0175others(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 | a0001c0001t0001g0200 | 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 | a0001c0003t0002g0188 | 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 | 46 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 46 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(43): 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 | a0001c0003t0001g0226 | 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 | a0001c0002t0001g0103a0001c0002t0001g0113 | 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 | a0001c0002t0010g0115 | 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 | a0001c0003t0001g0193 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0011 | 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 | 17 | a0001c0001t0001g0008a0001c0001t0001g0208a0001c0001t0001g0227others(14): 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 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049 | 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 | a0001c0002t0001g0057a0001c0002t0001g0066a0001c0002t0001g0067others(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 | a0001c0001t0001g0012a0001c0001t0001g0195a0001c0001t0001g0200others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0013others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0012 | 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 | 208 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.2872-1363A>T | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94878755 | ||||||
| chr8:94878885
|
T | G | 208 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): 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 | a0001c0001t0001g0267 | 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 | a0001c0003t0001g0181a0001c0003t0001g0197 | 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 | 165 | a0001c0001t0001g0008a0001c0001t0001g0208a0001c0001t0001g0227others(162): 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 | a0001c0001t0001g0185a0001c0001t0001g0242a0001c0001t0001g0266others(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 | 212 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(209): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): 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 | a0001c0003t0001g0284a0001c0003t0001g0285 | 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 | a0001c0001t0001g0195a0001c0001t0001g0205 | 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 | 165 | a0001c0001t0001g0008a0001c0001t0001g0208a0001c0001t0001g0227others(162): 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 | 6 | a0001c0001t0001g0186a0001c0001t0001g0215a0001c0001t0001g0217others(3): 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(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 | 207 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0015others(204): Show | 214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): 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 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0002t0001g0051others(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 | a0001c0001t0001g0299 | 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 | a0001c0003t0001g0286a0001c0003t0001g0287a0001c0003t0001g0288others(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 | a0001c0001t0001g0214a0001c0001t0001g0290 | 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 | a0001c0003t0001g0119a0001c0003t0001g0120 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2872-87T>G | INTS8 | ENSG00000164941.14 | transcript | ENST00000523731.6 | protein_coding | 26/26 | chr8 | 94880031 |