Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8630 |
| ensemblid | ENSG00000025423.11 |
| hgncid | 23316 |
| symbol | HSD17B6 |
| name | hydroxysteroid 17-beta dehydrogenase 6 |
| refseq_nuc | NM_003725.4 |
| refseq_prot | NP_003716.2 |
| ensembl_nuc | ENST00000322165.1 |
| ensembl_prot | ENSP00000318631.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 56763324 |
| end | 56787790 |
| strand | + |
| ver | v1.2 |
| region | chr12:56763324-56787790 |
| region5000 | chr12:56758324-56792790 |
| regionname0 | HSD17B6_chr12_56763324_56787790 |
| regionname5000 | HSD17B6_chr12_56758324_56792790 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 317 | 358 | 92 | 72 | 138 | 18 | 36 | 108 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | MWLYL others(312): Show |
chr12 | 56758324 | 56792790 |
| a0002 | 0/0 | 317 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | MWLYL others(312): Show |
chr12 | 56758324 | 56792790 |
| a0003 | 0/0 | 317 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | MWLYL others(312): Show |
chr12 | 56758324 | 56792790 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 951 | 356 | 90 | 72 | 138 | 18 | 36 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | ATGTG others(946): Show |
chr12 | 56758324 | 56792790 | ||
| a0001c0002 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | ATGTG others(946): Show |
chr12 | 56758324 | 56792790 | ||
| a0001c0003 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | ATGTG others(946): Show |
chr12 | 56758324 | 56792790 | ||
| a0002c0005 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | ATGTG others(946): Show |
chr12 | 56758324 | 56792790 | ||
| a0003c0004 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | ATGTG others(946): Show |
chr12 | 56758324 | 56792790 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1512 | 350 | 87 | 72 | 135 | 18 | 36 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0001c0001t0002 | 0/0 | 1512 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0001c0001t0003 | 0/0 | 1512 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0001c0001t0004 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0001c0001t0005 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0001c0002t0001 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0001c0003t0001 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0002c0005t0001 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| a0003c0004t0001 | 0/0 | 1512 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | AGCAG others(1507): Show |
chr12 | 56758324 | 56792790 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 4 | 6 | 2 | 2 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0003 | 0/0 | 6 | 2 | 2 | 2 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0004 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0001c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0002c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| a0003c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0232 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03927 | hp1 | a0002 | c0005 | t0001 | g0198 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG04228 | hp2 | a0003 | c0004 | t0001 | g0034 | SAS | STU | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ASW | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0043 | REF | REF | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0146 | REF | REF | HSD17B6_chr12_56758324_56792790 | HSD17B6 | chr12 | 56758324 | 56792790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56773956 | C | T | 1 | a0002 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.104C>T | p.Thr35Met | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/5 | 214/1512 | 104/954 | 35/317 | chr12 | 56773956 | |||
| chr12:56782096 | T | G | 1 | a0003 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.436T>G | p.Leu146Val | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/5 | 546/1512 | 436/954 | 146/317 | chr12 | 56782096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56773870 | G | A | 1 | a0001c0002 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.18G>A | p.Ala6Ala | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/5 | 128/1512 | 18/954 | 6/317 | chr12 | 56773870 | |||
| chr12:56774155 | G | A | 1 | a0001c0003 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.303G>A | p.Val101Val | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/5 | 413/1512 | 303/954 | 101/317 | chr12 | 56774155 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56787552 | T | A | 1 | a0001c0001t0004 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 5/5 | 210 | chr12 | 56787552 | ||||||
| chr12:56787567 | A | G | 1 | a0001c0001t0005 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 5/5 | 225 | chr12 | 56787567 | ||||||
| chr12:56787589 | G | C | 1 | a0001c0001t0002 | 2 | HG03453.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*247G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 5/5 | 247 | chr12 | 56787589 | ||||||
| chr12:56787747 | G | A | 1 | a0001c0001t0003 | 2 | HG00597.hp1 NA18983.hp2 |
3_prime_UTR_variant | MODIFIER | c.*405G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 5/5 | 405 | chr12 | 56787747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56763437 | T | TTG | 51 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(48): Show |
57 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-20+67_-20+68dupGT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | T | TTGTG | 13 | a0001c0001t0001g0030 a0001c0001t0001g0279 a0001c0001t0001g0280 others(10): Show |
14 | HG01106.hp2 HG02622.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+65_-20+68dupGT others(2): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | T | TTGTGTG | 5 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(2): Show |
5 | HG00544.hp1 HG04184.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+63_-20+68dupGT others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG00597.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.-20+59_-20+68dupGT others(8): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | TTG | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(32): Show |
42 | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-20+67_-20+68delGT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | TTGTG | T | 45 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
51 | HG00544.hp2 HG01109.hp2 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.-20+65_-20+68delGT others(2): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | TTGTGTG | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0044 others(8): Show |
13 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+63_-20+68delGT others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | TTGTGTGT others(1): Show |
T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+61_-20+68delGT others(6): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763437 | TTGTGTGT others(3): Show |
T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | HG00323.hp1 HG01081.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+59_-20+68delGT others(8): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56763437 | ||||||
| chr12:56763581 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+167T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56763581 | |||||||
| chr12:56763784 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-20+370G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56763784 | |||||||
| chr12:56763899 | C | T | 1 | a0001c0001t0001g0029 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-20+485C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56763899 | |||||||
| chr12:56763935 | G | C | 1 | a0001c0001t0001g0279 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-20+521G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56763935 | |||||||
| chr12:56764068 | C | CA | 6 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG00323.hp1 HG00642.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+676dupA | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56764068 | ||||||
| chr12:56764068 | C | CAA | 19 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
20 | HG01081.hp1 HG01891.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20+675_-20+676dup others(2): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56764068 | ||||||
| chr12:56764068 | C | CAAA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
7 | HG02056.hp2 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+674_-20+676dup others(3): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56764068 | ||||||
| chr12:56764068 | CA | C | 28 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0079 others(25): Show |
28 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-20+676delA | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56764068 | ||||||
| chr12:56764068 | CAA | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-20+675_-20+676del others(2): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56764068 | ||||||
| chr12:56764130 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-20+716A>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764130 | |||||||
| chr12:56764399 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-20+985C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764399 | |||||||
| chr12:56764432 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20+1018T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764432 | |||||||
| chr12:56764648 | T | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0031 others(23): Show |
28 | HG00323.hp1 HG01081.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-20+1234T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764648 | |||||||
| chr12:56764726 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-20+1312A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764726 | |||||||
| chr12:56764763 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-20+1349A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764763 | |||||||
| chr12:56764900 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0237 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-20+1486T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764900 | |||||||
| chr12:56764948 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0092 |
2 | HG01943.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-20+1534C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56764948 | |||||||
| chr12:56765187 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-20+1773A>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56765187 | |||||||
| chr12:56765211 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-20+1797C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56765211 | |||||||
| chr12:56765218 | C | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0037 others(15): Show |
20 | HG01074.hp2 HG01109.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20+1804C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56765218 | |||||||
| chr12:56765945 | A | G | 8 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | HG00609.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2531A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56765945 | |||||||
| chr12:56766071 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01099.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-20+2657T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56766071 | |||||||
| chr12:56766224 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-20+2810G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56766224 | |||||||
| chr12:56766300 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-20+2886T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56766300 | |||||||
| chr12:56766326 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG02257.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20+2912G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56766326 | |||||||
| chr12:56767139 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+3725C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767139 | |||||||
| chr12:56767141 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+3727C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767141 | |||||||
| chr12:56767242 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-20+3828G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767242 | |||||||
| chr12:56767251 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-20+3837G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767251 | |||||||
| chr12:56767294 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01109.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-20+3880C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767294 | |||||||
| chr12:56767328 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-20+3914C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767328 | |||||||
| chr12:56767373 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-20+3959C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767373 | |||||||
| chr12:56767401 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-20+3987C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767401 | |||||||
| chr12:56767626 | T | TATATA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-20+4213_-20+4217d others(7): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56767626 | ||||||
| chr12:56767632 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0252 |
2 | HG02976.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-20+4218T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767632 | |||||||
| chr12:56767750 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0044 others(12): Show |
17 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+4336C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767750 | |||||||
| chr12:56767753 | A | T | 1 | a0001c0001t0001g0285 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-20+4339A>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767753 | |||||||
| chr12:56767781 | ATGTATAT others(14): Show |
A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
16 | HG02074.hp2 NA18940.hp2 NA18945.hp1 others(13): Show |
intron_variant | MODIFIER | c.-20+4398_-20+4418d others(23): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56767781 | ||||||
| chr12:56767864 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-20+4450C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767864 | |||||||
| chr12:56767909 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-20+4495C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767909 | |||||||
| chr12:56767930 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02622.hp2 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-20+4516C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767930 | |||||||
| chr12:56767955 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0210 |
5 | HG00140.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+4541A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767955 | |||||||
| chr12:56767971 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-20+4557G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56767971 | |||||||
| chr12:56768128 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-20+4714C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56768128 | |||||||
| chr12:56768208 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-20+4794A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56768208 | |||||||
| chr12:56768767 | C | CG | 10 | a0001c0001t0001g0051 a0001c0001t0001g0068 a0001c0001t0001g0154 others(7): Show |
10 | HG00558.hp1 HG00597.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-5060dupG | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56768767 | ||||||
| chr12:56768881 | T | G | 1 | a0001c0001t0001g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19-4953T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56768881 | |||||||
| chr12:56768922 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19-4912A>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56768922 | |||||||
| chr12:56769103 | G | GT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-19-4714dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56769103 | ||||||
| chr12:56769103 | G | GTT | 26 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0077 others(23): Show |
27 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19-4715_-19-4714d others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56769103 | ||||||
| chr12:56769213 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-19-4621G>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56769213 | |||||||
| chr12:56769460 | G | C | 1 | a0001c0001t0001g0026 | 2 | NA18943.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-19-4374G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56769460 | |||||||
| chr12:56769480 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-19-4354A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56769480 | |||||||
| chr12:56769530 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-19-4304C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56769530 | |||||||
| chr12:56769532 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-19-4302C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56769532 | |||||||
| chr12:56769781 | C | CCA | 3 | a0001c0001t0001g0246 a0001c0001t0001g0253 a0001c0001t0001g0276 |
3 | HG00438.hp1 HG00558.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-19-4051_-19-4050d others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56769781 | ||||||
| chr12:56769882 | C | CT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-19-3950dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56769882 | ||||||
| chr12:56770025 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19-3809C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56770025 | |||||||
| chr12:56770219 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-3615A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56770219 | |||||||
| chr12:56770331 | A | G | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-3503A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56770331 | |||||||
| chr12:56770338 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0280 |
2 | NA19079.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-19-3496C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56770338 | |||||||
| chr12:56770344 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-19-3490G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56770344 | |||||||
| chr12:56770806 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-3028G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56770806 | |||||||
| chr12:56771124 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2710T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771124 | |||||||
| chr12:56771126 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2708A>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771126 | |||||||
| chr12:56771127 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2707G>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771127 | |||||||
| chr12:56771129 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2705C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771129 | |||||||
| chr12:56771130 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2704T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771130 | |||||||
| chr12:56771135 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2699G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771135 | |||||||
| chr12:56771136 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2698G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771136 | |||||||
| chr12:56771137 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2697C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771137 | |||||||
| chr12:56771143 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2691T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771143 | |||||||
| chr12:56771146 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2688G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771146 | |||||||
| chr12:56771147 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2687A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771147 | |||||||
| chr12:56771151 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2683T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771151 | |||||||
| chr12:56771153 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2681T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771153 | |||||||
| chr12:56771154 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2680T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771154 | |||||||
| chr12:56771155 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2679G>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771155 | |||||||
| chr12:56771162 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2672T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771162 | |||||||
| chr12:56771168 | A | T | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2666A>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771168 | |||||||
| chr12:56771170 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2664T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771170 | |||||||
| chr12:56771171 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2663C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771171 | |||||||
| chr12:56771172 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2662T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771172 | |||||||
| chr12:56771173 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2661A>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771173 | |||||||
| chr12:56771184 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2650T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771184 | |||||||
| chr12:56771185 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2649A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771185 | |||||||
| chr12:56771190 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2644C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771190 | |||||||
| chr12:56771191 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2643T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771191 | |||||||
| chr12:56771193 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2641C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771193 | |||||||
| chr12:56771202 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2632T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771202 | |||||||
| chr12:56771209 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2625C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771209 | |||||||
| chr12:56771210 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2624T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771210 | |||||||
| chr12:56771214 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2620T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771214 | |||||||
| chr12:56771220 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2614G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771220 | |||||||
| chr12:56771224 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2610T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771224 | |||||||
| chr12:56771229 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2605T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771229 | |||||||
| chr12:56771236 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2598T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771236 | |||||||
| chr12:56771237 | ACCACCTA others(3): Show |
A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2595_-19-2586d others(12): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56771237 | ||||||
| chr12:56771248 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2586C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771248 | |||||||
| chr12:56771252 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2582G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771252 | |||||||
| chr12:56771253 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2581C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771253 | |||||||
| chr12:56771254 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2580C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771254 | |||||||
| chr12:56771256 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2578T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771256 | |||||||
| chr12:56771261 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2573C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771261 | |||||||
| chr12:56771262 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2572T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771262 | |||||||
| chr12:56771263 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2571T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771263 | |||||||
| chr12:56771264 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2570T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771264 | |||||||
| chr12:56771266 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2568T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771266 | |||||||
| chr12:56771268 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2566C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771268 | |||||||
| chr12:56771269 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2565T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771269 | |||||||
| chr12:56771271 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19-2563T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771271 | |||||||
| chr12:56771448 | A | AT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0104 others(4): Show |
10 | HG00741.hp1 HG01358.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-2362dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56771448 | ||||||
| chr12:56771448 | AT | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.-19-2362delT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56771448 | ||||||
| chr12:56771448 | ATT | A | 7 | a0001c0001t0001g0084 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG00323.hp2 HG02015.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2363_-19-2362d others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56771448 | ||||||
| chr12:56771490 | G | A | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-19-2344G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771490 | |||||||
| chr12:56771586 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0168 |
2 | NA18945.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-19-2248G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56771586 | |||||||
| chr12:56772153 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-19-1681C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772153 | |||||||
| chr12:56772162 | G | A | 1 | a0001c0001t0001g0020 | 2 | NA19080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-19-1672G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772162 | |||||||
| chr12:56772357 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19-1477T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772357 | |||||||
| chr12:56772452 | T | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0060 |
2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-1382T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772452 | |||||||
| chr12:56772588 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0003c0004t0001g0034 |
3 | HG01978.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-19-1246C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772588 | |||||||
| chr12:56772629 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(77): Show |
94 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-19-1205G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772629 | |||||||
| chr12:56772697 | C | CA | 8 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0001g0113 others(5): Show |
8 | HG00738.hp1 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-1121dupA | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56772697 | ||||||
| chr12:56772703 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-1118_-19-1108d others(13): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56772703 | ||||||
| chr12:56772714 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0152 a0001c0001t0001g0239 others(1): Show |
4 | HG01106.hp1 HG04199.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1120G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772714 | |||||||
| chr12:56772714 | GA | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-19-1110delA | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 56772714 | ||||||
| chr12:56772715 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0075 a0001c0001t0001g0076 others(6): Show |
9 | HG01106.hp1 HG02486.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-1119A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772715 | |||||||
| chr12:56772837 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0280 |
2 | NA19079.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-19-997A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56772837 | |||||||
| chr12:56773115 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-19-719C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773115 | |||||||
| chr12:56773202 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0041 others(12): Show |
16 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-632C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773202 | |||||||
| chr12:56773319 | A | C | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-19-515A>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773319 | |||||||
| chr12:56773320 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-19-514C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773320 | |||||||
| chr12:56773410 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-19-424G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773410 | |||||||
| chr12:56773588 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19-246T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773588 | |||||||
| chr12:56773705 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0106 |
3 | HG01891.hp1 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-19-129G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773705 | |||||||
| chr12:56773726 | A | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0030 others(15): Show |
21 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19-108A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 1/4 | chr12 | 56773726 | |||||||
| chr12:56774236 | G | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
27 | HG00323.hp1 HG01081.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.313+71G>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56774236 | |||||||
| chr12:56774341 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
12 | HG00280.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+176A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56774341 | |||||||
| chr12:56774542 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.313+377T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56774542 | |||||||
| chr12:56774825 | T | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0030 others(15): Show |
21 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.313+660T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56774825 | |||||||
| chr12:56775044 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.313+879A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775044 | |||||||
| chr12:56775098 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0237 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.313+933T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775098 | |||||||
| chr12:56775103 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.313+938G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775103 | |||||||
| chr12:56775203 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.313+1038A>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775203 | |||||||
| chr12:56775322 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0209 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.313+1157A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775322 | |||||||
| chr12:56775363 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+1198G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775363 | |||||||
| chr12:56775374 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
153 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.313+1209T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775374 | |||||||
| chr12:56775641 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.313+1476C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775641 | |||||||
| chr12:56775878 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0041 others(10): Show |
14 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.313+1713C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56775878 | |||||||
| chr12:56776034 | G | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.313+1869G>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56776034 | |||||||
| chr12:56776304 | C | CT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
189 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.313+2157dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56776304 | ||||||
| chr12:56776304 | C | CTT | 22 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0030 others(19): Show |
25 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.313+2156_313+2157d others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56776304 | ||||||
| chr12:56776304 | CT | C | 6 | a0001c0001t0001g0128 a0001c0001t0001g0181 a0001c0001t0001g0183 others(3): Show |
6 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+2157delT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56776304 | ||||||
| chr12:56776386 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0202 |
2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.313+2221C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56776386 | |||||||
| chr12:56776556 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.313+2391C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56776556 | |||||||
| chr12:56776677 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.313+2512G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56776677 | |||||||
| chr12:56776710 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.313+2545G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56776710 | |||||||
| chr12:56776820 | C | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | NA18939.hp2 NA18941.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+2655C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56776820 | |||||||
| chr12:56776952 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.313+2787T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56776952 | |||||||
| chr12:56777245 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.313+3080A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777245 | |||||||
| chr12:56777320 | T | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0041 others(13): Show |
18 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.313+3155T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777320 | |||||||
| chr12:56777365 | A | ATTTTTT | 38 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0017 others(35): Show |
41 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.313+3210_313+3215d others(8): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56777365 | ||||||
| chr12:56777365 | A | ATTTTTTT | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
112 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.313+3209_313+3215d others(9): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56777365 | ||||||
| chr12:56777365 | A | ATTTTTTT others(1): Show |
15 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
18 | HG01257.hp2 HG01258.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.313+3208_313+3215d others(10): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56777365 | ||||||
| chr12:56777408 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.313+3243C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777408 | |||||||
| chr12:56777415 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.313+3250C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777415 | |||||||
| chr12:56777428 | G | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0234 |
3 | HG02258.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.313+3263G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777428 | |||||||
| chr12:56777435 | G | A | 2 | a0001c0001t0001g0007 a0001c0002t0001g0211 |
5 | HG02055.hp1 HG02559.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+3270G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777435 | |||||||
| chr12:56777594 | C | G | 4 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0001g0115 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+3429C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777594 | |||||||
| chr12:56777732 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
100 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.313+3567T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56777732 | |||||||
| chr12:56778053 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
5 | HG01074.hp2 HG01167.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+3888C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56778053 | |||||||
| chr12:56778101 | T | C | 7 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0001g0113 others(4): Show |
7 | HG00738.hp1 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-3873T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56778101 | |||||||
| chr12:56778155 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.314-3819T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56778155 | |||||||
| chr12:56778557 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
106 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.314-3417A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56778557 | |||||||
| chr12:56778614 | C | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0208 |
2 | NA19043.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.314-3360C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56778614 | |||||||
| chr12:56778674 | C | CT | 14 | a0001c0001t0001g0031 a0001c0001t0001g0055 a0001c0001t0001g0060 others(11): Show |
14 | HG01081.hp1 HG02074.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-3282dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56778674 | ||||||
| chr12:56778674 | CT | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(22): Show |
31 | HG00280.hp2 HG01169.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.314-3282delT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56778674 | ||||||
| chr12:56778787 | G | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(23): Show |
32 | HG00280.hp2 HG00738.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.314-3187G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56778787 | |||||||
| chr12:56779087 | AT | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
191 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.314-2876delT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56779087 | ||||||
| chr12:56779350 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0237 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.314-2624C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56779350 | |||||||
| chr12:56779437 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.314-2537C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56779437 | |||||||
| chr12:56779801 | C | CT | 138 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
157 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.314-2158dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56779801 | ||||||
| chr12:56779801 | C | CTT | 28 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(25): Show |
34 | HG00280.hp2 HG00738.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.314-2159_314-2158d others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56779801 | ||||||
| chr12:56780000 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0248 |
2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.314-1974C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780000 | |||||||
| chr12:56780090 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.314-1884C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780090 | |||||||
| chr12:56780616 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.314-1358T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780616 | |||||||
| chr12:56780646 | C | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0003c0004t0001g0034 |
3 | HG01978.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.314-1328C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780646 | |||||||
| chr12:56780739 | C | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(22): Show |
31 | HG00280.hp2 HG00738.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.314-1235C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780739 | |||||||
| chr12:56780776 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.314-1198G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780776 | |||||||
| chr12:56780836 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0003c0004t0001g0034 |
3 | HG01978.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.314-1138G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780836 | |||||||
| chr12:56780840 | C | CA | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(106): Show |
129 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.314-1110dupA | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56780840 | ||||||
| chr12:56780840 | C | CAA | 17 | a0001c0001t0001g0039 a0001c0001t0001g0111 a0001c0001t0001g0129 others(14): Show |
17 | HG01361.hp2 HG01934.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.314-1111_314-1110d others(4): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56780840 | ||||||
| chr12:56780840 | CA | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0028 others(17): Show |
23 | HG01069.hp2 HG01109.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.314-1110delA | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56780840 | ||||||
| chr12:56780966 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.314-1008T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56780966 | |||||||
| chr12:56781028 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.314-946C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56781028 | |||||||
| chr12:56781094 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.314-880G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56781094 | |||||||
| chr12:56781472 | GTATTT | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0237 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.314-499_314-495del others(5): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 56781472 | ||||||
| chr12:56781495 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.314-479C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56781495 | |||||||
| chr12:56781585 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0237 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.314-389C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56781585 | |||||||
| chr12:56781844 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.314-130T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56781844 | |||||||
| chr12:56781896 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.314-78A>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56781896 | |||||||
| chr12:56781906 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.314-68C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 2/4 | chr12 | 56781906 | |||||||
| chr12:56782305 | C | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(44): Show |
54 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.572+73C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782305 | |||||||
| chr12:56782315 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.572+83T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782315 | |||||||
| chr12:56782391 | C | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
193 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.572+159C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782391 | |||||||
| chr12:56782402 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
193 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.572+170G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782402 | |||||||
| chr12:56782596 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.572+364C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782596 | |||||||
| chr12:56782617 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.572+385C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782617 | |||||||
| chr12:56782660 | A | AT | 14 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0053 others(11): Show |
14 | HG00280.hp1 HG00741.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.572+448dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56782660 | ||||||
| chr12:56782660 | AT | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
110 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.572+448delT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56782660 | ||||||
| chr12:56782663 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.572+431T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782663 | |||||||
| chr12:56782681 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.572+449A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782681 | |||||||
| chr12:56782705 | G | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0234 others(1): Show |
8 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+473G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782705 | |||||||
| chr12:56782715 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.572+483A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56782715 | |||||||
| chr12:56783007 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.572+775A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783007 | |||||||
| chr12:56783039 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.572+807T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783039 | |||||||
| chr12:56783044 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.572+812T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783044 | |||||||
| chr12:56783093 | G | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0075 others(13): Show |
17 | HG00609.hp2 HG01109.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.572+861G>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783093 | |||||||
| chr12:56783130 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.572+898A>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783130 | |||||||
| chr12:56783152 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.572+920T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783152 | |||||||
| chr12:56783243 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0261 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.572+1011C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783243 | |||||||
| chr12:56783297 | C | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0003c0004t0001g0034 |
3 | HG01978.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.572+1065C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783297 | |||||||
| chr12:56783310 | GGGGGGCT others(42): Show |
G | 32 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0059 others(29): Show |
33 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.572+1129_572+1177d others(51): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56783310 | ||||||
| chr12:56783343 | G | A | 31 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0031 others(28): Show |
33 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.572+1111G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783343 | |||||||
| chr12:56783357 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.572+1125G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783357 | |||||||
| chr12:56783386 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.572+1154C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783386 | |||||||
| chr12:56783434 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.572+1202G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783434 | |||||||
| chr12:56783440 | C | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(48): Show |
58 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.572+1208C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783440 | |||||||
| chr12:56783477 | TGGCCGGG others(42): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.572+1258_572+1306d others(51): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56783477 | ||||||
| chr12:56783485 | C | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0037 others(15): Show |
20 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.572+1253C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783485 | |||||||
| chr12:56783514 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.572+1282G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783514 | |||||||
| chr12:56783521 | G | GCGGCCGG others(44): Show |
1 | a0001c0001t0001g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.572+1294_573-1277d others(53): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56783521 | ||||||
| chr12:56783526 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0260 |
2 | NA18966.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.572+1294C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783526 | |||||||
| chr12:56783547 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0126 a0001c0001t0001g0235 |
3 | HG02647.hp2 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.573-1306C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783547 | |||||||
| chr12:56783564 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0051 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.573-1289C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783564 | |||||||
| chr12:56783585 | C | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0031 others(29): Show |
34 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.573-1268C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783585 | |||||||
| chr12:56783620 | GCGGCTGG others(43): Show |
G | 30 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0031 others(27): Show |
32 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.573-1220_573-1171d others(52): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56783620 | ||||||
| chr12:56783622 | G | A | 48 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(45): Show |
55 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.573-1231G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783622 | |||||||
| chr12:56783630 | G | C | 1 | a0001c0001t0001g0007 | 3 | HG02559.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.573-1223G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783630 | |||||||
| chr12:56783633 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.573-1220T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783633 | |||||||
| chr12:56783643 | AC | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.573-1202delC | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56783643 | ||||||
| chr12:56783644 | CCCCCCCC others(42): Show |
C | 1 | a0001c0001t0001g0081 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.573-1202_573-1154d others(51): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56783644 | ||||||
| chr12:56783645 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.573-1208C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783645 | |||||||
| chr12:56783671 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.573-1182C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783671 | |||||||
| chr12:56783672 | G | A | 30 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0031 others(27): Show |
32 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.573-1181G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783672 | |||||||
| chr12:56783684 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0237 |
3 | HG02055.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.573-1169G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783684 | |||||||
| chr12:56783704 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.573-1149C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783704 | |||||||
| chr12:56783791 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573-1062G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783791 | |||||||
| chr12:56783792 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.573-1061G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783792 | |||||||
| chr12:56783794 | C | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0286 |
2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.573-1059C>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783794 | |||||||
| chr12:56783794 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0057 a0001c0001t0001g0061 others(2): Show |
6 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.573-1059C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783794 | |||||||
| chr12:56783814 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.573-1039G>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783814 | |||||||
| chr12:56783869 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG01358.hp1 HG01993.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.573-984C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783869 | |||||||
| chr12:56783925 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.573-928C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783925 | |||||||
| chr12:56783926 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.573-927G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783926 | |||||||
| chr12:56783949 | C | G | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0297 |
3 | HG00597.hp2 NA18987.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.573-904C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56783949 | |||||||
| chr12:56784020 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.573-833G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784020 | |||||||
| chr12:56784029 | A | G | 29 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0059 others(26): Show |
30 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.573-824A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784029 | |||||||
| chr12:56784034 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0149 |
3 | HG01081.hp2 HG01243.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.573-819A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784034 | |||||||
| chr12:56784037 | C | CG | 4 | a0001c0001t0001g0041 a0001c0001t0001g0138 a0001c0001t0001g0156 others(1): Show |
4 | HG01099.hp1 HG03098.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.573-812dupG | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56784037 | ||||||
| chr12:56784038 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.573-815G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784038 | |||||||
| chr12:56784075 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.573-778G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784075 | |||||||
| chr12:56784079 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.573-774G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784079 | |||||||
| chr12:56784086 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.573-767G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784086 | |||||||
| chr12:56784125 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0260 |
2 | NA18966.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.573-728C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784125 | |||||||
| chr12:56784130 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0106 |
3 | HG01891.hp1 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.573-723A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784130 | |||||||
| chr12:56784161 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.573-692C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784161 | |||||||
| chr12:56784175 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.573-678C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784175 | |||||||
| chr12:56784251 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.573-602C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784251 | |||||||
| chr12:56784280 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573-573C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784280 | |||||||
| chr12:56784285 | C | G | 1 | a0001c0001t0001g0011 | 2 | HG00140.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.573-568C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784285 | |||||||
| chr12:56784308 | TG | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0035 others(2): Show |
6 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-542delG | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56784308 | ||||||
| chr12:56784324 | G | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0115 |
2 | HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.573-529G>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784324 | |||||||
| chr12:56784379 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.573-474T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784379 | |||||||
| chr12:56784458 | C | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
101 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.573-395C>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784458 | |||||||
| chr12:56784478 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0042 others(12): Show |
21 | HG00642.hp2 HG00738.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.573-375C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784478 | |||||||
| chr12:56784479 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.573-374G>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784479 | |||||||
| chr12:56784545 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
106 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.573-308T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | chr12 | 56784545 | |||||||
| chr12:56784704 | CGAGGGAG others(5): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.573-134_573-123del others(12): Show |
HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 56784704 | ||||||
| chr12:56785168 | T | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0283 |
2 | NA18948.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.736+152T>A | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56785168 | |||||||
| chr12:56785319 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.736+303C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56785319 | |||||||
| chr12:56785556 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(12): Show |
20 | HG00280.hp2 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.736+540C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56785556 | |||||||
| chr12:56785755 | A | AC | 188 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
214 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.736+741dupC | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 56785755 | ||||||
| chr12:56786111 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.737-1014C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56786111 | |||||||
| chr12:56786249 | G | GT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0086 a0001c0001t0001g0091 others(6): Show |
10 | HG00140.hp1 HG01123.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.737-858dupT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 56786249 | ||||||
| chr12:56786249 | GT | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
111 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.737-858delT | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 56786249 | ||||||
| chr12:56786250 | T | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0093 a0001c0001t0001g0095 |
3 | HG02056.hp2 NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.737-875T>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56786250 | |||||||
| chr12:56786305 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.737-820A>G | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56786305 | |||||||
| chr12:56786342 | CG | C | 22 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0162 others(19): Show |
23 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.737-780delG | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 56786342 | ||||||
| chr12:56786692 | A | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0037 others(15): Show |
20 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.737-433A>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56786692 | |||||||
| chr12:56786972 | T | C | 29 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0059 others(26): Show |
30 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.737-153T>C | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56786972 | |||||||
| chr12:56787071 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
104 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.737-54C>T | HSD17B6 | ENSG00000025423.11 | transcript | ENST00000322165.1 | protein_coding | 4/4 | chr12 | 56787071 |