Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3082 |
|---|---|
| ensemblid | ENSG00000019991.18 |
| hgncid | 4893 |
| symbol | HGF |
| name | hepatocyte growth factor |
| refseq_nuc | NM_000601.6 |
| refseq_prot | NP_000592.3 |
| ensembl_nuc | ENST00000222390.11 |
| ensembl_prot | ENSP00000222390.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 81699010 |
| end | 81770047 |
| strand | - |
| ver | v1.2 |
| region | chr7:81699010-81770047 |
| region5000 | chr7:81694010-81775047 |
| regionname0 | HGF_chr7_81699010_81770047 |
| regionname5000 | HGF_chr7_81694010_81775047 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 728 | 267 | 83 | 46 | 100 | 4 | 32 | 70 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0002 | 0/0 | 728 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0003 | 0/0 | 728 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0004 | 0/0 | 728 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2187 | 225 | 54 | 43 | 93 | 4 | 29 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0002 | 0/0 | 2187 | 33 | 26 | 3 | 1 | 0 | 3 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0003 | 0/0 | 2187 | 3 | 0 | 2 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0004 | 0/0 | 2187 | 3 | 0 | 0 | 3 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0005 | 0/0 | 2187 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0006 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0007 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0008 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0009 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0010 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| c0011 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3648 | 145 | 23 | 25 | 67 | 3 | 27 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0002 | 1/1 | 3648 | 41 | 4 | 9 | 20 | 1 | 5 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0003 | 0/0 | 3648 | 35 | 13 | 10 | 11 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0004 | 0/0 | 3646 | 10 | 10 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0005 | 0/0 | 3646 | 9 | 9 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0006 | 0/0 | 3648 | 8 | 6 | 1 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0007 | 0/0 | 3648 | 5 | 4 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0008 | 0/0 | 3643 | 5 | 5 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0009 | 0/0 | 3646 | 4 | 4 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0010 | 0/0 | 3648 | 4 | 4 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0011 | 0/0 | 3648 | 2 | 0 | 2 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0012 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0013 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0014 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| t0015 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2187 | 225 | 54 | 43 | 93 | 4 | 29 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002 | 0/0 | 2187 | 33 | 26 | 3 | 1 | 0 | 3 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0004 | 0/0 | 2187 | 3 | 0 | 0 | 3 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0005 | 0/0 | 2187 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0007 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0008 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0009 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0011 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0002c0003 | 0/0 | 2187 | 3 | 0 | 2 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0003c0006 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0004c0010 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5834 | 130 | 21 | 23 | 60 | 3 | 23 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0002 | 1/1 | 5834 | 40 | 3 | 9 | 20 | 1 | 5 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0003 | 0/0 | 5834 | 29 | 8 | 9 | 11 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0004 | 0/0 | 5832 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0005 | 0/0 | 5832 | 8 | 8 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0006 | 0/0 | 5834 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0007 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0008 | 0/0 | 5829 | 5 | 5 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0009 | 0/0 | 5832 | 3 | 3 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0010 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0011 | 0/0 | 5834 | 2 | 0 | 2 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0012 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0013 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0001t0014 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0001 | 0/0 | 5834 | 5 | 2 | 0 | 1 | 0 | 2 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0002 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0003 | 0/0 | 5834 | 5 | 4 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0004 | 0/0 | 5832 | 9 | 9 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0005 | 0/0 | 5832 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0006 | 0/0 | 5834 | 3 | 1 | 1 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0007 | 0/0 | 5834 | 4 | 3 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0009 | 0/0 | 5832 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0010 | 0/0 | 5834 | 3 | 3 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0002t0015 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0004t0001 | 0/0 | 5834 | 3 | 0 | 0 | 3 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0005t0006 | 0/0 | 5834 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0007t0001 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0008t0001 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0009t0001 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0001c0011t0006 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0002c0003t0001 | 0/0 | 5834 | 3 | 0 | 2 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0003c0006t0001 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| a0004c0010t0003 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | copy fasta | chr7 | 81694010 | 81775047 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0006g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0011g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0004t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0005t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0008t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0009t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0011t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0002c0003t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0003c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0004c0010t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | GBR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0108 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01069 | hp1 | a0001 | c0002 | t0006 | g0090 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0154 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0091 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0105 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0059 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0131 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02027 | hp2 | a0001 | c0009 | t0001 | g0141 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02055 | hp1 | a0001 | c0002 | t0010 | g0103 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0182 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0255 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02165 | hp2 | a0001 | c0001 | t0013 | g0069 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0258 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0100 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0259 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02258 | hp2 | a0001 | c0002 | t0009 | g0253 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02280 | hp2 | a0001 | c0002 | t0007 | g0093 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0098 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0088 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0257 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0256 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02630 | hp2 | a0001 | c0002 | t0015 | g0094 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02647 | hp1 | a0001 | c0002 | t0007 | g0095 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02809 | hp2 | a0001 | c0011 | t0006 | g0097 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0096 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0133 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0101 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0112 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03017 | hp2 | a0003 | c0006 | t0001 | g0179 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0252 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0129 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03130 | hp1 | a0001 | c0002 | t0010 | g0104 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03130 | hp2 | a0001 | c0005 | t0006 | g0004 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0119 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0102 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03942 | hp1 | a0001 | c0002 | t0006 | g0089 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0099 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18984 | hp2 | a0001 | c0001 | t0012 | g0051 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19005 | hp1 | a0001 | c0007 | t0001 | g0079 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0120 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19058 | hp2 | a0001 | c0008 | t0001 | g0062 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0184 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19240 | hp1 | a0004 | c0010 | t0003 | g0202 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0066 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ASW | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0064 | SAS | GIH | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0010 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02486 | hp1 | a0001 | c0005 | t0006 | g0004 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0251 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | USA | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0212 | REF | REF | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0148 | REF | REF | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81705746
|
C | T | 1 | a0003 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1765G>A | p.Val589Ile | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 16/18 | 1841/5834 | 1765/2187 | 589/728 | chr7 | 81705746 | ||
| chr7:81729735
|
C | T | 1 | a0002 | 3 | HG01175.hp2 HG01361.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.910G>A | p.Glu304Lys | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/18 | 986/5834 | 910/2187 | 304/728 | chr7 | 81729735 | ||
| chr7:81752221
|
T | C | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.524A>G | p.Asn175Ser | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/18 | 600/5834 | 524/2187 | 175/728 | chr7 | 81752221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81705738
|
A | G | 1 | a0001c0007 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1773T>C | p.Asp591Asp | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 16/18 | 1849/5834 | 1773/2187 | 591/728 | chr7 | 81705738 | ||
| chr7:81706382
|
G | A | 1 | a0001c0004 | 3 | NA18946.hp1 NA18979.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.1662C>T | p.His554His | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/18 | 1738/5834 | 1662/2187 | 554/728 | chr7 | 81706382 | ||
| chr7:81743429
|
G | A | 1 | a0001c0008 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.789C>T | p.Pro263Pro | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/18 | 865/5834 | 789/2187 | 263/728 | chr7 | 81743429 | ||
| chr7:81745035
|
A | G | 2 | a0001c0005a0001c0011 | 3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.711T>C | p.His237His | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/18 | 787/5834 | 711/2187 | 237/728 | chr7 | 81745035 | ||
| chr7:81752157
|
T | C | 1 | a0001c0009 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.588A>G | p.Val196Val | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/18 | 664/5834 | 588/2187 | 196/728 | chr7 | 81752157 | ||
| chr7:81758726
|
T | C | 2 | a0001c0002a0001c0011 | 34 | HG00558.hp2 HG01069.hp1 HG01243.hp1 others(31): Show |
synonymous_variant | LOW | c.333A>G | p.Glu111Glu | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/18 | 409/5834 | 333/2187 | 111/728 | chr7 | 81758726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81699013
|
T | C | 1 | a0001c0001t0011 | 2 | HG00639.hp1 HG01106.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3568A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 3568 | chr7 | 81699013 | |||||
| chr7:81699165
|
A | T | 17 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(14): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*3416T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 3416 | chr7 | 81699165 | |||||
| chr7:81699477
|
C | A | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3104G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 3104 | chr7 | 81699477 | |||||
| chr7:81699720
|
C | T | 1 | a0001c0001t0013 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2861G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2861 | chr7 | 81699720 | |||||
| chr7:81699848
|
A | G | 1 | a0001c0001t0012 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2733T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2733 | chr7 | 81699848 | |||||
| chr7:81700351
|
A | G | 2 | a0001c0001t0010a0001c0002t0010 | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2230T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2230 | chr7 | 81700351 | |||||
| chr7:81700549
|
C | T | 2 | a0001c0001t0005a0001c0002t0005 | 9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2032G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2032 | chr7 | 81700549 | |||||
| chr7:81700605
|
G | A | 2 | a0001c0001t0010a0001c0002t0010 | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1976 | chr7 | 81700605 | |||||
| chr7:81700666
|
TAGG | T | 1 | a0001c0001t0008 | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1912_*1914delCCT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1912 | chr7 | 81700666 | |||||
| chr7:81700903
|
C | A | 3 | a0001c0001t0007a0001c0002t0007a0001c0002t0015 | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1678G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1678 | chr7 | 81700903 | |||||
| chr7:81700926
|
G | A | 4 | a0001c0001t0006a0001c0002t0006a0001c0005t0006others(1): Show | 8 | HG01069.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1655C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1655 | chr7 | 81700926 | |||||
| chr7:81700959
|
A | G | 2 | a0001c0001t0010a0001c0002t0010 | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1622T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1622 | chr7 | 81700959 | |||||
| chr7:81701064
|
C | G | 17 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(14): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1517G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1517 | chr7 | 81701064 | |||||
| chr7:81701311
|
C | T | 3 | a0001c0001t0003a0001c0002t0003a0004c0010t0003 | 35 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1270G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1270 | chr7 | 81701311 | |||||
| chr7:81701547
|
C | T | 4 | a0001c0001t0004a0001c0001t0005a0001c0002t0004others(1): Show | 19 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1034 | chr7 | 81701547 | |||||
| chr7:81701601
|
T | C | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 980 | chr7 | 81701601 | |||||
| chr7:81702053
|
TAA | T | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(4): Show | 28 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*526_*527delTT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 526 | chr7 | 81702053 | |||||
| chr7:81702069
|
G | A | 1 | a0001c0002t0015 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 512 | chr7 | 81702069 | |||||
| chr7:81702114
|
T | C | 1 | a0001c0001t0008 | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*467A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 467 | chr7 | 81702114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81702835
|
G | T | 5 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2011-78C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81702835 | ||||||
| chr7:81702897
|
T | C | 15 | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0027others(12): Show | 15 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.2011-140A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81702897 | ||||||
| chr7:81702917
|
T | C | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2011-160A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81702917 | ||||||
| chr7:81703239
|
C | CT | 10 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(7): Show | 10 | HG00140.hp2 HG01175.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.2011-483dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703239 | ||||||
| chr7:81703428
|
G | A | 1 | a0001c0001t0002g0212 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2011-671C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703428 | ||||||
| chr7:81703452
|
T | C | 1 | a0001c0002t0006g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2011-695A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703452 | ||||||
| chr7:81703677
|
T | A | 225 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(222): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2011-920A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703677 | ||||||
| chr7:81703862
|
C | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.2011-1105G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703862 | ||||||
| chr7:81704231
|
G | A | 3 | a0001c0001t0003g0220a0001c0001t0003g0224a0001c0001t0003g0240 | 3 | HG01123.hp2 HG02280.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2010+1159C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704231 | ||||||
| chr7:81704303
|
G | A | 5 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010+1087C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704303 | ||||||
| chr7:81704607
|
C | T | 5 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010+783G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704607 | ||||||
| chr7:81704962
|
C | T | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010+428G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704962 | ||||||
| chr7:81705033
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2010+357C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81705033 | ||||||
| chr7:81705208
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2010+182C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81705208 | ||||||
| chr7:81705277
|
T | C | 2 | a0001c0001t0002g0155a0001c0001t0002g0171 | 2 | NA18955.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2010+113A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81705277 | ||||||
| chr7:81705870
|
TA | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(208): Show | 216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1758-118delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81705870 | ||||||
| chr7:81705870
|
TAA | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0040a0001c0001t0001g0042others(8): Show | 11 | HG00544.hp1 HG01070.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1758-119_1758-118d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81705870 | ||||||
| chr7:81706014
|
G | T | 9 | a0001c0001t0005g0107a0001c0001t0005g0133a0001c0001t0005g0134others(6): Show | 9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1758-261C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81706014 | ||||||
| chr7:81706141
|
G | A | 2 | a0001c0001t0005g0107a0001c0001t0005g0142 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1757+146C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81706141 | ||||||
| chr7:81706144
|
C | T | 80 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1757+143G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81706144 | ||||||
| chr7:81706581
|
C | G | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617-154G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706581 | ||||||
| chr7:81706602
|
A | C | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617-175T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706602 | ||||||
| chr7:81706645
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0190 | 2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1617-218C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706645 | ||||||
| chr7:81706716
|
T | G | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-289A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706716 | ||||||
| chr7:81706935
|
A | C | 23 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(20): Show | 23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1616+355T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706935 | ||||||
| chr7:81706949
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(222): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1616+341G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706949 | ||||||
| chr7:81706974
|
G | GA | 23 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(20): Show | 23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1616+315dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706974 | ||||||
| chr7:81707068
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1616+222C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707068 | ||||||
| chr7:81707123
|
T | C | 29 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(26): Show | 29 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1616+167A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707123 | ||||||
| chr7:81707219
|
C | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0054others(6): Show | 9 | HG01074.hp1 HG01952.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.1616+71G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707219 | ||||||
| chr7:81707268
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0211 | 2 | HG00544.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1616+22T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707268 | ||||||
| chr7:81707464
|
C | T | 1 | a0001c0001t0008g0029 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1542-100G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707464 | ||||||
| chr7:81707490
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1542-126G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707490 | ||||||
| chr7:81707578
|
A | C | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1542-214T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707578 | ||||||
| chr7:81707816
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1542-452A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707816 | ||||||
| chr7:81707879
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1542-515A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707879 | ||||||
| chr7:81707906
|
G | T | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-542C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707906 | ||||||
| chr7:81707945
|
A | G | 3 | a0001c0001t0001g0178a0001c0001t0001g0214a0003c0006t0001g0179 | 3 | HG03017.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1542-581T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707945 | ||||||
| chr7:81708123
|
GT | G | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-760delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708123 | ||||||
| chr7:81708130
|
A | G | 23 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(20): Show | 23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1542-766T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708130 | ||||||
| chr7:81708258
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1542-894A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708258 | ||||||
| chr7:81708264
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1542-900C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708264 | ||||||
| chr7:81708297
|
A | G | 1 | a0003c0006t0001g0179 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1542-933T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708297 | ||||||
| chr7:81708310
|
A | C | 1 | a0001c0001t0002g0201 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1542-946T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708310 | ||||||
| chr7:81708524
|
C | CT | 15 | a0001c0001t0001g0115a0001c0001t0001g0214a0001c0001t0002g0087others(12): Show | 15 | HG00639.hp1 HG01099.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1542-1161dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | ||||||
| chr7:81708524
|
C | CTT | 26 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0036others(23): Show | 26 | HG01346.hp1 HG02109.hp2 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.1542-1162_1542-116 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | ||||||
| chr7:81708524
|
C | CTTT | 105 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(102): Show | 108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1542-1163_1542-116 others(7): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | ||||||
| chr7:81708524
|
C | CTTTT | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0022others(48): Show | 52 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.1542-1164_1542-116 others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | ||||||
| chr7:81708524
|
C | CTTTTTTT | 7 | a0001c0001t0001g0075a0001c0001t0008g0029a0001c0001t0008g0066others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542-1167_1542-116 others(11): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | ||||||
| chr7:81708524
|
CTTTTTTT | C | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-1167_1542-116 others(11): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | ||||||
| chr7:81708660
|
C | G | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1542-1296G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708660 | ||||||
| chr7:81708682
|
A | G | 2 | a0001c0002t0007g0105a0001c0002t0015g0094 | 2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1542-1318T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708682 | ||||||
| chr7:81708875
|
C | T | 33 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(30): Show | 33 | HG00280.hp2 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1541+1272G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708875 | ||||||
| chr7:81708956
|
A | G | 23 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(20): Show | 23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1541+1191T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708956 | ||||||
| chr7:81708980
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1541+1167T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708980 | ||||||
| chr7:81709104
|
A | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1541+1043T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709104 | ||||||
| chr7:81709334
|
A | G | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1541+813T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709334 | ||||||
| chr7:81709539
|
A | C | 1 | a0001c0002t0003g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1541+608T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709539 | ||||||
| chr7:81709666
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1541+481T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709666 | ||||||
| chr7:81709677
|
G | C | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1541+470C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709677 | ||||||
| chr7:81709689
|
A | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1541+458T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709689 | ||||||
| chr7:81709718
|
A | C | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1541+429T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709718 | ||||||
| chr7:81709891
|
C | T | 9 | a0001c0001t0003g0137a0001c0001t0003g0221a0001c0001t0003g0223others(6): Show | 9 | HG01243.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1541+256G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709891 | ||||||
| chr7:81709926
|
A | G | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1541+221T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709926 | ||||||
| chr7:81709988
|
A | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(189): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1541+159T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709988 | ||||||
| chr7:81710031
|
A | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0065 | 2 | HG01934.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1541+116T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81710031 | ||||||
| chr7:81710590
|
A | G | 23 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(20): Show | 23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1445-347T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81710590 | ||||||
| chr7:81710782
|
CATAAT | C | 19 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(16): Show | 19 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1445-544_1445-540d others(7): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81710782 | ||||||
| chr7:81710918
|
C | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(245): Show | 258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1444+563G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81710918 | ||||||
| chr7:81711191
|
G | A | 2 | a0001c0002t0003g0255a0004c0010t0003g0202 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1444+290C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711191 | ||||||
| chr7:81711199
|
C | T | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+282G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711199 | ||||||
| chr7:81711233
|
G | A | 1 | a0001c0001t0003g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1444+248C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711233 | ||||||
| chr7:81711456
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1444+25G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711456 | ||||||
| chr7:81711678
|
C | T | 1 | a0001c0001t0003g0232 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1406-159G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711678 | ||||||
| chr7:81711733
|
T | G | 1 | a0001c0001t0002g0087 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1406-214A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711733 | ||||||
| chr7:81711739
|
G | A | 1 | a0001c0002t0006g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1406-220C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711739 | ||||||
| chr7:81711746
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1406-227G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711746 | ||||||
| chr7:81711782
|
C | A | 1 | a0001c0001t0003g0217 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1406-263G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711782 | ||||||
| chr7:81711788
|
C | G | 1 | a0001c0001t0002g0171 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1406-269G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711788 | ||||||
| chr7:81711848
|
G | T | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1406-329C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711848 | ||||||
| chr7:81711870
|
C | G | 1 | a0001c0011t0006g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1406-351G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711870 | ||||||
| chr7:81711871
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1406-352A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711871 | ||||||
| chr7:81712210
|
C | T | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1406-691G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712210 | ||||||
| chr7:81712221
|
A | C | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1406-702T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712221 | ||||||
| chr7:81712339
|
C | A | 21 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(18): Show | 21 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1406-820G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712339 | ||||||
| chr7:81712465
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1406-946G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712465 | ||||||
| chr7:81712492
|
A | G | 1 | a0001c0001t0013g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1406-973T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712492 | ||||||
| chr7:81712546
|
A | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(186): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1406-1027T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712546 | ||||||
| chr7:81712722
|
C | T | 19 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(16): Show | 19 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1406-1203G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712722 | ||||||
| chr7:81712744
|
C | T | 1 | a0001c0001t0008g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1406-1225G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712744 | ||||||
| chr7:81712873
|
G | C | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1406-1354C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712873 | ||||||
| chr7:81713011
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1406-1492C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713011 | ||||||
| chr7:81713023
|
C | A | 2 | a0001c0001t0001g0056a0001c0008t0001g0062 | 2 | NA18982.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1406-1504G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713023 | ||||||
| chr7:81713298
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1406-1779C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713298 | ||||||
| chr7:81713537
|
C | CA | 214 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(211): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1406-2019dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713537 | ||||||
| chr7:81713631
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1406-2112G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713631 | ||||||
| chr7:81713692
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1406-2173C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713692 | ||||||
| chr7:81713777
|
T | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(186): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1406-2258A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713777 | ||||||
| chr7:81713858
|
T | A | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1406-2339A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713858 | ||||||
| chr7:81713890
|
T | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(186): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1406-2371A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713890 | ||||||
| chr7:81713989
|
C | CGT | 23 | a0001c0001t0002g0001a0001c0001t0002g0085a0001c0001t0002g0087others(20): Show | 26 | HG00609.hp2 HG00733.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1406-2472_1406-247 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | ||||||
| chr7:81713989
|
C | CGTGT | 3 | a0001c0001t0001g0197a0001c0001t0002g0145a0001c0001t0002g0201 | 3 | HG02015.hp2 HG02559.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1406-2474_1406-247 others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | ||||||
| chr7:81713989
|
CGT | C | 116 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 118 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1406-2472_1406-247 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | ||||||
| chr7:81713989
|
CGTGT | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0001g0236others(6): Show | 9 | HG02145.hp2 HG02615.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.1406-2474_1406-247 others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | ||||||
| chr7:81713989
|
CGTGTGT | C | 5 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0002t0001g0092others(2): Show | 5 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406-2476_1406-247 others(10): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | ||||||
| chr7:81713989
|
CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0009g0111a0001c0001t0009g0112a0001c0001t0010g0182others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-2478_1406-247 others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | ||||||
| chr7:81713989
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0001g0003a0001c0001t0001g0130 | 3 | HG00280.hp1 HG00741.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1406-2482_1406-247 others(16): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | ||||||
| chr7:81713991
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0078 | 2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1406-2472A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713991 | ||||||
| chr7:81713992
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1406-2473C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713992 | ||||||
| chr7:81714148
|
G | A | 3 | a0001c0001t0002g0128a0001c0001t0002g0149a0001c0001t0002g0152 | 3 | HG00642.hp2 HG01192.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1406-2629C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714148 | ||||||
| chr7:81714199
|
C | T | 7 | a0001c0001t0001g0075a0001c0001t0006g0006a0001c0002t0006g0088others(4): Show | 9 | HG01069.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1406-2680G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714199 | ||||||
| chr7:81714251
|
T | C | 1 | a0001c0002t0007g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1406-2732A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714251 | ||||||
| chr7:81714346
|
T | C | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1406-2827A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714346 | ||||||
| chr7:81714703
|
TA | T | 8 | a0001c0001t0001g0170a0001c0001t0002g0084a0001c0001t0002g0162others(5): Show | 8 | HG00558.hp1 HG00733.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1405+2528delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714703 | ||||||
| chr7:81715327
|
A | G | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1405+1905T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715327 | ||||||
| chr7:81715359
|
T | A | 1 | a0001c0001t0002g0201 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1405+1873A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715359 | ||||||
| chr7:81715362
|
A | G | 1 | a0001c0002t0001g0262 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1405+1870T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715362 | ||||||
| chr7:81715446
|
A | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0211 | 2 | HG00544.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1405+1786T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715446 | ||||||
| chr7:81715607
|
C | T | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405+1625G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715607 | ||||||
| chr7:81715754
|
C | A | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405+1478G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715754 | ||||||
| chr7:81715755
|
A | T | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405+1477T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715755 | ||||||
| chr7:81715908
|
G | A | 1 | a0001c0001t0002g0118 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1405+1324C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715908 | ||||||
| chr7:81716072
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1405+1160G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716072 | ||||||
| chr7:81716073
|
G | A | 2 | a0001c0005t0006g0004a0001c0011t0006g0097 | 3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1405+1159C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716073 | ||||||
| chr7:81716091
|
G | A | 2 | a0001c0005t0006g0004a0001c0011t0006g0097 | 3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1405+1141C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716091 | ||||||
| chr7:81716145
|
A | T | 1 | a0001c0001t0002g0127 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1405+1087T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716145 | ||||||
| chr7:81716189
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1405+1043T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716189 | ||||||
| chr7:81716269
|
C | T | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1405+963G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716269 | ||||||
| chr7:81716287
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0078 | 2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1405+945C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716287 | ||||||
| chr7:81716591
|
A | G | 2 | a0001c0005t0006g0004a0001c0011t0006g0097 | 3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1405+641T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716591 | ||||||
| chr7:81716617
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1405+615G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716617 | ||||||
| chr7:81716750
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1405+482C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716750 | ||||||
| chr7:81716769
|
T | C | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+463A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716769 | ||||||
| chr7:81716976
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1405+256T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716976 | ||||||
| chr7:81717104
|
G | A | 5 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405+128C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81717104 | ||||||
| chr7:81717369
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(194): Show | 202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
splice_region_variant&intron_variant | LOW | c.1272-4A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717369 | ||||||
| chr7:81717382
|
C | A | 1 | a0001c0002t0006g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1272-17G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717382 | ||||||
| chr7:81717485
|
T | C | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-120A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717485 | ||||||
| chr7:81717609
|
G | A | 223 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(220): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1272-244C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717609 | ||||||
| chr7:81717647
|
A | G | 1 | a0003c0006t0001g0179 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1272-282T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717647 | ||||||
| chr7:81718076
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1272-711G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718076 | ||||||
| chr7:81718232
|
T | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1272-867A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718232 | ||||||
| chr7:81718325
|
A | G | 1 | a0001c0001t0006g0006 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1272-960T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718325 | ||||||
| chr7:81718353
|
T | A | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-988A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718353 | ||||||
| chr7:81718392
|
GA | G | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1028delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718392 | ||||||
| chr7:81718430
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1272-1065G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718430 | ||||||
| chr7:81718437
|
TG | T | 6 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272-1073delC | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718437 | ||||||
| chr7:81718441
|
G | A | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1272-1076C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718441 | ||||||
| chr7:81718581
|
C | T | 5 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272-1216G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718581 | ||||||
| chr7:81718705
|
C | T | 9 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272-1340G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718705 | ||||||
| chr7:81718935
|
T | G | 1 | a0001c0001t0008g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1272-1570A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718935 | ||||||
| chr7:81719267
|
C | T | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1271+1478G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719267 | ||||||
| chr7:81719339
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1271+1406G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719339 | ||||||
| chr7:81719531
|
G | T | 1 | a0001c0009t0001g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1271+1214C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719531 | ||||||
| chr7:81719801
|
T | C | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1271+944A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719801 | ||||||
| chr7:81720096
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1271+649A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720096 | ||||||
| chr7:81720102
|
G | T | 1 | a0001c0007t0001g0079 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1271+643C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720102 | ||||||
| chr7:81720203
|
A | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(183): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1271+542T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720203 | ||||||
| chr7:81720356
|
C | A | 30 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(27): Show | 30 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1271+389G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720356 | ||||||
| chr7:81720374
|
C | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0198a0001c0001t0001g0213 | 3 | NA19005.hp2 NA19068.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1271+371G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720374 | ||||||
| chr7:81720536
|
A | G | 7 | a0001c0001t0007g0106a0001c0002t0003g0102a0001c0002t0007g0093others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1271+209T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720536 | ||||||
| chr7:81720892
|
A | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1169-45T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81720892 | ||||||
| chr7:81720907
|
G | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1169-60C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81720907 | ||||||
| chr7:81720973
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1169-126G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81720973 | ||||||
| chr7:81721048
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1169-201T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721048 | ||||||
| chr7:81721056
|
T | C | 1 | a0001c0001t0002g0124 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1169-209A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721056 | ||||||
| chr7:81721080
|
CTT | C | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1169-235_1169-234d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721080 | ||||||
| chr7:81721129
|
C | T | 260 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(257): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1169-282G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721129 | ||||||
| chr7:81721150
|
A | G | 5 | a0001c0001t0001g0165a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | HG00140.hp2 HG01175.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169-303T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721150 | ||||||
| chr7:81721164
|
G | A | 19 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(16): Show | 24 | HG00609.hp2 HG01123.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1169-317C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721164 | ||||||
| chr7:81721179
|
G | A | 7 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(4): Show | 8 | HG02486.hp1 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1169-332C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721179 | ||||||
| chr7:81721188
|
C | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0168 | 2 | HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1169-341G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721188 | ||||||
| chr7:81721221
|
T | C | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1169-374A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721221 | ||||||
| chr7:81721257
|
G | GA | 39 | a0001c0001t0004g0132a0001c0001t0005g0107a0001c0001t0005g0133others(36): Show | 40 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.1169-411dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721257 | ||||||
| chr7:81721451
|
T | G | 7 | a0001c0001t0007g0106a0001c0002t0003g0102a0001c0002t0007g0093others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169-604A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721451 | ||||||
| chr7:81721502
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1169-655G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721502 | ||||||
| chr7:81721714
|
T | C | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1169-867A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721714 | ||||||
| chr7:81721809
|
C | T | 226 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1169-962G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721809 | ||||||
| chr7:81721845
|
T | C | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1169-998A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721845 | ||||||
| chr7:81722010
|
A | AT | 7 | a0001c0001t0007g0106a0001c0002t0003g0102a0001c0002t0007g0093others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169-1164dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722010 | ||||||
| chr7:81722456
|
C | T | 7 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(4): Show | 8 | HG02486.hp1 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1169-1609G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722456 | ||||||
| chr7:81722616
|
C | G | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1169-1769G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722616 | ||||||
| chr7:81722800
|
C | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(183): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1169-1953G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722800 | ||||||
| chr7:81722813
|
C | CA | 174 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(171): Show | 177 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1169-1967dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722813 | ||||||
| chr7:81722813
|
C | CAA | 16 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0061others(13): Show | 16 | HG01071.hp1 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1169-1968_1169-196 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722813 | ||||||
| chr7:81722845
|
G | GTATATAT others(3): Show |
1 | a0001c0002t0010g0252 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1169-2008_1169-199 others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722845
|
G | GTATATAT others(5): Show |
1 | a0001c0002t0010g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1169-2010_1169-199 others(16): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722845
|
G | GTATATAT others(9): Show |
1 | a0001c0002t0009g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1169-2014_1169-199 others(20): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722845
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0004g0132a0001c0001t0009g0131a0001c0002t0004g0010 | 3 | HG01884.hp1 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1169-1999_1169-199 others(22): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722845
|
G | GTATATAT others(13): Show |
8 | a0001c0001t0005g0107a0001c0001t0005g0133a0001c0001t0005g0134others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1169-1999_1169-199 others(24): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722845
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0005g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1169-1999_1169-199 others(26): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722845
|
G | GTATATAT others(17): Show |
5 | a0001c0001t0005g0140a0001c0002t0004g0256a0001c0002t0004g0257others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1169-1999_1169-199 others(28): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722845
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0002g0201 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1169-1999_1169-199 others(34): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | ||||||
| chr7:81722854
|
T | TATATATA others(29): Show |
2 | a0001c0001t0007g0106a0001c0002t0015g0094 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1169-2008_1169-200 others(40): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | ||||||
| chr7:81722854
|
T | TATATATA others(31): Show |
2 | a0001c0002t0007g0093a0001c0002t0007g0095 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1169-2008_1169-200 others(42): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | ||||||
| chr7:81722854
|
T | TATATATA others(33): Show |
2 | a0001c0002t0003g0102a0001c0002t0007g0101 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1169-2008_1169-200 others(44): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | ||||||
| chr7:81722854
|
T | TATATATA others(35): Show |
1 | a0001c0002t0007g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1169-2008_1169-200 others(46): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | ||||||
| chr7:81722928
|
C | T | 1 | a0001c0002t0004g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1169-2081G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722928 | ||||||
| chr7:81722929
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG00280.hp2 HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1169-2082C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722929 | ||||||
| chr7:81723253
|
G | T | 26 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(23): Show | 26 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1169-2406C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723253 | ||||||
| chr7:81723255
|
A | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(183): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1169-2408T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723255 | ||||||
| chr7:81723270
|
G | A | 216 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(213): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1169-2423C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723270 | ||||||
| chr7:81723308
|
T | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(183): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1169-2461A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723308 | ||||||
| chr7:81723401
|
T | C | 185 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(182): Show | 189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1168+2489A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723401 | ||||||
| chr7:81723722
|
T | C | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168+2168A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723722 | ||||||
| chr7:81723744
|
G | A | 26 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(23): Show | 26 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168+2146C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723744 | ||||||
| chr7:81723801
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0073 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1168+2089A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723801 | ||||||
| chr7:81723841
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1168+2049A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723841 | ||||||
| chr7:81723910
|
G | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(183): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1168+1980C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723910 | ||||||
| chr7:81723913
|
G | T | 1 | a0001c0002t0004g0256 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1168+1977C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723913 | ||||||
| chr7:81723978
|
T | C | 3 | a0001c0002t0004g0098a0001c0002t0004g0119a0001c0002t0004g0120 | 3 | HG02451.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1168+1912A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723978 | ||||||
| chr7:81724245
|
G | T | 7 | a0001c0001t0007g0106a0001c0002t0003g0102a0001c0002t0007g0093others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1645C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724245 | ||||||
| chr7:81724349
|
G | T | 1 | a0001c0001t0002g0201 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168+1541C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724349 | ||||||
| chr7:81724696
|
G | A | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1168+1194C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724696 | ||||||
| chr7:81724940
|
A | G | 6 | a0001c0001t0004g0132a0001c0002t0004g0010a0001c0002t0004g0256others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+950T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724940 | ||||||
| chr7:81725026
|
A | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(3): Show | 6 | HG02015.hp1 HG02074.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+864T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725026 | ||||||
| chr7:81725300
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1168+590A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725300 | ||||||
| chr7:81725552
|
G | A | 4 | a0001c0001t0010g0182a0001c0002t0010g0103a0001c0002t0010g0104others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168+338C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725552 | ||||||
| chr7:81725750
|
G | A | 216 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(213): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1168+140C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725750 | ||||||
| chr7:81726080
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041-63T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726080 | ||||||
| chr7:81726133
|
T | A | 48 | a0001c0001t0001g0075a0001c0001t0001g0163a0001c0001t0001g0165others(45): Show | 50 | HG00140.hp2 HG00609.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1041-116A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726133 | ||||||
| chr7:81726158
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1041-141T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726158 | ||||||
| chr7:81726186
|
T | A | 36 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0001t0005g0107others(33): Show | 37 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1041-169A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726186 | ||||||
| chr7:81726336
|
A | G | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041-319T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726336 | ||||||
| chr7:81726356
|
T | C | 16 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0001g0242others(13): Show | 17 | HG00609.hp1 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1041-339A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726356 | ||||||
| chr7:81726454
|
T | A | 2 | a0001c0001t0001g0214a0003c0006t0001g0179 | 2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1041-437A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726454 | ||||||
| chr7:81726701
|
C | T | 226 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1041-684G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726701 | ||||||
| chr7:81727039
|
T | G | 2 | a0001c0001t0001g0025a0001c0001t0002g0201 | 2 | HG02559.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1041-1022A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727039 | ||||||
| chr7:81727048
|
TG | T | 8 | a0001c0001t0001g0192a0001c0001t0008g0029a0001c0001t0008g0066others(5): Show | 9 | HG02486.hp1 HG02809.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041-1032delC | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727048 | ||||||
| chr7:81727049
|
G | GT | 192 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(189): Show | 196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1041-1033dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727049 | ||||||
| chr7:81727073
|
T | C | 2 | a0002c0003t0001g0008a0002c0003t0001g0059 | 2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1041-1056A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727073 | ||||||
| chr7:81727085
|
A | C | 2 | a0002c0003t0001g0008a0002c0003t0001g0059 | 2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1041-1068T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727085 | ||||||
| chr7:81727187
|
C | T | 185 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(182): Show | 189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1041-1170G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727187 | ||||||
| chr7:81727197
|
C | T | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1041-1180G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727197 | ||||||
| chr7:81727210
|
GT | G | 223 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(220): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1041-1194delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727210 | ||||||
| chr7:81727271
|
C | T | 2 | a0001c0002t0007g0105a0001c0002t0015g0094 | 2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1041-1254G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727271 | ||||||
| chr7:81727339
|
G | T | 2 | a0001c0002t0002g0254a0001c0002t0006g0090 | 2 | HG01069.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1041-1322C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727339 | ||||||
| chr7:81727396
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1041-1379C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727396 | ||||||
| chr7:81727411
|
C | A | 9 | a0001c0001t0002g0201a0001c0001t0004g0132a0001c0002t0002g0254others(6): Show | 9 | HG01069.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041-1394G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727411 | ||||||
| chr7:81727553
|
T | A | 5 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-1536A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727553 | ||||||
| chr7:81727562
|
C | G | 6 | a0001c0001t0004g0132a0001c0002t0004g0010a0001c0002t0004g0256others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-1545G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727562 | ||||||
| chr7:81727576
|
A | AT | 16 | a0001c0001t0004g0132a0001c0001t0010g0182a0001c0002t0002g0254others(13): Show | 16 | HG01069.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1041-1560dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727576 | ||||||
| chr7:81727581
|
T | TA | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 209 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1041-1565dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727581 | ||||||
| chr7:81727591
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1041-1574G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727591 | ||||||
| chr7:81727739
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(203): Show | 211 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.1041-1722A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727739 | ||||||
| chr7:81727825
|
A | C | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1040+1780T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727825 | ||||||
| chr7:81727994
|
C | G | 9 | a0001c0001t0007g0106a0001c0001t0009g0131a0001c0001t0014g0129others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1040+1611G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727994 | ||||||
| chr7:81728033
|
T | G | 220 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(217): Show | 224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1040+1572A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728033 | ||||||
| chr7:81728541
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1040+1064G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728541 | ||||||
| chr7:81728710
|
C | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+895G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728710 | ||||||
| chr7:81728744
|
C | T | 33 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0001g0242others(30): Show | 34 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1040+861G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728744 | ||||||
| chr7:81728759
|
G | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(183): Show | 190 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1040+846C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728759 | ||||||
| chr7:81728873
|
G | A | 9 | a0001c0001t0005g0107a0001c0001t0005g0133a0001c0001t0005g0134others(6): Show | 9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1040+732C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728873 | ||||||
| chr7:81728910
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG00438.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1040+695G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728910 | ||||||
| chr7:81728992
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1040+613A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728992 | ||||||
| chr7:81729021
|
GATACTCA others(267): Show |
G | 195 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(192): Show | 199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.1040+310_1040+583d others(2): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81729021 | ||||||
| chr7:81729062
|
A | G | 6 | a0001c0001t0010g0182a0001c0002t0003g0102a0001c0002t0007g0101others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+543T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81729062 | ||||||
| chr7:81729396
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1040+209C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81729396 | ||||||
| chr7:81729800
|
CA | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-22delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81729800 | ||||||
| chr7:81729873
|
AT | A | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-95delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81729873 | ||||||
| chr7:81730187
|
G | A | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-408C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730187 | ||||||
| chr7:81730519
|
T | A | 9 | a0001c0001t0005g0107a0001c0001t0005g0133a0001c0001t0005g0134others(6): Show | 9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-740A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730519 | ||||||
| chr7:81730563
|
T | G | 3 | a0001c0001t0009g0131a0001c0002t0004g0251a0001c0002t0009g0253 | 3 | HG01884.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.866-784A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730563 | ||||||
| chr7:81730634
|
TA | T | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-856delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730634 | ||||||
| chr7:81730658
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0065others(3): Show | 6 | HG01934.hp1 HG01978.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-879T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730658 | ||||||
| chr7:81730689
|
C | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-910G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730689 | ||||||
| chr7:81731058
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.866-1279A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731058 | ||||||
| chr7:81731115
|
G | A | 9 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-1336C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731115 | ||||||
| chr7:81731463
|
A | G | 9 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-1684T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731463 | ||||||
| chr7:81731473
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.866-1694C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731473 | ||||||
| chr7:81731912
|
C | T | 5 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-2133G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731912 | ||||||
| chr7:81731947
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.866-2168G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731947 | ||||||
| chr7:81732067
|
C | A | 1 | a0001c0001t0008g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.866-2288G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732067 | ||||||
| chr7:81732200
|
C | A | 2 | a0001c0001t0005g0107a0001c0001t0005g0142 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.866-2421G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732200 | ||||||
| chr7:81732258
|
C | G | 6 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG00733.hp2 NA18982.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-2479G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732258 | ||||||
| chr7:81732311
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.866-2532G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732311 | ||||||
| chr7:81732451
|
G | A | 15 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.866-2672C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732451 | ||||||
| chr7:81732535
|
A | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0152 | 2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.866-2756T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732535 | ||||||
| chr7:81732564
|
G | A | 5 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.866-2785C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732564 | ||||||
| chr7:81732653
|
G | A | 15 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.866-2874C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732653 | ||||||
| chr7:81732874
|
C | T | 195 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(192): Show | 199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.866-3095G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732874 | ||||||
| chr7:81733068
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-3289G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733068 | ||||||
| chr7:81733090
|
T | G | 1 | a0001c0002t0007g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.866-3311A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733090 | ||||||
| chr7:81733173
|
A | C | 1 | a0001c0001t0002g0084 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.866-3394T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733173 | ||||||
| chr7:81733190
|
C | T | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-3411G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733190 | ||||||
| chr7:81733242
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.866-3463C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733242 | ||||||
| chr7:81733271
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(199): Show | 206 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.866-3492T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733271 | ||||||
| chr7:81733271
|
A | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0210 | 2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.866-3492T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733271 | ||||||
| chr7:81733438
|
C | A | 40 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(37): Show | 40 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.866-3659G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733438 | ||||||
| chr7:81733455
|
T | C | 16 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0001g0242others(13): Show | 17 | HG00609.hp1 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.866-3676A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733455 | ||||||
| chr7:81733763
|
A | G | 1 | a0001c0001t0003g0240 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.866-3984T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733763 | ||||||
| chr7:81733822
|
T | C | 3 | a0001c0001t0003g0229a0001c0001t0003g0234a0001c0001t0003g0243 | 3 | HG01257.hp2 HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.866-4043A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733822 | ||||||
| chr7:81734018
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(192): Show | 199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.866-4239C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734018 | ||||||
| chr7:81734054
|
T | C | 1 | a0001c0001t0006g0006 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.866-4275A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734054 | ||||||
| chr7:81734250
|
A | G | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.866-4471T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734250 | ||||||
| chr7:81734447
|
C | T | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.866-4668G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734447 | ||||||
| chr7:81734552
|
A | G | 3 | a0001c0001t0009g0131a0001c0002t0004g0251a0001c0002t0009g0253 | 3 | HG01884.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.866-4773T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734552 | ||||||
| chr7:81734581
|
T | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-4802A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734581 | ||||||
| chr7:81734625
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.866-4846G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734625 | ||||||
| chr7:81734791
|
A | G | 1 | a0001c0002t0004g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.866-5012T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734791 | ||||||
| chr7:81734813
|
G | A | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.866-5034C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734813 | ||||||
| chr7:81734871
|
C | T | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-5092G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734871 | ||||||
| chr7:81734948
|
C | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.866-5169G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734948 | ||||||
| chr7:81735119
|
C | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-5340G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735119 | ||||||
| chr7:81735298
|
A | G | 15 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.866-5519T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735298 | ||||||
| chr7:81735378
|
G | T | 36 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0001g0242others(33): Show | 38 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.866-5599C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735378 | ||||||
| chr7:81735489
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.866-5710T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735489 | ||||||
| chr7:81735874
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.866-6095T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735874 | ||||||
| chr7:81736098
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.866-6319T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736098 | ||||||
| chr7:81736107
|
C | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-6328G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736107 | ||||||
| chr7:81736260
|
C | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0110a0001c0002t0001g0248 | 3 | HG00639.hp2 HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.866-6481G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736260 | ||||||
| chr7:81736326
|
C | T | 2 | a0001c0002t0003g0099a0001c0002t0003g0100 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.866-6547G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736326 | ||||||
| chr7:81736473
|
A | G | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-6694T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736473 | ||||||
| chr7:81736512
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.866-6733T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736512 | ||||||
| chr7:81736549
|
T | C | 5 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-6770A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736549 | ||||||
| chr7:81736718
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.865+6635C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736718 | ||||||
| chr7:81736894
|
G | GGGGTGTG others(3): Show |
1 | a0001c0002t0007g0095 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.865+6458_865+6459i others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGGGTGTG others(5): Show |
3 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0015g0094 | 3 | HG02280.hp2 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.865+6458_865+6459i others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGT | 9 | a0001c0001t0002g0151a0001c0001t0002g0208a0001c0001t0002g0212others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.865+6457_865+6458d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGT | 4 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(1): Show | 4 | HG02965.hp2 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+6455_865+6458d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGTGT | 11 | a0001c0001t0003g0226a0001c0001t0005g0142a0001c0001t0008g0209others(8): Show | 12 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.865+6453_865+6458d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGTGTG others(1): Show |
38 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0035others(35): Show | 39 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.865+6451_865+6458d others(10): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGTGTG others(3): Show |
69 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0016others(66): Show | 70 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.865+6449_865+6458d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGTGTG others(5): Show |
61 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(58): Show | 62 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.865+6447_865+6458d others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGTGTG others(7): Show |
13 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0056others(10): Show | 13 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.865+6445_865+6458d others(16): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGTGTG others(9): Show |
6 | a0001c0001t0001g0211a0001c0001t0005g0133a0001c0001t0005g0134others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.865+6443_865+6458d others(18): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GGTGTGTG others(13): Show |
2 | a0001c0001t0001g0130a0001c0001t0005g0140 | 2 | HG02735.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.865+6439_865+6458d others(22): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GTGTGTGT others(4): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0057 | 2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.865+6458_865+6459i others(13): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GTGTGTGT others(6): Show |
1 | a0001c0002t0003g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+6458_865+6459i others(15): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81736894
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0236 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.865+6458_865+6459i others(17): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | ||||||
| chr7:81737765
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.865+5588C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81737765 | ||||||
| chr7:81737864
|
G | A | 15 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.865+5489C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81737864 | ||||||
| chr7:81738080
|
T | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(195): Show | 202 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.865+5273A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738080 | ||||||
| chr7:81738336
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+5017T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738336 | ||||||
| chr7:81738403
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.865+4950G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738403 | ||||||
| chr7:81738765
|
A | G | 14 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.865+4588T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738765 | ||||||
| chr7:81738909
|
AC | A | 8 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG00140.hp2 HG01175.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+4443delG | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738909 | ||||||
| chr7:81738962
|
T | C | 1 | a0001c0002t0005g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.865+4391A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738962 | ||||||
| chr7:81739111
|
T | C | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.865+4242A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739111 | ||||||
| chr7:81739119
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+4234T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739119 | ||||||
| chr7:81739138
|
A | G | 12 | a0001c0001t0004g0132a0001c0001t0010g0182a0001c0002t0003g0102others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.865+4215T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739138 | ||||||
| chr7:81739271
|
A | C | 2 | a0001c0001t0004g0132a0001c0002t0004g0010 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.865+4082T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739271 | ||||||
| chr7:81739361
|
T | G | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+3992A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739361 | ||||||
| chr7:81739432
|
G | GGACA | 7 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG02109.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.865+3917_865+3920d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739432 | ||||||
| chr7:81739569
|
AC | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(217): Show | 224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.865+3783delG | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739569 | ||||||
| chr7:81739636
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+3717T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739636 | ||||||
| chr7:81739673
|
T | C | 1 | a0001c0001t0013g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.865+3680A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739673 | ||||||
| chr7:81740103
|
A | G | 49 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 49 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.865+3250T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740103 | ||||||
| chr7:81740141
|
T | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+3212A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740141 | ||||||
| chr7:81740236
|
C | A | 1 | a0001c0001t0002g0159 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.865+3117G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740236 | ||||||
| chr7:81740395
|
G | C | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+2958C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740395 | ||||||
| chr7:81740435
|
C | T | 3 | a0001c0001t0009g0131a0001c0002t0004g0251a0001c0002t0009g0253 | 3 | HG01884.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.865+2918G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740435 | ||||||
| chr7:81740454
|
T | C | 14 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.865+2899A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740454 | ||||||
| chr7:81740948
|
G | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(202): Show | 209 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.865+2405C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740948 | ||||||
| chr7:81741054
|
A | T | 2 | a0001c0001t0003g0222a0001c0001t0003g0228 | 2 | HG01192.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.865+2299T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741054 | ||||||
| chr7:81741135
|
C | T | 1 | a0001c0002t0006g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.865+2218G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741135 | ||||||
| chr7:81741262
|
G | A | 8 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG00140.hp2 HG01175.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+2091C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741262 | ||||||
| chr7:81741286
|
A | AT | 14 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.865+2066dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741286 | ||||||
| chr7:81741288
|
T | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0045 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.865+2065A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741288 | ||||||
| chr7:81741384
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.865+1969A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741384 | ||||||
| chr7:81741458
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+1895C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741458 | ||||||
| chr7:81741526
|
G | T | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+1827C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741526 | ||||||
| chr7:81741583
|
C | CTG | 34 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(31): Show | 35 | HG00438.hp1 HG00544.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.865+1768_865+1769d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | ||||||
| chr7:81741583
|
C | CTGTG | 21 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 22 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.865+1766_865+1769d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | ||||||
| chr7:81741583
|
C | CTGTGTG | 10 | a0001c0001t0010g0182a0001c0002t0003g0102a0001c0002t0004g0256others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+1764_865+1769d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | ||||||
| chr7:81741583
|
C | G | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+1770G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | ||||||
| chr7:81741583
|
CTG | C | 7 | a0001c0001t0001g0075a0001c0001t0009g0111a0001c0001t0009g0112others(4): Show | 7 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.865+1768_865+1769d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | ||||||
| chr7:81741583
|
CTGTGTG | C | 5 | a0001c0001t0001g0165a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | HG00140.hp2 HG01175.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+1764_865+1769d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | ||||||
| chr7:81741720
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.865+1633G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741720 | ||||||
| chr7:81741744
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.865+1609C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741744 | ||||||
| chr7:81741922
|
G | C | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.865+1431C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741922 | ||||||
| chr7:81741938
|
C | CA | 173 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(170): Show | 177 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.865+1414dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741938 | ||||||
| chr7:81741938
|
C | CAA | 19 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0046others(16): Show | 19 | HG00140.hp2 HG01069.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.865+1413_865+1414d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741938 | ||||||
| chr7:81741938
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0009g0131a0001c0002t0009g0253 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.865+1403_865+1414d others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741938 | ||||||
| chr7:81741982
|
CAT | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01099.hp2 HG01433.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+1369_865+1370d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741982 | ||||||
| chr7:81742011
|
C | T | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.865+1342G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742011 | ||||||
| chr7:81742026
|
A | G | 1 | a0004c0010t0003g0202 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.865+1327T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742026 | ||||||
| chr7:81742064
|
T | C | 10 | a0001c0001t0007g0106a0001c0001t0009g0131a0001c0001t0014g0129others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.865+1289A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742064 | ||||||
| chr7:81742303
|
T | C | 217 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(214): Show | 221 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.865+1050A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742303 | ||||||
| chr7:81742615
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.865+738T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742615 | ||||||
| chr7:81742731
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+622T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742731 | ||||||
| chr7:81742763
|
A | G | 6 | a0001c0001t0004g0132a0001c0002t0004g0010a0001c0002t0004g0256others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.865+590T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742763 | ||||||
| chr7:81742840
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+513T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742840 | ||||||
| chr7:81743008
|
G | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0176a0001c0001t0001g0181others(1): Show | 4 | HG02165.hp1 HG02523.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+345C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81743008 | ||||||
| chr7:81743136
|
A | G | 220 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(217): Show | 224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.865+217T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81743136 | ||||||
| chr7:81743167
|
T | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.865+186A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81743167 | ||||||
| chr7:81743685
|
A | G | 2 | a0001c0005t0006g0004a0001c0011t0006g0097 | 3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.747-214T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81743685 | ||||||
| chr7:81744198
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(192): Show | 199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.747-727C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744198 | ||||||
| chr7:81744303
|
AT | A | 10 | a0001c0001t0007g0106a0001c0001t0009g0131a0001c0001t0014g0129others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+696delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744303 | ||||||
| chr7:81744303
|
ATT | A | 13 | a0001c0001t0001g0046a0001c0001t0004g0132a0001c0001t0010g0182others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.746+695_746+696del others(2): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744303 | ||||||
| chr7:81744303
|
ATTT | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(190): Show | 197 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.746+694_746+696del others(3): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744303 | ||||||
| chr7:81744364
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.746+636T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744364 | ||||||
| chr7:81744515
|
C | G | 1 | a0001c0002t0004g0257 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.746+485G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744515 | ||||||
| chr7:81744804
|
C | G | 4 | a0001c0001t0009g0131a0001c0002t0002g0254a0001c0002t0004g0251others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+196G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744804 | ||||||
| chr7:81744895
|
C | T | 2 | a0001c0001t0002g0151a0001c0001t0002g0183 | 2 | NA18969.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.746+105G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744895 | ||||||
| chr7:81745184
|
G | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(252): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.626-64C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745184 | ||||||
| chr7:81745503
|
T | C | 24 | a0001c0001t0004g0132a0001c0001t0007g0106a0001c0001t0009g0111others(21): Show | 24 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.626-383A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745503 | ||||||
| chr7:81745602
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.626-482A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745602 | ||||||
| chr7:81745649
|
A | G | 14 | a0001c0001t0004g0132a0001c0001t0009g0111a0001c0001t0009g0112others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.626-529T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745649 | ||||||
| chr7:81745735
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.626-615C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745735 | ||||||
| chr7:81745771
|
T | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0214others(1): Show | 4 | HG00140.hp2 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.626-651A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745771 | ||||||
| chr7:81745801
|
A | C | 10 | a0001c0001t0007g0106a0001c0001t0009g0131a0001c0001t0014g0129others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.626-681T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745801 | ||||||
| chr7:81745802
|
G | A | 1 | a0001c0001t0007g0106 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626-682C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745802 | ||||||
| chr7:81745881
|
A | G | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.626-761T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745881 | ||||||
| chr7:81745883
|
A | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01099.hp2 HG01433.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.626-763T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745883 | ||||||
| chr7:81745901
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.626-781A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745901 | ||||||
| chr7:81746032
|
G | T | 5 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.626-912C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746032 | ||||||
| chr7:81746132
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0214others(1): Show | 4 | HG00140.hp2 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.626-1012C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746132 | ||||||
| chr7:81746143
|
T | C | 1 | a0004c0010t0003g0202 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.626-1023A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746143 | ||||||
| chr7:81746266
|
A | C | 12 | a0001c0001t0004g0132a0001c0001t0007g0106a0001c0001t0014g0129others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.626-1146T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746266 | ||||||
| chr7:81746341
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0211a0001c0001t0003g0199 | 3 | HG00544.hp2 HG02040.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.626-1221C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746341 | ||||||
| chr7:81746354
|
G | GTCCA | 6 | a0001c0001t0010g0182a0001c0002t0003g0102a0001c0002t0007g0101others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.626-1238_626-1235d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746354 | ||||||
| chr7:81746376
|
G | C | 1 | a0001c0001t0002g0201 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.626-1256C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746376 | ||||||
| chr7:81746471
|
G | T | 4 | a0001c0001t0009g0131a0001c0002t0002g0254a0001c0002t0004g0251others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-1351C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746471 | ||||||
| chr7:81746538
|
G | A | 213 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(210): Show | 217 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.626-1418C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746538 | ||||||
| chr7:81746552
|
C | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0030others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.626-1432G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746552 | ||||||
| chr7:81746613
|
G | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(217): Show | 224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.626-1493C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746613 | ||||||
| chr7:81746628
|
T | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(194): Show | 201 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.626-1508A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746628 | ||||||
| chr7:81746630
|
G | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(194): Show | 201 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.626-1510C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746630 | ||||||
| chr7:81746631
|
T | C | 4 | a0001c0001t0009g0131a0001c0002t0002g0254a0001c0002t0004g0251others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-1511A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746631 | ||||||
| chr7:81747032
|
T | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-1912A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747032 | ||||||
| chr7:81747043
|
A | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(200): Show | 207 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.626-1923T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747043 | ||||||
| chr7:81747158
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.626-2038C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747158 | ||||||
| chr7:81747198
|
G | A | 1 | a0002c0003t0001g0008 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.626-2078C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747198 | ||||||
| chr7:81747263
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.626-2143G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747263 | ||||||
| chr7:81747296
|
A | G | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2176T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747296 | ||||||
| chr7:81747318
|
G | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2198C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747318 | ||||||
| chr7:81747333
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG01952.hp1 HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.626-2213G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747333 | ||||||
| chr7:81747334
|
G | A | 4 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0003g0222others(1): Show | 4 | HG01192.hp1 HG01346.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-2214C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747334 | ||||||
| chr7:81747334
|
G | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG01952.hp1 HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.626-2214C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747334 | ||||||
| chr7:81747368
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.626-2248A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747368 | ||||||
| chr7:81747388
|
A | G | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2268T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747388 | ||||||
| chr7:81747406
|
T | C | 16 | a0001c0001t0004g0132a0001c0001t0009g0131a0001c0001t0010g0182others(13): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.626-2286A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747406 | ||||||
| chr7:81747578
|
G | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2458C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747578 | ||||||
| chr7:81747724
|
C | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.626-2604G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747724 | ||||||
| chr7:81747815
|
C | T | 2 | a0001c0001t0004g0132a0001c0002t0004g0010 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.626-2695G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747815 | ||||||
| chr7:81748041
|
G | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2921C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748041 | ||||||
| chr7:81748147
|
T | C | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-3027A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748147 | ||||||
| chr7:81748302
|
A | C | 22 | a0001c0001t0004g0132a0001c0001t0007g0106a0001c0001t0009g0131others(19): Show | 22 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.626-3182T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748302 | ||||||
| chr7:81748347
|
T | C | 5 | a0001c0001t0007g0106a0001c0002t0007g0093a0001c0002t0007g0095others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.626-3227A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748347 | ||||||
| chr7:81748506
|
T | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-3386A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748506 | ||||||
| chr7:81748600
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.626-3480C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748600 | ||||||
| chr7:81748610
|
G | A | 4 | a0001c0001t0009g0131a0001c0002t0002g0254a0001c0002t0004g0251others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-3490C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748610 | ||||||
| chr7:81748663
|
T | TAAAAC | 190 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(187): Show | 193 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.625+3452_625+3456d others(7): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748663 | ||||||
| chr7:81748663
|
T | TAAAACAA others(3): Show |
15 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0028others(12): Show | 16 | HG01074.hp1 HG01074.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.625+3447_625+3456d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748663 | ||||||
| chr7:81748777
|
A | G | 1 | a0001c0009t0001g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.625+3343T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748777 | ||||||
| chr7:81749072
|
C | G | 2 | a0001c0001t0009g0111a0001c0001t0009g0112 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.625+3048G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749072 | ||||||
| chr7:81749165
|
G | GTCTT | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2951_625+2954d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749165 | ||||||
| chr7:81749182
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | NA18983.hp2 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.625+2938G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749182 | ||||||
| chr7:81749191
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.625+2929G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749191 | ||||||
| chr7:81749238
|
T | G | 10 | a0001c0001t0003g0137a0001c0001t0005g0107a0001c0001t0005g0133others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.625+2882A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749238 | ||||||
| chr7:81749356
|
G | A | 16 | a0001c0001t0004g0132a0001c0001t0009g0131a0001c0001t0010g0182others(13): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.625+2764C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749356 | ||||||
| chr7:81749432
|
A | G | 10 | a0001c0001t0003g0137a0001c0001t0005g0107a0001c0001t0005g0133others(7): Show | 10 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.625+2688T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749432 | ||||||
| chr7:81749518
|
G | A | 6 | a0001c0001t0004g0132a0001c0002t0004g0010a0001c0002t0004g0256others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+2602C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749518 | ||||||
| chr7:81749617
|
G | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2503C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749617 | ||||||
| chr7:81749626
|
A | G | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2494T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749626 | ||||||
| chr7:81749699
|
A | G | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2421T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749699 | ||||||
| chr7:81749713
|
C | T | 1 | a0001c0001t0013g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.625+2407G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749713 | ||||||
| chr7:81749751
|
C | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2369G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749751 | ||||||
| chr7:81749915
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.625+2205T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749915 | ||||||
| chr7:81749980
|
C | A | 1 | a0001c0001t0004g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.625+2140G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749980 | ||||||
| chr7:81750095
|
A | G | 1 | a0001c0002t0006g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.625+2025T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750095 | ||||||
| chr7:81750235
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0073 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.625+1885T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750235 | ||||||
| chr7:81750317
|
T | G | 1 | a0002c0003t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.625+1803A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750317 | ||||||
| chr7:81750405
|
C | G | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+1715G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750405 | ||||||
| chr7:81750406
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG00280.hp2 HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.625+1714C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750406 | ||||||
| chr7:81750598
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.625+1522A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750598 | ||||||
| chr7:81750649
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.625+1471C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750649 | ||||||
| chr7:81750737
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.625+1383C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750737 | ||||||
| chr7:81750818
|
G | GT | 214 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(211): Show | 218 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.625+1301dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750818 | ||||||
| chr7:81750861
|
G | A | 1 | a0001c0001t0003g0243 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.625+1259C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750861 | ||||||
| chr7:81750968
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.625+1152A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750968 | ||||||
| chr7:81751258
|
C | T | 256 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(253): Show | 266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.625+862G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751258 | ||||||
| chr7:81751336
|
G | A | 6 | a0001c0001t0007g0106a0001c0001t0014g0129a0001c0002t0007g0093others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+784C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751336 | ||||||
| chr7:81751368
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.625+752C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751368 | ||||||
| chr7:81751496
|
TCCATAG | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.625+618_625+623del others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751496 | ||||||
| chr7:81751503
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.625+617T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751503 | ||||||
| chr7:81751505
|
A | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.625+615T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751505 | ||||||
| chr7:81751521
|
TTGG | T | 22 | a0001c0001t0004g0132a0001c0001t0007g0106a0001c0001t0009g0131others(19): Show | 22 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.625+596_625+598del others(3): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751521 | ||||||
| chr7:81751593
|
A | G | 1 | a0001c0001t0003g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.625+527T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751593 | ||||||
| chr7:81751725
|
T | C | 6 | a0001c0001t0010g0182a0001c0002t0003g0102a0001c0002t0007g0101others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+395A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751725 | ||||||
| chr7:81751873
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.625+247G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751873 | ||||||
| chr7:81751879
|
G | A | 6 | a0001c0001t0010g0182a0001c0002t0003g0102a0001c0002t0007g0101others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+241C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751879 | ||||||
| chr7:81752010
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.625+110G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81752010 | ||||||
| chr7:81752340
|
T | G | 3 | a0001c0002t0006g0088a0001c0002t0006g0089a0001c0002t0006g0090 | 3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.483-78A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752340 | ||||||
| chr7:81752343
|
G | A | 3 | a0001c0002t0004g0098a0001c0002t0004g0119a0001c0002t0004g0120 | 3 | HG02451.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.483-81C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752343 | ||||||
| chr7:81752415
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.483-153A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752415 | ||||||
| chr7:81752596
|
C | G | 4 | a0001c0001t0009g0131a0001c0002t0002g0254a0001c0002t0004g0251others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-334G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752596 | ||||||
| chr7:81752737
|
G | A | 2 | a0001c0002t0003g0099a0001c0002t0003g0100 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.483-475C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752737 | ||||||
| chr7:81752903
|
A | T | 1 | a0001c0001t0009g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.483-641T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752903 | ||||||
| chr7:81752966
|
C | T | 1 | a0001c0002t0004g0119 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.483-704G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752966 | ||||||
| chr7:81753279
|
A | C | 2 | a0001c0001t0005g0107a0001c0001t0005g0142 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.483-1017T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753279 | ||||||
| chr7:81753318
|
ACAGGTAA others(3): Show |
A | 3 | a0001c0002t0006g0088a0001c0002t0006g0089a0001c0002t0006g0090 | 3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.483-1066_483-1057d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753318 | ||||||
| chr7:81753374
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(216): Show | 223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.483-1112G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753374 | ||||||
| chr7:81753378
|
T | C | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-1116A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753378 | ||||||
| chr7:81753379
|
G | A | 3 | a0001c0002t0006g0088a0001c0002t0006g0089a0001c0002t0006g0090 | 3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.483-1117C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753379 | ||||||
| chr7:81753458
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.483-1196C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753458 | ||||||
| chr7:81753467
|
A | C | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-1205T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753467 | ||||||
| chr7:81754028
|
C | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039 | 3 | HG01099.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.483-1766G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754028 | ||||||
| chr7:81754088
|
G | T | 1 | a0001c0002t0004g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.483-1826C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754088 | ||||||
| chr7:81754100
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0073 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.483-1838A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754100 | ||||||
| chr7:81754296
|
T | C | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.483-2034A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754296 | ||||||
| chr7:81754382
|
AT | A | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2121delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754382 | ||||||
| chr7:81754390
|
A | G | 1 | a0001c0001t0003g0227 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.483-2128T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754390 | ||||||
| chr7:81754483
|
C | A | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2221G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754483 | ||||||
| chr7:81754513
|
T | C | 1 | a0001c0002t0009g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.483-2251A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754513 | ||||||
| chr7:81754545
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.483-2283G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754545 | ||||||
| chr7:81754554
|
T | C | 4 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(1): Show | 4 | HG00558.hp2 HG02559.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2292A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754554 | ||||||
| chr7:81754626
|
T | C | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2364A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754626 | ||||||
| chr7:81754707
|
T | C | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2445A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754707 | ||||||
| chr7:81754880
|
C | G | 1 | a0001c0002t0009g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.482+2309G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754880 | ||||||
| chr7:81755142
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.482+2047T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755142 | ||||||
| chr7:81755155
|
G | C | 1 | a0001c0001t0002g0124 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.482+2034C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755155 | ||||||
| chr7:81755183
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(3): Show | 6 | HG02015.hp1 HG02074.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.482+2006G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755183 | ||||||
| chr7:81755222
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.482+1967T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755222 | ||||||
| chr7:81755267
|
C | G | 3 | a0001c0002t0006g0088a0001c0002t0006g0089a0001c0002t0006g0090 | 3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.482+1922G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755267 | ||||||
| chr7:81755398
|
A | C | 2 | a0001c0002t0002g0254a0001c0002t0004g0010 | 2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.482+1791T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755398 | ||||||
| chr7:81755406
|
A | AAGGGATT others(2): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1774_482+1782d others(11): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755406 | ||||||
| chr7:81755437
|
G | A | 3 | a0001c0002t0006g0088a0001c0002t0006g0089a0001c0002t0006g0090 | 3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.482+1752C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755437 | ||||||
| chr7:81755515
|
A | C | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.482+1674T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755515 | ||||||
| chr7:81755618
|
G | A | 4 | a0001c0001t0008g0029a0001c0001t0008g0066a0001c0001t0008g0068others(1): Show | 4 | HG02965.hp2 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1571C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755618 | ||||||
| chr7:81755685
|
T | C | 1 | a0001c0002t0004g0251 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.482+1504A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755685 | ||||||
| chr7:81755864
|
A | G | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+1325T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755864 | ||||||
| chr7:81755914
|
T | G | 1 | a0001c0002t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.482+1275A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755914 | ||||||
| chr7:81756229
|
T | A | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+960A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756229 | ||||||
| chr7:81756229
|
T | G | 4 | a0001c0002t0003g0102a0001c0002t0007g0101a0001c0002t0010g0103others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+960A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756229 | ||||||
| chr7:81756276
|
G | C | 6 | a0001c0002t0002g0254a0001c0002t0003g0091a0001c0002t0004g0010others(3): Show | 6 | HG01069.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.482+913C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756276 | ||||||
| chr7:81756546
|
T | C | 3 | a0001c0001t0005g0107a0001c0001t0005g0142a0001c0001t0005g0164 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.482+643A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756546 | ||||||
| chr7:81756579
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.482+610G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756579 | ||||||
| chr7:81756620
|
C | A | 1 | a0001c0002t0001g0261 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.482+569G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756620 | ||||||
| chr7:81756660
|
C | CA | 8 | a0001c0002t0003g0102a0001c0002t0004g0256a0001c0002t0004g0257others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.482+528dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756660 | ||||||
| chr7:81756749
|
C | T | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+440G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756749 | ||||||
| chr7:81756886
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.482+303C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756886 | ||||||
| chr7:81756901
|
C | CAGAAAG | 31 | a0001c0002t0001g0092a0001c0002t0001g0248a0001c0002t0001g0260others(28): Show | 31 | HG00558.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.482+287_482+288ins others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756901 | ||||||
| chr7:81756902
|
A | AGAAAGG | 3 | a0001c0002t0006g0088a0001c0002t0006g0089a0001c0002t0006g0090 | 3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.482+286_482+287ins others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756902 | ||||||
| chr7:81756952
|
C | G | 1 | a0001c0002t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.482+237G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756952 | ||||||
| chr7:81756981
|
A | G | 1 | a0001c0002t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.482+208T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756981 | ||||||
| chr7:81757056
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0003g0246a0001c0001t0003g0247 | 3 | HG00639.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.482+133G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757056 | ||||||
| chr7:81757063
|
G | A | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+126C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757063 | ||||||
| chr7:81757128
|
T | A | 1 | a0001c0001t0002g0002 | 3 | HG01123.hp1 HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.482+61A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757128 | ||||||
| chr7:81757167
|
C | T | 4 | a0001c0002t0003g0102a0001c0002t0007g0101a0001c0002t0010g0103others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+22G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757167 | ||||||
| chr7:81757550
|
G | T | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.368-247C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757550 | ||||||
| chr7:81757553
|
G | A | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.368-250C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757553 | ||||||
| chr7:81757769
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.368-466C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757769 | ||||||
| chr7:81757834
|
T | A | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.368-531A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757834 | ||||||
| chr7:81757854
|
T | C | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-551A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757854 | ||||||
| chr7:81757925
|
A | G | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.368-622T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757925 | ||||||
| chr7:81758025
|
CTA | C | 3 | a0001c0001t0005g0107a0001c0001t0005g0142a0001c0001t0005g0164 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.367+665_367+666del others(2): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758025 | ||||||
| chr7:81758060
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.367+632A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758060 | ||||||
| chr7:81758476
|
A | C | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.367+216T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758476 | ||||||
| chr7:81758516
|
A | G | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.367+176T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758516 | ||||||
| chr7:81759494
|
A | G | 1 | a0001c0001t0008g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.255-690T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759494 | ||||||
| chr7:81759598
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.255-794C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759598 | ||||||
| chr7:81759630
|
G | A | 3 | a0001c0002t0004g0257a0001c0002t0004g0258a0001c0002t0004g0259 | 3 | HG02257.hp1 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.255-826C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759630 | ||||||
| chr7:81759736
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.255-932G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759736 | ||||||
| chr7:81759741
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0003g0203 | 2 | NA18993.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.255-937A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759741 | ||||||
| chr7:81759768
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.255-964A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759768 | ||||||
| chr7:81759891
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.255-1087C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759891 | ||||||
| chr7:81759945
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0002t0003g0091 | 3 | HG01243.hp1 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.255-1141G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759945 | ||||||
| chr7:81759954
|
A | G | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255-1150T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759954 | ||||||
| chr7:81759996
|
G | A | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255-1192C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759996 | ||||||
| chr7:81760411
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.255-1607A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760411 | ||||||
| chr7:81760498
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.255-1694A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760498 | ||||||
| chr7:81760658
|
CAT | C | 2 | a0001c0001t0006g0006a0001c0001t0008g0209 | 3 | HG03209.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.255-1856_255-1855d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760658 | ||||||
| chr7:81760676
|
CGTGCGTG others(13): Show |
C | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255-1892_255-1873d others(22): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760676 | ||||||
| chr7:81760680
|
C | CGT | 16 | a0001c0001t0001g0021a0001c0001t0001g0249a0001c0001t0001g0250others(13): Show | 16 | HG00438.hp2 HG02027.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.255-1878_255-1877d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | ||||||
| chr7:81760680
|
CGT | C | 42 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 48 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.255-1878_255-1877d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | ||||||
| chr7:81760680
|
CGTGT | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(105): Show | 109 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.255-1880_255-1877d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | ||||||
| chr7:81760680
|
CGTGTGT | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0018others(55): Show | 61 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.255-1882_255-1877d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | ||||||
| chr7:81760680
|
CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0001g0075a0001c0001t0001g0206a0001c0001t0001g0207others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-1884_255-1877d others(10): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | ||||||
| chr7:81760680
|
CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0001g0076a0001c0001t0001g0213a0001c0001t0007g0106 | 3 | HG02735.hp1 NA19005.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.255-1886_255-1877d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | ||||||
| chr7:81760680
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0003g0245 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.255-1894_255-1877d others(20): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | ||||||
| chr7:81760682
|
T | TGC | 8 | a0001c0002t0003g0102a0001c0002t0004g0256a0001c0002t0004g0257others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.255-1879_255-1878i others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760682 | ||||||
| chr7:81760686
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.255-1882A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760686 | ||||||
| chr7:81760690
|
T | C | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-1886A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760690 | ||||||
| chr7:81760796
|
G | A | 3 | a0001c0002t0002g0254a0001c0002t0003g0255a0001c0002t0009g0253 | 3 | HG02145.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.254+1911C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760796 | ||||||
| chr7:81760847
|
T | C | 2 | a0001c0002t0004g0251a0001c0002t0010g0252 | 2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.254+1860A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760847 | ||||||
| chr7:81760921
|
T | C | 1 | a0001c0002t0004g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.254+1786A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760921 | ||||||
| chr7:81760971
|
G | A | 3 | a0001c0001t0006g0006a0001c0001t0008g0209a0001c0001t0009g0131 | 4 | HG01884.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+1736C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760971 | ||||||
| chr7:81761061
|
G | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0138a0001c0001t0001g0139others(8): Show | 12 | HG01433.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.254+1646C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761061 | ||||||
| chr7:81761165
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0130 | 3 | HG00280.hp1 HG00741.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.254+1542T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761165 | ||||||
| chr7:81761166
|
C | G | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.254+1541G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761166 | ||||||
| chr7:81761210
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.254+1497A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761210 | ||||||
| chr7:81761246
|
A | G | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.254+1461T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761246 | ||||||
| chr7:81761310
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.254+1397C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761310 | ||||||
| chr7:81761341
|
A | T | 2 | a0001c0002t0003g0102a0001c0002t0007g0101 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.254+1366T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761341 | ||||||
| chr7:81761555
|
T | TA | 21 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(18): Show | 21 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.254+1151dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761555 | ||||||
| chr7:81761555
|
TA | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0130a0001c0001t0003g0221others(4): Show | 7 | HG01192.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.254+1151delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761555 | ||||||
| chr7:81761659
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254+1048G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761659 | ||||||
| chr7:81761665
|
G | A | 2 | a0001c0001t0002g0212a0001c0002t0003g0091 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.254+1042C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761665 | ||||||
| chr7:81761709
|
T | C | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.254+998A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761709 | ||||||
| chr7:81762322
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+385C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762322 | ||||||
| chr7:81762355
|
C | T | 1 | a0001c0001t0014g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.254+352G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762355 | ||||||
| chr7:81762397
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.254+310T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762397 | ||||||
| chr7:81762519
|
C | T | 12 | a0001c0002t0001g0092a0001c0002t0003g0099a0001c0002t0003g0100others(9): Show | 12 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+188G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762519 | ||||||
| chr7:81762894
|
A | T | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-22T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81762894 | ||||||
| chr7:81763105
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.89-233A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763105 | ||||||
| chr7:81763310
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.89-438C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763310 | ||||||
| chr7:81763556
|
C | G | 2 | a0001c0002t0003g0255a0001c0002t0009g0253 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.89-684G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763556 | ||||||
| chr7:81763729
|
G | A | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.89-857C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763729 | ||||||
| chr7:81763812
|
C | T | 6 | a0001c0002t0003g0255a0001c0002t0004g0256a0001c0002t0004g0257others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-940G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763812 | ||||||
| chr7:81764069
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.89-1197G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764069 | ||||||
| chr7:81764152
|
T | C | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-1280A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764152 | ||||||
| chr7:81764320
|
C | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG01891.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.89-1448G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764320 | ||||||
| chr7:81764327
|
A | G | 1 | a0001c0002t0007g0101 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.89-1455T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764327 | ||||||
| chr7:81764457
|
T | C | 5 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG00558.hp2 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1585A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764457 | ||||||
| chr7:81764895
|
C | G | 1 | a0001c0001t0002g0124 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.89-2023G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764895 | ||||||
| chr7:81764989
|
A | G | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-2117T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764989 | ||||||
| chr7:81765018
|
G | A | 7 | a0001c0002t0002g0254a0001c0002t0003g0255a0001c0002t0004g0256others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2146C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765018 | ||||||
| chr7:81765047
|
T | C | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2175A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765047 | ||||||
| chr7:81765058
|
A | G | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 4 | NA18942.hp2 NA18977.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2186T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765058 | ||||||
| chr7:81765081
|
T | C | 4 | a0001c0002t0003g0102a0001c0002t0007g0101a0001c0002t0010g0103others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2209A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765081 | ||||||
| chr7:81765183
|
G | C | 5 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG00558.hp2 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2311C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765183 | ||||||
| chr7:81765300
|
A | C | 4 | a0001c0002t0003g0102a0001c0002t0007g0101a0001c0002t0010g0103others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2428T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765300 | ||||||
| chr7:81765364
|
A | C | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2492T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765364 | ||||||
| chr7:81765462
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG01952.hp1 HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.89-2590G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765462 | ||||||
| chr7:81765479
|
A | G | 7 | a0001c0002t0002g0254a0001c0002t0003g0255a0001c0002t0004g0256others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2607T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765479 | ||||||
| chr7:81765510
|
C | T | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2638G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765510 | ||||||
| chr7:81765511
|
A | G | 7 | a0001c0002t0002g0254a0001c0002t0003g0255a0001c0002t0004g0256others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2639T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765511 | ||||||
| chr7:81765547
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.89-2675G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765547 | ||||||
| chr7:81765588
|
T | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0218a0001c0001t0003g0217 | 3 | HG02129.hp1 NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.89-2716A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765588 | ||||||
| chr7:81765644
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.89-2772T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765644 | ||||||
| chr7:81765777
|
C | T | 16 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(13): Show | 16 | HG00558.hp2 HG01069.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-2905G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765777 | ||||||
| chr7:81765787
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.89-2915T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765787 | ||||||
| chr7:81765894
|
C | T | 5 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG00558.hp2 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3022G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765894 | ||||||
| chr7:81765901
|
G | C | 4 | a0001c0002t0004g0256a0001c0002t0004g0257a0001c0002t0004g0258others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-3029C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765901 | ||||||
| chr7:81766129
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.89-3257C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766129 | ||||||
| chr7:81766269
|
T | C | 29 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0241others(26): Show | 30 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-3397A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766269 | ||||||
| chr7:81766406
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.88+3478C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766406 | ||||||
| chr7:81766407
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.88+3477T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766407 | ||||||
| chr7:81766484
|
G | A | 1 | a0001c0002t0003g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+3400C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766484 | ||||||
| chr7:81766591
|
A | G | 1 | a0001c0002t0002g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.88+3293T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766591 | ||||||
| chr7:81767156
|
A | G | 12 | a0001c0002t0001g0092a0001c0002t0003g0099a0001c0002t0003g0100others(9): Show | 12 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+2728T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767156 | ||||||
| chr7:81767230
|
A | C | 1 | a0001c0001t0002g0118 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.88+2654T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767230 | ||||||
| chr7:81767249
|
A | G | 12 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(9): Show | 12 | HG00558.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+2635T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767249 | ||||||
| chr7:81767295
|
GA | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0109a0001c0001t0001g0110others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+2588delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767295 | ||||||
| chr7:81767718
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02148.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+2166T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767718 | ||||||
| chr7:81767761
|
G | T | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.88+2123C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767761 | ||||||
| chr7:81767792
|
A | T | 1 | a0001c0001t0007g0106 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.88+2092T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767792 | ||||||
| chr7:81767798
|
T | C | 1 | a0001c0002t0004g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.88+2086A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767798 | ||||||
| chr7:81767875
|
C | A | 1 | a0001c0002t0007g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.88+2009G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767875 | ||||||
| chr7:81767928
|
A | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02056.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.88+1956T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767928 | ||||||
| chr7:81768357
|
A | G | 4 | a0001c0002t0003g0091a0001c0002t0006g0088a0001c0002t0006g0089others(1): Show | 4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1527T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768357 | ||||||
| chr7:81768386
|
C | T | 32 | a0001c0002t0001g0092a0001c0002t0001g0248a0001c0002t0001g0260others(29): Show | 32 | HG00558.hp2 HG01069.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.88+1498G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768386 | ||||||
| chr7:81768444
|
A | G | 4 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(1): Show | 4 | NA18974.hp1 NA18987.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1440T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768444 | ||||||
| chr7:81768600
|
C | G | 3 | a0001c0002t0002g0254a0001c0002t0003g0255a0001c0002t0009g0253 | 3 | HG02145.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.88+1284G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768600 | ||||||
| chr7:81768601
|
A | G | 7 | a0001c0002t0002g0254a0001c0002t0003g0255a0001c0002t0004g0256others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+1283T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768601 | ||||||
| chr7:81768614
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 78 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.88+1270G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768614 | ||||||
| chr7:81768781
|
G | A | 7 | a0001c0002t0002g0254a0001c0002t0003g0255a0001c0002t0004g0256others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+1103C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768781 | ||||||
| chr7:81768784
|
T | C | 1 | a0001c0002t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.88+1100A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768784 | ||||||
| chr7:81768986
|
G | T | 1 | a0001c0002t0004g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.88+898C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768986 | ||||||
| chr7:81769017
|
GTTCCCAC others(7): Show |
G | 1 | a0001c0002t0009g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.88+853_88+866delTA others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769017 | ||||||
| chr7:81769040
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.88+844G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769040 | ||||||
| chr7:81769178
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.88+706T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769178 | ||||||
| chr7:81769199
|
A | T | 1 | a0001c0002t0004g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.88+685T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769199 | ||||||
| chr7:81769250
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.88+634G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769250 | ||||||
| chr7:81769328
|
C | A | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262 | 3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.88+556G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769328 | ||||||
| chr7:81769412
|
A | G | 1 | a0002c0003t0001g0008 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.88+472T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769412 | ||||||
| chr7:81769573
|
C | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG00438.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.88+311G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769573 | ||||||
| chr7:81769724
|
C | CA | 12 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(9): Show | 12 | HG00558.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+159dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769724 |