Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9375 |
|---|---|
| ensemblid | ENSG00000125304.10 |
| hgncid | 11865 |
| symbol | TM9SF2 |
| name | transmembrane 9 superfamily member 2 |
| refseq_nuc | NM_004800.3 |
| refseq_prot | NP_004791.1 |
| ensembl_nuc | ENST00000376387.5 |
| ensembl_prot | ENSP00000365567.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 99501472 |
| end | 99564048 |
| strand | + |
| ver | v1.2 |
| region | chr13:99501472-99564048 |
| region5000 | chr13:99496472-99569048 |
| regionname0 | TM9SF2_chr13_99501472_99564048 |
| regionname5000 | TM9SF2_chr13_99496472_99569048 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 663 | 332 | 86 | 52 | 138 | 18 | 36 | 102 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1992 | 323 | 78 | 52 | 137 | 18 | 36 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| c0002 | 0/0 | 1992 | 7 | 7 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| c0003 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| c0004 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1426 | 252 | 64 | 37 | 110 | 11 | 29 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0002 | 0/1 | 1426 | 59 | 7 | 13 | 27 | 6 | 5 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0003 | 0/0 | 1426 | 8 | 8 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0004 | 0/0 | 1426 | 7 | 7 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0005 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0006 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0007 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0008 | 0/0 | 1426 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0009 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| t0010 | 0/0 | 1426 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 10 | 0 | 0 | 7 | 3 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0004 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0006 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0024 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1992 | 323 | 78 | 52 | 137 | 18 | 36 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0002 | 0/0 | 1992 | 7 | 7 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0003 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0004 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3417 | 251 | 64 | 37 | 109 | 11 | 29 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0002 | 0/1 | 3417 | 58 | 6 | 13 | 27 | 6 | 5 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0003 | 0/0 | 3417 | 8 | 8 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0005 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0006 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0007 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0008 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0009 | 0/0 | 3417 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0001t0010 | 0/0 | 3417 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0002t0004 | 0/0 | 3417 | 7 | 7 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0003t0002 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| a0001c0004t0001 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | copy fasta | chr13 | 99496472 | 99569048 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 5 | 3 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0006 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0024 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0010g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0002t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | GBR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0210 | EUR | FIN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0130 | EUR | FIN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0093 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0096 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0200 | EUR | IBS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0264 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0259 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0260 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0263 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0080 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0103 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0031 | AFR | YRI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | YRI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18966 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0194 | AFR | LWK | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0261 | AFR | YRI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ASW | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ASW | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | TSI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0262 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | USA | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | USA | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0024 | REF | REF | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0006 | REF | REF | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:99552293
|
G | A | 1 | a0001c0003 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1455G>A | p.Thr485Thr | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/17 | 1590/3417 | 1455/1992 | 485/663 | chr13 | 99552293 | ||
| chr13:99559395
|
G | C | 1 | a0001c0002 | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
synonymous_variant | LOW | c.1785G>C | p.Thr595Thr | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/17 | 1920/3417 | 1785/1992 | 595/663 | chr13 | 99559395 | ||
| chr13:99559464
|
G | A | 1 | a0001c0004 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.1854G>A | p.Thr618Thr | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/17 | 1989/3417 | 1854/1992 | 618/663 | chr13 | 99559464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:99501568
|
C | T | 1 | a0001c0001t0010 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/17 | 39 | chr13 | 99501568 | |||||
| chr13:99563105
|
G | A | 1 | a0001c0001t0005 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 347 | chr13 | 99563105 | |||||
| chr13:99563358
|
A | C | 1 | a0001c0001t0009 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*600A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 600 | chr13 | 99563358 | |||||
| chr13:99563446
|
A | G | 1 | a0001c0001t0008 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*688A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 688 | chr13 | 99563446 | |||||
| chr13:99563451
|
C | G | 1 | a0001c0002t0004 | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*693C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 693 | chr13 | 99563451 | |||||
| chr13:99563454
|
A | G | 1 | a0001c0001t0007 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*696A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 696 | chr13 | 99563454 | |||||
| chr13:99563615
|
C | T | 1 | a0001c0001t0006 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*857C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 857 | chr13 | 99563615 | |||||
| chr13:99563705
|
G | A | 1 | a0001c0002t0004 | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 947 | chr13 | 99563705 | |||||
| chr13:99563763
|
A | G | 1 | a0001c0001t0003 | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1005A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 1005 | chr13 | 99563763 | |||||
| chr13:99563765
|
G | T | 3 | a0001c0001t0002a0001c0001t0007a0001c0003t0002 | 60 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1007G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 1007 | chr13 | 99563765 | |||||
| chr13:99563882
|
G | A | 1 | a0001c0002t0004 | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 17/17 | 1124 | chr13 | 99563882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:99501891
|
G | A | 1 | a0001c0002t0004g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.171+114G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99501891 | ||||||
| chr13:99502081
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.171+304G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502081 | ||||||
| chr13:99502117
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0033 | 3 | HG00639.hp2 HG03688.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.171+340G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502117 | ||||||
| chr13:99502200
|
AC | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.171+424delC | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502200 | ||||||
| chr13:99502229
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.171+452G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502229 | ||||||
| chr13:99502318
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+541T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502318 | ||||||
| chr13:99502475
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.171+698T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502475 | ||||||
| chr13:99502562
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.171+785C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502562 | ||||||
| chr13:99502823
|
T | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.171+1046T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502823 | ||||||
| chr13:99502912
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.171+1135A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99502912 | ||||||
| chr13:99503001
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.171+1224A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503001 | ||||||
| chr13:99503243
|
G | T | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+1466G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503243 | ||||||
| chr13:99503296
|
A | AC | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+1520dupC | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99503296 | |||||
| chr13:99503332
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(234): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.171+1555G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503332 | ||||||
| chr13:99503498
|
C | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 10 | HG01106.hp2 HG01257.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.171+1721C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503498 | ||||||
| chr13:99503535
|
C | T | 6 | a0001c0002t0004g0031a0001c0002t0004g0260a0001c0002t0004g0261others(3): Show | 6 | HG01891.hp2 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+1758C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503535 | ||||||
| chr13:99503568
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.171+1791G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503568 | ||||||
| chr13:99503637
|
G | T | 3 | a0001c0001t0001g0026a0001c0001t0002g0213a0001c0001t0002g0214 | 4 | HG02886.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1860G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503637 | ||||||
| chr13:99503665
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.171+1888G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503665 | ||||||
| chr13:99503709
|
C | CA | 11 | a0001c0001t0001g0015a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 12 | HG00140.hp2 HG00735.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+1955dupA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99503709 | |||||
| chr13:99503709
|
C | CAA | 31 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 38 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.171+1954_171+1955d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99503709 | |||||
| chr13:99503709
|
CA | C | 24 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(21): Show | 27 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.171+1955delA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99503709 | |||||
| chr13:99503730
|
A | AG | 18 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0023others(15): Show | 26 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.171+1953_171+1954i others(3): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503730 | ||||||
| chr13:99503730
|
A | G | 22 | a0001c0001t0001g0195a0001c0001t0002g0005a0001c0001t0002g0024others(19): Show | 27 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.171+1953A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503730 | ||||||
| chr13:99503732
|
A | AT | 9 | a0001c0001t0001g0018a0001c0001t0001g0107a0001c0001t0001g0108others(6): Show | 10 | HG00423.hp1 HG02027.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.171+1955_171+1956i others(3): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503732 | ||||||
| chr13:99503732
|
A | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0019others(65): Show | 79 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.171+1955A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503732 | ||||||
| chr13:99503821
|
A | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.171+2044A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503821 | ||||||
| chr13:99503928
|
C | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+2151C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503928 | ||||||
| chr13:99503935
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.171+2158T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503935 | ||||||
| chr13:99503976
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.171+2199C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99503976 | ||||||
| chr13:99504148
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.171+2371A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504148 | ||||||
| chr13:99504232
|
A | G | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+2455A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504232 | ||||||
| chr13:99504598
|
G | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01071.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.171+2821G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504598 | ||||||
| chr13:99504622
|
C | T | 25 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0024others(22): Show | 35 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.171+2845C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504622 | ||||||
| chr13:99504696
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.171+2919A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504696 | ||||||
| chr13:99504811
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.171+3034G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504811 | ||||||
| chr13:99504904
|
T | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.171+3127T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504904 | ||||||
| chr13:99504987
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+3210A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99504987 | ||||||
| chr13:99505004
|
CAAG | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+3234_171+3236d others(5): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99505004 | |||||
| chr13:99505152
|
C | CT | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(178): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.171+3392dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99505152 | |||||
| chr13:99505152
|
C | CTT | 6 | a0001c0001t0001g0022a0001c0001t0001g0068a0001c0001t0001g0114others(3): Show | 7 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+3391_171+3392d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99505152 | |||||
| chr13:99505355
|
G | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.171+3578G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99505355 | ||||||
| chr13:99505652
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+3875A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99505652 | ||||||
| chr13:99505669
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.171+3892A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99505669 | ||||||
| chr13:99505863
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.171+4086A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99505863 | ||||||
| chr13:99506436
|
G | T | 41 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(38): Show | 54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.171+4659G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99506436 | ||||||
| chr13:99506469
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG00099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.171+4692T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99506469 | ||||||
| chr13:99506804
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.171+5027A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99506804 | ||||||
| chr13:99506883
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.171+5106A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99506883 | ||||||
| chr13:99506961
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.171+5184A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99506961 | ||||||
| chr13:99506989
|
T | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02257.hp1 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.171+5212T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99506989 | ||||||
| chr13:99507108
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.171+5331T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99507108 | ||||||
| chr13:99507119
|
T | C | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.171+5342T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99507119 | ||||||
| chr13:99507173
|
A | G | 1 | a0001c0001t0001g0026 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.171+5396A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99507173 | ||||||
| chr13:99507240
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.171+5463C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99507240 | ||||||
| chr13:99507458
|
G | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.171+5681G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99507458 | ||||||
| chr13:99507698
|
T | C | 1 | a0001c0001t0003g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.171+5921T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99507698 | ||||||
| chr13:99508032
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.171+6255C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508032 | ||||||
| chr13:99508091
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(50): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.171+6314A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508091 | ||||||
| chr13:99508208
|
T | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.171+6431T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508208 | ||||||
| chr13:99508255
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.171+6478G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508255 | ||||||
| chr13:99508306
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.171+6529A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508306 | ||||||
| chr13:99508404
|
A | AAC | 63 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(60): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.171+6666_171+6667d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACAC | 21 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0035others(18): Show | 25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.171+6664_171+6667d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACAC | 26 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0075others(23): Show | 30 | HG00423.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.171+6662_171+6667d others(8): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACACA others(1): Show |
22 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0039others(19): Show | 24 | HG00621.hp2 HG01081.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.171+6660_171+6667d others(10): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACACA others(3): Show |
18 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0114others(15): Show | 24 | HG00558.hp2 HG00738.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.171+6658_171+6667d others(12): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACACA others(5): Show |
14 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(11): Show | 16 | HG00558.hp1 HG00597.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.171+6656_171+6667d others(14): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACACA others(7): Show |
11 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(8): Show | 11 | HG00323.hp2 HG01106.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+6654_171+6667d others(16): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACACA others(9): Show |
3 | a0001c0001t0001g0019a0001c0001t0001g0229a0001c0001t0002g0102 | 4 | HG01175.hp1 HG02723.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+6652_171+6667d others(18): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACACA others(11): Show |
3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0002t0004g0260 | 3 | HG02257.hp1 HG03098.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.171+6650_171+6667d others(20): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | AACACACA others(13): Show |
5 | a0001c0001t0001g0107a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02074.hp2 HG02300.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+6648_171+6667d others(22): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0169 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.171+6627_171+6628i others(17): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508404 | ||||||
| chr13:99508404
|
A | C | 1 | a0001c0001t0001g0170 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.171+6627A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508404 | ||||||
| chr13:99508404
|
AAC | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0071others(3): Show | 8 | HG01261.hp1 HG01934.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+6666_171+6667d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
AACAC | A | 28 | a0001c0001t0001g0067a0001c0001t0001g0168a0001c0001t0001g0249others(25): Show | 38 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.171+6664_171+6667d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508404
|
AACACAC | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0211 | 3 | HG01952.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.171+6662_171+6667d others(8): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508404 | |||||
| chr13:99508443
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.171+6667_171+6668i others(23): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508443 | |||||
| chr13:99508443
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0001g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.171+6667_171+6668i others(16): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508443 | |||||
| chr13:99508443
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.171+6667_171+6668i others(14): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99508443 | |||||
| chr13:99508443
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.171+6666A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508443 | ||||||
| chr13:99508444
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0122 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.171+6667_171+6668i others(13): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508444 | ||||||
| chr13:99508444
|
C | CACACACA others(6): Show |
2 | a0001c0001t0001g0126a0001c0001t0001g0170 | 2 | HG00609.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.171+6667_171+6668i others(15): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508444 | ||||||
| chr13:99508445
|
C | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.171+6668C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508445 | ||||||
| chr13:99508588
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+6811G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508588 | ||||||
| chr13:99508659
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.171+6882T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508659 | ||||||
| chr13:99508672
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171+6895A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508672 | ||||||
| chr13:99508706
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.171+6929A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508706 | ||||||
| chr13:99508859
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.171+7082C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99508859 | ||||||
| chr13:99509118
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+7341G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509118 | ||||||
| chr13:99509204
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.171+7427T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509204 | ||||||
| chr13:99509240
|
C | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | NA18975.hp1 NA18990.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.171+7463C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509240 | ||||||
| chr13:99509292
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.171+7515C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509292 | ||||||
| chr13:99509344
|
G | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.171+7567G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509344 | ||||||
| chr13:99509454
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.171+7677A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509454 | ||||||
| chr13:99509456
|
C | G | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.171+7679C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509456 | ||||||
| chr13:99509461
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.171+7684C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509461 | ||||||
| chr13:99509541
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0225 | 3 | HG03098.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.171+7764G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509541 | ||||||
| chr13:99509590
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.171+7813G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509590 | ||||||
| chr13:99509672
|
C | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0236a0001c0001t0001g0237others(5): Show | 9 | HG00609.hp1 HG02071.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+7895C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509672 | ||||||
| chr13:99509675
|
A | C | 1 | a0001c0001t0003g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171+7898A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509675 | ||||||
| chr13:99509708
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.172-7906G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509708 | ||||||
| chr13:99509757
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.172-7857G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509757 | ||||||
| chr13:99509809
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0045 | 3 | HG01074.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.172-7805G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509809 | ||||||
| chr13:99509954
|
G | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(153): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.172-7660G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99509954 | ||||||
| chr13:99510237
|
C | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-7377C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510237 | ||||||
| chr13:99510325
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0009g0096 | 3 | HG00099.hp1 HG01256.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.172-7289A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510325 | ||||||
| chr13:99510361
|
C | T | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.172-7253C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510361 | ||||||
| chr13:99510367
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.172-7247C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510367 | ||||||
| chr13:99510479
|
C | G | 1 | a0001c0001t0002g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.172-7135C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510479 | ||||||
| chr13:99510519
|
A | T | 1 | a0001c0001t0002g0190 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.172-7095A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510519 | ||||||
| chr13:99510545
|
T | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-7069T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510545 | ||||||
| chr13:99510710
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.172-6904G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510710 | ||||||
| chr13:99510792
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-6822A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510792 | ||||||
| chr13:99510795
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.172-6819C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510795 | ||||||
| chr13:99510823
|
C | G | 1 | a0001c0001t0002g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.172-6791C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510823 | ||||||
| chr13:99510857
|
T | G | 1 | a0001c0001t0002g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.172-6757T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99510857 | ||||||
| chr13:99511191
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172-6423A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511191 | ||||||
| chr13:99511257
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.172-6357T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511257 | ||||||
| chr13:99511276
|
C | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-6338C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511276 | ||||||
| chr13:99511299
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 6 | HG02572.hp1 HG02622.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-6315T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511299 | ||||||
| chr13:99511366
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.172-6248A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511366 | ||||||
| chr13:99511381
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.172-6233C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511381 | ||||||
| chr13:99511508
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.172-6106C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511508 | ||||||
| chr13:99511677
|
G | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0161 | 3 | NA18960.hp2 NA18995.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.172-5937G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511677 | ||||||
| chr13:99511806
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.172-5808A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99511806 | ||||||
| chr13:99512016
|
A | C | 1 | a0001c0001t0005g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.172-5598A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99512016 | ||||||
| chr13:99512387
|
A | G | 1 | a0001c0002t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172-5227A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99512387 | ||||||
| chr13:99512581
|
G | A | 43 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(40): Show | 56 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.172-5033G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99512581 | ||||||
| chr13:99512583
|
A | G | 9 | a0001c0001t0001g0027a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 10 | HG01106.hp2 HG01257.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-5031A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99512583 | ||||||
| chr13:99512612
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.172-5002C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99512612 | ||||||
| chr13:99512883
|
G | A | 1 | a0001c0002t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172-4731G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99512883 | ||||||
| chr13:99512893
|
T | C | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.172-4721T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99512893 | ||||||
| chr13:99513052
|
A | G | 1 | a0001c0001t0010g0093 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.172-4562A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513052 | ||||||
| chr13:99513066
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-4548G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513066 | ||||||
| chr13:99513131
|
T | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 10 | HG01106.hp2 HG01257.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-4483T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513131 | ||||||
| chr13:99513403
|
G | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.172-4211G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513403 | ||||||
| chr13:99513591
|
AC | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-4020delC | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99513591 | |||||
| chr13:99513633
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 10 | HG01106.hp2 HG01257.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-3981G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513633 | ||||||
| chr13:99513806
|
G | A | 43 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(40): Show | 56 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.172-3808G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513806 | ||||||
| chr13:99513841
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-3773A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513841 | ||||||
| chr13:99513886
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.172-3728G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513886 | ||||||
| chr13:99513912
|
TA | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(126): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.172-3700delA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99513912 | |||||
| chr13:99513937
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.172-3677C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513937 | ||||||
| chr13:99513939
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.172-3675G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99513939 | ||||||
| chr13:99514067
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.172-3547G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514067 | ||||||
| chr13:99514089
|
A | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.172-3525A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514089 | ||||||
| chr13:99514136
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.172-3478C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514136 | ||||||
| chr13:99514451
|
A | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0037others(3): Show | 8 | HG01981.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-3163A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514451 | ||||||
| chr13:99514541
|
G | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172-3073G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514541 | ||||||
| chr13:99514616
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.172-2998G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514616 | ||||||
| chr13:99514621
|
G | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.172-2993G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514621 | ||||||
| chr13:99514864
|
C | T | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.172-2750C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514864 | ||||||
| chr13:99514872
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.172-2742T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514872 | ||||||
| chr13:99514974
|
G | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.172-2640G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514974 | ||||||
| chr13:99515000
|
G | C | 43 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(40): Show | 56 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.172-2614G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515000 | ||||||
| chr13:99515115
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.172-2499A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515115 | ||||||
| chr13:99515239
|
T | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-2375T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515239 | ||||||
| chr13:99515375
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0037others(5): Show | 10 | HG01981.hp2 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-2239A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515375 | ||||||
| chr13:99515524
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.172-2090C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515524 | ||||||
| chr13:99515589
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2025G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515589 | ||||||
| chr13:99515694
|
G | A | 1 | a0001c0002t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172-1920G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515694 | ||||||
| chr13:99515734
|
G | GT | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(84): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.172-1864dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99515734 | |||||
| chr13:99515734
|
G | GTT | 8 | a0001c0001t0001g0026a0001c0001t0001g0052a0001c0001t0001g0062others(5): Show | 9 | HG01175.hp2 HG01975.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-1865_172-1864d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99515734 | |||||
| chr13:99515734
|
GT | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-1864delT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr13 | 99515734 | |||||
| chr13:99515761
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(182): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.172-1853T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515761 | ||||||
| chr13:99515772
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(145): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.172-1842G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515772 | ||||||
| chr13:99515881
|
T | G | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.172-1733T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515881 | ||||||
| chr13:99515889
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(145): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.172-1725C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515889 | ||||||
| chr13:99515890
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(182): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.172-1724A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515890 | ||||||
| chr13:99515893
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.172-1721C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515893 | ||||||
| chr13:99515899
|
A | T | 43 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(40): Show | 56 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.172-1715A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515899 | ||||||
| chr13:99516154
|
C | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.172-1460C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99516154 | ||||||
| chr13:99516157
|
G | A | 18 | a0001c0001t0001g0019a0001c0001t0001g0107a0001c0001t0001g0109others(15): Show | 19 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.172-1457G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99516157 | ||||||
| chr13:99516190
|
C | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0185 | 2 | HG00597.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.172-1424C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99516190 | ||||||
| chr13:99516627
|
T | C | 3 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG02056.hp2 HG02080.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.172-987T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99516627 | ||||||
| chr13:99517052
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.172-562G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99517052 | ||||||
| chr13:99517141
|
C | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-473C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99517141 | ||||||
| chr13:99517173
|
G | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.172-441G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99517173 | ||||||
| chr13:99517210
|
C | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01071.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.172-404C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99517210 | ||||||
| chr13:99517293
|
A | T | 2 | a0001c0002t0004g0262a0001c0002t0004g0263 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.172-321A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99517293 | ||||||
| chr13:99517467
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.172-147A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99517467 | ||||||
| chr13:99517571
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0019others(70): Show | 84 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.172-43G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99517571 | ||||||
| chr13:99517785
|
A | T | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.239+104A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99517785 | ||||||
| chr13:99517786
|
T | A | 1 | a0001c0001t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.239+105T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99517786 | ||||||
| chr13:99517827
|
ATCTTTTT others(9): Show |
A | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.239+152_239+167del others(16): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr13 | 99517827 | |||||
| chr13:99517857
|
A | G | 1 | a0001c0002t0004g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.239+176A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99517857 | ||||||
| chr13:99518017
|
C | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0143a0001c0001t0001g0152others(1): Show | 5 | HG02055.hp1 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+336C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518017 | ||||||
| chr13:99518087
|
A | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0118others(1): Show | 5 | HG02647.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+406A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518087 | ||||||
| chr13:99518172
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 5 | HG02572.hp1 HG02622.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+491C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518172 | ||||||
| chr13:99518292
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.239+611G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518292 | ||||||
| chr13:99518303
|
G | T | 1 | a0001c0001t0002g0209 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.239+622G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518303 | ||||||
| chr13:99518341
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.239+660G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518341 | ||||||
| chr13:99518378
|
T | C | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+697T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518378 | ||||||
| chr13:99518391
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.239+710G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518391 | ||||||
| chr13:99518650
|
G | A | 1 | a0001c0001t0001g0028 | 2 | NA18978.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.239+969G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518650 | ||||||
| chr13:99518740
|
G | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.239+1059G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518740 | ||||||
| chr13:99518763
|
A | AT | 12 | a0001c0001t0001g0223a0001c0001t0001g0232a0001c0001t0001g0245others(9): Show | 14 | HG00597.hp2 HG00735.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.239+1105dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr13 | 99518763 | |||||
| chr13:99518763
|
AT | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0019others(96): Show | 112 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.239+1105delT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr13 | 99518763 | |||||
| chr13:99518763
|
ATT | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0017others(52): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.239+1104_239+1105d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr13 | 99518763 | |||||
| chr13:99518763
|
ATTT | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 6 | HG02630.hp1 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+1103_239+1105d others(5): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr13 | 99518763 | |||||
| chr13:99518763
|
ATTTT | A | 6 | a0001c0002t0004g0031a0001c0002t0004g0260a0001c0002t0004g0261others(3): Show | 6 | HG01891.hp2 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.239+1102_239+1105d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr13 | 99518763 | |||||
| chr13:99518786
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.239+1105T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518786 | ||||||
| chr13:99518822
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.239+1141C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99518822 | ||||||
| chr13:99519067
|
T | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.240-969T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519067 | ||||||
| chr13:99519193
|
C | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.240-843C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519193 | ||||||
| chr13:99519263
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.240-773G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519263 | ||||||
| chr13:99519359
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.240-677A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519359 | ||||||
| chr13:99519662
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.240-374T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519662 | ||||||
| chr13:99519671
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(127): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.240-365G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519671 | ||||||
| chr13:99519684
|
TA | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.240-350delA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr13 | 99519684 | |||||
| chr13:99519689
|
G | A | 2 | a0001c0002t0004g0031a0001c0002t0004g0264 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.240-347G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519689 | ||||||
| chr13:99519701
|
G | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.240-335G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519701 | ||||||
| chr13:99519709
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.240-327A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519709 | ||||||
| chr13:99519872
|
T | C | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.240-164T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99519872 | ||||||
| chr13:99520021
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.240-15A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 2/16 | chr13 | 99520021 | ||||||
| chr13:99520212
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.333+83A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520212 | ||||||
| chr13:99520337
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.333+208G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520337 | ||||||
| chr13:99520364
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.333+235G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520364 | ||||||
| chr13:99520484
|
CCT | C | 7 | a0001c0001t0002g0003a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 12 | HG00544.hp2 HG03669.hp1 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.333+356_333+357del others(2): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520484 | ||||||
| chr13:99520569
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 5 | HG02572.hp1 HG02622.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+440A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520569 | ||||||
| chr13:99520576
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.333+447T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520576 | ||||||
| chr13:99520577
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.333+448T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520577 | ||||||
| chr13:99520638
|
A | C | 1 | a0001c0002t0004g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.333+509A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520638 | ||||||
| chr13:99520916
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(51): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.333+787C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520916 | ||||||
| chr13:99520917
|
G | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG01975.hp2 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+788G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99520917 | ||||||
| chr13:99521156
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333+1027T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521156 | ||||||
| chr13:99521165
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+1036G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521165 | ||||||
| chr13:99521232
|
T | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.333+1103T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521232 | ||||||
| chr13:99521575
|
G | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.333+1446G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521575 | ||||||
| chr13:99521604
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.333+1475A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521604 | ||||||
| chr13:99521642
|
A | C | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+1513A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521642 | ||||||
| chr13:99521667
|
G | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+1538G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521667 | ||||||
| chr13:99521674
|
C | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.333+1545C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521674 | ||||||
| chr13:99521701
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.333+1572T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521701 | ||||||
| chr13:99521772
|
T | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.333+1643T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521772 | ||||||
| chr13:99521776
|
A | G | 1 | a0001c0001t0008g0080 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.333+1647A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521776 | ||||||
| chr13:99521920
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.333+1791T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521920 | ||||||
| chr13:99521993
|
G | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.333+1864G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99521993 | ||||||
| chr13:99522002
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.333+1873C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522002 | ||||||
| chr13:99522038
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.333+1909C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522038 | ||||||
| chr13:99522107
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.333+1978G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522107 | ||||||
| chr13:99522194
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.333+2065T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522194 | ||||||
| chr13:99522468
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.333+2339G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522468 | ||||||
| chr13:99522512
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(236): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.333+2383G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522512 | ||||||
| chr13:99522549
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333+2420C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522549 | ||||||
| chr13:99522735
|
A | T | 1 | a0001c0001t0001g0248 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.333+2606A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522735 | ||||||
| chr13:99522757
|
A | T | 43 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(40): Show | 56 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.333+2628A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522757 | ||||||
| chr13:99522783
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333+2654G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522783 | ||||||
| chr13:99522880
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.333+2751T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99522880 | ||||||
| chr13:99523105
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.333+2976A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523105 | ||||||
| chr13:99523133
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.333+3004G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523133 | ||||||
| chr13:99523220
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.333+3091C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523220 | ||||||
| chr13:99523240
|
C | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+3111C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523240 | ||||||
| chr13:99523251
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.333+3122A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523251 | ||||||
| chr13:99523510
|
C | A | 2 | a0001c0001t0002g0176a0001c0001t0002g0177 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.333+3381C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523510 | ||||||
| chr13:99523705
|
A | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+3576A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523705 | ||||||
| chr13:99523909
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.333+3780G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99523909 | ||||||
| chr13:99524217
|
G | C | 1 | a0001c0001t0001g0245 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.333+4088G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524217 | ||||||
| chr13:99524219
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.333+4090G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524219 | ||||||
| chr13:99524283
|
G | A | 1 | a0001c0001t0001g0026 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.333+4154G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524283 | ||||||
| chr13:99524378
|
G | A | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+4249G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524378 | ||||||
| chr13:99524666
|
C | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.333+4537C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524666 | ||||||
| chr13:99524686
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.333+4557C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524686 | ||||||
| chr13:99524789
|
C | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+4660C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524789 | ||||||
| chr13:99524852
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.334-4615C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524852 | ||||||
| chr13:99524932
|
GAGAA | G | 7 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-4530_334-4527d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr13 | 99524932 | |||||
| chr13:99524964
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-4503A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524964 | ||||||
| chr13:99524971
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.334-4496G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99524971 | ||||||
| chr13:99525235
|
C | CTGTT | 17 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0067others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.334-4210_334-4207d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr13 | 99525235 | |||||
| chr13:99525455
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.334-4012T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525455 | ||||||
| chr13:99525466
|
TC | T | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-3998delC | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr13 | 99525466 | |||||
| chr13:99525553
|
A | AT | 60 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(57): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.334-3894dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr13 | 99525553 | |||||
| chr13:99525553
|
A | ATT | 8 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0273others(5): Show | 9 | HG01952.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-3895_334-3894d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr13 | 99525553 | |||||
| chr13:99525646
|
G | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.334-3821G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525646 | ||||||
| chr13:99525648
|
C | T | 3 | a0001c0001t0002g0206a0001c0001t0003g0267a0001c0001t0003g0271 | 3 | HG02922.hp1 HG02976.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.334-3819C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525648 | ||||||
| chr13:99525705
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.334-3762G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525705 | ||||||
| chr13:99525712
|
C | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.334-3755C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525712 | ||||||
| chr13:99525784
|
G | A | 2 | a0001c0001t0001g0132a0001c0002t0004g0259 | 2 | HG02630.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.334-3683G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525784 | ||||||
| chr13:99525833
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.334-3634G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525833 | ||||||
| chr13:99525834
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.334-3633C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525834 | ||||||
| chr13:99525844
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0108 | 2 | NA18962.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.334-3623C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525844 | ||||||
| chr13:99525918
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.334-3549G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525918 | ||||||
| chr13:99525993
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.334-3474T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525993 | ||||||
| chr13:99525998
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0165 | 2 | HG00423.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.334-3469T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525998 | ||||||
| chr13:99526011
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.334-3456G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526011 | ||||||
| chr13:99526131
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.334-3336C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526131 | ||||||
| chr13:99526132
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.334-3335C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526132 | ||||||
| chr13:99526203
|
G | A | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.334-3264G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526203 | ||||||
| chr13:99526311
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.334-3156G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526311 | ||||||
| chr13:99526373
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(150): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.334-3094A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526373 | ||||||
| chr13:99526443
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.334-3024A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526443 | ||||||
| chr13:99526660
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.334-2807G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526660 | ||||||
| chr13:99526670
|
T | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | NA18973.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.334-2797T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526670 | ||||||
| chr13:99526826
|
TG | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(126): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.334-2637delG | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr13 | 99526826 | |||||
| chr13:99526830
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.334-2637G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526830 | ||||||
| chr13:99526832
|
T | G | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.334-2635T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99526832 | ||||||
| chr13:99527032
|
A | T | 1 | a0001c0001t0002g0188 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.334-2435A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527032 | ||||||
| chr13:99527033
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.334-2434C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527033 | ||||||
| chr13:99527143
|
T | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.334-2324T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527143 | ||||||
| chr13:99527187
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.334-2280G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527187 | ||||||
| chr13:99527319
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.334-2148T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527319 | ||||||
| chr13:99527346
|
G | A | 1 | a0001c0001t0003g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.334-2121G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527346 | ||||||
| chr13:99527426
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0142 | 2 | NA18947.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.334-2041A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527426 | ||||||
| chr13:99527463
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.334-2004A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527463 | ||||||
| chr13:99527588
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-1879A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527588 | ||||||
| chr13:99527606
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.334-1861C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527606 | ||||||
| chr13:99527666
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-1801A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527666 | ||||||
| chr13:99527696
|
A | G | 3 | a0001c0001t0003g0265a0001c0001t0003g0268a0001c0001t0003g0270 | 3 | HG01891.hp1 HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.334-1771A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527696 | ||||||
| chr13:99527786
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.334-1681C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527786 | ||||||
| chr13:99527823
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.334-1644C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527823 | ||||||
| chr13:99527850
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.334-1617G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527850 | ||||||
| chr13:99527854
|
T | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.334-1613T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527854 | ||||||
| chr13:99527943
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.334-1524G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527943 | ||||||
| chr13:99527970
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.334-1497T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99527970 | ||||||
| chr13:99528138
|
C | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0057 | 3 | HG01243.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.334-1329C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99528138 | ||||||
| chr13:99528478
|
A | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-989A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99528478 | ||||||
| chr13:99528503
|
A | C | 1 | a0001c0001t0002g0179 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.334-964A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99528503 | ||||||
| chr13:99528825
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.334-642A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99528825 | ||||||
| chr13:99528899
|
A | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG00099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.334-568A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99528899 | ||||||
| chr13:99529011
|
T | C | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-456T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99529011 | ||||||
| chr13:99529030
|
GACACTT | G | 9 | a0001c0001t0001g0027a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 10 | HG01106.hp2 HG01257.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.334-435_334-430del others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr13 | 99529030 | |||||
| chr13:99529200
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.334-267G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99529200 | ||||||
| chr13:99529240
|
C | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0166others(1): Show | 4 | HG00738.hp1 HG01943.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-227C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99529240 | ||||||
| chr13:99529250
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334-217G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99529250 | ||||||
| chr13:99529645
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.461+51C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99529645 | ||||||
| chr13:99529661
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(128): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.461+67A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99529661 | ||||||
| chr13:99529858
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.461+264T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99529858 | ||||||
| chr13:99529987
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02572.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.461+393T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99529987 | ||||||
| chr13:99530080
|
CA | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(31): Show | 42 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.461+498delA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr13 | 99530080 | |||||
| chr13:99530147
|
T | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+553T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530147 | ||||||
| chr13:99530187
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0167 | 3 | HG02145.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.461+593G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530187 | ||||||
| chr13:99530195
|
C | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+601C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530195 | ||||||
| chr13:99530198
|
T | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+604T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530198 | ||||||
| chr13:99530249
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.461+655C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530249 | ||||||
| chr13:99530379
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.461+785G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530379 | ||||||
| chr13:99530660
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.461+1066A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530660 | ||||||
| chr13:99530759
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.461+1165A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530759 | ||||||
| chr13:99530774
|
G | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.461+1180G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530774 | ||||||
| chr13:99530856
|
CAT | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.461+1264_461+1265d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr13 | 99530856 | |||||
| chr13:99530946
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.461+1352C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530946 | ||||||
| chr13:99530981
|
C | A | 1 | a0001c0001t0001g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.461+1387C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99530981 | ||||||
| chr13:99531009
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.461+1415C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531009 | ||||||
| chr13:99531022
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 10 | HG01106.hp2 HG01257.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.461+1428G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531022 | ||||||
| chr13:99531156
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.461+1562C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531156 | ||||||
| chr13:99531216
|
G | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.461+1622G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531216 | ||||||
| chr13:99531297
|
A | G | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.461+1703A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531297 | ||||||
| chr13:99531402
|
T | G | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.461+1808T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531402 | ||||||
| chr13:99531517
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.461+1923A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531517 | ||||||
| chr13:99531581
|
G | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0088others(1): Show | 4 | HG00735.hp2 HG00738.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.461+1987G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531581 | ||||||
| chr13:99531611
|
A | C | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.461+2017A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531611 | ||||||
| chr13:99531763
|
C | T | 6 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG01975.hp2 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.461+2169C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531763 | ||||||
| chr13:99531765
|
A | G | 1 | a0001c0001t0001g0012 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.461+2171A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99531765 | ||||||
| chr13:99532014
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.461+2420A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532014 | ||||||
| chr13:99532113
|
G | T | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.461+2519G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532113 | ||||||
| chr13:99532137
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(132): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.461+2543C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532137 | ||||||
| chr13:99532145
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.461+2551G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532145 | ||||||
| chr13:99532153
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.461+2559G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532153 | ||||||
| chr13:99532166
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.461+2572C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532166 | ||||||
| chr13:99532208
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.461+2614T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532208 | ||||||
| chr13:99532267
|
G | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0177 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.461+2673G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532267 | ||||||
| chr13:99532340
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.461+2746G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532340 | ||||||
| chr13:99532341
|
C | T | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.461+2747C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532341 | ||||||
| chr13:99532442
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.461+2848C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532442 | ||||||
| chr13:99532453
|
G | A | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.461+2859G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532453 | ||||||
| chr13:99532499
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.461+2905G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532499 | ||||||
| chr13:99532537
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0045 | 3 | HG01074.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.461+2943A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532537 | ||||||
| chr13:99532664
|
G | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(183): Show | 221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.461+3070G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532664 | ||||||
| chr13:99532788
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.461+3194C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532788 | ||||||
| chr13:99532805
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.461+3211A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99532805 | ||||||
| chr13:99533297
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.462-3311G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533297 | ||||||
| chr13:99533298
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.462-3310C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533298 | ||||||
| chr13:99533314
|
C | G | 1 | a0001c0001t0003g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.462-3294C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533314 | ||||||
| chr13:99533400
|
T | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0170others(1): Show | 4 | HG02015.hp1 NA18612.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.462-3208T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533400 | ||||||
| chr13:99533423
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0007g0103 | 2 | HG02148.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.462-3185C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533423 | ||||||
| chr13:99533511
|
G | A | 1 | a0001c0002t0004g0262 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.462-3097G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533511 | ||||||
| chr13:99533523
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.462-3085A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533523 | ||||||
| chr13:99533752
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 5 | HG02572.hp1 HG02622.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-2856G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533752 | ||||||
| chr13:99533785
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.462-2823C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533785 | ||||||
| chr13:99533871
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.462-2737A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533871 | ||||||
| chr13:99533964
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.462-2644T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533964 | ||||||
| chr13:99533998
|
C | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.462-2610C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99533998 | ||||||
| chr13:99534324
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.462-2284A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534324 | ||||||
| chr13:99534502
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.462-2106T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534502 | ||||||
| chr13:99534544
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02056.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.462-2064A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534544 | ||||||
| chr13:99534565
|
A | G | 6 | a0001c0002t0004g0031a0001c0002t0004g0260a0001c0002t0004g0261others(3): Show | 6 | HG01891.hp2 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.462-2043A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534565 | ||||||
| chr13:99534680
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.462-1928A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534680 | ||||||
| chr13:99534704
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.462-1904G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534704 | ||||||
| chr13:99534875
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.462-1733C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534875 | ||||||
| chr13:99534996
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.462-1612T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99534996 | ||||||
| chr13:99535090
|
T | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.462-1518T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535090 | ||||||
| chr13:99535445
|
C | T | 43 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(40): Show | 56 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.462-1163C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535445 | ||||||
| chr13:99535486
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.462-1122A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535486 | ||||||
| chr13:99535488
|
A | G | 43 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(40): Show | 56 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.462-1120A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535488 | ||||||
| chr13:99535559
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.462-1049A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535559 | ||||||
| chr13:99535813
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(73): Show | 88 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.462-795C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535813 | ||||||
| chr13:99535839
|
A | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0248 | 2 | HG00735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.462-769A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535839 | ||||||
| chr13:99535937
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.462-671A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535937 | ||||||
| chr13:99535938
|
ACAGTATT others(6): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.462-669_462-657del others(13): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535938 | ||||||
| chr13:99535953
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.462-655G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535953 | ||||||
| chr13:99535996
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.462-612G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99535996 | ||||||
| chr13:99536228
|
C | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0019others(64): Show | 78 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.462-380C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99536228 | ||||||
| chr13:99536299
|
G | T | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.462-309G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99536299 | ||||||
| chr13:99536303
|
T | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.462-305T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99536303 | ||||||
| chr13:99536331
|
A | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(73): Show | 88 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.462-277A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | chr13 | 99536331 | ||||||
| chr13:99536569
|
TG | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.462-36delG | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr13 | 99536569 | |||||
| chr13:99536966
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.591+229A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 5/16 | chr13 | 99536966 | ||||||
| chr13:99537140
|
A | ATT | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.591+404_591+405dup others(2): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr13 | 99537140 | |||||
| chr13:99537273
|
C | T | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-466C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 5/16 | chr13 | 99537273 | ||||||
| chr13:99538223
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.716+360G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538223 | ||||||
| chr13:99538250
|
A | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.716+387A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538250 | ||||||
| chr13:99538257
|
A | G | 10 | a0001c0001t0001g0112a0001c0001t0002g0025a0001c0001t0002g0186others(7): Show | 11 | HG00423.hp1 HG01081.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.716+394A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538257 | ||||||
| chr13:99538283
|
C | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.716+420C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538283 | ||||||
| chr13:99538340
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.716+477C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538340 | ||||||
| chr13:99538373
|
T | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.716+510T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538373 | ||||||
| chr13:99538451
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.716+588A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538451 | ||||||
| chr13:99538783
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.717-663C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538783 | ||||||
| chr13:99538786
|
G | T | 1 | a0001c0001t0001g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.717-660G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538786 | ||||||
| chr13:99538893
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.717-553T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99538893 | ||||||
| chr13:99539173
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.717-273G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99539173 | ||||||
| chr13:99539209
|
C | CA | 8 | a0001c0001t0001g0136a0001c0001t0003g0265a0001c0001t0003g0266others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.717-225dupA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr13 | 99539209 | |||||
| chr13:99539210
|
A | C | 7 | a0001c0001t0002g0003a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 12 | HG00544.hp2 HG03669.hp1 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.717-236A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99539210 | ||||||
| chr13:99539210
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0221 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.717-222_717-211del others(12): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr13 | 99539210 | |||||
| chr13:99539222
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.717-224G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 6/16 | chr13 | 99539222 | ||||||
| chr13:99539886
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(50): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.828+329G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99539886 | ||||||
| chr13:99540088
|
G | A | 5 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0262others(2): Show | 5 | HG01891.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+531G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99540088 | ||||||
| chr13:99540156
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0061a0001c0001t0001g0062 | 4 | HG02970.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-558T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99540156 | ||||||
| chr13:99540225
|
T | C | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-489T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99540225 | ||||||
| chr13:99540247
|
C | T | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.829-467C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99540247 | ||||||
| chr13:99540396
|
T | TA | 34 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(31): Show | 38 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.829-302dupA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr13 | 99540396 | |||||
| chr13:99540396
|
TA | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(77): Show | 92 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.829-302delA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr13 | 99540396 | |||||
| chr13:99540466
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.829-248A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99540466 | ||||||
| chr13:99540495
|
CT | C | 63 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0044others(60): Show | 78 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.829-201delT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr13 | 99540495 | |||||
| chr13:99540536
|
T | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.829-178T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99540536 | ||||||
| chr13:99540614
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0142a0001c0001t0001g0150 | 3 | NA18947.hp1 NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.829-100G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 7/16 | chr13 | 99540614 | ||||||
| chr13:99541131
|
T | G | 2 | a0001c0001t0002g0176a0001c0001t0002g0177 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.908+338T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 8/16 | chr13 | 99541131 | ||||||
| chr13:99541326
|
A | G | 5 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0262others(2): Show | 5 | HG01891.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-233A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 8/16 | chr13 | 99541326 | ||||||
| chr13:99541331
|
A | C | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.909-228A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 8/16 | chr13 | 99541331 | ||||||
| chr13:99541500
|
G | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0143a0001c0001t0001g0152others(1): Show | 5 | HG02055.hp1 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.909-59G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 8/16 | chr13 | 99541500 | ||||||
| chr13:99541798
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1017+131A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99541798 | ||||||
| chr13:99541906
|
T | C | 5 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0198others(2): Show | 5 | HG01243.hp1 HG02486.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+239T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99541906 | ||||||
| chr13:99541915
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1017+248C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99541915 | ||||||
| chr13:99541948
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1017+281A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99541948 | ||||||
| chr13:99541953
|
C | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1017+286C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99541953 | ||||||
| chr13:99542083
|
G | A | 1 | a0001c0003t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1017+416G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542083 | ||||||
| chr13:99542109
|
C | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0118others(1): Show | 5 | HG02647.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+442C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542109 | ||||||
| chr13:99542149
|
C | CA | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(85): Show | 100 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1017+500dupA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr13 | 99542149 | |||||
| chr13:99542149
|
CA | C | 19 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0072others(16): Show | 21 | HG00621.hp1 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1017+500delA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr13 | 99542149 | |||||
| chr13:99542149
|
CAA | C | 38 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(35): Show | 51 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1017+499_1017+500d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr13 | 99542149 | |||||
| chr13:99542168
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1017+501T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542168 | ||||||
| chr13:99542194
|
G | C | 5 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0262others(2): Show | 5 | HG01891.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+527G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542194 | ||||||
| chr13:99542263
|
C | G | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1017+596C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542263 | ||||||
| chr13:99542399
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1017+732A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542399 | ||||||
| chr13:99542497
|
G | T | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1017+830G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542497 | ||||||
| chr13:99542584
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017+917C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99542584 | ||||||
| chr13:99543003
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1018-860A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543003 | ||||||
| chr13:99543028
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1018-835C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543028 | ||||||
| chr13:99543368
|
C | T | 5 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0262others(2): Show | 5 | HG01891.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-495C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543368 | ||||||
| chr13:99543533
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1018-330G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543533 | ||||||
| chr13:99543622
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0141 | 2 | HG04199.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.1018-241A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543622 | ||||||
| chr13:99543639
|
C | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(76): Show | 91 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1018-224C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543639 | ||||||
| chr13:99543717
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1018-146A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543717 | ||||||
| chr13:99543721
|
T | A | 5 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0262others(2): Show | 5 | HG01891.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-142T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 9/16 | chr13 | 99543721 | ||||||
| chr13:99544136
|
G | A | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150+141G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544136 | ||||||
| chr13:99544300
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1150+305G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544300 | ||||||
| chr13:99544342
|
C | CA | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 35 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1150+358dupA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr13 | 99544342 | |||||
| chr13:99544354
|
C | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 118 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1150+359C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544354 | ||||||
| chr13:99544356
|
A | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0118others(3): Show | 7 | HG01192.hp1 HG02109.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+361A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544356 | ||||||
| chr13:99544361
|
C | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+366C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544361 | ||||||
| chr13:99544452
|
T | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+457T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544452 | ||||||
| chr13:99544698
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1150+703G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544698 | ||||||
| chr13:99544725
|
A | G | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150+730A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544725 | ||||||
| chr13:99544801
|
A | C | 1 | a0001c0001t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1150+806A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544801 | ||||||
| chr13:99544816
|
T | C | 42 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1150+821T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99544816 | ||||||
| chr13:99545177
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0037others(5): Show | 10 | HG01981.hp2 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150+1182A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99545177 | ||||||
| chr13:99545242
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+1247A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99545242 | ||||||
| chr13:99545445
|
G | A | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150+1450G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99545445 | ||||||
| chr13:99545574
|
C | CT | 42 | a0001c0001t0001g0122a0001c0001t0001g0161a0001c0001t0001g0195others(39): Show | 55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1151-1400dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr13 | 99545574 | |||||
| chr13:99545817
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1151-1168G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99545817 | ||||||
| chr13:99545858
|
C | G | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1151-1127C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99545858 | ||||||
| chr13:99546162
|
G | A | 7 | a0001c0001t0001g0085a0001c0001t0001g0225a0001c0001t0001g0228others(4): Show | 7 | HG01975.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-823G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546162 | ||||||
| chr13:99546180
|
G | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG01975.hp2 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-805G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546180 | ||||||
| chr13:99546216
|
G | C | 5 | a0001c0001t0001g0223a0001c0002t0004g0031a0001c0002t0004g0262others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-769G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546216 | ||||||
| chr13:99546310
|
C | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-675C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546310 | ||||||
| chr13:99546352
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1151-633T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546352 | ||||||
| chr13:99546442
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1151-543G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546442 | ||||||
| chr13:99546463
|
C | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1151-522C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546463 | ||||||
| chr13:99546534
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1151-451T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546534 | ||||||
| chr13:99546567
|
G | GT | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0113others(4): Show | 7 | HG01175.hp1 HG01192.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-405dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr13 | 99546567 | |||||
| chr13:99546694
|
A | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-291A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546694 | ||||||
| chr13:99546718
|
G | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151-267G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546718 | ||||||
| chr13:99546917
|
T | C | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1151-68T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546917 | ||||||
| chr13:99546970
|
C | T | 109 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(106): Show | 131 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1151-15C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546970 | ||||||
| chr13:99547487
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1270+383C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99547487 | ||||||
| chr13:99547596
|
G | A | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1270+492G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99547596 | ||||||
| chr13:99547610
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1270+506C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99547610 | ||||||
| chr13:99547918
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(50): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1270+814T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99547918 | ||||||
| chr13:99548057
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1270+953T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548057 | ||||||
| chr13:99548112
|
TAC | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1270+1009_1270+101 others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548112 | ||||||
| chr13:99548118
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0119 | 4 | HG02647.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+1014A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548118 | ||||||
| chr13:99548232
|
C | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1271-933C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548232 | ||||||
| chr13:99548255
|
G | T | 1 | a0001c0001t0001g0010 | 2 | HG03688.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1271-910G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548255 | ||||||
| chr13:99548389
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1271-776G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548389 | ||||||
| chr13:99548440
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1271-725A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548440 | ||||||
| chr13:99548561
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1271-604A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548561 | ||||||
| chr13:99548617
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1271-548A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548617 | ||||||
| chr13:99548772
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(151): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1271-393C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99548772 | ||||||
| chr13:99549118
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1271-47G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 11/16 | chr13 | 99549118 | ||||||
| chr13:99549386
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(154): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1328+164A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99549386 | ||||||
| chr13:99549462
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1328+240C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99549462 | ||||||
| chr13:99549505
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1328+283C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99549505 | ||||||
| chr13:99549571
|
CAT | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1328+352_1328+353d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr13 | 99549571 | |||||
| chr13:99549756
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1328+534A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99549756 | ||||||
| chr13:99549819
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG00621.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1328+597C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99549819 | ||||||
| chr13:99549892
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1328+670C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99549892 | ||||||
| chr13:99549952
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(143): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1328+730C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99549952 | ||||||
| chr13:99550025
|
T | A | 4 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0170others(1): Show | 4 | HG02015.hp1 NA18612.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1328+803T>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550025 | ||||||
| chr13:99550047
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(142): Show | 170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1328+825G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550047 | ||||||
| chr13:99550115
|
C | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(48): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1328+893C>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550115 | ||||||
| chr13:99550189
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1328+967A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550189 | ||||||
| chr13:99550421
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 35 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1328+1199C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550421 | ||||||
| chr13:99550590
|
T | C | 45 | a0001c0001t0001g0195a0001c0001t0001g0236a0001c0001t0001g0237others(42): Show | 58 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1328+1368T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550590 | ||||||
| chr13:99550599
|
C | G | 7 | a0001c0001t0002g0003a0001c0001t0002g0187a0001c0001t0002g0188others(4): Show | 12 | HG00544.hp2 HG03669.hp1 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.1328+1377C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550599 | ||||||
| chr13:99550684
|
A | G | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1328+1462A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550684 | ||||||
| chr13:99550873
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1329-1294C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99550873 | ||||||
| chr13:99550901
|
TA | T | 8 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0002t0004g0031others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329-1264delA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr13 | 99550901 | |||||
| chr13:99551104
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1329-1063A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551104 | ||||||
| chr13:99551202
|
C | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01192.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1329-965C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551202 | ||||||
| chr13:99551256
|
A | C | 1 | a0001c0001t0001g0050 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1329-911A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551256 | ||||||
| chr13:99551319
|
C | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(84): Show | 108 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1329-848C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551319 | ||||||
| chr13:99551549
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1329-618G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551549 | ||||||
| chr13:99551554
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329-613A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551554 | ||||||
| chr13:99551622
|
A | G | 3 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG00099.hp1 HG01256.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1329-545A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551622 | ||||||
| chr13:99551739
|
T | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329-428T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551739 | ||||||
| chr13:99551913
|
A | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 35 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1329-254A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551913 | ||||||
| chr13:99551930
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1329-237A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551930 | ||||||
| chr13:99551939
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329-228G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99551939 | ||||||
| chr13:99552002
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1329-165T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99552002 | ||||||
| chr13:99552156
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1329-11G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 12/16 | chr13 | 99552156 | ||||||
| chr13:99552353
|
A | C | 1 | a0001c0002t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1488+27A>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99552353 | ||||||
| chr13:99552428
|
G | C | 1 | a0001c0001t0001g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1488+102G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99552428 | ||||||
| chr13:99552442
|
G | A | 1 | a0001c0001t0007g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1488+116G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99552442 | ||||||
| chr13:99552591
|
A | ACATT | 59 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(56): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1488+290_1488+293d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr13 | 99552591 | |||||
| chr13:99552824
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1488+498G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99552824 | ||||||
| chr13:99552881
|
G | C | 1 | a0001c0002t0004g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1488+555G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99552881 | ||||||
| chr13:99553052
|
C | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0177 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1488+726C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99553052 | ||||||
| chr13:99553078
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 35 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1488+752C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99553078 | ||||||
| chr13:99553240
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1488+914G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99553240 | ||||||
| chr13:99553269
|
G | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(23): Show | 33 | HG01074.hp1 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1488+943G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99553269 | ||||||
| chr13:99553755
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1489-549G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99553755 | ||||||
| chr13:99554124
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1489-180C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99554124 | ||||||
| chr13:99554241
|
G | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(73): Show | 88 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1489-63G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99554241 | ||||||
| chr13:99554275
|
T | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 12 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1489-29T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 13/16 | chr13 | 99554275 | ||||||
| chr13:99554800
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1640+345G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 14/16 | chr13 | 99554800 | ||||||
| chr13:99554838
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1640+383C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 14/16 | chr13 | 99554838 | ||||||
| chr13:99555003
|
G | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(152): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1641-533G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 14/16 | chr13 | 99555003 | ||||||
| chr13:99555107
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1641-429C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 14/16 | chr13 | 99555107 | ||||||
| chr13:99555125
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1641-411A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 14/16 | chr13 | 99555125 | ||||||
| chr13:99555481
|
G | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0107a0001c0001t0001g0109others(14): Show | 18 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1641-55G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 14/16 | chr13 | 99555481 | ||||||
| chr13:99555490
|
C | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1641-46C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 14/16 | chr13 | 99555490 | ||||||
| chr13:99555984
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1752+337A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99555984 | ||||||
| chr13:99556066
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1752+419A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556066 | ||||||
| chr13:99556163
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+516A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556163 | ||||||
| chr13:99556177
|
A | ATATT | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1752+531_1752+534d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99556177 | |||||
| chr13:99556283
|
A | G | 44 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(41): Show | 59 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1752+636A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556283 | ||||||
| chr13:99556451
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1752+804C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556451 | ||||||
| chr13:99556548
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1752+901A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556548 | ||||||
| chr13:99556571
|
T | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0118others(1): Show | 5 | HG02647.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1752+924T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556571 | ||||||
| chr13:99556574
|
C | CT | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(142): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1752+942dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99556574 | |||||
| chr13:99556574
|
C | CTT | 116 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0018others(113): Show | 143 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1752+941_1752+942d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99556574 | |||||
| chr13:99556574
|
C | CTTT | 6 | a0001c0001t0001g0112a0001c0001t0001g0143a0001c0001t0002g0176others(3): Show | 6 | HG00423.hp1 HG01243.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1752+940_1752+942d others(5): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99556574 | |||||
| chr13:99556574
|
CT | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+942delT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99556574 | |||||
| chr13:99556615
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+968G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556615 | ||||||
| chr13:99556707
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1752+1060C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556707 | ||||||
| chr13:99556736
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+1089A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556736 | ||||||
| chr13:99556876
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1752+1229G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556876 | ||||||
| chr13:99557066
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1752+1419G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99557066 | ||||||
| chr13:99557430
|
T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1752+1783T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99557430 | ||||||
| chr13:99557531
|
G | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-1832G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99557531 | ||||||
| chr13:99557618
|
C | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0215a0001c0001t0001g0216others(6): Show | 10 | HG01106.hp2 HG01257.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1753-1745C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99557618 | ||||||
| chr13:99557635
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1753-1728A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99557635 | ||||||
| chr13:99557880
|
C | CA | 27 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 34 | HG01074.hp1 HG01074.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1753-1475dupA | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99557880 | |||||
| chr13:99557977
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-1386A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99557977 | ||||||
| chr13:99557979
|
C | G | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1753-1384C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99557979 | ||||||
| chr13:99558179
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1753-1184A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99558179 | ||||||
| chr13:99558344
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-1019A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99558344 | ||||||
| chr13:99558356
|
T | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1753-1007T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99558356 | ||||||
| chr13:99558587
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0101 | 3 | HG02647.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1753-776C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99558587 | ||||||
| chr13:99558658
|
C | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-705C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99558658 | ||||||
| chr13:99558722
|
TTG | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(48): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1753-623_1753-622d others(4): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99558722 | |||||
| chr13:99558722
|
TTGTG | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-625_1753-622d others(6): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr13 | 99558722 | |||||
| chr13:99559016
|
T | C | 1 | a0001c0001t0002g0196 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1753-347T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99559016 | ||||||
| chr13:99559208
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-155A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99559208 | ||||||
| chr13:99559235
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1753-128G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99559235 | ||||||
| chr13:99559257
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | NA18988.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1753-106T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99559257 | ||||||
| chr13:99559830
|
C | CT | 47 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0049others(44): Show | 62 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1924+310dupT | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr13 | 99559830 | |||||
| chr13:99560180
|
G | A | 2 | a0001c0002t0004g0260a0001c0002t0004g0261 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1924+646G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560180 | ||||||
| chr13:99560233
|
G | A | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1924+699G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560233 | ||||||
| chr13:99560347
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0118others(1): Show | 5 | HG02647.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1924+813G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560347 | ||||||
| chr13:99560360
|
G | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1924+826G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560360 | ||||||
| chr13:99560363
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1924+829T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560363 | ||||||
| chr13:99560712
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1924+1178C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560712 | ||||||
| chr13:99560743
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0101a0001c0001t0001g0118others(1): Show | 5 | HG02647.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1924+1209G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560743 | ||||||
| chr13:99560914
|
C | T | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1924+1380C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560914 | ||||||
| chr13:99560932
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(151): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1924+1398C>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560932 | ||||||
| chr13:99560943
|
G | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0019others(67): Show | 81 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1924+1409G>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560943 | ||||||
| chr13:99560973
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1924+1439G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99560973 | ||||||
| chr13:99561051
|
A | T | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1924+1517A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561051 | ||||||
| chr13:99561052
|
T | C | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1924+1518T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561052 | ||||||
| chr13:99561304
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1925-1387C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561304 | ||||||
| chr13:99561443
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1925-1248A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561443 | ||||||
| chr13:99561465
|
T | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0059 | 3 | HG02080.hp2 HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1925-1226T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561465 | ||||||
| chr13:99561622
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1925-1069G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561622 | ||||||
| chr13:99561688
|
TCCTTTAA others(15): Show |
T | 8 | a0001c0001t0003g0265a0001c0001t0003g0266a0001c0001t0003g0267others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1925-1001_1925-980 others(25): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr13 | 99561688 | |||||
| chr13:99561736
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(241): Show | 292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1925-955T>C | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561736 | ||||||
| chr13:99561761
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1925-930A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561761 | ||||||
| chr13:99561895
|
A | G | 7 | a0001c0002t0004g0031a0001c0002t0004g0259a0001c0002t0004g0260others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1925-796A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99561895 | ||||||
| chr13:99562018
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1925-673A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99562018 | ||||||
| chr13:99562109
|
A | T | 46 | a0001c0001t0001g0195a0001c0001t0002g0003a0001c0001t0002g0005others(43): Show | 61 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1925-582A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99562109 | ||||||
| chr13:99562219
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1925-472G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99562219 | ||||||
| chr13:99562287
|
A | G | 1 | a0001c0001t0002g0007 | 3 | HG01069.hp2 HG01071.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1925-404A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99562287 | ||||||
| chr13:99562322
|
T | G | 4 | a0001c0001t0001g0107a0001c0001t0001g0124a0001c0001t0001g0126others(1): Show | 4 | HG00609.hp2 HG02074.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1925-369T>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99562322 | ||||||
| chr13:99562356
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1925-335G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | chr13 | 99562356 | ||||||
| chr13:99562563
|
A | ATTCCCGG others(29): Show |
1 | a0001c0001t0001g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1925-125_1925-90du others(37): Show |
TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr13 | 99562563 |