Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3293 |
|---|---|
| ensemblid | ENSG00000130948.10 |
| hgncid | 5212 |
| symbol | HSD17B3 |
| name | hydroxysteroid 17-beta dehydrogenase 3 |
| refseq_nuc | NM_000197.2 |
| refseq_prot | NP_000188.1 |
| ensembl_nuc | ENST00000375263.8 |
| ensembl_prot | ENSP00000364412.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 96235306 |
| end | 96302176 |
| strand | - |
| ver | v1.2 |
| region | chr9:96235306-96302176 |
| region5000 | chr9:96230306-96307176 |
| regionname0 | HSD17B3_chr9_96235306_96302176 |
| regionname5000 | HSD17B3_chr9_96230306_96307176 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 310 | 294 | 69 | 64 | 109 | 11 | 39 | 75 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0002 | 0/0 | 310 | 58 | 5 | 7 | 39 | 1 | 6 | 29 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0003 | 0/0 | 310 | 15 | 0 | 0 | 11 | 0 | 4 | 9 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0004 | 0/0 | 310 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0005 | 0/0 | 310 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0006 | 0/0 | 310 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0007 | 0/0 | 310 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0008 | 0/0 | 310 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0009 | 0/0 | 310 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 933 | 292 | 68 | 64 | 108 | 11 | 39 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0002 | 0/0 | 933 | 58 | 5 | 7 | 39 | 1 | 6 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0003 | 0/0 | 933 | 15 | 0 | 0 | 11 | 0 | 4 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0004 | 0/0 | 933 | 2 | 0 | 1 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0005 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0006 | 0/0 | 933 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0007 | 0/0 | 933 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0008 | 0/0 | 933 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0009 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0010 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| c0011 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 227 | 225 | 59 | 54 | 61 | 12 | 37 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| t0002 | 0/0 | 227 | 103 | 15 | 18 | 63 | 0 | 7 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| t0003 | 0/0 | 227 | 30 | 0 | 2 | 27 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| t0004 | 0/0 | 227 | 16 | 0 | 0 | 11 | 0 | 5 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 933 | 292 | 68 | 64 | 108 | 11 | 39 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0001c0009 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0001c0010 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0002c0002 | 0/0 | 933 | 58 | 5 | 7 | 39 | 1 | 6 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0003c0003 | 0/0 | 933 | 15 | 0 | 0 | 11 | 0 | 4 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0004c0004 | 0/0 | 933 | 2 | 0 | 1 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0005c0005 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0006c0006 | 0/0 | 933 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0007c0008 | 0/0 | 933 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0008c0011 | 0/0 | 933 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0009c0007 | 0/0 | 933 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1159 | 191 | 55 | 49 | 41 | 11 | 33 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0001c0001t0002 | 0/0 | 1159 | 74 | 13 | 13 | 43 | 0 | 5 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0001c0001t0003 | 0/0 | 1159 | 27 | 0 | 2 | 24 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0001c0009t0003 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0001c0010t0001 | 0/0 | 1159 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0002c0002t0001 | 0/0 | 1159 | 29 | 3 | 3 | 18 | 1 | 4 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0002c0002t0002 | 0/0 | 1159 | 27 | 2 | 4 | 19 | 0 | 2 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0002c0002t0003 | 0/0 | 1159 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0003c0003t0004 | 0/0 | 1159 | 15 | 0 | 0 | 11 | 0 | 4 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0004c0004t0001 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0004c0004t0002 | 0/0 | 1159 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0005c0005t0002 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0006c0006t0004 | 0/0 | 1159 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0007c0008t0001 | 0/0 | 1159 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0008c0011t0001 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| a0009c0007t0001 | 0/0 | 1159 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | copy fasta | chr9 | 96230306 | 96307176 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0009t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0001c0010t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0003c0003t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0004c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0004c0004t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0005c0005t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0006c0006t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0007c0008t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0008c0011t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| a0009c0007t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0314 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0338 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00621 | hp2 | a0003 | c0003 | t0004 | g0260 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0362 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0363 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0277 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0370 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0371 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01192 | hp2 | a0004 | c0004 | t0002 | g0374 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01952 | hp1 | a0007 | c0008 | t0001 | g0154 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0302 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0333 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02071 | hp2 | a0003 | c0003 | t0004 | g0261 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0340 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | CDX | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | CDX | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02300 | hp1 | a0009 | c0007 | t0001 | g0208 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0327 | EAS | KHV | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0367 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0361 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02683 | hp2 | a0003 | c0003 | t0004 | g0263 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0359 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02976 | hp1 | a0001 | c0010 | t0001 | g0010 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0360 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0365 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0373 | AFR | ESN | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0368 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0366 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0348 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03704 | hp2 | a0006 | c0006 | t0004 | g0257 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0369 | SAS | PJL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03834 | hp1 | a0003 | c0003 | t0004 | g0258 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03942 | hp1 | a0003 | c0003 | t0004 | g0270 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04115 | hp1 | a0003 | c0003 | t0004 | g0271 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | BEB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0372 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0357 | AFR | YRI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0326 | EAS | CHB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | CHB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | CHB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18939 | hp1 | a0003 | c0003 | t0004 | g0262 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0353 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18956 | hp2 | a0003 | c0003 | t0004 | g0269 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18963 | hp1 | a0008 | c0011 | t0001 | g0178 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18966 | hp2 | a0003 | c0003 | t0004 | g0267 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18970 | hp2 | a0001 | c0009 | t0003 | g0238 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18980 | hp2 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0325 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18990 | hp2 | a0003 | c0003 | t0004 | g0264 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18991 | hp1 | a0003 | c0003 | t0004 | g0265 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0354 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18998 | hp1 | a0003 | c0003 | t0004 | g0256 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19007 | hp2 | a0003 | c0003 | t0004 | g0266 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0317 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19065 | hp2 | a0003 | c0003 | t0004 | g0268 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19066 | hp2 | a0004 | c0004 | t0001 | g0225 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19067 | hp1 | a0005 | c0005 | t0002 | g0272 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19074 | hp2 | a0003 | c0003 | t0004 | g0259 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19076 | hp2 | a0002 | c0002 | t0003 | g0250 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0301 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | YRI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0356 | AFR | ASW | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0185 | EUR | TSI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | TSI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | USA | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | USA | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | LWK | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0051 | REF | REF | HSD17B3_chr9_96230306_96307176 | HSD17B3 | chr9 | 96230306 | 96307176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96235528
|
C | T | 3 | a0002a0006a0008 | 60 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(57): Show |
missense_variant | MODERATE | c.865G>A | p.Gly289Ser | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 11/11 | 937/1159 | 865/933 | 289/310 | chr9 | 96235528 | ||
| chr9:96244382
|
C | T | 1 | a0007 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.619G>A | p.Ala207Thr | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/11 | 691/1159 | 619/933 | 207/310 | chr9 | 96244382 | ||
| chr9:96249768
|
T | C | 1 | a0008 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.472A>G | p.Ile158Val | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/11 | 544/1159 | 472/933 | 158/310 | chr9 | 96249768 | ||
| chr9:96252848
|
C | T | 1 | a0009 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.340G>A | p.Glu114Lys | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/11 | 412/1159 | 340/933 | 114/310 | chr9 | 96252848 | ||
| chr9:96301966
|
T | C | 1 | a0004 | 2 | HG01192.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.139A>G | p.Met47Val | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/11 | 211/1159 | 139/933 | 47/310 | chr9 | 96301966 | ||
| chr9:96302014
|
C | T | 2 | a0003a0006 | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
missense_variant | MODERATE | c.91G>A | p.Val31Ile | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/11 | 163/1159 | 91/933 | 31/310 | chr9 | 96302014 | ||
| chr9:96302032
|
C | T | 1 | a0005 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.73G>A | p.Val25Met | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/11 | 145/1159 | 73/933 | 25/310 | chr9 | 96302032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96235568
|
C | T | 1 | a0001c0009 | 1 | NA18970.hp2 | splice_region_variant&synonymous_variant | LOW | c.825G>A | p.Ala275Ala | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 11/11 | 897/1159 | 825/933 | 275/310 | chr9 | 96235568 | ||
| chr9:96240776
|
G | A | 1 | a0001c0010 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.804C>T | p.Cys268Cys | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/11 | 876/1159 | 804/933 | 268/310 | chr9 | 96240776 | ||
| chr9:96298422
|
C | T | 2 | a0003c0003a0006c0006 | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
synonymous_variant | LOW | c.195G>A | p.Ser65Ser | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/11 | 267/1159 | 195/933 | 65/310 | chr9 | 96298422 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96302114
|
C | G | 2 | a0003c0003t0004a0006c0006t0004 | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/11 | 10 | chr9 | 96302114 | |||||
| chr9:96302133
|
T | C | 3 | a0001c0001t0003a0001c0009t0003a0002c0002t0003 | 30 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-29A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/11 | 29 | chr9 | 96302133 | |||||
| chr9:96302143
|
T | C | 6 | a0001c0001t0002a0002c0002t0002a0003c0003t0004others(3): Show | 119 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(116): Show |
5_prime_UTR_variant | MODIFIER | c.-39A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/11 | 39 | chr9 | 96302143 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:96235628
|
ATCTTTGT others(2): Show |
A | 157 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0021others(154): Show | 157 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.823-67_823-59delCC others(7): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96235628 | ||||||
| chr9:96235779
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.823-209A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96235779 | ||||||
| chr9:96235811
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0003g0231a0001c0009t0003g0238 | 3 | NA18970.hp2 NA18983.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.823-241A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96235811 | ||||||
| chr9:96235906
|
A | C | 2 | a0001c0001t0001g0149a0001c0001t0002g0368 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.823-336T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96235906 | ||||||
| chr9:96236003
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.823-433A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236003 | ||||||
| chr9:96236037
|
C | T | 162 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0021others(159): Show | 162 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.823-467G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236037 | ||||||
| chr9:96236081
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-511T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236081 | ||||||
| chr9:96236186
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0036others(1): Show | 4 | HG01243.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-616G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236186 | ||||||
| chr9:96236249
|
G | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(122): Show | 125 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.823-679C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236249 | ||||||
| chr9:96236346
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.823-776C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236346 | ||||||
| chr9:96236378
|
A | G | 15 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0111others(12): Show | 15 | HG00673.hp1 HG02155.hp1 HG04184.hp2 others(12): Show |
intron_variant | MODIFIER | c.823-808T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236378 | ||||||
| chr9:96236410
|
G | A | 1 | a0002c0002t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823-840C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236410 | ||||||
| chr9:96236514
|
C | CATAA | 89 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.823-948_823-945dup others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236514 | ||||||
| chr9:96236514
|
C | CATAAATA others(1): Show |
102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 102 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.823-952_823-945dup others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236514 | ||||||
| chr9:96236514
|
C | CATAAATA others(5): Show |
18 | a0001c0001t0001g0033a0001c0001t0001g0127a0001c0001t0001g0158others(15): Show | 18 | HG00280.hp2 HG00544.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.823-956_823-945dup others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236514 | ||||||
| chr9:96236514
|
C | CATAAATA others(9): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0128a0001c0001t0001g0147others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-960_823-945dup others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236514 | ||||||
| chr9:96236514
|
CATAA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0160others(3): Show | 6 | HG02683.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-948_823-945del others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236514 | ||||||
| chr9:96236514
|
CATAAATA others(9): Show |
C | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823-960_823-945del others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236514 | ||||||
| chr9:96236688
|
G | T | 8 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0145others(5): Show | 8 | HG00323.hp2 HG01255.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-1118C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236688 | ||||||
| chr9:96236689
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.823-1119G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96236689 | ||||||
| chr9:96237061
|
G | A | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00423.hp1 HG01070.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.823-1491C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237061 | ||||||
| chr9:96237109
|
C | G | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823-1539G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237109 | ||||||
| chr9:96237110
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00423.hp1 HG01070.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.823-1540C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237110 | ||||||
| chr9:96237110
|
G | C | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.823-1540C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237110 | ||||||
| chr9:96237135
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823-1565G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237135 | ||||||
| chr9:96237269
|
T | C | 1 | a0001c0001t0002g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823-1699A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237269 | ||||||
| chr9:96237542
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00423.hp1 HG01070.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.823-1972C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237542 | ||||||
| chr9:96237568
|
T | C | 107 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0028others(104): Show | 107 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.823-1998A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96237568 | ||||||
| chr9:96238061
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.823-2491C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96238061 | ||||||
| chr9:96238244
|
G | A | 76 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0036others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.822+2514C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96238244 | ||||||
| chr9:96238300
|
T | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0021others(155): Show | 158 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.822+2458A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96238300 | ||||||
| chr9:96238352
|
A | T | 1 | a0002c0002t0002g0338 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.822+2406T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96238352 | ||||||
| chr9:96238637
|
G | A | 76 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0036others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.822+2121C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96238637 | ||||||
| chr9:96238690
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.822+2068A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96238690 | ||||||
| chr9:96238729
|
G | A | 1 | a0002c0002t0002g0327 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.822+2029C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96238729 | ||||||
| chr9:96239213
|
C | T | 56 | a0002c0002t0001g0030a0002c0002t0001g0058a0002c0002t0001g0063others(53): Show | 56 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.822+1545G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239213 | ||||||
| chr9:96239243
|
C | T | 195 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(192): Show | 195 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.822+1515G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239243 | ||||||
| chr9:96239271
|
G | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0158a0001c0001t0001g0169others(1): Show | 4 | HG01952.hp1 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+1487C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239271 | ||||||
| chr9:96239430
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.822+1328A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239430 | ||||||
| chr9:96239453
|
T | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0036others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.822+1305A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239453 | ||||||
| chr9:96239761
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.822+997C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239761 | ||||||
| chr9:96239837
|
T | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.822+921A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239837 | ||||||
| chr9:96239844
|
GT | G | 157 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0021others(154): Show | 157 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.822+913delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239844 | ||||||
| chr9:96239903
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00423.hp1 HG01070.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.822+855G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239903 | ||||||
| chr9:96239971
|
C | A | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 325 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.822+787G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96239971 | ||||||
| chr9:96240060
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0130others(8): Show | 11 | HG01069.hp2 HG01099.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.822+698G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240060 | ||||||
| chr9:96240113
|
C | T | 1 | a0001c0001t0002g0343 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.822+645G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240113 | ||||||
| chr9:96240146
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0002g0355 | 3 | HG02922.hp2 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.822+612C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240146 | ||||||
| chr9:96240312
|
G | A | 271 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 271 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.822+446C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240312 | ||||||
| chr9:96240473
|
C | G | 271 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 271 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.822+285G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240473 | ||||||
| chr9:96240572
|
G | A | 76 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0036others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.822+186C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240572 | ||||||
| chr9:96240603
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0036others(2): Show | 5 | HG01243.hp2 HG02040.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+155G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240603 | ||||||
| chr9:96240719
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.822+39G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 10/10 | chr9 | 96240719 | ||||||
| chr9:96240950
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.673-43G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96240950 | ||||||
| chr9:96240982
|
C | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 325 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.673-75G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96240982 | ||||||
| chr9:96241251
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0075 | 2 | NA18959.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.673-344A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241251 | ||||||
| chr9:96241303
|
T | A | 1 | a0001c0001t0001g0209 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.673-396A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241303 | ||||||
| chr9:96241375
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(47): Show | 50 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.673-468A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241375 | ||||||
| chr9:96241656
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.673-749G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241656 | ||||||
| chr9:96241802
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.673-895C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241802 | ||||||
| chr9:96241890
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00423.hp1 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.673-983C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241890 | ||||||
| chr9:96241957
|
C | A | 271 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 271 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.673-1050G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241957 | ||||||
| chr9:96241961
|
A | AAAAAGAA others(6): Show |
1 | a0001c0001t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.673-1055_673-1054i others(15): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
A | AAAAG | 61 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(58): Show | 61 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.673-1058_673-1055d others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
A | AAAAGAAA others(1): Show |
60 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0018others(57): Show | 60 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.673-1062_673-1055d others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
A | AAAAGAAA others(5): Show |
65 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0022others(62): Show | 65 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.673-1066_673-1055d others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
A | AAAAGAAA others(9): Show |
48 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(45): Show | 48 | HG00609.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.673-1070_673-1055d others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
A | AAAAGAAA others(13): Show |
25 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0055others(22): Show | 25 | HG00323.hp1 HG01175.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.673-1074_673-1055d others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
A | AAAAGAAA others(17): Show |
7 | a0001c0001t0001g0147a0001c0001t0001g0196a0001c0001t0001g0220others(4): Show | 7 | HG00621.hp2 HG01109.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-1078_673-1055d others(26): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
AAAAG | A | 30 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0101others(27): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.673-1058_673-1055d others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
AAAAGAAA others(1): Show |
A | 4 | a0001c0001t0001g0082a0001c0001t0002g0290a0002c0002t0002g0314others(1): Show | 4 | HG00408.hp2 HG02027.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-1062_673-1055d others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
AAAAGAAA others(5): Show |
A | 1 | a0001c0001t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.673-1066_673-1055d others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241961
|
AAAAGAAA others(9): Show |
A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.673-1070_673-1055d others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241961 | ||||||
| chr9:96241974
|
A | AAAGAAAG others(4): Show |
1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.673-1078_673-1068d others(13): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96241974 | ||||||
| chr9:96242003
|
A | AAGAAAGA others(3): Show |
2 | a0001c0001t0001g0120a0003c0003t0004g0263 | 2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.673-1097_673-1096i others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242003 | ||||||
| chr9:96242005
|
G | GAGAA | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.673-1102_673-1099d others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242005 | ||||||
| chr9:96242007
|
G | A | 2 | a0002c0002t0001g0173a0003c0003t0004g0269 | 2 | NA18956.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.673-1100C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242007 | ||||||
| chr9:96242008
|
A | AGAAAGAA others(22): Show |
1 | a0003c0003t0004g0269 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.673-1102_673-1101i others(31): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242008 | ||||||
| chr9:96242032
|
T | TA | 76 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0036others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.673-1126dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242032 | ||||||
| chr9:96242412
|
C | A | 55 | a0002c0002t0001g0058a0002c0002t0001g0063a0002c0002t0001g0064others(52): Show | 55 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.673-1505G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242412 | ||||||
| chr9:96242449
|
C | T | 4 | a0003c0003t0004g0256a0003c0003t0004g0264a0003c0003t0004g0265others(1): Show | 4 | NA18990.hp2 NA18991.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-1542G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242449 | ||||||
| chr9:96242598
|
G | A | 1 | a0001c0001t0002g0364 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.673-1691C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242598 | ||||||
| chr9:96242766
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0066 | 2 | HG00438.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.672+1563A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242766 | ||||||
| chr9:96242914
|
C | G | 1 | a0001c0001t0002g0356 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.672+1415G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96242914 | ||||||
| chr9:96243133
|
G | A | 2 | a0001c0001t0001g0120a0003c0003t0004g0263 | 2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.672+1196C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243133 | ||||||
| chr9:96243320
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.672+1009G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243320 | ||||||
| chr9:96243425
|
G | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.672+904C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243425 | ||||||
| chr9:96243576
|
A | G | 1 | a0001c0001t0001g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.672+753T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243576 | ||||||
| chr9:96243639
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0002g0348 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.672+690C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243639 | ||||||
| chr9:96243699
|
A | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.672+630T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243699 | ||||||
| chr9:96243741
|
G | C | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.672+588C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243741 | ||||||
| chr9:96243778
|
G | A | 55 | a0002c0002t0001g0058a0002c0002t0001g0063a0002c0002t0001g0064others(52): Show | 55 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.672+551C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96243778 | ||||||
| chr9:96244176
|
C | G | 1 | a0001c0001t0002g0285 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.672+153G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96244176 | ||||||
| chr9:96244207
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.672+122G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96244207 | ||||||
| chr9:96244296
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 53 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.672+33A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 9/10 | chr9 | 96244296 | ||||||
| chr9:96244416
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.607-22G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244416 | ||||||
| chr9:96244417
|
C | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0180a0001c0001t0002g0368others(1): Show | 4 | HG02280.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-23G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244417 | ||||||
| chr9:96244442
|
G | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0180a0001c0001t0002g0368 | 3 | HG02280.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.607-48C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244442 | ||||||
| chr9:96244478
|
C | T | 1 | a0001c0001t0002g0373 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.607-84G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244478 | ||||||
| chr9:96244518
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0158 | 2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.607-124G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244518 | ||||||
| chr9:96244534
|
T | C | 5 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0155others(2): Show | 5 | HG01255.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-140A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244534 | ||||||
| chr9:96244597
|
A | C | 3 | a0002c0002t0002g0360a0002c0002t0002g0366a0007c0008t0001g0154 | 3 | HG01952.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.607-203T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244597 | ||||||
| chr9:96244607
|
T | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(190): Show | 193 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.607-213A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244607 | ||||||
| chr9:96244663
|
C | CA | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0160others(4): Show | 7 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.607-270dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244663 | ||||||
| chr9:96244675
|
C | T | 193 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(190): Show | 193 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.607-281G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244675 | ||||||
| chr9:96244796
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0180a0001c0001t0002g0368others(1): Show | 4 | HG02280.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-402G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244796 | ||||||
| chr9:96244885
|
C | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0013others(186): Show | 189 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.606+460G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96244885 | ||||||
| chr9:96245125
|
G | A | 55 | a0002c0002t0001g0058a0002c0002t0001g0063a0002c0002t0001g0064others(52): Show | 55 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.606+220C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96245125 | ||||||
| chr9:96245216
|
C | G | 1 | a0002c0002t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.606+129G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 8/10 | chr9 | 96245216 | ||||||
| chr9:96245542
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.525-116C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245542 | ||||||
| chr9:96245560
|
G | T | 1 | a0007c0008t0001g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.525-134C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245560 | ||||||
| chr9:96245561
|
C | T | 1 | a0007c0008t0001g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.525-135G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245561 | ||||||
| chr9:96245607
|
G | A | 2 | a0001c0001t0002g0310a0004c0004t0002g0374 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.525-181C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245607 | ||||||
| chr9:96245625
|
G | A | 321 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(318): Show | 321 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.525-199C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245625 | ||||||
| chr9:96245691
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.525-265A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245691 | ||||||
| chr9:96245948
|
T | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.525-522A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245948 | ||||||
| chr9:96245950
|
A | G | 1 | a0001c0001t0002g0351 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.525-524T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245950 | ||||||
| chr9:96245967
|
C | T | 4 | a0003c0003t0004g0260a0003c0003t0004g0262a0003c0003t0004g0267others(1): Show | 4 | HG00621.hp2 NA18939.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-541G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96245967 | ||||||
| chr9:96246112
|
G | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0180a0001c0001t0002g0368 | 3 | HG02280.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.524+444C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96246112 | ||||||
| chr9:96246161
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 255 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.524+395C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96246161 | ||||||
| chr9:96246276
|
T | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.524+280A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96246276 | ||||||
| chr9:96246447
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.524+109G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 7/10 | chr9 | 96246447 | ||||||
| chr9:96246672
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0133 | 2 | HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.490-82C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96246672 | ||||||
| chr9:96246727
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0204a0001c0001t0002g0306 | 3 | HG00673.hp1 NA18975.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.490-137C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96246727 | ||||||
| chr9:96246935
|
T | C | 1 | a0002c0002t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.490-345A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96246935 | ||||||
| chr9:96247066
|
T | C | 1 | a0002c0002t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.490-476A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247066 | ||||||
| chr9:96247077
|
C | T | 1 | a0002c0002t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.490-487G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247077 | ||||||
| chr9:96247127
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-537C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247127 | ||||||
| chr9:96247281
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.490-691A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247281 | ||||||
| chr9:96247351
|
C | T | 8 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0145others(5): Show | 8 | HG00323.hp2 HG01255.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-761G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247351 | ||||||
| chr9:96247671
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(47): Show | 50 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.490-1081A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247671 | ||||||
| chr9:96247706
|
A | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0102 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-1116T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247706 | ||||||
| chr9:96247785
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG02280.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-1195G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247785 | ||||||
| chr9:96247875
|
C | T | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(262): Show | 265 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.490-1285G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247875 | ||||||
| chr9:96247890
|
G | A | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 265 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.490-1300C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96247890 | ||||||
| chr9:96248158
|
G | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0180a0001c0001t0002g0368 | 3 | HG02280.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.490-1568C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248158 | ||||||
| chr9:96248330
|
G | A | 1 | a0001c0001t0003g0242 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.489+1421C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248330 | ||||||
| chr9:96248570
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 60 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.489+1181A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248570 | ||||||
| chr9:96248635
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.489+1116C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248635 | ||||||
| chr9:96248739
|
A | T | 2 | a0002c0002t0001g0011a0002c0002t0001g0012 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+1012T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248739 | ||||||
| chr9:96248907
|
A | AT | 91 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0037others(88): Show | 91 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.489+843dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248907 | ||||||
| chr9:96248907
|
A | T | 2 | a0002c0002t0001g0011a0002c0002t0001g0012 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+844T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248907 | ||||||
| chr9:96248907
|
AT | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+843delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96248907 | ||||||
| chr9:96249020
|
C | T | 34 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 34 | HG00423.hp1 HG01070.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.489+731G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96249020 | ||||||
| chr9:96249398
|
T | G | 2 | a0002c0002t0002g0370a0002c0002t0002g0371 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.489+353A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96249398 | ||||||
| chr9:96249473
|
A | C | 1 | a0002c0002t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.489+278T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96249473 | ||||||
| chr9:96249495
|
C | G | 1 | a0001c0001t0002g0275 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.489+256G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96249495 | ||||||
| chr9:96249511
|
G | C | 1 | a0001c0010t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.489+240C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96249511 | ||||||
| chr9:96249644
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.489+107C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 6/10 | chr9 | 96249644 | ||||||
| chr9:96249832
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.454-46T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96249832 | ||||||
| chr9:96249872
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.454-86A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96249872 | ||||||
| chr9:96249894
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.454-108G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96249894 | ||||||
| chr9:96249995
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 60 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.454-209G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96249995 | ||||||
| chr9:96250070
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 53 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.454-284G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250070 | ||||||
| chr9:96250126
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0102 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.454-340C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250126 | ||||||
| chr9:96250202
|
G | A | 1 | a0001c0001t0002g0319 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.454-416C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250202 | ||||||
| chr9:96250216
|
G | C | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 325 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.454-430C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250216 | ||||||
| chr9:96250246
|
C | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(56): Show | 59 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.454-460G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250246 | ||||||
| chr9:96250420
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.454-634C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250420 | ||||||
| chr9:96250456
|
A | C | 1 | a0002c0002t0001g0090 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.454-670T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250456 | ||||||
| chr9:96250615
|
A | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 60 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.453+803T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250615 | ||||||
| chr9:96250717
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0149a0001c0001t0001g0180others(1): Show | 4 | HG02280.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+701C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250717 | ||||||
| chr9:96250748
|
C | A | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.453+670G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250748 | ||||||
| chr9:96250748
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.453+670G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250748 | ||||||
| chr9:96250788
|
T | C | 1 | a0001c0001t0002g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.453+630A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250788 | ||||||
| chr9:96250867
|
G | A | 1 | a0001c0001t0002g0286 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.453+551C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250867 | ||||||
| chr9:96250887
|
C | CAA | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(56): Show | 59 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.453+529_453+530dup others(2): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250887 | ||||||
| chr9:96250894
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.453+524T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250894 | ||||||
| chr9:96250968
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(50): Show | 53 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.453+450A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96250968 | ||||||
| chr9:96251091
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.453+327A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251091 | ||||||
| chr9:96251105
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.453+313G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251105 | ||||||
| chr9:96251195
|
G | A | 25 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0046others(22): Show | 25 | HG00423.hp1 HG01515.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.453+223C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251195 | ||||||
| chr9:96251257
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+161C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251257 | ||||||
| chr9:96251279
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0102 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.453+139C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251279 | ||||||
| chr9:96251320
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.453+98T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251320 | ||||||
| chr9:96251334
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(54): Show | 57 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.453+84G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251334 | ||||||
| chr9:96251381
|
A | G | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 325 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.453+37T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 5/10 | chr9 | 96251381 | ||||||
| chr9:96252024
|
TGCACGCG others(3): Show |
T | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.386-549_386-540del others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252024 | ||||||
| chr9:96252058
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-573T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252058 | ||||||
| chr9:96252111
|
C | CAACT | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(49): Show | 52 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.386-630_386-627dup others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252111 | ||||||
| chr9:96252271
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.385+532C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252271 | ||||||
| chr9:96252429
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.385+374C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252429 | ||||||
| chr9:96252486
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.385+317A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252486 | ||||||
| chr9:96252530
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0097a0001c0001t0002g0316others(5): Show | 8 | NA18747.hp1 NA18747.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+273C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252530 | ||||||
| chr9:96252542
|
CA | C | 8 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0087others(5): Show | 8 | HG01069.hp2 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+260delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252542 | ||||||
| chr9:96252554
|
A | G | 4 | a0001c0010t0001g0010a0002c0002t0002g0360a0002c0002t0002g0366others(1): Show | 4 | HG01952.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+249T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252554 | ||||||
| chr9:96252583
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.385+220C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252583 | ||||||
| chr9:96252655
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.385+148C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252655 | ||||||
| chr9:96252698
|
ATGGTTTG others(3): Show |
A | 1 | a0003c0003t0004g0269 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.385+95_385+104delA others(9): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 4/10 | chr9 | 96252698 | ||||||
| chr9:96252916
|
C | T | 1 | a0001c0001t0002g0355 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.278-6G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96252916 | ||||||
| chr9:96252963
|
G | A | 5 | a0001c0001t0002g0329a0001c0001t0003g0229a0001c0001t0003g0237others(2): Show | 5 | HG00423.hp1 NA18944.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-53C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96252963 | ||||||
| chr9:96252977
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(47): Show | 50 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.278-67G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96252977 | ||||||
| chr9:96253156
|
A | C | 1 | a0001c0001t0001g0216 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.278-246T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96253156 | ||||||
| chr9:96253157
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.278-247C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96253157 | ||||||
| chr9:96253549
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(49): Show | 52 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.278-639T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96253549 | ||||||
| chr9:96253607
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.278-697G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96253607 | ||||||
| chr9:96253653
|
G | A | 7 | a0002c0002t0001g0069a0002c0002t0001g0090a0002c0002t0002g0288others(4): Show | 7 | HG00621.hp1 HG01993.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-743C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96253653 | ||||||
| chr9:96253813
|
T | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(236): Show | 239 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.278-903A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96253813 | ||||||
| chr9:96253839
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0002g0355 | 3 | HG02922.hp2 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.278-929G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96253839 | ||||||
| chr9:96254122
|
C | T | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 310 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.277+746G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96254122 | ||||||
| chr9:96254421
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(51): Show | 54 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.277+447C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96254421 | ||||||
| chr9:96254507
|
T | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0002g0334others(2): Show | 5 | HG00558.hp2 HG00609.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+361A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96254507 | ||||||
| chr9:96254614
|
A | C | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 323 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.277+254T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96254614 | ||||||
| chr9:96254638
|
C | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(56): Show | 59 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.277+230G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 3/10 | chr9 | 96254638 | ||||||
| chr9:96255045
|
G | A | 1 | a0001c0001t0001g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.202-102C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255045 | ||||||
| chr9:96255130
|
G | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0037others(9): Show | 12 | HG01255.hp1 HG01884.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-187C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255130 | ||||||
| chr9:96255353
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.202-410G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255353 | ||||||
| chr9:96255367
|
C | CT | 26 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0043others(23): Show | 26 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-425dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
C | CTT | 11 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0060others(8): Show | 11 | HG01361.hp2 HG02083.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-426_202-425dup others(2): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
C | CTTT | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0082others(4): Show | 7 | HG01358.hp2 HG01981.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-427_202-425dup others(3): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0048a0001c0001t0001g0101a0001c0001t0001g0108others(8): Show | 11 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-434_202-425dup others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0078a0001c0001t0001g0209others(1): Show | 4 | HG00438.hp1 HG00733.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-435_202-425dup others(11): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0001g0054a0001c0001t0001g0198a0001c0001t0001g0215others(1): Show | 4 | HG01346.hp1 HG01361.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-436_202-425dup others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0332 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.202-437_202-425dup others(13): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-455_202-425dup others(31): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CT | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0115a0001c0001t0001g0124others(8): Show | 11 | HG00558.hp2 HG00673.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.202-425delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTT | C | 8 | a0001c0001t0001g0083a0001c0001t0001g0111a0001c0001t0001g0133others(5): Show | 8 | HG00408.hp1 HG00673.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-427_202-425del others(3): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTT | C | 18 | a0001c0001t0001g0046a0001c0001t0001g0132a0001c0001t0001g0138others(15): Show | 18 | HG01192.hp2 HG01261.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.202-428_202-425del others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTT | C | 29 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0039others(26): Show | 29 | HG01069.hp2 HG01099.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.202-429_202-425del others(5): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTT | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0035others(15): Show | 18 | HG00323.hp2 HG00423.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.202-430_202-425del others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT | C | 32 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0028others(29): Show | 32 | HG01169.hp1 HG01257.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.202-431_202-425del others(7): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(1): Show |
C | 12 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0020others(9): Show | 12 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-432_202-425del others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0195a0001c0001t0001g0223a0001c0001t0002g0275 | 3 | HG03710.hp1 NA18994.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.202-434_202-425del others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0129a0001c0001t0001g0156a0001c0001t0002g0331 | 3 | HG03041.hp1 NA18940.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.202-435_202-425del others(11): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0040a0001c0001t0001g0160a0001c0001t0001g0167 | 3 | HG02523.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.202-436_202-425del others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0161 | 3 | HG02895.hp1 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.202-437_202-425del others(13): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.202-438_202-425del others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0175a0001c0001t0002g0337 | 2 | HG00738.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.202-439_202-425del others(15): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0084a0002c0002t0001g0011a0002c0002t0001g0012others(1): Show | 4 | HG01243.hp2 HG01952.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-440_202-425del others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(10): Show |
C | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0037others(10): Show | 13 | HG00621.hp1 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.202-441_202-425del others(17): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(11): Show |
C | 63 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0149others(60): Show | 63 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.202-442_202-425del others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(12): Show |
C | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.202-443_202-425del others(19): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.202-444_202-425del others(20): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(14): Show |
C | 4 | a0001c0001t0001g0146a0001c0001t0002g0313a0001c0001t0002g0362others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-445_202-425del others(21): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0002g0320 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.202-446_202-425del others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255367
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.202-447_202-425del others(23): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255367 | ||||||
| chr9:96255411
|
A | G | 1 | a0002c0002t0001g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.202-468T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255411 | ||||||
| chr9:96255433
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.202-490T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255433 | ||||||
| chr9:96255589
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0002g0316a0001c0001t0002g0330others(1): Show | 4 | NA18747.hp1 NA18747.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-646G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255589 | ||||||
| chr9:96255622
|
G | A | 1 | a0002c0002t0001g0194 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.202-679C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255622 | ||||||
| chr9:96255626
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0002g0348 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.202-683C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255626 | ||||||
| chr9:96255704
|
G | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 325 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.202-761C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255704 | ||||||
| chr9:96255797
|
C | G | 1 | a0001c0001t0002g0286 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.202-854G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255797 | ||||||
| chr9:96255802
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 297 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.202-859G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255802 | ||||||
| chr9:96255850
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.202-907C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255850 | ||||||
| chr9:96255950
|
G | A | 1 | a0002c0002t0002g0338 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.202-1007C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255950 | ||||||
| chr9:96255998
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.202-1055A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255998 | ||||||
| chr9:96255999
|
C | G | 89 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0023others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.202-1056G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96255999 | ||||||
| chr9:96256139
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.202-1196C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256139 | ||||||
| chr9:96256160
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(135): Show | 138 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.202-1217T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256160 | ||||||
| chr9:96256330
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.202-1387A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256330 | ||||||
| chr9:96256334
|
A | T | 1 | a0001c0010t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.202-1391T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256334 | ||||||
| chr9:96256393
|
G | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.202-1450C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256393 | ||||||
| chr9:96256452
|
G | A | 1 | a0001c0001t0002g0355 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.202-1509C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256452 | ||||||
| chr9:96256544
|
G | A | 1 | a0001c0001t0002g0329 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.202-1601C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256544 | ||||||
| chr9:96256892
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 297 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.202-1949T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96256892 | ||||||
| chr9:96257177
|
T | C | 22 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0059others(19): Show | 22 | HG00423.hp1 HG01515.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.202-2234A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96257177 | ||||||
| chr9:96257395
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.202-2452C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96257395 | ||||||
| chr9:96257436
|
C | A | 1 | a0002c0002t0002g0301 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.202-2493G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96257436 | ||||||
| chr9:96257628
|
C | A | 2 | a0002c0002t0001g0011a0002c0002t0001g0012 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.202-2685G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96257628 | ||||||
| chr9:96257710
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.202-2767A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96257710 | ||||||
| chr9:96257929
|
G | T | 1 | a0001c0001t0002g0346 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.202-2986C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96257929 | ||||||
| chr9:96257960
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.202-3017C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96257960 | ||||||
| chr9:96258230
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.202-3287C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96258230 | ||||||
| chr9:96258957
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.202-4014G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96258957 | ||||||
| chr9:96259225
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0002g0368 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.202-4282C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259225 | ||||||
| chr9:96259226
|
G | A | 13 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0072others(10): Show | 13 | HG00558.hp1 HG00609.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.202-4283C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259226 | ||||||
| chr9:96259300
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 176 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.202-4357T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259300 | ||||||
| chr9:96259318
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.202-4375C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259318 | ||||||
| chr9:96259379
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.202-4436T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259379 | ||||||
| chr9:96259439
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0010t0001g0010 | 3 | HG02976.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202-4496C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259439 | ||||||
| chr9:96259497
|
C | T | 1 | a0002c0002t0002g0333 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.202-4554G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259497 | ||||||
| chr9:96259547
|
C | G | 6 | a0001c0001t0001g0192a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | HG00735.hp2 HG01074.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-4604G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259547 | ||||||
| chr9:96259649
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.202-4706T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259649 | ||||||
| chr9:96259659
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.202-4716A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259659 | ||||||
| chr9:96259706
|
A | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0031others(38): Show | 41 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.202-4763T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259706 | ||||||
| chr9:96259715
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.202-4772G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259715 | ||||||
| chr9:96259725
|
G | GA | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.202-4783dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259725 | ||||||
| chr9:96259778
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.202-4835A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259778 | ||||||
| chr9:96259794
|
A | G | 1 | a0002c0002t0002g0353 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.202-4851T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259794 | ||||||
| chr9:96259846
|
C | T | 2 | a0002c0002t0001g0011a0002c0002t0001g0012 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.202-4903G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259846 | ||||||
| chr9:96259911
|
T | C | 1 | a0002c0002t0002g0301 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.202-4968A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259911 | ||||||
| chr9:96259921
|
A | G | 1 | a0002c0002t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.202-4978T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96259921 | ||||||
| chr9:96260097
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.202-5154G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96260097 | ||||||
| chr9:96260171
|
T | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 9 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-5228A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96260171 | ||||||
| chr9:96260249
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0003g0245 | 2 | HG00408.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.202-5306T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96260249 | ||||||
| chr9:96260482
|
T | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202-5539A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96260482 | ||||||
| chr9:96260709
|
G | A | 31 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0111others(28): Show | 31 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.202-5766C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96260709 | ||||||
| chr9:96260955
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 283 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.202-6012C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96260955 | ||||||
| chr9:96261066
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.202-6123T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261066 | ||||||
| chr9:96261175
|
T | C | 203 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0017others(200): Show | 203 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.202-6232A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261175 | ||||||
| chr9:96261209
|
T | TCTGCTGC others(12): Show |
297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 297 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.202-6267_202-6266i others(21): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261209 | ||||||
| chr9:96261247
|
G | A | 41 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(38): Show | 41 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.202-6304C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261247 | ||||||
| chr9:96261393
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.202-6450C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261393 | ||||||
| chr9:96261438
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.202-6495C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261438 | ||||||
| chr9:96261580
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.202-6637A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261580 | ||||||
| chr9:96261678
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.202-6735G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96261678 | ||||||
| chr9:96262229
|
C | CT | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 27 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.202-7287dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262229 | ||||||
| chr9:96262229
|
CT | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0017others(204): Show | 207 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.202-7287delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262229 | ||||||
| chr9:96262229
|
CTT | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0146a0001c0001t0001g0167others(3): Show | 6 | HG02486.hp1 HG02523.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-7288_202-7287d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262229 | ||||||
| chr9:96262347
|
C | T | 1 | a0003c0003t0004g0271 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.202-7404G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262347 | ||||||
| chr9:96262433
|
G | A | 5 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0002g0334others(2): Show | 5 | HG02027.hp1 HG02056.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-7490C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262433 | ||||||
| chr9:96262649
|
A | G | 26 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 26 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.202-7706T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262649 | ||||||
| chr9:96262724
|
T | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(67): Show | 70 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.202-7781A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262724 | ||||||
| chr9:96262882
|
A | G | 27 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 27 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-7939T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262882 | ||||||
| chr9:96262947
|
T | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.202-8004A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96262947 | ||||||
| chr9:96263013
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.202-8070A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263013 | ||||||
| chr9:96263015
|
T | C | 3 | a0002c0002t0001g0069a0002c0002t0002g0278a0002c0002t0002g0354 | 3 | HG03017.hp2 NA18966.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.202-8072A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263015 | ||||||
| chr9:96263336
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0019others(8): Show | 11 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-8393G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263336 | ||||||
| chr9:96263524
|
T | C | 1 | a0001c0001t0002g0279 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.202-8581A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263524 | ||||||
| chr9:96263553
|
TA | T | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(327): Show | 330 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.202-8611delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263553 | ||||||
| chr9:96263665
|
C | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0147others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-8722G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263665 | ||||||
| chr9:96263682
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.202-8739A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263682 | ||||||
| chr9:96263772
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.202-8829G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263772 | ||||||
| chr9:96263842
|
T | C | 42 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0001t0001g0193others(39): Show | 42 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.202-8899A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263842 | ||||||
| chr9:96263971
|
A | C | 1 | a0001c0001t0002g0313 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.202-9028T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263971 | ||||||
| chr9:96263972
|
T | C | 1 | a0002c0002t0002g0278 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.202-9029A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96263972 | ||||||
| chr9:96264160
|
G | C | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.202-9217C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264160 | ||||||
| chr9:96264238
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.202-9295T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264238 | ||||||
| chr9:96264248
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0002g0367 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.202-9305G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264248 | ||||||
| chr9:96264309
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.202-9366T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264309 | ||||||
| chr9:96264332
|
G | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202-9389C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264332 | ||||||
| chr9:96264432
|
A | C | 15 | a0001c0001t0001g0031a0001c0001t0001g0159a0001c0001t0001g0164others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-9489T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264432 | ||||||
| chr9:96264503
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.202-9560G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264503 | ||||||
| chr9:96264680
|
T | C | 217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(214): Show | 217 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.202-9737A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264680 | ||||||
| chr9:96264932
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(113): Show | 116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.202-9989A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264932 | ||||||
| chr9:96264948
|
T | A | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 185 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.202-10005A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96264948 | ||||||
| chr9:96265206
|
CA | C | 11 | a0001c0001t0001g0089a0001c0001t0001g0125a0001c0001t0001g0127others(8): Show | 11 | HG01109.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-10264delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96265206 | ||||||
| chr9:96265321
|
T | A | 173 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(170): Show | 173 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.202-10378A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96265321 | ||||||
| chr9:96265532
|
A | G | 188 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(185): Show | 188 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.202-10589T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96265532 | ||||||
| chr9:96265878
|
C | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.202-10935G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96265878 | ||||||
| chr9:96265916
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.202-10973G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96265916 | ||||||
| chr9:96266313
|
C | G | 1 | a0001c0001t0002g0298 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.202-11370G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266313 | ||||||
| chr9:96266511
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.202-11568G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266511 | ||||||
| chr9:96266532
|
A | AGTGCTGA others(4): Show |
1 | a0001c0001t0001g0195 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.202-11600_202-1159 others(15): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266532 | ||||||
| chr9:96266545
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.202-11602G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266545 | ||||||
| chr9:96266604
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.202-11661A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266604 | ||||||
| chr9:96266638
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | NA18612.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.202-11695C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266638 | ||||||
| chr9:96266647
|
G | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 10 | HG01884.hp2 HG01952.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-11704C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266647 | ||||||
| chr9:96266911
|
G | T | 1 | a0002c0002t0001g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.202-11968C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96266911 | ||||||
| chr9:96267007
|
C | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 10 | HG01884.hp2 HG01952.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-12064G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267007 | ||||||
| chr9:96267149
|
A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.202-12206T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267149 | ||||||
| chr9:96267157
|
AT | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.202-12215delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267157 | ||||||
| chr9:96267157
|
ATT | A | 9 | a0002c0002t0001g0064a0002c0002t0001g0098a0002c0002t0001g0099others(6): Show | 9 | NA18960.hp1 NA18963.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-12216_202-1221 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267157 | ||||||
| chr9:96267196
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.202-12253C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267196 | ||||||
| chr9:96267226
|
G | A | 1 | a0009c0007t0001g0208 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.202-12283C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267226 | ||||||
| chr9:96267264
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.202-12321G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267264 | ||||||
| chr9:96267265
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.202-12322T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267265 | ||||||
| chr9:96267266
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.202-12323G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267266 | ||||||
| chr9:96267270
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.202-12327A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267270 | ||||||
| chr9:96267280
|
C | G | 1 | a0002c0002t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.202-12337G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267280 | ||||||
| chr9:96267311
|
C | G | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 10 | HG01884.hp2 HG01952.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-12368G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267311 | ||||||
| chr9:96267338
|
A | T | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.202-12395T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267338 | ||||||
| chr9:96267533
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.202-12590C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267533 | ||||||
| chr9:96267675
|
C | T | 51 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0001g0157others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.202-12732G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267675 | ||||||
| chr9:96267712
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-12769A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267712 | ||||||
| chr9:96267761
|
A | G | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.202-12818T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96267761 | ||||||
| chr9:96268073
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.202-13130G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268073 | ||||||
| chr9:96268184
|
C | A | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.202-13241G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268184 | ||||||
| chr9:96268214
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.202-13271C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268214 | ||||||
| chr9:96268291
|
A | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(7): Show | 10 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-13348T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268291 | ||||||
| chr9:96268389
|
G | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.202-13446C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268389 | ||||||
| chr9:96268450
|
T | C | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.202-13507A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268450 | ||||||
| chr9:96268538
|
T | TCTTACAG others(1): Show |
24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.202-13603_202-1359 others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268538 | ||||||
| chr9:96268592
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.202-13649G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268592 | ||||||
| chr9:96268686
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.202-13743G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268686 | ||||||
| chr9:96268874
|
A | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-13931T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268874 | ||||||
| chr9:96268898
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.202-13955C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96268898 | ||||||
| chr9:96269072
|
TA | T | 68 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0022others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.202-14130delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269072 | ||||||
| chr9:96269086
|
G | A | 1 | a0002c0002t0002g0369 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.202-14143C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269086 | ||||||
| chr9:96269346
|
G | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(122): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.202-14403C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269346 | ||||||
| chr9:96269357
|
A | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202-14414T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269357 | ||||||
| chr9:96269526
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.202-14583A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269526 | ||||||
| chr9:96269567
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.202-14624G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269567 | ||||||
| chr9:96269594
|
T | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(122): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.202-14651A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269594 | ||||||
| chr9:96269749
|
C | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.202-14806G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269749 | ||||||
| chr9:96269858
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.202-14915G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269858 | ||||||
| chr9:96269872
|
C | A | 48 | a0001c0001t0001g0091a0001c0001t0001g0110a0001c0001t0002g0306others(45): Show | 48 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.202-14929G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269872 | ||||||
| chr9:96269909
|
G | GA | 8 | a0001c0001t0001g0082a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02074.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-14967dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269909 | ||||||
| chr9:96269909
|
GA | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.202-14967delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96269909 | ||||||
| chr9:96270111
|
C | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.202-15168G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270111 | ||||||
| chr9:96270113
|
G | A | 2 | a0002c0002t0001g0058a0002c0002t0001g0064 | 2 | NA18969.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.202-15170C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270113 | ||||||
| chr9:96270197
|
A | G | 8 | a0002c0002t0001g0058a0002c0002t0001g0064a0002c0002t0001g0098others(5): Show | 8 | NA18960.hp1 NA18969.hp1 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-15254T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270197 | ||||||
| chr9:96270247
|
T | TAC | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.202-15306_202-1530 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270247 | ||||||
| chr9:96270269
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-15326G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270269 | ||||||
| chr9:96270269
|
CAGAGAG | C | 8 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 8 | HG01243.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-15332_202-1532 others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270269 | ||||||
| chr9:96270271
|
G | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 182 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.202-15328C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270271 | ||||||
| chr9:96270273
|
G | C | 2 | a0001c0001t0001g0192a0001c0001t0002g0368 | 2 | HG03486.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.202-15330C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270273 | ||||||
| chr9:96270390
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.202-15447C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270390 | ||||||
| chr9:96270575
|
A | C | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.202-15632T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270575 | ||||||
| chr9:96270642
|
G | C | 54 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0159others(51): Show | 54 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.202-15699C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270642 | ||||||
| chr9:96270760
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.202-15817A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270760 | ||||||
| chr9:96270936
|
G | C | 68 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0028others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.202-15993C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270936 | ||||||
| chr9:96270953
|
C | CG | 71 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0015others(68): Show | 71 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.202-16011dupC | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270953 | ||||||
| chr9:96270953
|
CG | C | 121 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(118): Show | 121 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.202-16011delC | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270953 | ||||||
| chr9:96270956
|
G | C | 2 | a0002c0002t0001g0094a0003c0003t0004g0271 | 2 | HG02040.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.202-16013C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270956 | ||||||
| chr9:96270959
|
G | C | 2 | a0001c0001t0001g0163a0001c0001t0002g0367 | 2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.202-16016C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270959 | ||||||
| chr9:96270959
|
G | GGGT | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.202-16017_202-1601 others(7): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96270959 | ||||||
| chr9:96271052
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(135): Show | 138 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.202-16109C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271052 | ||||||
| chr9:96271168
|
A | G | 2 | a0001c0001t0002g0332a0001c0001t0003g0241 | 2 | HG00597.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.202-16225T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271168 | ||||||
| chr9:96271192
|
G | T | 126 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(123): Show | 126 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.202-16249C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271192 | ||||||
| chr9:96271309
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.202-16366C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271309 | ||||||
| chr9:96271413
|
T | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.202-16470A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271413 | ||||||
| chr9:96271578
|
C | T | 1 | a0001c0001t0003g0252 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.202-16635G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271578 | ||||||
| chr9:96271635
|
G | C | 54 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0159others(51): Show | 54 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.202-16692C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271635 | ||||||
| chr9:96271745
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202-16802A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96271745 | ||||||
| chr9:96272096
|
C | T | 50 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0159others(47): Show | 50 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.202-17153G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272096 | ||||||
| chr9:96272304
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.202-17361C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272304 | ||||||
| chr9:96272373
|
A | ATC | 5 | a0001c0001t0001g0040a0001c0001t0001g0100a0001c0001t0001g0138others(2): Show | 5 | HG01261.hp2 HG02523.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-17432_202-1743 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTC | 10 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0087others(7): Show | 10 | HG00423.hp2 HG01256.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-17434_202-1743 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTC | 3 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0002g0285 | 3 | HG02148.hp2 HG03130.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.202-17436_202-1743 others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(1): Show |
7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0184others(4): Show | 7 | HG02622.hp2 HG02698.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-17438_202-1743 others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(3): Show |
8 | a0001c0001t0001g0055a0001c0001t0001g0119a0001c0001t0001g0150others(5): Show | 8 | HG00408.hp1 HG01517.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-17440_202-1743 others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(17): Show |
2 | a0002c0002t0001g0011a0002c0002t0001g0012 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.202-17431_202-1743 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(5): Show |
10 | a0001c0001t0001g0110a0001c0001t0001g0156a0001c0001t0001g0166others(7): Show | 10 | HG00738.hp1 HG01099.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-17442_202-1743 others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(7): Show |
14 | a0001c0001t0001g0003a0001c0001t0001g0085a0001c0001t0001g0114others(11): Show | 14 | HG00280.hp1 HG00621.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.202-17444_202-1743 others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(9): Show |
18 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0120others(15): Show | 18 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-17446_202-1743 others(20): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(11): Show |
9 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0133others(6): Show | 9 | HG00544.hp1 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-17448_202-1743 others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(13): Show |
15 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0021others(12): Show | 15 | HG00323.hp1 HG01069.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-17450_202-1743 others(24): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(15): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.202-17452_202-1743 others(26): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(17): Show |
8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0164others(5): Show | 8 | HG01346.hp2 HG01934.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-17454_202-1743 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(19): Show |
6 | a0001c0001t0001g0027a0001c0001t0001g0183a0001c0001t0001g0197others(3): Show | 6 | HG00642.hp1 HG01346.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-17456_202-1743 others(30): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(21): Show |
2 | a0002c0002t0002g0301a0003c0003t0004g0263 | 2 | HG02683.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.202-17458_202-1743 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(23): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0191a0004c0004t0001g0225 | 3 | HG01192.hp1 HG02630.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.202-17460_202-1743 others(34): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(25): Show |
4 | a0001c0001t0003g0236a0002c0002t0002g0317a0002c0002t0002g0325others(1): Show | 4 | HG02300.hp1 NA18989.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-17462_202-1743 others(36): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(27): Show |
1 | a0001c0001t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.202-17431_202-1743 others(38): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(29): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0312 | 3 | HG02895.hp1 HG02897.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.202-17431_202-1743 others(40): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(31): Show |
2 | a0001c0001t0001g0140a0002c0002t0002g0353 | 2 | HG00544.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.202-17431_202-1743 others(42): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272373
|
A | ATCTCTCT others(39): Show |
1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.202-17431_202-1743 others(50): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272373 | ||||||
| chr9:96272375
|
C | CTCTCTCT others(20): Show |
1 | a0001c0001t0001g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.202-17433_202-1743 others(31): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272375 | ||||||
| chr9:96272398
|
T | TCTCTCTC others(57): Show |
1 | a0001c0001t0002g0299 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.202-17456_202-1745 others(68): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272398 | ||||||
| chr9:96272405
|
C | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0199 | 2 | HG01175.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.202-17462G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTA | 5 | a0001c0001t0001g0043a0001c0001t0001g0097a0001c0001t0002g0341others(2): Show | 5 | HG03017.hp1 HG03688.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0003g0239 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0001g0086 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(3): Show |
2 | a0001c0001t0003g0231a0001c0009t0003g0238 | 2 | NA18970.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(7): Show |
1 | a0003c0003t0004g0264 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0168a0003c0003t0004g0268 | 2 | NA18906.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(7): Show |
4 | a0001c0001t0001g0162a0001c0001t0002g0335a0002c0002t0002g0278others(1): Show | 4 | HG03453.hp1 NA18966.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(9): Show |
1 | a0003c0003t0004g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(20): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(11): Show |
1 | a0002c0002t0002g0372 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(26): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0002g0329 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(9): Show |
2 | a0001c0001t0001g0179a0001c0001t0001g0220 | 2 | HG00597.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(20): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(13): Show |
1 | a0001c0001t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(24): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(15): Show |
2 | a0001c0001t0002g0297a0001c0001t0003g0240 | 2 | NA18960.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(26): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0203 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
1 | a0002c0002t0001g0224 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(9): Show |
2 | a0001c0001t0001g0155a0001c0001t0002g0373 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(20): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(11): Show |
6 | a0001c0001t0001g0219a0001c0001t0002g0283a0001c0001t0003g0241others(3): Show | 6 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(13): Show |
1 | a0001c0001t0002g0331 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(24): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0106 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0001g0202 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(30): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0132 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(23): Show |
1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(34): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(11): Show |
3 | a0001c0001t0002g0332a0001c0001t0003g0244a0003c0003t0004g0266 | 3 | HG00597.hp2 HG04184.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(13): Show |
1 | a0001c0001t0001g0218 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(24): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(17): Show |
3 | a0001c0001t0001g0109a0001c0001t0003g0249a0002c0002t0002g0333 | 3 | HG02015.hp1 NA18612.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(23): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0124 | 2 | HG03654.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(34): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(29): Show |
1 | a0002c0002t0002g0350 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(40): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(13): Show |
1 | a0001c0001t0001g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(24): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(15): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG03490.hp2 HG03492.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(26): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(17): Show |
2 | a0001c0001t0001g0113a0001c0001t0003g0233 | 2 | HG01123.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(19): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG01255.hp1 HG02109.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(30): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
3 | a0001c0001t0001g0148a0001c0001t0001g0213a0001c0001t0003g0251 | 3 | HG00738.hp2 NA18995.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(25): Show |
1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(36): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(27): Show |
1 | a0002c0002t0002g0288 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(38): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0002g0279 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(40): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(15): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0149a0001c0001t0001g0188others(2): Show | 5 | HG00733.hp1 HG00741.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(26): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(17): Show |
5 | a0001c0001t0001g0193a0001c0001t0001g0222a0001c0001t0002g0281others(2): Show | 5 | HG00408.hp2 HG00642.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0123 | 2 | HG02486.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(30): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0211 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(17): Show |
1 | a0002c0002t0002g0366 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(19): Show |
6 | a0001c0001t0001g0139a0001c0001t0001g0206a0001c0001t0001g0215others(3): Show | 6 | HG01168.hp2 HG01361.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(30): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
3 | a0001c0001t0001g0190a0001c0001t0002g0311a0001c0001t0003g0242 | 3 | HG00673.hp2 HG00735.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(25): Show |
1 | a0001c0001t0002g0336 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(36): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0001g0104 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(40): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(33): Show |
1 | a0001c0001t0002g0287 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(44): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(19): Show |
4 | a0001c0001t0001g0116a0001c0001t0001g0180a0001c0001t0001g0186others(1): Show | 4 | HG02280.hp2 HG02602.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(30): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
6 | a0001c0001t0001g0101a0001c0001t0001g0111a0001c0001t0001g0115others(3): Show | 6 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(23): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0137a0002c0002t0001g0121 | 3 | HG03831.hp2 NA18953.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(34): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(25): Show |
4 | a0001c0001t0002g0323a0002c0002t0001g0058a0002c0002t0001g0064others(1): Show | 4 | NA18960.hp1 NA18969.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-17463_202-1746 others(36): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0002g0307 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(38): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(21): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0176 | 2 | HG01496.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(32): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(23): Show |
2 | a0001c0001t0001g0141a0001c0001t0002g0367 | 2 | HG02572.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(34): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(25): Show |
2 | a0001c0001t0002g0304a0003c0003t0004g0261 | 2 | HG02071.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(36): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0002g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(38): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(23): Show |
2 | a0001c0001t0001g0147a0001c0001t0002g0321 | 2 | HG01109.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(34): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0002g0320 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(38): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(31): Show |
1 | a0001c0001t0002g0313 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(42): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(33): Show |
2 | a0001c0001t0001g0163a0002c0002t0002g0302 | 2 | HG01993.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(44): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(25): Show |
3 | a0001c0001t0001g0146a0001c0001t0002g0303a0002c0002t0002g0371 | 3 | HG01169.hp2 HG03098.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(36): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0002g0290 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(40): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(31): Show |
1 | a0001c0001t0002g0319 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(42): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(33): Show |
1 | a0002c0002t0002g0305 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(44): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(45): Show |
1 | a0001c0001t0002g0308 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(56): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(27): Show |
2 | a0001c0001t0001g0209a0002c0002t0002g0370 | 2 | HG01167.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(38): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(29): Show |
1 | a0002c0002t0002g0327 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(40): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(31): Show |
2 | a0001c0001t0001g0131a0001c0001t0002g0300 | 2 | HG02080.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(42): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(35): Show |
2 | a0001c0001t0002g0289a0002c0002t0002g0326 | 2 | NA18612.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(46): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(31): Show |
1 | a0005c0005t0002g0272 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(42): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(51): Show |
1 | a0001c0001t0002g0309 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(62): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(33): Show |
1 | a0001c0001t0001g0029 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(44): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(35): Show |
1 | a0003c0003t0004g0258 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(46): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(39): Show |
1 | a0001c0001t0002g0286 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(50): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(39): Show |
1 | a0001c0001t0002g0322 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(50): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(45): Show |
1 | a0002c0002t0002g0328 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(56): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(35): Show |
1 | a0002c0002t0002g0318 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.202-17463_202-1746 others(46): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(43): Show |
2 | a0001c0001t0002g0310a0004c0004t0002g0374 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(54): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(43): Show |
2 | a0001c0001t0002g0316a0003c0003t0004g0271 | 2 | HG04115.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.202-17463_202-1746 others(54): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
C | CTCTCTCT others(49): Show |
1 | a0002c0002t0002g0280 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.202-17463_202-1746 others(60): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
CTA | C | 20 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0039others(17): Show | 20 | HG00438.hp2 HG01257.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.202-17464_202-1746 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
CTATA | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0047others(3): Show | 6 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-17466_202-1746 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
CTATATA | C | 7 | a0001c0001t0001g0056a0001c0001t0001g0102a0001c0001t0001g0195others(4): Show | 7 | HG00741.hp2 HG03017.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-17468_202-1746 others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0033a0001c0001t0001g0037a0002c0002t0001g0030 | 3 | HG01884.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.202-17470_202-1746 others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
CTATATAT others(5): Show |
C | 1 | a0001c0001t0002g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.202-17474_202-1746 others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272405
|
CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202-17478_202-1746 others(20): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272405 | ||||||
| chr9:96272407
|
A | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.202-17464T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272407 | ||||||
| chr9:96272409
|
A | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.202-17466T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272409 | ||||||
| chr9:96272411
|
A | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.202-17468T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272411 | ||||||
| chr9:96272413
|
A | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0013others(73): Show | 76 | HG00438.hp2 HG00733.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.202-17470T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272413 | ||||||
| chr9:96272415
|
A | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0033others(52): Show | 55 | HG01070.hp1 HG01071.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.202-17472T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272415 | ||||||
| chr9:96272417
|
A | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0033others(30): Show | 33 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.202-17474T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272417 | ||||||
| chr9:96272419
|
A | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0070others(14): Show | 17 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.202-17476T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272419 | ||||||
| chr9:96272421
|
A | C | 11 | a0001c0001t0001g0054a0001c0001t0001g0084a0001c0001t0001g0205others(8): Show | 11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-17478T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272421 | ||||||
| chr9:96272423
|
A | C | 10 | a0001c0001t0001g0054a0001c0001t0001g0084a0001c0001t0001g0205others(7): Show | 10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-17480T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272423 | ||||||
| chr9:96272425
|
A | C | 9 | a0001c0001t0001g0054a0001c0001t0001g0205a0001c0001t0001g0207others(6): Show | 9 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-17482T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272425 | ||||||
| chr9:96272427
|
A | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0210 | 2 | NA18967.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.202-17484T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272427 | ||||||
| chr9:96272429
|
A | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0210 | 2 | NA18967.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.202-17486T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272429 | ||||||
| chr9:96272431
|
A | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0210 | 2 | NA18967.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.202-17488T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272431 | ||||||
| chr9:96272433
|
A | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0210 | 2 | NA18967.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.202-17490T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272433 | ||||||
| chr9:96272446
|
T | A | 60 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0028others(57): Show | 60 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.202-17503A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272446 | ||||||
| chr9:96272446
|
TA | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0120a0002c0002t0001g0144 | 3 | HG00323.hp1 HG00323.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.202-17504delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272446 | ||||||
| chr9:96272447
|
A | AT | 4 | a0001c0001t0001g0053a0001c0001t0001g0193a0001c0001t0003g0240others(1): Show | 4 | HG02015.hp2 HG02738.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-17505_202-1750 others(5): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272447 | ||||||
| chr9:96272448
|
A | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.202-17505T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272448 | ||||||
| chr9:96272449
|
A | AAT | 7 | a0001c0001t0001g0014a0001c0001t0002g0295a0001c0001t0002g0296others(4): Show | 7 | HG00408.hp2 HG02486.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-17508_202-1750 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272449 | ||||||
| chr9:96272449
|
A | T | 2 | a0001c0001t0002g0312a0002c0002t0001g0144 | 2 | HG02698.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.202-17506T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272449 | ||||||
| chr9:96272625
|
G | A | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG00642.hp2 HG00741.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-17682C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272625 | ||||||
| chr9:96272757
|
T | C | 1 | a0002c0002t0001g0064 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.202-17814A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272757 | ||||||
| chr9:96272810
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.202-17867C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272810 | ||||||
| chr9:96272904
|
T | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(134): Show | 137 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.202-17961A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272904 | ||||||
| chr9:96272904
|
T | C | 1 | a0001c0001t0002g0336 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.202-17961A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272904 | ||||||
| chr9:96272949
|
A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.202-18006T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272949 | ||||||
| chr9:96272980
|
T | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(75): Show | 78 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.202-18037A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96272980 | ||||||
| chr9:96273066
|
A | G | 1 | a0002c0002t0002g0354 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.202-18123T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273066 | ||||||
| chr9:96273174
|
C | T | 138 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(135): Show | 138 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.202-18231G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273174 | ||||||
| chr9:96273185
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202-18242C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273185 | ||||||
| chr9:96273234
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.202-18291A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273234 | ||||||
| chr9:96273247
|
TAGTCCAC others(11): Show |
T | 1 | a0005c0005t0002g0272 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.202-18322_202-1830 others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273247 | ||||||
| chr9:96273385
|
T | C | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.202-18442A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273385 | ||||||
| chr9:96273764
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.202-18821T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273764 | ||||||
| chr9:96273845
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.202-18902G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96273845 | ||||||
| chr9:96274279
|
A | C | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.202-19336T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274279 | ||||||
| chr9:96274386
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(132): Show | 135 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.202-19443C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274386 | ||||||
| chr9:96274410
|
G | A | 1 | a0001c0001t0002g0348 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.202-19467C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274410 | ||||||
| chr9:96274423
|
T | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.202-19480A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274423 | ||||||
| chr9:96274439
|
C | T | 8 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 8 | HG01243.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-19496G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274439 | ||||||
| chr9:96274456
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.202-19513T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274456 | ||||||
| chr9:96274474
|
A | G | 2 | a0001c0001t0002g0290a0002c0002t0001g0071 | 2 | HG02027.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.202-19531T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274474 | ||||||
| chr9:96274520
|
T | G | 211 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(208): Show | 211 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.202-19577A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274520 | ||||||
| chr9:96274614
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.202-19671G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96274614 | ||||||
| chr9:96275093
|
G | GA | 26 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(23): Show | 26 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.202-20151dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96275093 | ||||||
| chr9:96275748
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.202-20805C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96275748 | ||||||
| chr9:96275832
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0009 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.202-20889C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96275832 | ||||||
| chr9:96275974
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202-21031G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96275974 | ||||||
| chr9:96275976
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-21033T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96275976 | ||||||
| chr9:96276049
|
T | G | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.202-21106A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276049 | ||||||
| chr9:96276107
|
T | TA | 127 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 127 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.202-21165dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276107 | ||||||
| chr9:96276107
|
T | TAA | 64 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(61): Show | 64 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.202-21166_202-2116 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276107 | ||||||
| chr9:96276107
|
T | TAAA | 23 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0029others(20): Show | 23 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.202-21167_202-2116 others(7): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276107 | ||||||
| chr9:96276107
|
T | TAAAA | 7 | a0001c0001t0001g0169a0001c0001t0003g0242a0002c0002t0001g0224others(4): Show | 7 | HG00673.hp2 HG02683.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-21168_202-2116 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276107 | ||||||
| chr9:96276129
|
A | AC | 23 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0191others(20): Show | 23 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.202-21187_202-2118 others(5): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276129 | ||||||
| chr9:96276145
|
G | A | 215 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(212): Show | 215 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.202-21202C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276145 | ||||||
| chr9:96276152
|
C | T | 367 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(364): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.202-21209G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276152 | ||||||
| chr9:96276162
|
T | C | 9 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 9 | HG01884.hp2 HG01952.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.202-21219A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276162 | ||||||
| chr9:96276213
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-21270G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276213 | ||||||
| chr9:96276230
|
C | A | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.202-21287G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276230 | ||||||
| chr9:96276231
|
A | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0125a0001c0001t0001g0127others(7): Show | 10 | HG01109.hp1 HG01255.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-21288T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276231 | ||||||
| chr9:96276277
|
T | C | 1 | a0002c0002t0001g0143 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.202-21334A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276277 | ||||||
| chr9:96276533
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.202-21590T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276533 | ||||||
| chr9:96276627
|
A | G | 215 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(212): Show | 215 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.202-21684T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276627 | ||||||
| chr9:96276647
|
CA | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(134): Show | 137 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.202-21705delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276647 | ||||||
| chr9:96276700
|
C | T | 49 | a0001c0001t0001g0141a0001c0001t0001g0159a0001c0001t0001g0164others(46): Show | 49 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.201+21716G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276700 | ||||||
| chr9:96276972
|
T | C | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 325 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.201+21444A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96276972 | ||||||
| chr9:96277062
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.201+21354C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277062 | ||||||
| chr9:96277156
|
A | G | 367 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(364): Show | 367 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.201+21260T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277156 | ||||||
| chr9:96277200
|
C | CA | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(302): Show | 305 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.201+21215dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277200 | ||||||
| chr9:96277200
|
C | CAA | 15 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0002g0274others(12): Show | 15 | HG01978.hp2 HG02071.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+21214_201+2121 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277200 | ||||||
| chr9:96277211
|
G | A | 215 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(212): Show | 215 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.201+21205C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277211 | ||||||
| chr9:96277391
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.201+21025A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277391 | ||||||
| chr9:96277394
|
T | A | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.201+21022A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277394 | ||||||
| chr9:96277395
|
A | T | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.201+21021T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277395 | ||||||
| chr9:96277419
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.201+20997C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277419 | ||||||
| chr9:96277643
|
G | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 325 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.201+20773C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277643 | ||||||
| chr9:96277672
|
A | AATAAAAA others(3): Show |
1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.201+20743_201+2074 others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277672 | ||||||
| chr9:96277672
|
A | AATAAAAA others(2): Show |
217 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(214): Show | 217 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.201+20743_201+2074 others(13): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277672 | ||||||
| chr9:96277768
|
C | T | 8 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 8 | HG01243.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+20648G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277768 | ||||||
| chr9:96277798
|
C | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+20618G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277798 | ||||||
| chr9:96277819
|
G | GAATT | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 324 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.201+20596_201+2059 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277819 | ||||||
| chr9:96277835
|
G | GCA | 7 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0001g0053others(4): Show | 7 | HG01175.hp2 HG02074.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.201+20579_201+2058 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
G | GCACA | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0168others(9): Show | 12 | HG01952.hp1 HG01993.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.201+20577_201+2058 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
G | GCACACA | 42 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0028others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+20575_201+2058 others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
G | GCACACAC others(1): Show |
24 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0054others(21): Show | 24 | HG00621.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.201+20573_201+2058 others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
G | GCACACAC others(3): Show |
11 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0181others(8): Show | 11 | HG00408.hp2 HG00609.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+20571_201+2058 others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
GCA | G | 52 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0086others(49): Show | 52 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.201+20579_201+2058 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
GCACA | G | 14 | a0001c0001t0001g0087a0001c0001t0002g0306a0001c0001t0002g0329others(11): Show | 14 | HG00408.hp1 HG02155.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.201+20577_201+2058 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
GCACACA | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(41): Show | 44 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.201+20575_201+2058 others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277835
|
GCACACAC others(3): Show |
G | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 71 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.201+20571_201+2058 others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277835 | ||||||
| chr9:96277837
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.201+20579T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277837 | ||||||
| chr9:96277847
|
A | G | 1 | a0001c0001t0002g0339 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.201+20569T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277847 | ||||||
| chr9:96277880
|
T | G | 1 | a0001c0001t0003g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.201+20536A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96277880 | ||||||
| chr9:96278219
|
T | G | 55 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0159others(52): Show | 55 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.201+20197A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278219 | ||||||
| chr9:96278319
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0017others(134): Show | 137 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.201+20097C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278319 | ||||||
| chr9:96278397
|
A | C | 1 | a0001c0001t0003g0242 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.201+20019T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278397 | ||||||
| chr9:96278479
|
A | G | 1 | a0006c0006t0004g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.201+19937T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278479 | ||||||
| chr9:96278488
|
T | A | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.201+19928A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278488 | ||||||
| chr9:96278786
|
T | C | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 24 | HG01070.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.201+19630A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278786 | ||||||
| chr9:96278832
|
A | T | 8 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 8 | HG01243.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+19584T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278832 | ||||||
| chr9:96278861
|
C | T | 1 | a0007c0008t0001g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.201+19555G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278861 | ||||||
| chr9:96278969
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.201+19447C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278969 | ||||||
| chr9:96278981
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.201+19435C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278981 | ||||||
| chr9:96278992
|
T | C | 2 | a0001c0001t0002g0310a0004c0004t0002g0374 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.201+19424A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96278992 | ||||||
| chr9:96279302
|
T | C | 1 | a0001c0001t0002g0289 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.201+19114A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279302 | ||||||
| chr9:96279314
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.201+19102C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279314 | ||||||
| chr9:96279364
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.201+19052C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279364 | ||||||
| chr9:96279468
|
A | G | 1 | a0001c0001t0002g0348 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.201+18948T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279468 | ||||||
| chr9:96279776
|
C | CT | 18 | a0001c0001t0001g0129a0001c0001t0002g0307a0003c0003t0004g0256others(15): Show | 18 | HG00621.hp2 HG02071.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.201+18639dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279776 | ||||||
| chr9:96279810
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.201+18606G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279810 | ||||||
| chr9:96279852
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0168others(1): Show | 4 | HG02280.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+18564G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279852 | ||||||
| chr9:96279854
|
C | A | 14 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0165others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.201+18562G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279854 | ||||||
| chr9:96279856
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.201+18560C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279856 | ||||||
| chr9:96279915
|
G | A | 72 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(69): Show | 72 | HG00438.hp1 HG00609.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.201+18501C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279915 | ||||||
| chr9:96279942
|
T | C | 17 | a0001c0001t0001g0129a0003c0003t0004g0256a0003c0003t0004g0258others(14): Show | 17 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(14): Show |
intron_variant | MODIFIER | c.201+18474A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279942 | ||||||
| chr9:96279944
|
C | T | 198 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.201+18472G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279944 | ||||||
| chr9:96279980
|
A | T | 1 | a0002c0002t0003g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.201+18436T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96279980 | ||||||
| chr9:96280051
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.201+18365C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96280051 | ||||||
| chr9:96280058
|
T | C | 207 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(204): Show | 207 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.201+18358A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96280058 | ||||||
| chr9:96280065
|
G | A | 2 | a0001c0001t0001g0091a0009c0007t0001g0208 | 2 | HG02300.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.201+18351C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96280065 | ||||||
| chr9:96280501
|
C | T | 4 | a0001c0001t0001g0067a0002c0002t0001g0058a0002c0002t0001g0063others(1): Show | 4 | NA18948.hp2 NA18969.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+17915G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96280501 | ||||||
| chr9:96280506
|
G | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+17910C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96280506 | ||||||
| chr9:96280826
|
A | G | 61 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.201+17590T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96280826 | ||||||
| chr9:96280887
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.201+17529T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96280887 | ||||||
| chr9:96281309
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.201+17107T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281309 | ||||||
| chr9:96281357
|
C | T | 10 | a0001c0001t0002g0355a0001c0001t0002g0356a0001c0001t0002g0357others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+17059G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281357 | ||||||
| chr9:96281540
|
T | G | 198 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.201+16876A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281540 | ||||||
| chr9:96281563
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.201+16853G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281563 | ||||||
| chr9:96281750
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.201+16666G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281750 | ||||||
| chr9:96281838
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.201+16578C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281838 | ||||||
| chr9:96281927
|
C | CTGCTTGT others(16): Show |
1 | a0002c0002t0002g0318 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.201+16466_201+1648 others(27): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281927 | ||||||
| chr9:96281928
|
T | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+16488A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96281928 | ||||||
| chr9:96282083
|
T | C | 11 | a0003c0003t0004g0258a0003c0003t0004g0259a0003c0003t0004g0260others(8): Show | 11 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+16333A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282083 | ||||||
| chr9:96282183
|
G | C | 1 | a0001c0001t0002g0283 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.201+16233C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282183 | ||||||
| chr9:96282205
|
G | A | 11 | a0003c0003t0004g0258a0003c0003t0004g0259a0003c0003t0004g0260others(8): Show | 11 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+16211C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282205 | ||||||
| chr9:96282257
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.201+16159T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282257 | ||||||
| chr9:96282305
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+16111C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282305 | ||||||
| chr9:96282347
|
T | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+16069A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282347 | ||||||
| chr9:96282509
|
A | G | 1 | a0002c0002t0002g0360 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.201+15907T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282509 | ||||||
| chr9:96282580
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0066 | 2 | HG00438.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.201+15836A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282580 | ||||||
| chr9:96282614
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.201+15802C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282614 | ||||||
| chr9:96282992
|
C | CT | 60 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0044others(57): Show | 60 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.201+15423dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96282992
|
C | CTT | 19 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0164others(16): Show | 19 | HG00735.hp1 HG01175.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.201+15422_201+1542 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96282992
|
CT | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.201+15423delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96282992
|
CTT | C | 8 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 8 | HG01243.hp2 HG02922.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+15422_201+1542 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96282992
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0021a0001c0001t0002g0307a0002c0002t0002g0302 | 3 | HG01256.hp2 HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.201+15412_201+1542 others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96282992
|
CTTTTTTT others(6): Show |
C | 76 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(73): Show | 76 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.201+15411_201+1542 others(17): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96282992
|
CTTTTTTT others(7): Show |
C | 42 | a0001c0001t0001g0091a0001c0001t0002g0306a0001c0001t0002g0329others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+15410_201+1542 others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96282992
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0243 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.201+15409_201+1542 others(19): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96282992 | ||||||
| chr9:96283095
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.201+15321A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283095 | ||||||
| chr9:96283173
|
C | T | 196 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 196 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.201+15243G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283173 | ||||||
| chr9:96283177
|
G | GTAC | 3 | a0001c0001t0001g0013a0001c0001t0001g0038a0001c0001t0001g0061 | 3 | HG01975.hp2 HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.201+15236_201+1523 others(7): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283177 | ||||||
| chr9:96283248
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.201+15168T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283248 | ||||||
| chr9:96283249
|
C | G | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.201+15167G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283249 | ||||||
| chr9:96283257
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.201+15159T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283257 | ||||||
| chr9:96283258
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.201+15158T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283258 | ||||||
| chr9:96283297
|
G | A | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0160others(2): Show | 5 | HG02451.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+15119C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283297 | ||||||
| chr9:96283445
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.201+14971A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283445 | ||||||
| chr9:96283522
|
T | C | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+14894A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283522 | ||||||
| chr9:96283728
|
GTTGTC | G | 9 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 9 | HG01884.hp2 HG01952.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.201+14683_201+1468 others(9): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283728 | ||||||
| chr9:96283885
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.201+14531C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283885 | ||||||
| chr9:96283910
|
C | CCTGCTGA others(11): Show |
1 | a0001c0001t0001g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.201+14505_201+1450 others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283910 | ||||||
| chr9:96283999
|
T | C | 16 | a0001c0001t0001g0028a0001c0001t0002g0286a0001c0001t0002g0289others(13): Show | 16 | HG00609.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+14417A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96283999 | ||||||
| chr9:96284035
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.201+14381A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284035 | ||||||
| chr9:96284215
|
T | TA | 9 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0057others(6): Show | 9 | HG00438.hp2 HG01981.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+14200dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
T | TAAA | 13 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0166others(10): Show | 13 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.201+14198_201+1420 others(7): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
T | TAAAA | 36 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(33): Show | 36 | HG00639.hp2 HG01167.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.201+14197_201+1420 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
T | TAAAAA | 9 | a0001c0001t0001g0164a0001c0001t0001g0190a0001c0001t0001g0191others(6): Show | 9 | HG00280.hp2 HG00735.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+14196_201+1420 others(9): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
TA | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0049a0001c0001t0001g0055others(15): Show | 18 | HG00621.hp2 HG02071.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.201+14200delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
TAA | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG00544.hp2 HG01175.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+14199_201+1420 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
TAAA | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.201+14198_201+1420 others(7): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
TAAAA | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0116others(7): Show | 10 | HG01255.hp2 HG02071.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+14197_201+1420 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284215
|
TAAAAA | T | 115 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(112): Show | 115 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.201+14196_201+1420 others(9): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284215 | ||||||
| chr9:96284218
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.201+14198T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284218 | ||||||
| chr9:96284241
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.201+14175C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284241 | ||||||
| chr9:96284481
|
G | T | 11 | a0003c0003t0004g0258a0003c0003t0004g0259a0003c0003t0004g0260others(8): Show | 11 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+13935C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284481 | ||||||
| chr9:96284726
|
G | A | 1 | a0001c0001t0002g0312 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.201+13690C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284726 | ||||||
| chr9:96284841
|
A | AT | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(277): Show | 280 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.201+13574dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284841 | ||||||
| chr9:96284841
|
A | ATT | 21 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0002g0291others(18): Show | 21 | HG00621.hp2 HG01515.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.201+13573_201+1357 others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284841 | ||||||
| chr9:96284899
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.201+13517G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284899 | ||||||
| chr9:96284955
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.201+13461G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96284955 | ||||||
| chr9:96285027
|
C | T | 122 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(119): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.201+13389G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285027 | ||||||
| chr9:96285028
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.201+13388C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285028 | ||||||
| chr9:96285041
|
G | A | 9 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(6): Show | 9 | HG01243.hp2 HG02257.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.201+13375C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285041 | ||||||
| chr9:96285429
|
T | C | 2 | a0003c0003t0004g0263a0003c0003t0004g0270 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.201+12987A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285429 | ||||||
| chr9:96285469
|
A | C | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.201+12947T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285469 | ||||||
| chr9:96285473
|
T | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+12943A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285473 | ||||||
| chr9:96285494
|
G | A | 59 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(56): Show | 59 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.201+12922C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285494 | ||||||
| chr9:96285556
|
G | C | 2 | a0003c0003t0004g0263a0003c0003t0004g0270 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.201+12860C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285556 | ||||||
| chr9:96285591
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.201+12825G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285591 | ||||||
| chr9:96285721
|
A | G | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+12695T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285721 | ||||||
| chr9:96285776
|
T | A | 1 | a0001c0001t0002g0291 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.201+12640A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96285776 | ||||||
| chr9:96286002
|
T | G | 1 | a0001c0001t0003g0255 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.201+12414A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286002 | ||||||
| chr9:96286060
|
A | G | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+12356T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286060 | ||||||
| chr9:96286071
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.201+12345G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286071 | ||||||
| chr9:96286125
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.201+12291G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286125 | ||||||
| chr9:96286176
|
T | G | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+12240A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286176 | ||||||
| chr9:96286308
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.201+12108G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286308 | ||||||
| chr9:96286609
|
G | C | 1 | a0001c0001t0002g0291 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.201+11807C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286609 | ||||||
| chr9:96286639
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.201+11777T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286639 | ||||||
| chr9:96286702
|
C | A | 1 | a0002c0002t0002g0371 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.201+11714G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286702 | ||||||
| chr9:96286702
|
CA | C | 56 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.201+11713delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286702 | ||||||
| chr9:96286703
|
A | C | 1 | a0002c0002t0002g0371 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.201+11713T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286703 | ||||||
| chr9:96286713
|
C | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.201+11703G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286713 | ||||||
| chr9:96286761
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.201+11655G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286761 | ||||||
| chr9:96286957
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.201+11459C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286957 | ||||||
| chr9:96286997
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201+11419G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96286997 | ||||||
| chr9:96287014
|
C | T | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+11402G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287014 | ||||||
| chr9:96287024
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.201+11392G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287024 | ||||||
| chr9:96287047
|
C | G | 1 | a0002c0002t0002g0338 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.201+11369G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287047 | ||||||
| chr9:96287210
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+11206A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287210 | ||||||
| chr9:96287332
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.201+11084G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287332 | ||||||
| chr9:96287359
|
G | A | 2 | a0001c0001t0001g0180a0007c0008t0001g0154 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.201+11057C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287359 | ||||||
| chr9:96287419
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.201+10997A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287419 | ||||||
| chr9:96287485
|
C | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0076others(1): Show | 4 | HG02698.hp1 HG03688.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+10931G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287485 | ||||||
| chr9:96287486
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(8): Show | 11 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.201+10930C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287486 | ||||||
| chr9:96287520
|
C | A | 9 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(6): Show | 9 | HG01243.hp2 HG02257.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.201+10896G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287520 | ||||||
| chr9:96287571
|
A | G | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+10845T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287571 | ||||||
| chr9:96287582
|
C | T | 1 | a0002c0002t0001g0185 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.201+10834G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287582 | ||||||
| chr9:96287687
|
G | A | 1 | a0001c0001t0003g0232 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.201+10729C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287687 | ||||||
| chr9:96287691
|
G | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+10725C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287691 | ||||||
| chr9:96287704
|
C | T | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+10712G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287704 | ||||||
| chr9:96287709
|
C | CTAAA | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+10703_201+1070 others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287709 | ||||||
| chr9:96287818
|
C | A | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+10598G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287818 | ||||||
| chr9:96287869
|
C | CA | 11 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0062others(8): Show | 11 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.201+10546dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287869 | ||||||
| chr9:96287869
|
CA | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.201+10546delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96287869 | ||||||
| chr9:96288040
|
A | G | 2 | a0001c0001t0001g0180a0007c0008t0001g0154 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.201+10376T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288040 | ||||||
| chr9:96288048
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+10368G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288048 | ||||||
| chr9:96288191
|
C | T | 2 | a0001c0001t0001g0180a0007c0008t0001g0154 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.201+10225G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288191 | ||||||
| chr9:96288316
|
C | T | 1 | a0001c0001t0002g0365 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+10100G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288316 | ||||||
| chr9:96288340
|
G | A | 1 | a0002c0002t0002g0325 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.201+10076C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288340 | ||||||
| chr9:96288449
|
C | A | 1 | a0001c0001t0001g0205 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.201+9967G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288449 | ||||||
| chr9:96288489
|
C | T | 1 | a0002c0002t0002g0278 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.201+9927G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288489 | ||||||
| chr9:96288512
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.201+9904T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288512 | ||||||
| chr9:96288522
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.201+9894A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288522 | ||||||
| chr9:96288551
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.201+9865G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288551 | ||||||
| chr9:96288597
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+9819T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288597 | ||||||
| chr9:96288613
|
A | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+9803T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288613 | ||||||
| chr9:96288763
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.201+9653G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288763 | ||||||
| chr9:96288829
|
G | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+9587C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288829 | ||||||
| chr9:96288853
|
C | T | 19 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.201+9563G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288853 | ||||||
| chr9:96288858
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.201+9558T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288858 | ||||||
| chr9:96288889
|
A | T | 45 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0168others(42): Show | 45 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.201+9527T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288889 | ||||||
| chr9:96288915
|
T | C | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+9501A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288915 | ||||||
| chr9:96288931
|
C | T | 139 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(136): Show | 139 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.201+9485G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288931 | ||||||
| chr9:96288936
|
CA | C | 316 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.201+9479delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96288936 | ||||||
| chr9:96289004
|
G | A | 123 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(120): Show | 123 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.201+9412C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289004 | ||||||
| chr9:96289109
|
T | TA | 194 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(191): Show | 194 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.201+9306dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289109 | ||||||
| chr9:96289127
|
G | GA | 19 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.201+9288dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289127 | ||||||
| chr9:96289142
|
G | A | 197 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.201+9274C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289142 | ||||||
| chr9:96289156
|
G | A | 19 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.201+9260C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289156 | ||||||
| chr9:96289192
|
G | GGT | 30 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(27): Show | 30 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.201+9222_201+9223d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289192 | ||||||
| chr9:96289192
|
G | GGTGTGT | 5 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0170others(2): Show | 5 | HG02257.hp2 HG03041.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+9218_201+9223d others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289192 | ||||||
| chr9:96289192
|
GGTGTGT | G | 4 | a0001c0001t0002g0273a0001c0001t0002g0276a0001c0001t0002g0282others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+9218_201+9223d others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289192 | ||||||
| chr9:96289192
|
GGTGTGTG others(1): Show |
G | 172 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(169): Show | 172 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.201+9216_201+9223d others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289192 | ||||||
| chr9:96289192
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG00642.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.201+9214_201+9223d others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289192 | ||||||
| chr9:96289192
|
GGTGTGTG others(9): Show |
G | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+9208_201+9223d others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289192 | ||||||
| chr9:96289206
|
T | C | 1 | a0002c0002t0002g0353 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.201+9210A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289206 | ||||||
| chr9:96289260
|
G | A | 42 | a0001c0001t0001g0091a0001c0001t0002g0306a0001c0001t0002g0329others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+9156C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289260 | ||||||
| chr9:96289471
|
C | G | 43 | a0001c0001t0001g0091a0001c0001t0002g0306a0001c0001t0002g0329others(40): Show | 43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.201+8945G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289471 | ||||||
| chr9:96289709
|
G | A | 89 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(86): Show | 89 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.201+8707C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289709 | ||||||
| chr9:96289712
|
C | A | 17 | a0001c0001t0002g0367a0003c0003t0004g0256a0003c0003t0004g0258others(14): Show | 17 | HG00621.hp2 HG02071.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.201+8704G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289712 | ||||||
| chr9:96289715
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG02922.hp1 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+8701C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289715 | ||||||
| chr9:96289716
|
A | G | 1 | a0001c0001t0002g0292 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.201+8700T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289716 | ||||||
| chr9:96289836
|
G | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.201+8580C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96289836 | ||||||
| chr9:96290029
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.201+8387A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290029 | ||||||
| chr9:96290055
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201+8361G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290055 | ||||||
| chr9:96290061
|
T | C | 74 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(71): Show | 74 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.201+8355A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290061 | ||||||
| chr9:96290083
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.201+8333T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290083 | ||||||
| chr9:96290084
|
C | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.201+8332G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290084 | ||||||
| chr9:96290164
|
C | G | 83 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(80): Show | 83 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.201+8252G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290164 | ||||||
| chr9:96290166
|
T | A | 1 | a0001c0001t0003g0226 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.201+8250A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290166 | ||||||
| chr9:96290189
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.201+8227G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290189 | ||||||
| chr9:96290258
|
C | T | 65 | a0001c0001t0001g0091a0001c0001t0001g0181a0001c0001t0001g0182others(62): Show | 65 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.201+8158G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290258 | ||||||
| chr9:96290267
|
G | A | 1 | a0001c0001t0002g0312 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.201+8149C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290267 | ||||||
| chr9:96290287
|
A | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0168 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.201+8129T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290287 | ||||||
| chr9:96290303
|
G | A | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+8113C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290303 | ||||||
| chr9:96290456
|
C | CCT | 36 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0158others(33): Show | 36 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.201+7959_201+7960i others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CCTT | 19 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.201+7959_201+7960i others(5): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CCTTT | 4 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0167others(1): Show | 4 | HG02572.hp2 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+7959_201+7960i others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CT | 117 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(114): Show | 117 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.201+7959dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTT | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.201+7958_201+7959d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTT | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(83): Show | 86 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.201+7957_201+7959d others(5): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTTT | 25 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(22): Show | 25 | HG00280.hp1 HG00423.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.201+7956_201+7959d others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTTTTTT others(3): Show |
1 | a0006c0006t0004g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.201+7950_201+7959d others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTTTTTT others(5): Show |
1 | a0003c0003t0004g0263 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.201+7948_201+7959d others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTTTTTT others(6): Show |
5 | a0003c0003t0004g0258a0003c0003t0004g0261a0003c0003t0004g0262others(2): Show | 5 | HG02071.hp2 HG03834.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+7947_201+7959d others(15): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTTTTTT others(7): Show |
5 | a0003c0003t0004g0260a0003c0003t0004g0266a0003c0003t0004g0269others(2): Show | 5 | HG00621.hp2 HG03942.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+7946_201+7959d others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTTTTTT others(8): Show |
2 | a0003c0003t0004g0259a0003c0003t0004g0265 | 2 | NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.201+7945_201+7959d others(17): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290456
|
C | CTTTTTTT others(10): Show |
1 | a0003c0003t0004g0264 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.201+7943_201+7959d others(19): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290456 | ||||||
| chr9:96290480
|
C | T | 21 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(18): Show | 21 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.201+7936G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290480 | ||||||
| chr9:96290517
|
T | C | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.201+7899A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290517 | ||||||
| chr9:96290731
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.201+7685C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290731 | ||||||
| chr9:96290995
|
C | T | 2 | a0001c0001t0001g0120a0002c0002t0001g0144 | 2 | HG00323.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.201+7421G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96290995 | ||||||
| chr9:96291207
|
C | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+7209G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291207 | ||||||
| chr9:96291340
|
C | G | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+7076G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291340 | ||||||
| chr9:96291476
|
A | G | 1 | a0001c0001t0003g0254 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.201+6940T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291476 | ||||||
| chr9:96291506
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.201+6910A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291506 | ||||||
| chr9:96291514
|
C | T | 2 | a0001c0001t0001g0180a0007c0008t0001g0154 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.201+6902G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291514 | ||||||
| chr9:96291689
|
G | T | 1 | a0001c0001t0002g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.201+6727C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291689 | ||||||
| chr9:96291731
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+6685G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291731 | ||||||
| chr9:96291786
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.201+6630C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291786 | ||||||
| chr9:96291884
|
G | A | 42 | a0001c0001t0001g0091a0001c0001t0002g0306a0001c0001t0002g0329others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+6532C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96291884 | ||||||
| chr9:96292167
|
G | A | 1 | a0002c0002t0002g0326 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.201+6249C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292167 | ||||||
| chr9:96292289
|
T | C | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+6127A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292289 | ||||||
| chr9:96292322
|
T | C | 61 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.201+6094A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292322 | ||||||
| chr9:96292390
|
G | T | 1 | a0003c0003t0004g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.201+6026C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292390 | ||||||
| chr9:96292642
|
C | T | 58 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(55): Show | 58 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.201+5774G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292642 | ||||||
| chr9:96292856
|
C | T | 3 | a0003c0003t0004g0258a0003c0003t0004g0271a0006c0006t0004g0257 | 3 | HG03704.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.201+5560G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292856 | ||||||
| chr9:96292883
|
T | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+5533A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292883 | ||||||
| chr9:96292967
|
G | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0117others(6): Show | 9 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.201+5449C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96292967 | ||||||
| chr9:96293006
|
T | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0001g0150others(1): Show | 4 | HG00738.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+5410A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293006 | ||||||
| chr9:96293118
|
G | A | 1 | a0001c0001t0001g0136 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.201+5298C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293118 | ||||||
| chr9:96293159
|
G | A | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+5257C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293159 | ||||||
| chr9:96293308
|
G | A | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+5108C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293308 | ||||||
| chr9:96293345
|
G | C | 1 | a0001c0001t0002g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.201+5071C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293345 | ||||||
| chr9:96293488
|
C | T | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.201+4928G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293488 | ||||||
| chr9:96293516
|
T | TCTCTCCT others(18): Show |
8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+4875_201+4899d others(27): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293516 | ||||||
| chr9:96293585
|
C | T | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+4831G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293585 | ||||||
| chr9:96293616
|
C | T | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+4800G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293616 | ||||||
| chr9:96293661
|
A | ATG | 5 | a0001c0001t0001g0014a0001c0001t0001g0180a0001c0001t0002g0367others(2): Show | 5 | HG01106.hp2 HG01952.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+4753_201+4754d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293661 | ||||||
| chr9:96293661
|
ATG | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+4753_201+4754d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293661 | ||||||
| chr9:96293673
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.201+4743C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293673 | ||||||
| chr9:96293709
|
G | A | 61 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.201+4707C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293709 | ||||||
| chr9:96293722
|
A | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.201+4694T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293722 | ||||||
| chr9:96293791
|
C | CA | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+4624dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293791 | ||||||
| chr9:96293809
|
A | G | 9 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(6): Show | 9 | HG01243.hp2 HG02257.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.201+4607T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293809 | ||||||
| chr9:96293865
|
C | T | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+4551G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293865 | ||||||
| chr9:96293927
|
A | G | 82 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.201+4489T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293927 | ||||||
| chr9:96293941
|
A | G | 1 | a0001c0001t0002g0311 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.201+4475T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96293941 | ||||||
| chr9:96294112
|
C | T | 1 | a0002c0002t0001g0194 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.201+4304G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294112 | ||||||
| chr9:96294153
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.201+4263C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294153 | ||||||
| chr9:96294250
|
C | CA | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.201+4165dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294250 | ||||||
| chr9:96294266
|
A | C | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+4150T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294266 | ||||||
| chr9:96294388
|
T | C | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+4028A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294388 | ||||||
| chr9:96294598
|
G | A | 42 | a0001c0001t0001g0091a0001c0001t0002g0306a0001c0001t0002g0329others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.201+3818C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294598 | ||||||
| chr9:96294633
|
G | A | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0162others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+3783C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294633 | ||||||
| chr9:96294698
|
C | T | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.201+3718G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294698 | ||||||
| chr9:96294742
|
C | T | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+3674G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294742 | ||||||
| chr9:96294845
|
G | A | 1 | a0001c0001t0003g0253 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.201+3571C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294845 | ||||||
| chr9:96294965
|
C | T | 1 | a0002c0002t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.201+3451G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294965 | ||||||
| chr9:96294995
|
C | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.201+3421G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96294995 | ||||||
| chr9:96295002
|
CT | C | 70 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0130others(67): Show | 70 | HG00280.hp2 HG00597.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.201+3413delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295002 | ||||||
| chr9:96295002
|
CTT | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.201+3412_201+3413d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295002 | ||||||
| chr9:96295002
|
CTTT | C | 34 | a0001c0001t0001g0026a0001c0001t0001g0119a0001c0001t0001g0180others(31): Show | 34 | HG00621.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.201+3411_201+3413d others(5): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295002 | ||||||
| chr9:96295081
|
A | G | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+3335T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295081 | ||||||
| chr9:96295196
|
G | A | 1 | a0002c0002t0001g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.201+3220C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295196 | ||||||
| chr9:96295209
|
G | A | 2 | a0001c0001t0001g0180a0007c0008t0001g0154 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.201+3207C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295209 | ||||||
| chr9:96295279
|
A | G | 56 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.201+3137T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295279 | ||||||
| chr9:96295299
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02451.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+3117G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295299 | ||||||
| chr9:96295313
|
T | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.201+3103A>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295313 | ||||||
| chr9:96295320
|
GTTTGTT | G | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+3090_201+3095d others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295320 | ||||||
| chr9:96295342
|
G | GT | 4 | a0001c0001t0001g0164a0001c0001t0001g0193a0001c0001t0001g0200others(1): Show | 4 | HG02572.hp2 HG02738.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+3073dupA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295342 | ||||||
| chr9:96295348
|
G | T | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.201+3068C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295348 | ||||||
| chr9:96295356
|
C | T | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+3060G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295356 | ||||||
| chr9:96295391
|
A | G | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG00735.hp2 HG01074.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+3025T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295391 | ||||||
| chr9:96295465
|
G | A | 22 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(19): Show | 22 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.201+2951C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295465 | ||||||
| chr9:96295512
|
G | A | 40 | a0001c0001t0001g0091a0001c0001t0002g0329a0001c0001t0002g0330others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.201+2904C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295512 | ||||||
| chr9:96295758
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.201+2658C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295758 | ||||||
| chr9:96295818
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.201+2598G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295818 | ||||||
| chr9:96295864
|
C | G | 1 | a0008c0011t0001g0178 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.201+2552G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295864 | ||||||
| chr9:96295864
|
C | T | 1 | a0002c0002t0002g0353 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.201+2552G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96295864 | ||||||
| chr9:96296109
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0167 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.201+2307G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296109 | ||||||
| chr9:96296110
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.201+2306C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296110 | ||||||
| chr9:96296142
|
A | C | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+2274T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296142 | ||||||
| chr9:96296169
|
G | A | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+2247C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296169 | ||||||
| chr9:96296255
|
AAAG | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.201+2158_201+2160d others(5): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296255 | ||||||
| chr9:96296306
|
G | A | 2 | a0001c0001t0001g0180a0007c0008t0001g0154 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.201+2110C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296306 | ||||||
| chr9:96296317
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.201+2099G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296317 | ||||||
| chr9:96296681
|
T | C | 1 | a0001c0001t0002g0311 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.201+1735A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296681 | ||||||
| chr9:96296707
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.201+1709A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296707 | ||||||
| chr9:96296712
|
C | T | 2 | a0001c0001t0003g0235a0001c0001t0003g0236 | 2 | NA18989.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.201+1704G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296712 | ||||||
| chr9:96296759
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.201+1657G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96296759 | ||||||
| chr9:96297030
|
C | CA | 32 | a0001c0001t0001g0027a0001c0001t0001g0081a0001c0001t0001g0082others(29): Show | 32 | HG00280.hp1 HG00558.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.201+1385dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297030 | ||||||
| chr9:96297030
|
CA | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.201+1385delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297030 | ||||||
| chr9:96297043
|
A | C | 2 | a0001c0001t0001g0044a0002c0002t0002g0369 | 2 | HG01934.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.201+1373T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297043 | ||||||
| chr9:96297341
|
CT | C | 276 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(273): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.201+1074delA | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297341 | ||||||
| chr9:96297341
|
CTT | C | 21 | a0001c0001t0001g0108a0001c0001t0001g0116a0001c0001t0001g0162others(18): Show | 21 | HG00621.hp2 HG01515.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.201+1073_201+1074d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297341 | ||||||
| chr9:96297347
|
T | C | 1 | a0001c0001t0002g0336 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.201+1069A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297347 | ||||||
| chr9:96297348
|
T | C | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+1068A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297348 | ||||||
| chr9:96297617
|
G | A | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.201+799C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297617 | ||||||
| chr9:96297636
|
C | T | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+780G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297636 | ||||||
| chr9:96297637
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.201+779C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297637 | ||||||
| chr9:96297903
|
G | A | 74 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(71): Show | 74 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.201+513C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297903 | ||||||
| chr9:96297948
|
C | G | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0162others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+468G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96297948 | ||||||
| chr9:96298111
|
T | C | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.201+305A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96298111 | ||||||
| chr9:96298286
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.201+130A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96298286 | ||||||
| chr9:96298299
|
C | T | 14 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0165others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.201+117G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96298299 | ||||||
| chr9:96298330
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.201+86A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96298330 | ||||||
| chr9:96298378
|
A | G | 46 | a0001c0001t0001g0091a0001c0001t0001g0155a0001c0001t0001g0156others(43): Show | 46 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.201+38T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 2/10 | chr9 | 96298378 | ||||||
| chr9:96298600
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.155-138C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96298600 | ||||||
| chr9:96298676
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.155-214A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96298676 | ||||||
| chr9:96298761
|
C | T | 40 | a0001c0001t0001g0091a0001c0001t0002g0329a0001c0001t0002g0330others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.155-299G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96298761 | ||||||
| chr9:96298770
|
G | A | 40 | a0001c0001t0001g0091a0001c0001t0002g0329a0001c0001t0002g0330others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.155-308C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96298770 | ||||||
| chr9:96298785
|
G | T | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.155-323C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96298785 | ||||||
| chr9:96298913
|
C | A | 55 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(52): Show | 55 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.155-451G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96298913 | ||||||
| chr9:96299088
|
G | T | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.155-626C>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299088 | ||||||
| chr9:96299153
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.155-691C>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299153 | ||||||
| chr9:96299189
|
G | A | 1 | a0007c0008t0001g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.155-727C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299189 | ||||||
| chr9:96299336
|
A | G | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.155-874T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299336 | ||||||
| chr9:96299598
|
C | G | 2 | a0003c0003t0004g0267a0003c0003t0004g0268 | 2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.155-1136G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299598 | ||||||
| chr9:96299602
|
A | G | 62 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(59): Show | 62 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.155-1140T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299602 | ||||||
| chr9:96299679
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.155-1217T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299679 | ||||||
| chr9:96299690
|
A | G | 37 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(34): Show | 37 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.155-1228T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299690 | ||||||
| chr9:96299780
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.155-1318C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299780 | ||||||
| chr9:96299844
|
C | G | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.155-1382G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299844 | ||||||
| chr9:96299889
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.155-1427A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299889 | ||||||
| chr9:96299980
|
G | A | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0162others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-1518C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299980 | ||||||
| chr9:96299995
|
C | G | 2 | a0001c0001t0001g0180a0007c0008t0001g0154 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.155-1533G>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96299995 | ||||||
| chr9:96300063
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.155-1601G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300063 | ||||||
| chr9:96300080
|
AGTGCTAC others(37): Show |
A | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.155-1662_155-1619d others(46): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300080 | ||||||
| chr9:96300100
|
G | A | 22 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(19): Show | 22 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-1638C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300100 | ||||||
| chr9:96300152
|
T | C | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.155-1690A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300152 | ||||||
| chr9:96300209
|
G | GAC | 42 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(39): Show | 42 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.154+1740_154+1741d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACAC | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 86 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.154+1738_154+1741d others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACAC | 46 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(43): Show | 46 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.154+1736_154+1741d others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACACA others(1): Show |
35 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0070others(32): Show | 35 | HG00544.hp2 HG00642.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.154+1734_154+1741d others(10): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACACA others(3): Show |
23 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0167others(20): Show | 23 | HG00408.hp1 HG00639.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+1732_154+1741d others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACACA others(5): Show |
9 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(6): Show | 9 | HG01168.hp2 HG01361.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+1730_154+1741d others(14): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACACA others(7): Show |
3 | a0001c0001t0001g0207a0001c0001t0001g0216a0002c0002t0002g0372 | 3 | HG04204.hp2 NA18968.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.154+1728_154+1741d others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACACA others(9): Show |
3 | a0001c0001t0001g0209a0001c0001t0001g0210a0009c0007t0001g0208 | 3 | HG02300.hp1 NA18967.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.154+1726_154+1741d others(18): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACACA others(11): Show |
2 | a0001c0001t0001g0211a0001c0001t0001g0217 | 2 | HG02132.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.154+1724_154+1741d others(20): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
G | GACACACA others(13): Show |
1 | a0001c0001t0001g0212 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.154+1722_154+1741d others(22): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
GAC | G | 24 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.154+1740_154+1741d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
GACAC | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0085others(11): Show | 14 | HG00597.hp2 HG01243.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+1738_154+1741d others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
GACACAC | G | 17 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0182others(14): Show | 17 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.154+1736_154+1741d others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
GACACACA others(3): Show |
G | 5 | a0001c0001t0002g0329a0001c0001t0002g0330a0001c0001t0002g0331others(2): Show | 5 | HG02155.hp1 HG03704.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+1732_154+1741d others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300209
|
GACACACA others(7): Show |
G | 1 | a0001c0001t0001g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154+1728_154+1741d others(16): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300209 | ||||||
| chr9:96300250
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154+1700_154+1701i others(17): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300250 | ||||||
| chr9:96300253
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.154+1697_154+1698i others(13): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300253 | ||||||
| chr9:96300300
|
CCCAAACA others(331): Show |
C | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(81): Show | 84 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.154+1313_154+1650d others(2): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300300 | ||||||
| chr9:96300332
|
A | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+1619T>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300332 | ||||||
| chr9:96300463
|
A | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.154+1488T>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300463 | ||||||
| chr9:96300593
|
T | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+1358A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300593 | ||||||
| chr9:96300605
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.154+1346G>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300605 | ||||||
| chr9:96300607
|
T | TTG | 26 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(23): Show | 26 | HG00544.hp1 HG00621.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.154+1342_154+1343d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300607 | ||||||
| chr9:96300607
|
T | TTGTGTG | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+1338_154+1343d others(8): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300607 | ||||||
| chr9:96300607
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.154+1334_154+1343d others(12): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300607 | ||||||
| chr9:96300607
|
TTG | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(87): Show | 90 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.154+1342_154+1343d others(4): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300607 | ||||||
| chr9:96300607
|
TTGTG | T | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG01884.hp2 HG01952.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+1340_154+1343d others(6): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300607 | ||||||
| chr9:96300670
|
T | C | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+1281A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300670 | ||||||
| chr9:96300767
|
A | G | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+1184T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300767 | ||||||
| chr9:96300896
|
T | TA | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+1054dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300896 | ||||||
| chr9:96300955
|
T | G | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+996A>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96300955 | ||||||
| chr9:96301004
|
T | C | 64 | a0001c0001t0001g0091a0001c0001t0001g0180a0001c0001t0001g0181others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.154+947A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301004 | ||||||
| chr9:96301077
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.154+874G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301077 | ||||||
| chr9:96301414
|
T | TAAAAATA others(301): Show |
1 | a0001c0001t0001g0092 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(308): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(302): Show |
1 | a0001c0001t0001g0093 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(309): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(311): Show |
1 | a0002c0002t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(318): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(318): Show |
8 | a0001c0001t0001g0097a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 8 | HG00735.hp2 HG01074.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+536_154+537ins others(325): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(319): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0101a0001c0001t0001g0102others(25): Show | 28 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.154+536_154+537ins others(326): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(320): Show |
37 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(34): Show | 37 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.154+536_154+537ins others(327): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(321): Show |
13 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(10): Show | 13 | HG00423.hp2 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.154+536_154+537ins others(328): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(322): Show |
1 | a0001c0001t0002g0352 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(329): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(323): Show |
2 | a0002c0002t0001g0151a0002c0002t0001g0152 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.154+536_154+537ins others(330): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(324): Show |
1 | a0001c0001t0001g0176 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154+536_154+537ins others(331): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(325): Show |
2 | a0001c0001t0001g0003a0001c0001t0001g0153 | 2 | HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154+536_154+537ins others(332): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(326): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+536_154+537ins others(333): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(327): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01243.hp1 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.154+536_154+537ins others(334): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(328): Show |
1 | a0001c0001t0001g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(335): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(329): Show |
1 | a0001c0010t0001g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(336): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(330): Show |
1 | a0002c0002t0001g0011 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(337): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(331): Show |
1 | a0002c0002t0001g0012 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154+536_154+537ins others(338): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(319): Show |
1 | a0001c0001t0001g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(326): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301414
|
T | TAAAAATA others(304): Show |
1 | a0001c0001t0002g0365 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154+536_154+537ins others(311): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301414 | ||||||
| chr9:96301450
|
C | T | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.154+501G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301450 | ||||||
| chr9:96301451
|
G | A | 24 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(21): Show | 24 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.154+500C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301451 | ||||||
| chr9:96301519
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.154+432A>G | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301519 | ||||||
| chr9:96301547
|
C | T | 1 | a0001c0001t0002g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.154+404G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301547 | ||||||
| chr9:96301572
|
G | A | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+379C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301572 | ||||||
| chr9:96301680
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.154+271G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301680 | ||||||
| chr9:96301686
|
G | A | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+265C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301686 | ||||||
| chr9:96301710
|
C | CA | 97 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(94): Show | 97 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.154+240dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301710 | ||||||
| chr9:96301710
|
C | CAA | 8 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG00597.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+239_154+240dup others(2): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301710 | ||||||
| chr9:96301710
|
CA | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(11): Show | 14 | HG00323.hp1 HG01243.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+240delT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301710 | ||||||
| chr9:96301754
|
G | A | 23 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(20): Show | 23 | HG00621.hp2 HG02071.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+197C>T | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301754 | ||||||
| chr9:96301758
|
A | G | 1 | a0002c0002t0001g0185 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.154+193T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301758 | ||||||
| chr9:96301830
|
A | G | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.154+121T>C | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301830 | ||||||
| chr9:96301835
|
C | T | 16 | a0003c0003t0004g0256a0003c0003t0004g0258a0003c0003t0004g0259others(13): Show | 16 | HG00621.hp2 HG02071.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.154+116G>A | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301835 | ||||||
| chr9:96301920
|
C | CA | 45 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(42): Show | 45 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.154+30dupT | HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | 96301920 |