Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1989 | 323 | 78 | 52 | 137 | 18 | 36 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | ATGAG others(1984): Show |
chr13 | 99496472 | 99569048 | ||
| a0001c0002 | 0/0 | 1989 | 7 | 7 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | ATGAG others(1984): Show |
chr13 | 99496472 | 99569048 | ||
| a0001c0003 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | ATGAG others(1984): Show |
chr13 | 99496472 | 99569048 | ||
| a0001c0004 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | ATGAG others(1984): Show |
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 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0002 | 0/1 | 3417 | 58 | 6 | 13 | 27 | 6 | 5 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0003 | 0/0 | 3417 | 8 | 8 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0005 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 1 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0006 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0007 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0008 | 0/0 | 3417 | 1 | 0 | 0 | 0 | 0 | 1 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0009 | 0/0 | 3417 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0001t0010 | 0/0 | 3417 | 1 | 0 | 1 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0002t0004 | 0/0 | 3417 | 7 | 7 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0003t0002 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
chr13 | 99496472 | 99569048 |
| a0001c0004t0001 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | AGCGC others(3412): Show |
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 | 0/0 | 2 | 0 | 0 | 0 | 2 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | g0203 | 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 | g0201 | 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 | g0202 | 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 | g0024 | 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 | g0024 | 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 | a0001 | c0001 | t0002 | g0200 | REF | REF | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | TM9SF2_chr13_99496472_99569048 | TM9SF2 | chr13 | 99496472 | 99569048 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0002 a0001c0001t0007 a0001c0003t0002 |
59 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(56): 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0001g0010 a0001c0001t0001g0033 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): 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 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0260 a0001c0002t0004g0261 others(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 | a0001c0001t0001g0026 a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0023 others(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 | 21 | a0001c0001t0001g0195 a0001c0001t0002g0005 a0001c0001t0002g0024 others(18): Show |
26 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(23): 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 | a0001c0001t0001g0018 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
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 | 24 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0024 others(21): Show |
34 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(31): 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(177): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): 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 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0114 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 40 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(37): Show |
53 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(50): 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 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | 1 | a0001c0001t0002g0024 | 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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0108 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0229 a0001c0001t0002g0102 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0002t0004g0260 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0071 others(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 | 27 | a0001c0001t0001g0067 a0001c0001t0001g0168 a0001c0001t0001g0249 others(24): Show |
37 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(34): 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 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0002g0211 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0101 |
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 | 1 | a0001c0001t0002g0024 | 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 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0225 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0045 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0009g0096 |
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 | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0001g0026 a0001c0001t0001g0101 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0161 |
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 | 42 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): 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 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | 42 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): 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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.172-2993G>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99514621 | |||||||
| chr13:99514864 | C | T | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | 42 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): 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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0037 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0001g0062 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | 42 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.172-1715A>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 1/16 | chr13 | 99515899 | |||||||
| chr13:99516154 | C | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): 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 | a0001c0001t0001g0019 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0183 a0001c0001t0002g0185 |
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 | a0001c0001t0001g0137 a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
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 | a0001c0002t0004g0262 a0001c0002t0004g0263 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): 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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0232 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0260 a0001c0002t0004g0261 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0002t0004g0031 a0001c0002t0004g0264 |
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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0187 a0001c0001t0002g0188 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(235): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): 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 | 42 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0002g0201 | 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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): 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 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0067 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | 59 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0038 others(56): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(69): 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 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0273 others(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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): 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 | a0001c0001t0002g0206 a0001c0001t0003g0267 a0001c0001t0003g0271 |
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 | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.334-3762G>A | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 3/16 | chr13 | 99525705 | |||||||
| chr13:99525712 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): 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 | a0001c0001t0001g0132 a0001c0002t0004g0259 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0165 |
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 | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0001t0001g0110 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0101 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0268 a0001c0001t0003g0270 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0057 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0167 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0088 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): 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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): 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 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0045 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0058 a0001c0001t0007g0103 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0260 a0001c0002t0004g0261 others(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 | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | 42 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): 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 | 42 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): 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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0245 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(39): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0112 a0001c0001t0002g0025 a0001c0001t0002g0186 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0136 a0001c0001t0003g0265 a0001c0001t0003g0266 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0187 a0001c0001t0002g0188 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0262 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0062 |
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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0002g0203 | 1 | HG00140.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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | 62 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0044 others(59): Show |
77 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(74): 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 | a0001c0001t0001g0110 a0001c0001t0001g0142 a0001c0001t0001g0150 |
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 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0262 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0198 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(35): Show |
50 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(47): 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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0262 others(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 | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0262 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0141 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0262 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 96 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
117 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(114): 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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0118 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): 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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | 41 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0037 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | 41 | a0001c0001t0001g0122 a0001c0001t0001g0161 a0001c0001t0001g0195 others(38): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): 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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0225 a0001c0001t0001g0228 others(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 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | a0001c0001t0001g0223 a0001c0002t0004g0031 a0001c0002t0004g0262 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0113 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | 108 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(105): Show |
130 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1151-15C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 10/16 | chr13 | 99546970 | |||||||
| chr13:99547487 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0119 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 44 | a0001c0001t0001g0195 a0001c0001t0001g0236 a0001c0001t0001g0237 others(41): Show |
57 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(54): 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 | a0001c0001t0002g0003 a0001c0001t0002g0187 a0001c0001t0002g0188 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0002t0004g0031 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | 86 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
107 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(104): 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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0094 a0001c0001t0001g0095 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0107 a0001c0001t0001g0109 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0101 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | 43 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(40): Show |
58 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1752+636A>G | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556283 | |||||||
| chr13:99556451 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1752+804C>T | TM9SF2 | ENSG00000125304.10 | transcript | ENST00000376387.5 | protein_coding | 15/16 | chr13 | 99556451 | |||||||
| chr13:99556548 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): 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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(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 | 115 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(112): Show |
142 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(139): 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 | a0001c0001t0001g0112 a0001c0001t0001g0143 a0001c0001t0002g0176 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
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 | 46 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0049 others(43): Show |
61 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(58): 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 | a0001c0002t0004g0260 a0001c0002t0004g0261 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0118 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): 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 | a0001c0001t0001g0026 a0001c0001t0001g0101 a0001c0001t0001g0118 others(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 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0059 |
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 | a0001c0001t0003g0265 a0001c0001t0003g0266 a0001c0001t0003g0267 others(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 | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): 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 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0002t0004g0031 a0001c0002t0004g0259 a0001c0002t0004g0260 others(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 | 45 | a0001c0001t0001g0195 a0001c0001t0002g0003 a0001c0001t0002g0005 others(42): Show |
60 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(57): 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 | a0001c0001t0001g0107 a0001c0001t0001g0124 a0001c0001t0001g0126 others(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 |