Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51170 |
|---|---|
| ensemblid | ENSG00000198189.11 |
| hgncid | 22960 |
| symbol | HSD17B11 |
| name | hydroxysteroid 17-beta dehydrogenase 11 |
| refseq_nuc | NM_016245.5 |
| refseq_prot | NP_057329.3 |
| ensembl_nuc | ENST00000358290.9 |
| ensembl_prot | ENSP00000351035.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 87336515 |
| end | 87391188 |
| strand | - |
| ver | v1.2 |
| region | chr4:87336515-87391188 |
| region5000 | chr4:87331515-87396188 |
| regionname0 | HSD17B11_chr4_87336515_87391188 |
| regionname5000 | HSD17B11_chr4_87331515_87396188 |
| 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 | 1/0 | 300 | 386 | 99 | 70 | 166 | 14 | 36 | 128 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0002 | 0/1 | 300 | 4 | 1 | 0 | 0 | 0 | 2 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| 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 | 1/0 | 903 | 285 | 38 | 44 | 165 | 6 | 31 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| c0002 | 0/0 | 903 | 81 | 43 | 25 | 0 | 8 | 5 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| c0003 | 0/0 | 903 | 13 | 12 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| c0004 | 0/1 | 903 | 4 | 1 | 0 | 0 | 0 | 2 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| c0005 | 0/0 | 903 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| c0006 | 0/0 | 903 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| c0007 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| c0008 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| 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 | 1/0 | 880 | 168 | 15 | 25 | 95 | 7 | 25 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0002 | 0/1 | 880 | 72 | 8 | 31 | 23 | 4 | 5 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0003 | 0/0 | 879 | 61 | 15 | 8 | 36 | 0 | 2 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0004 | 0/0 | 879 | 35 | 27 | 2 | 1 | 1 | 4 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0005 | 0/0 | 884 | 12 | 11 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0006 | 0/0 | 881 | 11 | 0 | 0 | 10 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0007 | 0/0 | 881 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0008 | 0/0 | 882 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0009 | 0/0 | 881 | 5 | 5 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0010 | 0/0 | 881 | 4 | 1 | 1 | 1 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0011 | 0/0 | 882 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0012 | 0/0 | 880 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0013 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0014 | 0/0 | 880 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0015 | 0/0 | 880 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0016 | 0/0 | 880 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| t0017 | 0/0 | 880 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| 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 | 1/0 | 903 | 285 | 38 | 44 | 165 | 6 | 31 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002 | 0/0 | 903 | 81 | 43 | 25 | 0 | 8 | 5 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0003 | 0/0 | 903 | 13 | 12 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0005 | 0/0 | 903 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0006 | 0/0 | 903 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0007 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0008 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0002c0004 | 0/1 | 903 | 4 | 1 | 0 | 0 | 0 | 2 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1782 | 129 | 2 | 13 | 94 | 1 | 18 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0002 | 0/0 | 1782 | 57 | 4 | 22 | 23 | 3 | 5 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0003 | 0/0 | 1781 | 54 | 11 | 5 | 36 | 0 | 2 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0004 | 0/0 | 1781 | 10 | 2 | 2 | 1 | 1 | 4 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0005 | 0/0 | 1786 | 10 | 9 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0006 | 0/0 | 1783 | 11 | 0 | 0 | 10 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0007 | 0/0 | 1783 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0009 | 0/0 | 1783 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0010 | 0/0 | 1783 | 3 | 0 | 1 | 1 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0015 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0001t0016 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0001 | 0/0 | 1782 | 35 | 12 | 12 | 0 | 6 | 5 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0002 | 0/0 | 1782 | 13 | 4 | 8 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0003 | 0/0 | 1781 | 4 | 1 | 3 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0004 | 0/0 | 1781 | 18 | 18 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0005 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0008 | 0/0 | 1784 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0009 | 0/0 | 1783 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0010 | 0/0 | 1783 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0011 | 0/0 | 1784 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0012 | 0/0 | 1782 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0014 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0002t0017 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0003t0002 | 0/0 | 1782 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0003t0003 | 0/0 | 1781 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0003t0004 | 0/0 | 1781 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0003t0008 | 0/0 | 1784 | 5 | 5 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0003t0013 | 0/0 | 1781 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0005t0004 | 0/0 | 1781 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0006t0004 | 0/0 | 1781 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0006t0005 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0007t0001 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0001c0008t0009 | 0/0 | 1783 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0002c0004t0001 | 0/0 | 1782 | 3 | 1 | 0 | 0 | 0 | 2 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| a0002c0004t0002 | 0/1 | 1782 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | copy fasta | chr4 | 87331515 | 87396188 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0004g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0009g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0009g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0009g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0010g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0010g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0010g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0015g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0001t0016g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0004g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0009g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0012g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0012g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0014g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0002t0017g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0004g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0004g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0003t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0005t0004g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0005t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0005t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0006t0004g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0006t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0007t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0001c0008t0009g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0002c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0002c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0002c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| a0002c0004t0002g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0183 | EUR | GBR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | GBR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0255 | EUR | FIN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0017 | EUR | FIN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00323 | hp2 | a0001 | c0002 | t0014 | g0018 | EUR | FIN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG00741 | hp2 | a0001 | c0002 | t0012 | g0262 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0148 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01081 | hp1 | a0001 | c0002 | t0012 | g0257 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0028 | AMR | PUR | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0146 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0357 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0358 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0147 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0282 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0010 | EUR | IBS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0259 | EUR | IBS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | IBS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0347 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0281 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02055 | hp1 | a0001 | c0002 | t0011 | g0152 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0166 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0170 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02145 | hp1 | a0001 | c0002 | t0009 | g0356 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02145 | hp2 | a0001 | c0002 | t0010 | g0013 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | CDX | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0275 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0138 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0373 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02280 | hp2 | a0001 | c0002 | t0004 | g0367 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0363 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0133 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0167 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0348 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0364 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02622 | hp1 | a0001 | c0003 | t0008 | g0294 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02622 | hp2 | a0001 | c0002 | t0017 | g0185 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02630 | hp1 | a0001 | c0003 | t0003 | g0131 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0378 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02647 | hp1 | a0001 | c0003 | t0004 | g0365 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0371 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0267 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0268 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02717 | hp2 | a0001 | c0005 | t0004 | g0370 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0376 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0266 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02738 | hp2 | a0002 | c0004 | t0001 | g0270 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0379 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0350 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02818 | hp2 | a0001 | c0005 | t0004 | g0369 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02886 | hp1 | a0001 | c0005 | t0004 | g0374 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02886 | hp2 | a0001 | c0003 | t0003 | g0132 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02895 | hp1 | a0001 | c0002 | t0011 | g0150 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02896 | hp1 | a0001 | c0006 | t0004 | g0368 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02896 | hp2 | a0001 | c0003 | t0008 | g0293 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02897 | hp2 | a0001 | c0003 | t0008 | g0291 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0366 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0380 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0352 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0119 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02970 | hp2 | a0001 | c0003 | t0008 | g0292 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02976 | hp1 | a0001 | c0003 | t0008 | g0295 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0136 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0375 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0343 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0135 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0349 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03139 | hp2 | a0001 | c0003 | t0004 | g0344 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03195 | hp2 | a0001 | c0002 | t0008 | g0288 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0153 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0077 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03225 | hp2 | a0001 | c0002 | t0011 | g0151 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0362 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0372 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | ESN | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03540 | hp2 | a0001 | c0006 | t0005 | g0160 | AFR | GWD | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0345 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0360 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0181 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0361 | SAS | BEB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04228 | hp1 | a0001 | c0001 | t0015 | g0080 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0346 | AFR | YRI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | CHB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | YRI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18973 | hp2 | a0001 | c0001 | t0010 | g0012 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19000 | hp2 | a0001 | c0007 | t0001 | g0340 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | LWK | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0354 | AFR | LWK | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | LWK | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0351 | AFR | LWK | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0355 | AFR | YRI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | YRI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0137 | AFR | ASW | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20129 | hp2 | a0001 | c0008 | t0009 | g0353 | AFR | ASW | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0329 | EUR | TSI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0182 | EUR | TSI | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20905 | hp1 | a0002 | c0004 | t0001 | g0273 | SAS | GIH | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | GIH | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0085 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0134 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02486 | hp2 | a0001 | c0003 | t0013 | g0009 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | MSL | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | USA | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | USA | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0377 | AFR | USA | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | USA | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0149 | AFR | LWK | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | LWK | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0004 | t0002 | g0072 | REF | REF | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0274 | REF | REF | HSD17B11_chr4_87331515_87396188 | HSD17B11 | chr4 | 87331515 | 87396188 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87337331
|
C | T | 1 | a0002 | 4 | HG02257.hp2 HG02738.hp2 NA20905.hp1 others(1): Show |
missense_variant | MODERATE | c.848G>A | p.Arg283Gln | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 7/7 | 966/1782 | 848/903 | 283/300 | chr4 | 87337331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87357332
|
T | G | 2 | a0001c0003a0001c0006 | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
synonymous_variant | LOW | c.642A>C | p.Thr214Thr | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/7 | 760/1782 | 642/903 | 214/300 | chr4 | 87357332 | ||
| chr4:87372732
|
C | T | 1 | a0001c0008 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.534G>A | p.Ser178Ser | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/7 | 652/1782 | 534/903 | 178/300 | chr4 | 87372732 | ||
| chr4:87372735
|
G | A | 3 | a0001c0002a0001c0003a0001c0005 | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
synonymous_variant | LOW | c.531C>T | p.Val177Val | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/7 | 649/1782 | 531/903 | 177/300 | chr4 | 87372735 | ||
| chr4:87372774
|
A | G | 1 | a0001c0007 | 1 | NA19000.hp2 | synonymous_variant | LOW | c.492T>C | p.His164His | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/7 | 610/1782 | 492/903 | 164/300 | chr4 | 87372774 | ||
| chr4:87372786
|
C | T | 1 | a0001c0005 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.480G>A | p.Thr160Thr | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/7 | 598/1782 | 480/903 | 160/300 | chr4 | 87372786 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87336547
|
A | T | 1 | a0001c0001t0015 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*729T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 7/7 | 729 | chr4 | 87336547 | |||||
| chr4:87336568
|
T | TAA | 9 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(6): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*707_*708insTT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 7/7 | 707 | chr4 | 87336568 | |||||
| chr4:87336620
|
A | G | 2 | a0001c0002t0012a0001c0002t0014 | 3 | HG00323.hp2 HG00741.hp2 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*656T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 7/7 | 656 | chr4 | 87336620 | |||||
| chr4:87336740
|
G | A | 1 | a0001c0002t0017 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*536C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 7/7 | 536 | chr4 | 87336740 | |||||
| chr4:87391099
|
G | GT | 3 | a0001c0001t0006a0001c0001t0010a0001c0002t0010 | 15 | HG00621.hp2 HG01257.hp1 HG01515.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-30dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/7 | 30 | chr4 | 87391099 | |||||
| chr4:87391099
|
G | GTT | 4 | a0001c0001t0005a0001c0002t0005a0001c0002t0011others(1): Show | 15 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-31_-30dupAA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/7 | 30 | chr4 | 87391099 | |||||
| chr4:87391099
|
GT | G | 13 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(10): Show | 108 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
5_prime_UTR_variant | MODIFIER | c.-30delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/7 | 30 | chr4 | 87391099 | |||||
| chr4:87391101
|
T | G | 1 | a0001c0001t0016 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/7 | 31 | chr4 | 87391101 | |||||
| chr4:87391141
|
A | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(10): Show | 146 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
5_prime_UTR_variant | MODIFIER | c.-71T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/7 | 71 | chr4 | 87391141 | |||||
| chr4:87391179
|
A | T | 1 | a0001c0003t0013 | 1 | HG02486.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/7 | chr4 | 87391179 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:87337460
|
A | C | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.813-94T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87337460 | ||||||
| chr4:87337499
|
T | C | 39 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(36): Show | 39 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.813-133A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87337499 | ||||||
| chr4:87337750
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.813-384G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87337750 | ||||||
| chr4:87337822
|
C | G | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.813-456G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87337822 | ||||||
| chr4:87337856
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(306): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.813-490C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87337856 | ||||||
| chr4:87337944
|
G | A | 1 | a0001c0002t0001g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.813-578C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87337944 | ||||||
| chr4:87338033
|
C | T | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.813-667G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338033 | ||||||
| chr4:87338034
|
G | A | 7 | a0001c0001t0001g0227a0001c0002t0001g0277a0001c0002t0001g0278others(4): Show | 7 | HG01074.hp2 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.813-668C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338034 | ||||||
| chr4:87338061
|
C | G | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.813-695G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338061 | ||||||
| chr4:87338094
|
A | G | 39 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(36): Show | 39 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.813-728T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338094 | ||||||
| chr4:87338181
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.813-815G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338181 | ||||||
| chr4:87338220
|
C | G | 1 | a0001c0001t0001g0253 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.813-854G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338220 | ||||||
| chr4:87338224
|
A | AC | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.813-859dupG | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338224 | ||||||
| chr4:87338311
|
G | C | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.813-945C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338311 | ||||||
| chr4:87338382
|
T | G | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.813-1016A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338382 | ||||||
| chr4:87338466
|
A | G | 2 | a0001c0002t0001g0260a0001c0002t0001g0261 | 2 | HG01099.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.813-1100T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338466 | ||||||
| chr4:87338676
|
C | G | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.813-1310G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338676 | ||||||
| chr4:87338702
|
A | T | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.813-1336T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338702 | ||||||
| chr4:87338720
|
A | G | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.813-1354T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338720 | ||||||
| chr4:87338826
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(61): Show | 67 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.813-1460G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338826 | ||||||
| chr4:87338827
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.813-1461C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338827 | ||||||
| chr4:87338886
|
G | A | 6 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0076others(3): Show | 6 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.813-1520C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338886 | ||||||
| chr4:87338949
|
T | A | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.812+1541A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87338949 | ||||||
| chr4:87339010
|
CT | C | 5 | a0001c0001t0003g0108a0001c0001t0003g0127a0001c0001t0003g0128others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.812+1479delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339010 | ||||||
| chr4:87339015
|
A | G | 5 | a0001c0001t0003g0108a0001c0001t0003g0127a0001c0001t0003g0128others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.812+1475T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339015 | ||||||
| chr4:87339017
|
T | A | 1 | a0001c0001t0001g0238 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.812+1473A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339017 | ||||||
| chr4:87339108
|
C | T | 20 | a0001c0002t0001g0006a0001c0002t0001g0255a0001c0002t0001g0256others(17): Show | 21 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.812+1382G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339108 | ||||||
| chr4:87339111
|
A | G | 180 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(177): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.812+1379T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339111 | ||||||
| chr4:87339112
|
G | C | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.812+1378C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339112 | ||||||
| chr4:87339190
|
A | T | 23 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(20): Show | 25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.812+1300T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339190 | ||||||
| chr4:87339195
|
C | T | 5 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.812+1295G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339195 | ||||||
| chr4:87339372
|
C | T | 2 | a0001c0001t0003g0101a0001c0001t0003g0102 | 2 | NA18952.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.812+1118G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339372 | ||||||
| chr4:87339373
|
G | A | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.812+1117C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339373 | ||||||
| chr4:87339406
|
C | T | 3 | a0001c0005t0004g0369a0001c0005t0004g0370a0001c0005t0004g0374 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.812+1084G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339406 | ||||||
| chr4:87339506
|
A | C | 1 | a0001c0001t0003g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.812+984T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339506 | ||||||
| chr4:87339694
|
G | A | 3 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152 | 3 | HG02055.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.812+796C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339694 | ||||||
| chr4:87339713
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.812+777T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339713 | ||||||
| chr4:87339750
|
G | T | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.812+740C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339750 | ||||||
| chr4:87339835
|
T | C | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.812+655A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339835 | ||||||
| chr4:87339840
|
A | G | 1 | a0001c0002t0001g0183 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.812+650T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339840 | ||||||
| chr4:87339974
|
G | A | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.812+516C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339974 | ||||||
| chr4:87339990
|
C | T | 29 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(26): Show | 29 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.812+500G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87339990 | ||||||
| chr4:87340031
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.812+459G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87340031 | ||||||
| chr4:87340079
|
AT | A | 20 | a0001c0002t0001g0006a0001c0002t0001g0255a0001c0002t0001g0256others(17): Show | 21 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.812+410delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87340079 | ||||||
| chr4:87340149
|
A | G | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.812+341T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87340149 | ||||||
| chr4:87340222
|
T | C | 32 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(29): Show | 32 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.812+268A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87340222 | ||||||
| chr4:87340264
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(71): Show | 77 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.812+226A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87340264 | ||||||
| chr4:87340339
|
C | A | 1 | a0001c0002t0008g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.812+151G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 6/6 | chr4 | 87340339 | ||||||
| chr4:87340676
|
A | C | 52 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(49): Show | 54 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.696-70T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87340676 | ||||||
| chr4:87340849
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.696-243A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87340849 | ||||||
| chr4:87340854
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.696-248C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87340854 | ||||||
| chr4:87341237
|
T | C | 1 | a0001c0001t0001g0320 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.696-631A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341237 | ||||||
| chr4:87341321
|
G | A | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-715C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341321 | ||||||
| chr4:87341471
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.696-865A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341471 | ||||||
| chr4:87341529
|
T | C | 3 | a0001c0002t0003g0146a0001c0002t0003g0147a0001c0002t0003g0148 | 3 | HG01070.hp2 HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.696-923A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341529 | ||||||
| chr4:87341621
|
G | A | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1015C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341621 | ||||||
| chr4:87341629
|
G | A | 3 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152 | 3 | HG02055.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.696-1023C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341629 | ||||||
| chr4:87341640
|
C | T | 42 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(39): Show | 42 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.696-1034G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341640 | ||||||
| chr4:87341876
|
AATAG | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(61): Show | 67 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.696-1274_696-1271d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341876 | ||||||
| chr4:87341885
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.696-1279T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341885 | ||||||
| chr4:87341950
|
T | C | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1344A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87341950 | ||||||
| chr4:87342109
|
G | A | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1503C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342109 | ||||||
| chr4:87342307
|
A | G | 32 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(29): Show | 32 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.696-1701T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342307 | ||||||
| chr4:87342337
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.696-1731C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342337 | ||||||
| chr4:87342376
|
C | T | 15 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(12): Show | 15 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.696-1770G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342376 | ||||||
| chr4:87342381
|
C | CA | 20 | a0001c0001t0001g0241a0001c0001t0001g0302a0001c0001t0001g0309others(17): Show | 20 | HG01192.hp2 HG02027.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.696-1776dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342381 | ||||||
| chr4:87342381
|
C | CAA | 14 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0003g0139others(11): Show | 15 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.696-1777_696-1776d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342381 | ||||||
| chr4:87342381
|
CA | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0223a0001c0001t0001g0269others(5): Show | 8 | HG00323.hp1 HG01099.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-1776delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342381 | ||||||
| chr4:87342381
|
CAA | C | 14 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.696-1777_696-1776d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342381 | ||||||
| chr4:87342381
|
CAAA | C | 15 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(12): Show | 15 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.696-1778_696-1776d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342381 | ||||||
| chr4:87342404
|
T | G | 1 | a0001c0001t0004g0362 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.696-1798A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342404 | ||||||
| chr4:87342445
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.696-1839C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342445 | ||||||
| chr4:87342462
|
T | TTTGG | 28 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(25): Show | 28 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.696-1860_696-1857d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342462 | ||||||
| chr4:87342603
|
A | G | 6 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(3): Show | 6 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1997T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342603 | ||||||
| chr4:87342608
|
GA | G | 6 | a0001c0001t0001g0180a0001c0001t0006g0166a0001c0002t0011g0150others(3): Show | 6 | HG00609.hp1 HG02055.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-2003delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342608 | ||||||
| chr4:87342645
|
G | A | 3 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152 | 3 | HG02055.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.696-2039C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342645 | ||||||
| chr4:87342712
|
A | G | 28 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(25): Show | 28 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.696-2106T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342712 | ||||||
| chr4:87342786
|
C | CA | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-2181dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342786 | ||||||
| chr4:87342794
|
T | C | 28 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(25): Show | 28 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.696-2188A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342794 | ||||||
| chr4:87342911
|
C | T | 32 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(29): Show | 32 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.696-2305G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342911 | ||||||
| chr4:87342945
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.696-2339T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87342945 | ||||||
| chr4:87343026
|
A | C | 28 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(25): Show | 28 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.696-2420T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343026 | ||||||
| chr4:87343052
|
A | T | 28 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(25): Show | 28 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.696-2446T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343052 | ||||||
| chr4:87343299
|
A | G | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-2693T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343299 | ||||||
| chr4:87343435
|
T | C | 8 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0301others(5): Show | 8 | NA18949.hp1 NA18951.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-2829A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343435 | ||||||
| chr4:87343451
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.696-2845G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343451 | ||||||
| chr4:87343462
|
G | A | 242 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(239): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.696-2856C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343462 | ||||||
| chr4:87343473
|
G | A | 1 | a0001c0001t0003g0121 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.696-2867C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343473 | ||||||
| chr4:87343496
|
C | T | 1 | a0001c0001t0004g0373 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.696-2890G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343496 | ||||||
| chr4:87343547
|
C | CT | 180 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(177): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.696-2942dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343547 | ||||||
| chr4:87343547
|
CT | C | 36 | a0001c0001t0001g0217a0001c0001t0001g0249a0001c0001t0002g0036others(33): Show | 36 | HG00639.hp2 HG01069.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.696-2942delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343547 | ||||||
| chr4:87343557
|
T | C | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-2951A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343557 | ||||||
| chr4:87343610
|
C | T | 27 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(24): Show | 27 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.696-3004G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343610 | ||||||
| chr4:87343700
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.696-3094T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343700 | ||||||
| chr4:87343704
|
C | T | 48 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(45): Show | 49 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.696-3098G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343704 | ||||||
| chr4:87343751
|
T | C | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-3145A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343751 | ||||||
| chr4:87343767
|
C | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0066 | 2 | HG02027.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.696-3161G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343767 | ||||||
| chr4:87343842
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.696-3236G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343842 | ||||||
| chr4:87343908
|
G | A | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-3302C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87343908 | ||||||
| chr4:87344070
|
A | T | 7 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0228others(4): Show | 7 | HG00408.hp1 HG01978.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.696-3464T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344070 | ||||||
| chr4:87344094
|
C | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(70): Show | 74 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.696-3488G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344094 | ||||||
| chr4:87344145
|
A | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(70): Show | 74 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.696-3539T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344145 | ||||||
| chr4:87344230
|
C | A | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-3624G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344230 | ||||||
| chr4:87344259
|
A | G | 1 | a0001c0002t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.696-3653T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344259 | ||||||
| chr4:87344304
|
T | C | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-3698A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344304 | ||||||
| chr4:87344340
|
A | G | 5 | a0001c0003t0002g0028a0001c0003t0004g0344a0001c0003t0004g0364others(2): Show | 5 | HG01192.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-3734T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344340 | ||||||
| chr4:87344348
|
G | C | 1 | a0001c0002t0001g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.696-3742C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344348 | ||||||
| chr4:87344461
|
G | C | 5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0216others(2): Show | 5 | NA18943.hp1 NA18947.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-3855C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344461 | ||||||
| chr4:87344785
|
G | A | 51 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(48): Show | 52 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.696-4179C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344785 | ||||||
| chr4:87344854
|
C | T | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-4248G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344854 | ||||||
| chr4:87344890
|
T | C | 2 | a0001c0001t0004g0357a0001c0001t0004g0358 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.696-4284A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344890 | ||||||
| chr4:87344913
|
C | A | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-4307G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344913 | ||||||
| chr4:87344930
|
A | G | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-4324T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344930 | ||||||
| chr4:87344977
|
G | C | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.696-4371C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87344977 | ||||||
| chr4:87345042
|
T | C | 5 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-4436A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87345042 | ||||||
| chr4:87345137
|
G | A | 95 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(92): Show | 99 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.696-4531C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87345137 | ||||||
| chr4:87345199
|
AG | A | 6 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(3): Show | 6 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-4594delC | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87345199 | ||||||
| chr4:87345366
|
G | A | 8 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(5): Show | 9 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-4760C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87345366 | ||||||
| chr4:87345379
|
C | G | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-4773G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87345379 | ||||||
| chr4:87345555
|
C | G | 1 | a0001c0002t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.696-4949G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87345555 | ||||||
| chr4:87345779
|
C | A | 2 | a0001c0001t0005g0164a0001c0001t0009g0346 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.696-5173G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87345779 | ||||||
| chr4:87346103
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.696-5497T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346103 | ||||||
| chr4:87346136
|
A | C | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-5530T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346136 | ||||||
| chr4:87346227
|
C | A | 14 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(11): Show | 14 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.696-5621G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346227 | ||||||
| chr4:87346386
|
C | T | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-5780G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346386 | ||||||
| chr4:87346387
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(62): Show | 68 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.696-5781C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346387 | ||||||
| chr4:87346414
|
C | A | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-5808G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346414 | ||||||
| chr4:87346414
|
C | T | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-5808G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346414 | ||||||
| chr4:87346520
|
C | T | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-5914G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346520 | ||||||
| chr4:87346723
|
C | G | 52 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(49): Show | 54 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.696-6117G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346723 | ||||||
| chr4:87346795
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(61): Show | 65 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.696-6189G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346795 | ||||||
| chr4:87346825
|
G | C | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-6219C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346825 | ||||||
| chr4:87346874
|
A | T | 1 | a0001c0002t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.696-6268T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346874 | ||||||
| chr4:87346883
|
A | G | 10 | a0001c0002t0001g0289a0001c0002t0004g0348a0001c0002t0004g0349others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-6277T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346883 | ||||||
| chr4:87346887
|
A | G | 1 | a0001c0002t0001g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.696-6281T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346887 | ||||||
| chr4:87346894
|
T | A | 6 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(3): Show | 6 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-6288A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346894 | ||||||
| chr4:87346928
|
G | GTTTA | 47 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.696-6326_696-6323d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87346928 | ||||||
| chr4:87347059
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | NA18984.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.696-6453T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347059 | ||||||
| chr4:87347091
|
TTAGTATT others(6048): Show |
T | 61 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(58): Show | 62 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.695+4133_696-6486d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347091 | ||||||
| chr4:87347103
|
A | AT | 55 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(52): Show | 57 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.696-6498dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347103 | ||||||
| chr4:87347103
|
A | ATT | 8 | a0001c0001t0004g0008a0001c0001t0004g0359a0001c0001t0004g0360others(5): Show | 9 | HG00099.hp2 HG02809.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-6499_696-6498d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347103 | ||||||
| chr4:87347103
|
A | ATTTTT | 9 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0001g0269others(6): Show | 9 | HG00609.hp2 HG00738.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-6502_696-6498d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347103 | ||||||
| chr4:87347103
|
ATTTTTTT others(13): Show |
A | 3 | a0001c0002t0004g0376a0001c0002t0004g0377a0001c0002t0004g0378 | 3 | HG02630.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.696-6517_696-6498d others(22): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347103 | ||||||
| chr4:87347115
|
T | TTC | 22 | a0001c0001t0001g0242a0001c0001t0002g0051a0001c0002t0001g0002others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.696-6510_696-6509i others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347115 | ||||||
| chr4:87347116
|
C | CT | 17 | a0001c0001t0001g0178a0001c0001t0001g0231a0001c0001t0001g0232others(14): Show | 17 | HG00423.hp1 HG01978.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.696-6511dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347116 | ||||||
| chr4:87347116
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(146): Show | 155 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.696-6510G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347116 | ||||||
| chr4:87347117
|
T | C | 4 | a0001c0001t0002g0016a0001c0001t0002g0029a0001c0001t0002g0046others(1): Show | 4 | HG01517.hp1 HG03098.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-6511A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347117 | ||||||
| chr4:87347117
|
T | TC | 3 | a0001c0001t0001g0198a0001c0001t0001g0207a0001c0001t0006g0171 | 3 | HG00438.hp1 NA19006.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.696-6512_696-6511i others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347117 | ||||||
| chr4:87347117
|
T | TTC | 61 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(58): Show | 64 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.696-6512_696-6511i others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347117 | ||||||
| chr4:87347117
|
T | TTTTC | 50 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(47): Show | 51 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.696-6512_696-6511i others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347117 | ||||||
| chr4:87347189
|
A | C | 110 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.696-6583T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347189 | ||||||
| chr4:87347251
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.696-6645A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347251 | ||||||
| chr4:87347261
|
C | A | 4 | a0001c0001t0001g0314a0001c0001t0001g0326a0001c0001t0001g0328others(1): Show | 4 | NA18946.hp1 NA18969.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-6655G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347261 | ||||||
| chr4:87347281
|
G | C | 1 | a0001c0002t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.696-6675C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347281 | ||||||
| chr4:87347289
|
C | A | 1 | a0001c0002t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.696-6683G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347289 | ||||||
| chr4:87347314
|
C | T | 1 | a0001c0001t0004g0359 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.696-6708G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347314 | ||||||
| chr4:87347670
|
T | G | 1 | a0001c0001t0002g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.696-7064A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347670 | ||||||
| chr4:87347723
|
T | C | 1 | a0001c0001t0003g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.696-7117A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347723 | ||||||
| chr4:87347768
|
G | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(79): Show | 84 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.696-7162C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347768 | ||||||
| chr4:87347951
|
C | T | 1 | a0001c0002t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.696-7345G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87347951 | ||||||
| chr4:87348050
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246 | 5 | NA18941.hp1 NA18959.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-7444T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348050 | ||||||
| chr4:87348066
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696-7460C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348066 | ||||||
| chr4:87348067
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696-7461A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348067 | ||||||
| chr4:87348069
|
G | C | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696-7463C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348069 | ||||||
| chr4:87348087
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696-7481G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348087 | ||||||
| chr4:87348093
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696-7487C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348093 | ||||||
| chr4:87348095
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696-7489T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348095 | ||||||
| chr4:87348102
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.696-7496A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348102 | ||||||
| chr4:87348113
|
GA | G | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-7508delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348113 | ||||||
| chr4:87348153
|
T | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246 | 5 | NA18941.hp1 NA18959.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-7547A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348153 | ||||||
| chr4:87348202
|
C | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(70): Show | 74 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.696-7596G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348202 | ||||||
| chr4:87348261
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246 | 5 | NA18941.hp1 NA18959.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-7655A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348261 | ||||||
| chr4:87348415
|
T | G | 93 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(90): Show | 97 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.696-7809A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348415 | ||||||
| chr4:87348443
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(61): Show | 65 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.696-7837G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348443 | ||||||
| chr4:87348447
|
A | G | 110 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(107): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.696-7841T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348447 | ||||||
| chr4:87348487
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.696-7881G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348487 | ||||||
| chr4:87348492
|
T | C | 1 | a0001c0002t0004g0355 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.696-7886A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348492 | ||||||
| chr4:87348551
|
A | T | 1 | a0001c0002t0004g0377 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.696-7945T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348551 | ||||||
| chr4:87348602
|
A | G | 1 | a0001c0001t0003g0094 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.696-7996T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348602 | ||||||
| chr4:87348785
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.696-8179G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348785 | ||||||
| chr4:87348842
|
A | ATCCCTT | 248 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(245): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.696-8237_696-8236i others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348842 | ||||||
| chr4:87348844
|
T | TAA | 248 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(245): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.696-8239_696-8238i others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348844 | ||||||
| chr4:87348935
|
A | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(61): Show | 65 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.696-8329T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87348935 | ||||||
| chr4:87349026
|
G | A | 6 | a0001c0001t0001g0212a0001c0001t0001g0221a0001c0001t0002g0037others(3): Show | 6 | HG00544.hp1 HG00621.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+8253C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349026 | ||||||
| chr4:87349056
|
G | A | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+8223C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349056 | ||||||
| chr4:87349087
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.695+8192A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349087 | ||||||
| chr4:87349167
|
C | A | 1 | a0001c0002t0010g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.695+8112G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349167 | ||||||
| chr4:87349197
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(62): Show | 68 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.695+8082C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349197 | ||||||
| chr4:87349237
|
A | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01069.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.695+8042T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349237 | ||||||
| chr4:87349345
|
T | C | 1 | a0001c0002t0004g0375 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.695+7934A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349345 | ||||||
| chr4:87349515
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.695+7764C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349515 | ||||||
| chr4:87349519
|
G | T | 94 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(91): Show | 98 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.695+7760C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349519 | ||||||
| chr4:87349579
|
T | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.695+7700A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349579 | ||||||
| chr4:87349719
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.695+7560C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349719 | ||||||
| chr4:87349728
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.695+7551C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349728 | ||||||
| chr4:87349863
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.695+7416C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349863 | ||||||
| chr4:87349955
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.695+7324G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87349955 | ||||||
| chr4:87350171
|
G | A | 3 | a0001c0002t0004g0376a0001c0002t0004g0377a0001c0002t0004g0378 | 3 | HG02630.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.695+7108C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350171 | ||||||
| chr4:87350246
|
T | C | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+7033A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350246 | ||||||
| chr4:87350426
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | NA18982.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.695+6853C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350426 | ||||||
| chr4:87350563
|
G | T | 1 | a0001c0001t0002g0044 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.695+6716C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350563 | ||||||
| chr4:87350586
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.695+6693A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350586 | ||||||
| chr4:87350637
|
T | C | 52 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(49): Show | 54 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.695+6642A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350637 | ||||||
| chr4:87350751
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.695+6528C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350751 | ||||||
| chr4:87350775
|
G | C | 7 | a0001c0001t0001g0227a0001c0002t0001g0277a0001c0002t0001g0278others(4): Show | 7 | HG01074.hp2 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+6504C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350775 | ||||||
| chr4:87350965
|
T | C | 2 | a0001c0001t0001g0325a0001c0001t0001g0335 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.695+6314A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87350965 | ||||||
| chr4:87351046
|
C | G | 1 | a0001c0001t0001g0220 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.695+6233G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351046 | ||||||
| chr4:87351076
|
A | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(249): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.695+6203T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351076 | ||||||
| chr4:87351079
|
G | A | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.695+6200C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351079 | ||||||
| chr4:87351080
|
C | T | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.695+6199G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351080 | ||||||
| chr4:87351216
|
C | T | 1 | a0001c0002t0004g0345 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.695+6063G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351216 | ||||||
| chr4:87351250
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0320a0001c0001t0001g0321others(2): Show | 6 | HG02040.hp2 NA18943.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+6029C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351250 | ||||||
| chr4:87351480
|
C | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(70): Show | 74 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.695+5799G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351480 | ||||||
| chr4:87351579
|
G | C | 2 | a0001c0002t0002g0022a0001c0002t0002g0023 | 2 | HG00642.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.695+5700C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351579 | ||||||
| chr4:87351601
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.695+5678C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351601 | ||||||
| chr4:87351616
|
G | A | 1 | a0001c0002t0001g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695+5663C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351616 | ||||||
| chr4:87351643
|
A | G | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.695+5636T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351643 | ||||||
| chr4:87351662
|
T | C | 2 | a0001c0001t0002g0042a0001c0001t0002g0066 | 2 | HG02027.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.695+5617A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351662 | ||||||
| chr4:87351679
|
T | C | 3 | a0001c0005t0004g0369a0001c0005t0004g0370a0001c0005t0004g0374 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.695+5600A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351679 | ||||||
| chr4:87351793
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.695+5486G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351793 | ||||||
| chr4:87351853
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.695+5426G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87351853 | ||||||
| chr4:87352193
|
C | T | 1 | a0001c0005t0004g0374 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.695+5086G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352193 | ||||||
| chr4:87352235
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.695+5044G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352235 | ||||||
| chr4:87352379
|
C | T | 1 | a0001c0002t0002g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.695+4900G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352379 | ||||||
| chr4:87352390
|
T | G | 1 | a0001c0002t0002g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.695+4889A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352390 | ||||||
| chr4:87352398
|
C | T | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.695+4881G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352398 | ||||||
| chr4:87352430
|
C | T | 1 | a0001c0002t0004g0345 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.695+4849G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352430 | ||||||
| chr4:87352433
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0004g0372 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.695+4846C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352433 | ||||||
| chr4:87352444
|
G | A | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.695+4835C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352444 | ||||||
| chr4:87352535
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.695+4744T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352535 | ||||||
| chr4:87352580
|
C | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(61): Show | 67 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.695+4699G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352580 | ||||||
| chr4:87352589
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.695+4690C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352589 | ||||||
| chr4:87352603
|
A | G | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.695+4676T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352603 | ||||||
| chr4:87352656
|
G | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(62): Show | 68 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.695+4623C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352656 | ||||||
| chr4:87352664
|
C | A | 1 | a0001c0002t0002g0026 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.695+4615G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352664 | ||||||
| chr4:87352721
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01069.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.695+4558A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352721 | ||||||
| chr4:87352722
|
C | T | 4 | a0001c0001t0001g0226a0001c0001t0002g0033a0001c0001t0002g0035others(1): Show | 4 | HG01069.hp2 HG01175.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+4557G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352722 | ||||||
| chr4:87352723
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.695+4556C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352723 | ||||||
| chr4:87352723
|
G | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01069.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.695+4556C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352723 | ||||||
| chr4:87352724
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01069.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.695+4555A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352724 | ||||||
| chr4:87352727
|
C | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01069.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.695+4552G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352727 | ||||||
| chr4:87352728
|
C | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01069.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.695+4551G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352728 | ||||||
| chr4:87352777
|
C | T | 2 | a0001c0001t0003g0109a0001c0001t0003g0110 | 2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.695+4502G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352777 | ||||||
| chr4:87352784
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.695+4495C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352784 | ||||||
| chr4:87352895
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(62): Show | 68 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.695+4384G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352895 | ||||||
| chr4:87352896
|
G | A | 6 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0003g0139others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+4383C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352896 | ||||||
| chr4:87352923
|
G | C | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.695+4356C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352923 | ||||||
| chr4:87352965
|
C | T | 1 | a0001c0002t0004g0352 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.695+4314G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352965 | ||||||
| chr4:87352981
|
G | T | 4 | a0001c0001t0001g0197a0001c0001t0002g0082a0001c0001t0003g0093others(1): Show | 4 | HG00735.hp1 HG02280.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+4298C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352981 | ||||||
| chr4:87352986
|
C | T | 1 | a0001c0002t0004g0345 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.695+4293G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87352986 | ||||||
| chr4:87353045
|
G | A | 1 | a0001c0001t0015g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.695+4234C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353045 | ||||||
| chr4:87353187
|
C | T | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+4092G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353187 | ||||||
| chr4:87353421
|
T | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(315): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.695+3858A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353421 | ||||||
| chr4:87353445
|
A | G | 26 | a0001c0002t0001g0006a0001c0002t0001g0255a0001c0002t0001g0256others(23): Show | 27 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.695+3834T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353445 | ||||||
| chr4:87353588
|
T | G | 57 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(54): Show | 58 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.695+3691A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353588 | ||||||
| chr4:87353703
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.695+3576G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353703 | ||||||
| chr4:87353731
|
A | AG | 52 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(49): Show | 54 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.695+3547dupC | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353731 | ||||||
| chr4:87353733
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.695+3546C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353733 | ||||||
| chr4:87353848
|
C | T | 1 | a0001c0002t0002g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.695+3431G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353848 | ||||||
| chr4:87353884
|
T | C | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+3395A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353884 | ||||||
| chr4:87353947
|
C | T | 41 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(38): Show | 43 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.695+3332G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353947 | ||||||
| chr4:87353989
|
C | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(68): Show | 72 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.695+3290G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87353989 | ||||||
| chr4:87354027
|
T | C | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+3252A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354027 | ||||||
| chr4:87354037
|
C | T | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+3242G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354037 | ||||||
| chr4:87354111
|
C | A | 53 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(50): Show | 54 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.695+3168G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354111 | ||||||
| chr4:87354214
|
G | A | 182 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(179): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.695+3065C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354214 | ||||||
| chr4:87354231
|
C | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.695+3048G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354231 | ||||||
| chr4:87354236
|
C | G | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+3043G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354236 | ||||||
| chr4:87354240
|
C | T | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+3039G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354240 | ||||||
| chr4:87354307
|
A | T | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+2972T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354307 | ||||||
| chr4:87354347
|
T | C | 53 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(50): Show | 54 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.695+2932A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354347 | ||||||
| chr4:87354362
|
G | C | 2 | a0001c0001t0001g0318a0001c0001t0006g0173 | 2 | NA18963.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.695+2917C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354362 | ||||||
| chr4:87354547
|
T | G | 53 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(50): Show | 54 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.695+2732A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354547 | ||||||
| chr4:87354556
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.695+2723T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354556 | ||||||
| chr4:87354587
|
C | G | 1 | a0001c0002t0004g0354 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.695+2692G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354587 | ||||||
| chr4:87354629
|
C | T | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+2650G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354629 | ||||||
| chr4:87354642
|
C | CA | 6 | a0001c0001t0005g0159a0001c0001t0005g0163a0001c0001t0005g0164others(3): Show | 6 | HG00639.hp2 HG00733.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.695+2636dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354642 | ||||||
| chr4:87354650
|
AT | A | 7 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(4): Show | 7 | HG02258.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+2628delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354650 | ||||||
| chr4:87354651
|
T | A | 46 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(43): Show | 47 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.695+2628A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354651 | ||||||
| chr4:87354657
|
A | T | 3 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152 | 3 | HG02055.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.695+2622T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354657 | ||||||
| chr4:87354659
|
AT | A | 3 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152 | 3 | HG02055.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.695+2619delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354659 | ||||||
| chr4:87354660
|
T | A | 64 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(61): Show | 65 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.695+2619A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354660 | ||||||
| chr4:87354737
|
A | G | 4 | a0001c0002t0001g0181a0001c0002t0001g0182a0001c0002t0001g0183others(1): Show | 4 | HG00099.hp1 HG01261.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+2542T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354737 | ||||||
| chr4:87354822
|
T | G | 1 | a0001c0001t0002g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.695+2457A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354822 | ||||||
| chr4:87354927
|
C | A | 1 | a0001c0002t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.695+2352G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354927 | ||||||
| chr4:87354949
|
C | CA | 77 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(74): Show | 80 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.695+2329dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354949 | ||||||
| chr4:87354949
|
C | CAA | 52 | a0001c0001t0001g0200a0001c0001t0001g0246a0001c0001t0001g0308others(49): Show | 53 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.695+2328_695+2329d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354949 | ||||||
| chr4:87354949
|
CA | C | 106 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(103): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.695+2329delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354949 | ||||||
| chr4:87354949
|
CAA | C | 10 | a0001c0001t0001g0238a0001c0001t0001g0297a0001c0001t0002g0016others(7): Show | 10 | HG01884.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.695+2328_695+2329d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87354949 | ||||||
| chr4:87355132
|
T | C | 4 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+2147A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355132 | ||||||
| chr4:87355426
|
C | T | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+1853G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355426 | ||||||
| chr4:87355462
|
A | G | 2 | a0001c0001t0003g0101a0001c0001t0003g0102 | 2 | NA18952.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.695+1817T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355462 | ||||||
| chr4:87355524
|
GA | G | 10 | a0001c0001t0001g0318a0001c0003t0002g0028a0001c0003t0003g0131others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.695+1754delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355524 | ||||||
| chr4:87355553
|
T | C | 64 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(61): Show | 65 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.695+1726A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355553 | ||||||
| chr4:87355728
|
A | G | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+1551T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355728 | ||||||
| chr4:87355765
|
G | T | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+1514C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355765 | ||||||
| chr4:87355883
|
AAC | A | 52 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(49): Show | 54 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.695+1394_695+1395d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355883 | ||||||
| chr4:87355903
|
CAA | C | 81 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(78): Show | 82 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.695+1374_695+1375d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355903 | ||||||
| chr4:87355915
|
AAAAC | A | 7 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0003g0139others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+1360_695+1363d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355915 | ||||||
| chr4:87355994
|
TC | T | 4 | a0001c0001t0001g0199a0001c0001t0001g0310a0001c0001t0003g0116others(1): Show | 4 | NA18954.hp1 NA18957.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.695+1284delG | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87355994 | ||||||
| chr4:87356030
|
G | A | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.695+1249C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356030 | ||||||
| chr4:87356051
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.695+1228A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356051 | ||||||
| chr4:87356137
|
G | A | 58 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(55): Show | 59 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.695+1142C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356137 | ||||||
| chr4:87356138
|
A | G | 58 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(55): Show | 59 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.695+1141T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356138 | ||||||
| chr4:87356162
|
G | A | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+1117C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356162 | ||||||
| chr4:87356273
|
T | C | 58 | a0001c0001t0001g0249a0001c0001t0005g0154a0001c0001t0005g0155others(55): Show | 59 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.695+1006A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356273 | ||||||
| chr4:87356580
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(315): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.695+699T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356580 | ||||||
| chr4:87356618
|
G | A | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+661C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356618 | ||||||
| chr4:87356745
|
T | C | 4 | a0001c0001t0001g0176a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | NA18982.hp2 NA18985.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+534A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356745 | ||||||
| chr4:87356775
|
G | A | 111 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.695+504C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356775 | ||||||
| chr4:87356904
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.695+375A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87356904 | ||||||
| chr4:87357105
|
T | C | 12 | a0001c0001t0001g0188a0001c0001t0001g0213a0001c0001t0001g0214others(9): Show | 12 | HG02165.hp1 NA18943.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.695+174A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87357105 | ||||||
| chr4:87357231
|
G | T | 6 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(3): Show | 6 | HG00609.hp2 HG01175.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+48C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 5/6 | chr4 | 87357231 | ||||||
| chr4:87357854
|
A | AT | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.558-439_558-438ins others(1): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357854 | ||||||
| chr4:87357855
|
C | A | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.558-439G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357855 | ||||||
| chr4:87357891
|
T | G | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.558-475A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357891 | ||||||
| chr4:87357948
|
A | ATTT | 4 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0001g0308others(1): Show | 4 | NA18949.hp1 NA18951.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.558-533_558-532ins others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTT | 3 | a0001c0001t0001g0321a0001c0001t0001g0334a0001c0001t0001g0336 | 3 | NA18957.hp2 NA18984.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.558-533_558-532ins others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTTT | 14 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0269others(11): Show | 14 | HG00738.hp2 HG03704.hp2 HG04204.hp1 others(11): Show |
intron_variant | MODIFIER | c.558-533_558-532ins others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTTTT | 19 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0287others(16): Show | 19 | HG00621.hp1 HG00673.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.558-533_558-532ins others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTTTT others(1): Show |
14 | a0001c0001t0001g0007a0001c0001t0001g0180a0001c0001t0001g0189others(11): Show | 15 | HG00609.hp1 HG01981.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-533_558-532ins others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0176a0001c0001t0001g0194a0001c0001t0001g0300others(5): Show | 8 | HG01175.hp1 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.558-533_558-532ins others(9): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0002g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.558-533_558-532ins others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.558-533_558-532ins others(13): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0002g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.558-533_558-532ins others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
AATTTTTT others(1): Show |
A | 8 | a0001c0001t0001g0214a0001c0001t0001g0250a0001c0001t0001g0251others(5): Show | 8 | HG00597.hp2 NA18947.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.558-540_558-533del others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357948
|
AATTTTTT others(5): Show |
A | 1 | a0001c0002t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.558-544_558-533del others(12): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357948 | ||||||
| chr4:87357949
|
A | AT | 59 | a0001c0001t0001g0209a0001c0001t0001g0232a0001c0001t0001g0236others(56): Show | 59 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.558-534dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATT | 12 | a0001c0001t0002g0015a0001c0001t0002g0039a0001c0001t0002g0056others(9): Show | 13 | HG00099.hp2 HG01361.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.558-535_558-534dup others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTT | 7 | a0001c0001t0001g0226a0001c0001t0004g0361a0001c0001t0016g0149others(4): Show | 7 | HG00741.hp1 HG02273.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.558-536_558-534dup others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT | 33 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(30): Show | 33 | HG00597.hp1 HG01261.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.558-540_558-534dup others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(1): Show |
24 | a0001c0001t0001g0197a0001c0001t0001g0205a0001c0001t0001g0208others(21): Show | 25 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.558-541_558-534dup others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0002g0031a0001c0001t0003g0092a0001c0001t0003g0095others(5): Show | 8 | HG00642.hp2 HG01978.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.558-542_558-534dup others(9): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0198a0001c0001t0001g0207 | 2 | HG00438.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.558-543_558-534dup others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(4): Show |
2 | a0001c0002t0001g0006a0001c0002t0001g0264 | 3 | HG00733.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.558-544_558-534dup others(11): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(5): Show |
2 | a0001c0002t0012g0257a0001c0002t0012g0262 | 2 | HG00741.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.558-545_558-534dup others(12): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(6): Show |
2 | a0001c0002t0001g0258a0001c0002t0001g0263 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.558-546_558-534dup others(13): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.558-547_558-534dup others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(8): Show |
1 | a0001c0002t0001g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.558-548_558-534dup others(15): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | ATTTTTTT others(9): Show |
2 | a0001c0002t0001g0260a0001c0002t0014g0018 | 2 | HG00323.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.558-549_558-534dup others(16): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
A | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(65): Show | 69 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.558-533T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
AT | A | 40 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0188others(37): Show | 40 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.558-534delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
ATTTTTTT others(1): Show |
A | 5 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 7 | HG02071.hp1 HG02602.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.558-541_558-534del others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.558-549_558-534del others(16): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357949
|
ATTTTTTT others(11): Show |
A | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.558-551_558-534del others(18): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357949 | ||||||
| chr4:87357953
|
T | A | 1 | a0001c0006t0005g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.558-537A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357953 | ||||||
| chr4:87357954
|
T | A | 5 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-538A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357954 | ||||||
| chr4:87357968
|
T | A | 9 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(6): Show | 9 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.558-552A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357968 | ||||||
| chr4:87357986
|
G | C | 41 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(38): Show | 42 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.558-570C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87357986 | ||||||
| chr4:87358022
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(179): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.558-606A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358022 | ||||||
| chr4:87358061
|
C | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-645G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358061 | ||||||
| chr4:87358062
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-646G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358062 | ||||||
| chr4:87358071
|
C | A | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-655G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358071 | ||||||
| chr4:87358072
|
C | G | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-656G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358072 | ||||||
| chr4:87358074
|
GC | G | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-659delG | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358074 | ||||||
| chr4:87358085
|
C | T | 4 | a0001c0001t0001g0287a0001c0001t0001g0300a0001c0001t0001g0305others(1): Show | 4 | NA18951.hp1 NA18959.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.558-669G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358085 | ||||||
| chr4:87358086
|
G | C | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.558-670C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358086 | ||||||
| chr4:87358087
|
C | A | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.558-671G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358087 | ||||||
| chr4:87358110
|
C | T | 1 | a0001c0002t0009g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.558-694G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358110 | ||||||
| chr4:87358117
|
A | G | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.558-701T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358117 | ||||||
| chr4:87358151
|
C | T | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-735G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358151 | ||||||
| chr4:87358188
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0006g0168 | 2 | NA18980.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.558-772G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358188 | ||||||
| chr4:87358253
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.558-837C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358253 | ||||||
| chr4:87358412
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-996C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358412 | ||||||
| chr4:87358413
|
C | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-997G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358413 | ||||||
| chr4:87358536
|
C | T | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-1120G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358536 | ||||||
| chr4:87358558
|
C | T | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-1142G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358558 | ||||||
| chr4:87358652
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.558-1236G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358652 | ||||||
| chr4:87358785
|
T | A | 3 | a0001c0002t0003g0146a0001c0002t0003g0147a0001c0002t0003g0148 | 3 | HG01070.hp2 HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.558-1369A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358785 | ||||||
| chr4:87358786
|
A | T | 6 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.558-1370T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358786 | ||||||
| chr4:87358791
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(168): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.558-1375T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358791 | ||||||
| chr4:87358794
|
T | A | 2 | a0001c0001t0002g0029a0001c0002t0010g0013 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.558-1378A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358794 | ||||||
| chr4:87358795
|
T | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(169): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.558-1379A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358795 | ||||||
| chr4:87358796
|
A | T | 2 | a0001c0001t0003g0139a0001c0001t0003g0140 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.558-1380T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358796 | ||||||
| chr4:87358802
|
A | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(63): Show | 69 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.558-1386T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358802 | ||||||
| chr4:87358829
|
A | G | 1 | a0001c0001t0001g0329 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.558-1413T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358829 | ||||||
| chr4:87358835
|
T | A | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-1419A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358835 | ||||||
| chr4:87358949
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(186): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.558-1533C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358949 | ||||||
| chr4:87358971
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-1555A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87358971 | ||||||
| chr4:87359030
|
G | T | 1 | a0001c0001t0001g0238 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.558-1614C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359030 | ||||||
| chr4:87359181
|
T | C | 14 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(11): Show | 14 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.558-1765A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359181 | ||||||
| chr4:87359227
|
T | C | 5 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.558-1811A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359227 | ||||||
| chr4:87359253
|
T | TA | 4 | a0001c0001t0001g0197a0001c0001t0002g0082a0001c0001t0003g0093others(1): Show | 4 | HG00735.hp1 HG02280.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.558-1838dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359253 | ||||||
| chr4:87359350
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(172): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.558-1934G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359350 | ||||||
| chr4:87359497
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.558-2081C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359497 | ||||||
| chr4:87359565
|
C | T | 1 | a0001c0003t0008g0295 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.558-2149G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359565 | ||||||
| chr4:87359573
|
A | T | 4 | a0001c0003t0003g0131a0001c0003t0003g0132a0001c0003t0003g0133others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.558-2157T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359573 | ||||||
| chr4:87359674
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(170): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.558-2258T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359674 | ||||||
| chr4:87359868
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-2452T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359868 | ||||||
| chr4:87359885
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-2469T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359885 | ||||||
| chr4:87359927
|
G | T | 1 | a0001c0001t0002g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.558-2511C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359927 | ||||||
| chr4:87359947
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(170): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.558-2531T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87359947 | ||||||
| chr4:87360009
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.558-2593T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360009 | ||||||
| chr4:87360030
|
G | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(296): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.558-2614C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360030 | ||||||
| chr4:87360139
|
G | GT | 190 | a0001c0001t0001g0001a0001c0001t0001g0176a0001c0001t0001g0177others(187): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.558-2724dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360139 | ||||||
| chr4:87360212
|
A | G | 2 | a0001c0001t0001g0318a0001c0001t0006g0173 | 2 | NA18963.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.558-2796T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360212 | ||||||
| chr4:87360212
|
AAT | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(170): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.558-2798_558-2797d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360212 | ||||||
| chr4:87360272
|
T | G | 5 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-2856A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360272 | ||||||
| chr4:87360326
|
T | C | 1 | a0001c0002t0011g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.558-2910A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360326 | ||||||
| chr4:87360417
|
G | C | 1 | a0001c0002t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.558-3001C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360417 | ||||||
| chr4:87360685
|
T | C | 2 | a0001c0001t0004g0357a0001c0001t0004g0358 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.558-3269A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360685 | ||||||
| chr4:87360832
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-3416T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360832 | ||||||
| chr4:87360864
|
C | T | 18 | a0001c0002t0001g0002a0001c0002t0001g0184a0001c0002t0001g0187others(15): Show | 20 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.558-3448G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360864 | ||||||
| chr4:87360869
|
A | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(170): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.558-3453T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360869 | ||||||
| chr4:87360882
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.558-3466C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360882 | ||||||
| chr4:87360959
|
T | C | 15 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.558-3543A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87360959 | ||||||
| chr4:87361489
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0002g0081 | 3 | HG00609.hp2 HG01175.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.558-4073G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361489 | ||||||
| chr4:87361505
|
T | C | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.558-4089A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361505 | ||||||
| chr4:87361557
|
G | A | 168 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(165): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.558-4141C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361557 | ||||||
| chr4:87361560
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-4144C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361560 | ||||||
| chr4:87361636
|
G | A | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.558-4220C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361636 | ||||||
| chr4:87361638
|
G | A | 17 | a0001c0001t0004g0372a0001c0001t0004g0373a0001c0001t0005g0154others(14): Show | 17 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.558-4222C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361638 | ||||||
| chr4:87361644
|
G | A | 52 | a0001c0001t0004g0372a0001c0001t0004g0373a0001c0001t0005g0154others(49): Show | 53 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.558-4228C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361644 | ||||||
| chr4:87361683
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.558-4267G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361683 | ||||||
| chr4:87361684
|
G | A | 2 | a0001c0001t0003g0127a0001c0001t0003g0130 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.558-4268C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361684 | ||||||
| chr4:87361698
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.558-4282G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361698 | ||||||
| chr4:87361741
|
T | C | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.558-4325A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361741 | ||||||
| chr4:87361829
|
A | G | 1 | a0002c0004t0001g0273 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.558-4413T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361829 | ||||||
| chr4:87361858
|
A | C | 8 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 8 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.558-4442T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361858 | ||||||
| chr4:87361897
|
G | A | 23 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(20): Show | 25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.558-4481C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361897 | ||||||
| chr4:87361903
|
A | T | 1 | a0001c0003t0013g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.558-4487T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87361903 | ||||||
| chr4:87362075
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.558-4659C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362075 | ||||||
| chr4:87362263
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | NA18984.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.558-4847C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362263 | ||||||
| chr4:87362353
|
C | T | 8 | a0001c0001t0001g0241a0001c0001t0001g0283a0001c0001t0002g0004others(5): Show | 9 | HG01123.hp2 HG01192.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.558-4937G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362353 | ||||||
| chr4:87362621
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(247): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.558-5205A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362621 | ||||||
| chr4:87362673
|
C | T | 6 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0001g0261others(3): Show | 6 | HG00323.hp2 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.558-5257G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362673 | ||||||
| chr4:87362757
|
A | G | 1 | a0001c0002t0002g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.558-5341T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362757 | ||||||
| chr4:87362771
|
C | T | 3 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152 | 3 | HG02055.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.558-5355G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362771 | ||||||
| chr4:87362802
|
G | A | 9 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.558-5386C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362802 | ||||||
| chr4:87362906
|
G | A | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0311others(3): Show | 6 | HG00408.hp2 NA18949.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.558-5490C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362906 | ||||||
| chr4:87362944
|
T | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0189others(146): Show | 153 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.558-5528A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87362944 | ||||||
| chr4:87363130
|
A | T | 62 | a0001c0001t0002g0032a0001c0001t0003g0139a0001c0001t0003g0140others(59): Show | 63 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.558-5714T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363130 | ||||||
| chr4:87363171
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.558-5755C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363171 | ||||||
| chr4:87363306
|
A | G | 15 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(12): Show | 15 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.558-5890T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363306 | ||||||
| chr4:87363464
|
G | A | 2 | a0001c0001t0003g0139a0001c0001t0003g0140 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.558-6048C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363464 | ||||||
| chr4:87363731
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-6315T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363731 | ||||||
| chr4:87363744
|
G | A | 9 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.558-6328C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363744 | ||||||
| chr4:87363749
|
G | C | 9 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.558-6333C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363749 | ||||||
| chr4:87363749
|
G | T | 1 | a0001c0003t0013g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.558-6333C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363749 | ||||||
| chr4:87363751
|
C | A | 56 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(53): Show | 57 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.558-6335G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363751 | ||||||
| chr4:87363787
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.558-6371C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363787 | ||||||
| chr4:87363820
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(314): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.558-6404T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363820 | ||||||
| chr4:87363965
|
G | A | 1 | a0001c0002t0001g0002 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.558-6549C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87363965 | ||||||
| chr4:87364070
|
T | A | 96 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(93): Show | 100 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.558-6654A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364070 | ||||||
| chr4:87364143
|
TTTTTG | T | 55 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.558-6732_558-6728d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364143 | ||||||
| chr4:87364171
|
T | A | 19 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.558-6755A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364171 | ||||||
| chr4:87364202
|
G | A | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.558-6786C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364202 | ||||||
| chr4:87364270
|
G | GA | 26 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(23): Show | 26 | HG00544.hp2 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-6855dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364270 | ||||||
| chr4:87364270
|
GA | G | 6 | a0001c0001t0001g0176a0001c0001t0001g0228a0001c0001t0001g0300others(3): Show | 6 | HG01993.hp1 HG02735.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.558-6855delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364270 | ||||||
| chr4:87364270
|
GAA | G | 53 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(50): Show | 54 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.558-6856_558-6855d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364270 | ||||||
| chr4:87364271
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.558-6855T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364271 | ||||||
| chr4:87364285
|
A | G | 1 | a0001c0001t0007g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.558-6869T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364285 | ||||||
| chr4:87364296
|
C | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(139): Show | 146 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.558-6880G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364296 | ||||||
| chr4:87364313
|
T | A | 1 | a0001c0001t0001g0324 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.558-6897A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364313 | ||||||
| chr4:87364412
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.558-6996C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364412 | ||||||
| chr4:87364546
|
T | C | 1 | a0001c0001t0007g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.558-7130A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364546 | ||||||
| chr4:87364652
|
G | C | 50 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.558-7236C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364652 | ||||||
| chr4:87364759
|
T | G | 27 | a0001c0002t0001g0006a0001c0002t0001g0255a0001c0002t0001g0256others(24): Show | 28 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.558-7343A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364759 | ||||||
| chr4:87364871
|
T | C | 5 | a0001c0001t0001g0287a0001c0001t0001g0300a0001c0001t0001g0305others(2): Show | 5 | HG00673.hp2 NA18951.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-7455A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364871 | ||||||
| chr4:87364919
|
A | C | 3 | a0001c0005t0004g0369a0001c0005t0004g0370a0001c0005t0004g0374 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.558-7503T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87364919 | ||||||
| chr4:87365041
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.558-7625G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365041 | ||||||
| chr4:87365106
|
T | A | 47 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.557+7603A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365106 | ||||||
| chr4:87365157
|
G | A | 5 | a0001c0001t0002g0003a0001c0001t0002g0048a0001c0001t0002g0049others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.557+7552C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365157 | ||||||
| chr4:87365202
|
A | G | 9 | a0001c0001t0001g0241a0001c0001t0001g0283a0001c0001t0002g0004others(6): Show | 10 | HG01123.hp2 HG01192.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.557+7507T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365202 | ||||||
| chr4:87365211
|
G | A | 50 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.557+7498C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365211 | ||||||
| chr4:87365221
|
T | C | 50 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.557+7488A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365221 | ||||||
| chr4:87365257
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(133): Show | 140 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.557+7452G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365257 | ||||||
| chr4:87365367
|
G | T | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.557+7342C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365367 | ||||||
| chr4:87365457
|
A | G | 1 | a0001c0001t0003g0101 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.557+7252T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365457 | ||||||
| chr4:87365525
|
C | T | 3 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379 | 3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.557+7184G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365525 | ||||||
| chr4:87365644
|
C | A | 2 | a0001c0001t0003g0104a0001c0001t0003g0105 | 2 | HG02027.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.557+7065G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365644 | ||||||
| chr4:87365678
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(88): Show | 94 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.557+7031A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365678 | ||||||
| chr4:87365750
|
T | TA | 238 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(235): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.557+6958dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365750 | ||||||
| chr4:87365771
|
A | C | 1 | a0001c0002t0008g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.557+6938T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365771 | ||||||
| chr4:87365773
|
G | A | 50 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.557+6936C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365773 | ||||||
| chr4:87365831
|
G | GA | 84 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(81): Show | 87 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.557+6877dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87365831 | ||||||
| chr4:87366015
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(63): Show | 69 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.557+6694G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366015 | ||||||
| chr4:87366034
|
T | C | 5 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.557+6675A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366034 | ||||||
| chr4:87366037
|
G | T | 1 | a0001c0002t0008g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.557+6672C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366037 | ||||||
| chr4:87366083
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(88): Show | 94 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.557+6626G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366083 | ||||||
| chr4:87366132
|
C | T | 3 | a0001c0005t0004g0369a0001c0005t0004g0370a0001c0005t0004g0374 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.557+6577G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366132 | ||||||
| chr4:87366211
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(139): Show | 146 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.557+6498T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366211 | ||||||
| chr4:87366263
|
T | A | 1 | a0001c0001t0002g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.557+6446A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366263 | ||||||
| chr4:87366264
|
A | T | 1 | a0001c0001t0002g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.557+6445T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366264 | ||||||
| chr4:87366300
|
C | T | 1 | a0001c0001t0003g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.557+6409G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366300 | ||||||
| chr4:87366446
|
C | T | 98 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(95): Show | 102 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.557+6263G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366446 | ||||||
| chr4:87366632
|
T | C | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+6077A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366632 | ||||||
| chr4:87366760
|
T | C | 3 | a0001c0002t0011g0150a0001c0002t0011g0151a0001c0002t0011g0152 | 3 | HG02055.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.557+5949A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366760 | ||||||
| chr4:87366841
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(139): Show | 146 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.557+5868C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366841 | ||||||
| chr4:87366865
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.557+5844C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366865 | ||||||
| chr4:87366929
|
AT | A | 27 | a0001c0002t0001g0006a0001c0002t0001g0255a0001c0002t0001g0256others(24): Show | 28 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.557+5779delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87366929 | ||||||
| chr4:87367302
|
T | C | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+5407A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87367302 | ||||||
| chr4:87367447
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(238): Show | 249 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.557+5262A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87367447 | ||||||
| chr4:87367589
|
A | C | 2 | a0001c0001t0001g0325a0001c0001t0001g0335 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.557+5120T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87367589 | ||||||
| chr4:87367917
|
T | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.557+4792A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87367917 | ||||||
| chr4:87368045
|
C | T | 1 | a0001c0001t0003g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.557+4664G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368045 | ||||||
| chr4:87368055
|
T | C | 2 | a0001c0003t0003g0132a0001c0003t0013g0009 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557+4654A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368055 | ||||||
| chr4:87368083
|
C | T | 98 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(95): Show | 102 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.557+4626G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368083 | ||||||
| chr4:87368084
|
G | A | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.557+4625C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368084 | ||||||
| chr4:87368100
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(238): Show | 249 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.557+4609T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368100 | ||||||
| chr4:87368114
|
A | G | 2 | a0001c0003t0002g0028a0001c0003t0013g0009 | 2 | HG01192.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.557+4595T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368114 | ||||||
| chr4:87368145
|
G | A | 9 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.557+4564C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368145 | ||||||
| chr4:87368190
|
A | G | 50 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.557+4519T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368190 | ||||||
| chr4:87368242
|
G | T | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+4467C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368242 | ||||||
| chr4:87368261
|
G | A | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.557+4448C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368261 | ||||||
| chr4:87368445
|
T | C | 6 | a0001c0002t0001g0277a0001c0002t0001g0278a0001c0002t0001g0279others(3): Show | 6 | HG01074.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+4264A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368445 | ||||||
| chr4:87368497
|
A | T | 2 | a0001c0002t0002g0020a0001c0002t0002g0021 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.557+4212T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368497 | ||||||
| chr4:87368523
|
T | C | 50 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.557+4186A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368523 | ||||||
| chr4:87368562
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(88): Show | 94 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.557+4147C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368562 | ||||||
| chr4:87368606
|
A | T | 50 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.557+4103T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368606 | ||||||
| chr4:87368613
|
G | A | 3 | a0001c0005t0004g0369a0001c0005t0004g0370a0001c0005t0004g0374 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.557+4096C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368613 | ||||||
| chr4:87368623
|
C | T | 7 | a0001c0001t0002g0015a0001c0001t0002g0032a0001c0001t0002g0039others(4): Show | 7 | NA18961.hp1 NA18962.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.557+4086G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368623 | ||||||
| chr4:87368696
|
C | T | 1 | a0001c0001t0007g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.557+4013G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368696 | ||||||
| chr4:87368739
|
C | T | 2 | a0001c0001t0004g0357a0001c0001t0004g0358 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.557+3970G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368739 | ||||||
| chr4:87368767
|
G | A | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+3942C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368767 | ||||||
| chr4:87368796
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0235 | 2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.557+3913G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368796 | ||||||
| chr4:87368994
|
A | C | 4 | a0001c0001t0005g0156a0001c0001t0005g0162a0001c0001t0005g0163others(1): Show | 4 | HG00639.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+3715T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87368994 | ||||||
| chr4:87369010
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.557+3699A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369010 | ||||||
| chr4:87369093
|
T | G | 1 | a0001c0001t0004g0362 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.557+3616A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369093 | ||||||
| chr4:87369113
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(139): Show | 146 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.557+3596C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369113 | ||||||
| chr4:87369260
|
C | A | 21 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(18): Show | 21 | HG01192.hp2 HG02258.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.557+3449G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369260 | ||||||
| chr4:87369407
|
GA | G | 21 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(18): Show | 21 | HG01192.hp2 HG02258.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.557+3301delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369407 | ||||||
| chr4:87369429
|
A | ATTC | 47 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.557+3277_557+3279d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369429 | ||||||
| chr4:87369432
|
C | CT | 72 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(69): Show | 75 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.557+3276dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369432 | ||||||
| chr4:87369434
|
T | TC | 25 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(22): Show | 25 | HG01192.hp2 HG02055.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.557+3274_557+3275i others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369434 | ||||||
| chr4:87369507
|
C | T | 23 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(20): Show | 25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.557+3202G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369507 | ||||||
| chr4:87369514
|
G | C | 10 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(7): Show | 10 | HG02258.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.557+3195C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369514 | ||||||
| chr4:87369568
|
G | A | 51 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(48): Show | 52 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.557+3141C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369568 | ||||||
| chr4:87369588
|
C | A | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+3121G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369588 | ||||||
| chr4:87369729
|
C | A | 3 | a0001c0002t0002g0077a0001c0002t0004g0379a0001c0002t0004g0380 | 3 | HG02809.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.557+2980G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369729 | ||||||
| chr4:87369788
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.557+2921C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369788 | ||||||
| chr4:87369796
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.557+2913C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369796 | ||||||
| chr4:87369799
|
C | T | 19 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.557+2910G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369799 | ||||||
| chr4:87369856
|
A | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(67): Show | 73 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.557+2853T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87369856 | ||||||
| chr4:87370002
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.557+2707T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370002 | ||||||
| chr4:87370042
|
A | T | 3 | a0001c0002t0002g0077a0001c0002t0004g0379a0001c0002t0004g0380 | 3 | HG02809.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.557+2667T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370042 | ||||||
| chr4:87370081
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0189others(247): Show | 258 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.557+2628T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370081 | ||||||
| chr4:87370287
|
G | A | 51 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(48): Show | 52 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.557+2422C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370287 | ||||||
| chr4:87370383
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0189others(247): Show | 258 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.557+2326A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370383 | ||||||
| chr4:87370428
|
A | T | 2 | a0001c0001t0001g0180a0001c0001t0006g0166 | 2 | HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.557+2281T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370428 | ||||||
| chr4:87370446
|
T | C | 3 | a0001c0001t0004g0008a0001c0001t0004g0360a0001c0001t0004g0361 | 4 | HG00099.hp2 HG03669.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.557+2263A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370446 | ||||||
| chr4:87370448
|
T | C | 21 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(18): Show | 21 | HG01192.hp2 HG02258.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.557+2261A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370448 | ||||||
| chr4:87370518
|
C | T | 10 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(7): Show | 10 | HG02258.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.557+2191G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370518 | ||||||
| chr4:87370541
|
G | C | 21 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(18): Show | 21 | HG01192.hp2 HG02258.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.557+2168C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370541 | ||||||
| chr4:87370577
|
G | A | 21 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(18): Show | 21 | HG01192.hp2 HG02258.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.557+2132C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370577 | ||||||
| chr4:87370581
|
A | AT | 66 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(63): Show | 69 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.557+2127dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370581 | ||||||
| chr4:87370608
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(139): Show | 146 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.557+2101T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370608 | ||||||
| chr4:87370720
|
ATATTATT others(324): Show |
A | 72 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(69): Show | 73 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.557+1658_557+1988d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370720 | ||||||
| chr4:87370741
|
TTATTA | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(67): Show | 73 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.557+1963_557+1967d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370741 | ||||||
| chr4:87370748
|
TATTA | T | 56 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(53): Show | 58 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.557+1957_557+1960d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370748 | ||||||
| chr4:87370749
|
A | AT | 7 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG00544.hp1 HG02074.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.557+1959dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370749 | ||||||
| chr4:87370749
|
A | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(68): Show | 74 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.557+1960T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370749 | ||||||
| chr4:87370751
|
TA | T | 39 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(36): Show | 41 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.557+1957delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370751 | ||||||
| chr4:87370752
|
A | AT | 23 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0192others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.557+1956dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370752 | ||||||
| chr4:87370752
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(5): Show | 8 | HG00544.hp1 HG02074.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.557+1957T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370752 | ||||||
| chr4:87370753
|
TTA | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(66): Show | 72 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.557+1954_557+1955d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370753 | ||||||
| chr4:87370755
|
A | AT | 15 | a0001c0001t0001g0188a0001c0001t0001g0214a0001c0001t0001g0215others(12): Show | 15 | HG02165.hp1 HG03669.hp2 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.557+1953dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
A | ATTAT | 9 | a0001c0001t0001g0213a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG01496.hp1 NA18963.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.557+1953_557+1954i others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
A | ATTATTAT | 18 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0253others(15): Show | 19 | HG01168.hp2 HG02040.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.557+1953_557+1954i others(9): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
A | ATTATTAT others(6): Show |
1 | a0001c0001t0001g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.557+1953_557+1954i others(15): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
A | ATTATTAT others(3): Show |
2 | a0001c0001t0001g0327a0001c0001t0003g0118 | 2 | HG02080.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.557+1953_557+1954i others(12): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
A | ATTATTTT | 18 | a0001c0001t0001g0180a0001c0001t0001g0190a0001c0001t0001g0287others(15): Show | 18 | HG00609.hp1 HG04204.hp1 NA18612.hp2 others(15): Show |
intron_variant | MODIFIER | c.557+1953_557+1954i others(9): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
A | ATTATTTT others(4): Show |
1 | a0001c0001t0001g0235 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.557+1953_557+1954i others(13): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
A | T | 50 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0189others(47): Show | 50 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.557+1954T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370755
|
AT | A | 94 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(91): Show | 98 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.557+1953delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370755 | ||||||
| chr4:87370756
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.557+1953A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370756 | ||||||
| chr4:87370756
|
T | TA | 10 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0001g0249others(7): Show | 10 | HG00609.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.557+1952_557+1953i others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370756 | ||||||
| chr4:87370756
|
T | TTATTATT others(6): Show |
1 | a0001c0001t0004g0362 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.557+1952_557+1953i others(15): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370756 | ||||||
| chr4:87370757
|
T | TATTATTA | 5 | a0001c0001t0001g0299a0001c0001t0001g0302a0001c0001t0001g0308others(2): Show | 5 | HG00673.hp2 NA18949.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.557+1951_557+1952i others(9): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370757 | ||||||
| chr4:87370758
|
T | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(66): Show | 72 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.557+1951A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370758 | ||||||
| chr4:87370759
|
T | A | 8 | a0001c0002t0001g0289a0001c0002t0004g0348a0001c0002t0004g0349others(5): Show | 8 | HG02451.hp2 HG02615.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.557+1950A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370759 | ||||||
| chr4:87370760
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0302 | 2 | NA19054.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.557+1949A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370760 | ||||||
| chr4:87370761
|
T | A | 3 | a0001c0001t0002g0029a0001c0001t0002g0056a0001c0001t0002g0068 | 3 | HG01361.hp1 HG02004.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.557+1948A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370761 | ||||||
| chr4:87370762
|
T | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(67): Show | 73 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.557+1947A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370762 | ||||||
| chr4:87370812
|
G | C | 3 | a0001c0001t0003g0142a0001c0001t0003g0143a0001c0001t0003g0144 | 3 | HG00639.hp1 HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.557+1897C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370812 | ||||||
| chr4:87370816
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.557+1893C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370816 | ||||||
| chr4:87370819
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(63): Show | 69 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.557+1890G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370819 | ||||||
| chr4:87370880
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.557+1829C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370880 | ||||||
| chr4:87370913
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.557+1796G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370913 | ||||||
| chr4:87370943
|
G | A | 8 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0301others(5): Show | 8 | NA18949.hp1 NA18951.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.557+1766C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370943 | ||||||
| chr4:87370995
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(68): Show | 74 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.557+1714C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87370995 | ||||||
| chr4:87371048
|
G | A | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.557+1661C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371048 | ||||||
| chr4:87371074
|
A | G | 21 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(18): Show | 21 | HG01192.hp2 HG02258.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.557+1635T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371074 | ||||||
| chr4:87371079
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(67): Show | 73 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.557+1630T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371079 | ||||||
| chr4:87371181
|
C | T | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+1528G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371181 | ||||||
| chr4:87371232
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(63): Show | 69 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.557+1477A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371232 | ||||||
| chr4:87371263
|
T | G | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+1446A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371263 | ||||||
| chr4:87371341
|
G | T | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+1368C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371341 | ||||||
| chr4:87371868
|
C | T | 91 | a0001c0001t0001g0249a0001c0002t0001g0002a0001c0002t0001g0006others(88): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.557+841G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371868 | ||||||
| chr4:87371920
|
C | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0196a0001c0001t0002g0081others(1): Show | 4 | HG00609.hp2 HG01175.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.557+789G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371920 | ||||||
| chr4:87371922
|
A | G | 2 | a0001c0002t0003g0146a0001c0002t0003g0147 | 2 | HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.557+787T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371922 | ||||||
| chr4:87371943
|
T | A | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.557+766A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371943 | ||||||
| chr4:87371961
|
G | A | 16 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(13): Show | 16 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.557+748C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371961 | ||||||
| chr4:87371978
|
T | C | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.557+731A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87371978 | ||||||
| chr4:87372008
|
C | T | 90 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(87): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.557+701G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372008 | ||||||
| chr4:87372013
|
C | A | 19 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.557+696G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372013 | ||||||
| chr4:87372017
|
C | T | 1 | a0001c0002t0001g0006 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.557+692G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372017 | ||||||
| chr4:87372018
|
G | A | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | NA18971.hp2 NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.557+691C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372018 | ||||||
| chr4:87372086
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.557+623G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372086 | ||||||
| chr4:87372104
|
G | A | 90 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(87): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.557+605C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372104 | ||||||
| chr4:87372142
|
C | T | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+567G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372142 | ||||||
| chr4:87372192
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.557+517C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372192 | ||||||
| chr4:87372196
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.557+513A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372196 | ||||||
| chr4:87372199
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.557+510G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372199 | ||||||
| chr4:87372200
|
G | A | 16 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(13): Show | 16 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.557+509C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372200 | ||||||
| chr4:87372225
|
T | A | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.557+484A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372225 | ||||||
| chr4:87372242
|
C | CA | 31 | a0001c0001t0001g0176a0001c0001t0001g0198a0001c0001t0001g0216others(28): Show | 31 | HG00438.hp1 HG00621.hp1 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.557+466dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372242 | ||||||
| chr4:87372242
|
CA | C | 67 | a0001c0001t0001g0223a0001c0001t0001g0236a0001c0001t0001g0237others(64): Show | 69 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.557+466delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372242 | ||||||
| chr4:87372242
|
CAAAAAAA | C | 84 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(81): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.557+460_557+466del others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372242 | ||||||
| chr4:87372242
|
CAAAAAAA others(3): Show |
C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.557+457_557+466del others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372242 | ||||||
| chr4:87372274
|
C | T | 1 | a0001c0002t0009g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.557+435G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372274 | ||||||
| chr4:87372287
|
TTC | T | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.557+420_557+421del others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372287 | ||||||
| chr4:87372350
|
A | T | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.557+359T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372350 | ||||||
| chr4:87372493
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.557+216A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372493 | ||||||
| chr4:87372566
|
C | A | 5 | a0001c0002t0001g0181a0001c0002t0001g0182a0001c0002t0001g0183others(2): Show | 5 | HG00099.hp1 HG01261.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.557+143G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372566 | ||||||
| chr4:87372593
|
A | G | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.557+116T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 4/6 | chr4 | 87372593 | ||||||
| chr4:87372840
|
G | GA | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.451-26dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87372840 | ||||||
| chr4:87372947
|
C | G | 1 | a0001c0001t0002g0070 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.451-132G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87372947 | ||||||
| chr4:87373207
|
G | A | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.451-392C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373207 | ||||||
| chr4:87373284
|
G | A | 1 | a0001c0002t0011g0150 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.451-469C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373284 | ||||||
| chr4:87373336
|
TA | T | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.451-522delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373336 | ||||||
| chr4:87373493
|
C | T | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-678G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373493 | ||||||
| chr4:87373611
|
A | G | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.451-796T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373611 | ||||||
| chr4:87373640
|
C | G | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.451-825G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373640 | ||||||
| chr4:87373810
|
AT | A | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.450+888delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373810 | ||||||
| chr4:87373856
|
C | G | 80 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(77): Show | 82 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.450+843G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373856 | ||||||
| chr4:87373888
|
A | AG | 3 | a0001c0003t0003g0131a0001c0003t0003g0132a0001c0003t0003g0133 | 3 | HG02572.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.450+810dupC | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373888 | ||||||
| chr4:87373999
|
T | C | 1 | a0001c0002t0004g0345 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.450+700A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87373999 | ||||||
| chr4:87374100
|
G | A | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.450+599C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87374100 | ||||||
| chr4:87374281
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.450+418G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87374281 | ||||||
| chr4:87374356
|
T | G | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.450+343A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87374356 | ||||||
| chr4:87374379
|
G | A | 1 | a0001c0002t0004g0380 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.450+320C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87374379 | ||||||
| chr4:87374387
|
G | A | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.450+312C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87374387 | ||||||
| chr4:87374634
|
A | G | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.450+65T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87374634 | ||||||
| chr4:87374672
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0326 | 2 | NA18946.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.450+27G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 3/6 | chr4 | 87374672 | ||||||
| chr4:87374899
|
A | AT | 89 | a0001c0001t0001g0206a0001c0001t0001g0236a0001c0001t0002g0031others(86): Show | 92 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.319-70dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87374899 | ||||||
| chr4:87374940
|
C | T | 78 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(75): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.319-110G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87374940 | ||||||
| chr4:87374994
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.319-164T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87374994 | ||||||
| chr4:87375004
|
T | C | 16 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(13): Show | 16 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.319-174A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375004 | ||||||
| chr4:87375058
|
C | T | 55 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(52): Show | 57 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.319-228G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375058 | ||||||
| chr4:87375084
|
A | G | 16 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(13): Show | 16 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.319-254T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375084 | ||||||
| chr4:87375107
|
T | C | 78 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(75): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.319-277A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375107 | ||||||
| chr4:87375142
|
G | T | 9 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-312C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375142 | ||||||
| chr4:87375203
|
C | T | 78 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(75): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.319-373G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375203 | ||||||
| chr4:87375213
|
C | A | 78 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(75): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.319-383G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375213 | ||||||
| chr4:87375219
|
T | C | 4 | a0001c0002t0001g0181a0001c0002t0001g0182a0001c0002t0001g0183others(1): Show | 4 | HG00099.hp1 HG01261.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-389A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375219 | ||||||
| chr4:87375265
|
C | T | 4 | a0001c0003t0003g0131a0001c0003t0003g0132a0001c0003t0003g0133others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.319-435G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375265 | ||||||
| chr4:87375301
|
G | A | 4 | a0001c0001t0001g0287a0001c0001t0001g0300a0001c0001t0001g0305others(1): Show | 4 | NA18951.hp1 NA18959.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.319-471C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375301 | ||||||
| chr4:87375436
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(305): Show | 317 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.319-606C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375436 | ||||||
| chr4:87375464
|
G | T | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-634C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375464 | ||||||
| chr4:87375469
|
C | T | 9 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-639G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375469 | ||||||
| chr4:87375515
|
G | A | 19 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.319-685C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375515 | ||||||
| chr4:87375532
|
C | G | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-702G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375532 | ||||||
| chr4:87375553
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.319-723G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375553 | ||||||
| chr4:87375629
|
T | A | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-799A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375629 | ||||||
| chr4:87375681
|
C | T | 16 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(13): Show | 16 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.319-851G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375681 | ||||||
| chr4:87375695
|
C | G | 1 | a0001c0001t0002g0014 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.319-865G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375695 | ||||||
| chr4:87375697
|
C | T | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-867G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375697 | ||||||
| chr4:87375728
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.319-898G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375728 | ||||||
| chr4:87375835
|
A | ATTTC | 174 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(171): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.319-1006_319-1005i others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375835 | ||||||
| chr4:87375879
|
A | C | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-1049T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87375879 | ||||||
| chr4:87376216
|
C | G | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.319-1386G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376216 | ||||||
| chr4:87376301
|
C | T | 1 | a0001c0006t0004g0368 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.319-1471G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376301 | ||||||
| chr4:87376388
|
C | T | 19 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.319-1558G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376388 | ||||||
| chr4:87376443
|
T | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(71): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.319-1613A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376443 | ||||||
| chr4:87376503
|
C | CA | 91 | a0001c0001t0001g0176a0001c0001t0001g0188a0001c0001t0001g0193others(88): Show | 92 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.319-1674dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376503 | ||||||
| chr4:87376503
|
C | CAA | 6 | a0001c0001t0001g0298a0001c0001t0005g0161a0001c0001t0007g0137others(3): Show | 6 | HG01070.hp2 HG02145.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-1675_319-1674d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376503 | ||||||
| chr4:87376503
|
CA | C | 7 | a0001c0001t0001g0204a0001c0001t0002g0003a0001c0001t0002g0014others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.319-1674delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376503 | ||||||
| chr4:87376503
|
CAAAA | C | 11 | a0001c0002t0001g0296a0001c0003t0004g0364a0001c0003t0004g0365others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.319-1677_319-1674d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376503 | ||||||
| chr4:87376520
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.319-1690T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376520 | ||||||
| chr4:87376522
|
AC | A | 8 | a0001c0002t0001g0002a0001c0002t0001g0184a0001c0002t0001g0268others(5): Show | 10 | HG00323.hp1 HG00741.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-1693delG | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376522 | ||||||
| chr4:87376523
|
C | A | 66 | a0001c0002t0001g0006a0001c0002t0001g0181a0001c0002t0001g0182others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.319-1693G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376523 | ||||||
| chr4:87376556
|
G | GAAATAT | 94 | a0001c0002t0001g0002a0001c0002t0001g0006a0001c0002t0001g0181others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.319-1732_319-1727d others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376556 | ||||||
| chr4:87376679
|
A | AT | 175 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(172): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.319-1850dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376679 | ||||||
| chr4:87376762
|
T | C | 3 | a0001c0003t0003g0131a0001c0003t0003g0132a0001c0003t0003g0133 | 3 | HG02572.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.319-1932A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87376762 | ||||||
| chr4:87377097
|
G | T | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-2267C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377097 | ||||||
| chr4:87377108
|
T | C | 173 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(170): Show | 178 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.319-2278A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377108 | ||||||
| chr4:87377174
|
G | A | 19 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.319-2344C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377174 | ||||||
| chr4:87377263
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.319-2433T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377263 | ||||||
| chr4:87377427
|
G | A | 2 | a0001c0002t0003g0146a0001c0002t0003g0147 | 2 | HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.319-2597C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377427 | ||||||
| chr4:87377429
|
G | C | 16 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(13): Show | 16 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.319-2599C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377429 | ||||||
| chr4:87377449
|
C | CA | 91 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(88): Show | 94 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.319-2620dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377449 | ||||||
| chr4:87377449
|
CAA | C | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-2621_319-2620d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377449 | ||||||
| chr4:87377693
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.319-2863A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377693 | ||||||
| chr4:87377698
|
C | T | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-2868G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377698 | ||||||
| chr4:87377746
|
A | G | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-2916T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377746 | ||||||
| chr4:87377870
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.319-3040C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377870 | ||||||
| chr4:87377919
|
C | A | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-3089G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377919 | ||||||
| chr4:87377993
|
C | A | 1 | a0001c0002t0002g0076 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.319-3163G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87377993 | ||||||
| chr4:87378010
|
T | C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-3180A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378010 | ||||||
| chr4:87378115
|
C | G | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-3285G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378115 | ||||||
| chr4:87378232
|
T | C | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3402A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378232 | ||||||
| chr4:87378510
|
A | T | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3680T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378510 | ||||||
| chr4:87378548
|
C | A | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+3707G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378548 | ||||||
| chr4:87378552
|
C | T | 21 | a0001c0002t0001g0296a0001c0002t0004g0380a0001c0002t0005g0153others(18): Show | 21 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.318+3703G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378552 | ||||||
| chr4:87378573
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+3682A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378573 | ||||||
| chr4:87378715
|
C | CT | 16 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0003g0131others(13): Show | 16 | HG01192.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.318+3539dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378715 | ||||||
| chr4:87378730
|
C | A | 15 | a0001c0002t0001g0289a0001c0002t0001g0290a0001c0002t0003g0085others(12): Show | 15 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.318+3525G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378730 | ||||||
| chr4:87378778
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.318+3477G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378778 | ||||||
| chr4:87378793
|
G | A | 19 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(16): Show | 19 | HG01192.hp2 HG02055.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.318+3462C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378793 | ||||||
| chr4:87378794
|
ATT | A | 60 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(57): Show | 62 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.318+3459_318+3460d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378794 | ||||||
| chr4:87378797
|
T | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0242 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.318+3458A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378797 | ||||||
| chr4:87378797
|
TTA | T | 93 | a0001c0001t0001g0249a0001c0001t0003g0139a0001c0001t0003g0140others(90): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.318+3456_318+3457d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378797 | ||||||
| chr4:87378797
|
TTATA | T | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.318+3454_318+3457d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378797 | ||||||
| chr4:87378810
|
T | A | 3 | a0001c0001t0001g0242a0001c0002t0001g0267a0001c0002t0004g0367 | 3 | HG02129.hp1 HG02280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.318+3445A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378810 | ||||||
| chr4:87378812
|
A | T | 3 | a0001c0001t0001g0242a0001c0002t0001g0267a0001c0002t0004g0367 | 3 | HG02129.hp1 HG02280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.318+3443T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378812 | ||||||
| chr4:87378816
|
T | A | 2 | a0001c0002t0001g0267a0001c0002t0004g0367 | 2 | HG02280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.318+3439A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378816 | ||||||
| chr4:87378817
|
AAAATATA others(19): Show |
A | 1 | a0001c0001t0001g0303 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.318+3412_318+3437d others(28): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378817 | ||||||
| chr4:87378817
|
AAAATATA others(41): Show |
A | 2 | a0001c0001t0001g0193a0001c0002t0001g0259 | 2 | HG01516.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.318+3390_318+3437d others(50): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378817 | ||||||
| chr4:87378817
|
AAAATATA others(79): Show |
A | 5 | a0001c0002t0001g0263a0001c0002t0001g0264a0001c0002t0001g0265others(2): Show | 5 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3352_318+3437d others(88): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378817 | ||||||
| chr4:87378819
|
A | T | 2 | a0001c0002t0001g0267a0001c0002t0004g0367 | 2 | HG02280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.318+3436T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378819 | ||||||
| chr4:87378819
|
AATATATA others(7): Show |
A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.318+3422_318+3435d others(16): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378819 | ||||||
| chr4:87378819
|
AATATATA others(107): Show |
A | 2 | a0001c0002t0005g0153a0001c0002t0011g0152 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.318+3322_318+3435d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378819 | ||||||
| chr4:87378823
|
TATATATA others(37): Show |
T | 8 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0277others(5): Show | 8 | HG00280.hp2 HG01074.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3388_318+3431d others(46): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378823 | ||||||
| chr4:87378823
|
TATATATA others(65): Show |
T | 2 | a0001c0002t0002g0020a0001c0002t0002g0021 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.318+3360_318+3431d others(74): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378823 | ||||||
| chr4:87378823
|
TATATATA others(75): Show |
T | 1 | a0001c0002t0009g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.318+3350_318+3431d others(84): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378823 | ||||||
| chr4:87378823
|
TATATATA others(89): Show |
T | 9 | a0001c0002t0001g0289a0001c0002t0004g0348a0001c0002t0004g0349others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+3336_318+3431d others(98): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378823 | ||||||
| chr4:87378823
|
TATATATA others(99): Show |
T | 3 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0010g0013 | 3 | HG00642.hp1 HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.318+3326_318+3431d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378823 | ||||||
| chr4:87378825
|
TATATAAA others(49): Show |
T | 1 | a0001c0003t0004g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.318+3374_318+3429d others(58): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378825 | ||||||
| chr4:87378827
|
TATAAATA others(85): Show |
T | 3 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286 | 3 | HG03486.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.318+3336_318+3427d others(94): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378827 | ||||||
| chr4:87378827
|
TATAAATA others(95): Show |
T | 10 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0290others(7): Show | 10 | HG00323.hp2 HG00741.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.318+3326_318+3427d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378827 | ||||||
| chr4:87378831
|
A | T | 45 | a0001c0001t0001g0309a0001c0001t0016g0149a0001c0002t0001g0002others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.318+3424T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378831 | ||||||
| chr4:87378831
|
AAT | A | 7 | a0001c0001t0002g0031a0001c0001t0004g0372a0001c0001t0005g0155others(4): Show | 7 | HG00639.hp2 HG01978.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+3422_318+3423d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378831 | ||||||
| chr4:87378831
|
AATATATA others(31): Show |
A | 3 | a0001c0001t0002g0033a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG01069.hp2 HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.318+3386_318+3423d others(40): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378831 | ||||||
| chr4:87378833
|
T | A | 45 | a0001c0001t0001g0309a0001c0001t0016g0149a0001c0002t0001g0002others(42): Show | 48 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.318+3422A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378833 | ||||||
| chr4:87378833
|
T | TATATATA others(3): Show |
1 | a0001c0001t0005g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.318+3421_318+3422i others(12): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378833 | ||||||
| chr4:87378833
|
T | TATATATA others(95): Show |
1 | a0001c0001t0002g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.318+3421_318+3422i others(104): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378833 | ||||||
| chr4:87378833
|
T | TATATATA others(119): Show |
2 | a0001c0001t0002g0048a0001c0001t0002g0049 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.318+3421_318+3422i others(128): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378833 | ||||||
| chr4:87378833
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.318+3410_318+3421d others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378833 | ||||||
| chr4:87378835
|
T | A | 1 | a0001c0002t0001g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.318+3420A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378835 | ||||||
| chr4:87378835
|
T | TATATATA others(63): Show |
1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+3419_318+3420i others(72): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378835 | ||||||
| chr4:87378835
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0003g0096 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.318+3410_318+3419d others(12): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378835 | ||||||
| chr4:87378837
|
T | A | 1 | a0001c0002t0002g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.318+3418A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378837 | ||||||
| chr4:87378839
|
T | A | 1 | a0001c0001t0001g0341 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.318+3416A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378839 | ||||||
| chr4:87378841
|
T | A | 52 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(49): Show | 53 | HG00597.hp2 HG00609.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.318+3414A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378841 | ||||||
| chr4:87378841
|
T | TAA | 5 | a0001c0001t0002g0029a0001c0001t0007g0135a0001c0001t0007g0136others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+3413_318+3414i others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378841 | ||||||
| chr4:87378843
|
T | A | 65 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(62): Show | 67 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.318+3412A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378843 | ||||||
| chr4:87378843
|
TAA | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(49): Show | 53 | HG00597.hp2 HG00609.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.318+3410_318+3411d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378843 | ||||||
| chr4:87378845
|
A | AATATACA others(5): Show |
2 | a0001c0001t0004g0357a0001c0001t0004g0358 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.318+3409_318+3410i others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378845 | ||||||
| chr4:87378845
|
A | T | 123 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(120): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.318+3410T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378845 | ||||||
| chr4:87378845
|
AAT | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0359a0001c0001t0004g0360others(2): Show | 6 | HG00099.hp2 HG03239.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+3408_318+3409d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378845 | ||||||
| chr4:87378845
|
AATATATA others(19): Show |
A | 8 | a0001c0001t0003g0094a0001c0001t0003g0108a0001c0001t0003g0124others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3384_318+3409d others(28): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378845 | ||||||
| chr4:87378846
|
A | C | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.318+3409T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378846 | ||||||
| chr4:87378847
|
T | A | 1 | a0001c0001t0001g0315 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.318+3408A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378847 | ||||||
| chr4:87378848
|
ATATATAT others(108): Show |
A | 1 | a0001c0002t0011g0150 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.318+3292_318+3406d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378848 | ||||||
| chr4:87378850
|
ATATATAA others(104): Show |
A | 3 | a0001c0005t0004g0369a0001c0005t0004g0370a0001c0005t0004g0374 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.318+3294_318+3404d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378850 | ||||||
| chr4:87378850
|
ATATATAA others(106): Show |
A | 9 | a0001c0002t0001g0296a0001c0003t0002g0028a0001c0003t0004g0364others(6): Show | 9 | HG01192.hp2 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+3292_318+3404d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378850 | ||||||
| chr4:87378850
|
ATATATAA others(107): Show |
A | 1 | a0001c0002t0011g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.318+3291_318+3404d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378850 | ||||||
| chr4:87378853
|
T | A | 5 | a0001c0001t0002g0029a0001c0001t0007g0135a0001c0001t0007g0136others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+3402A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378853 | ||||||
| chr4:87378853
|
T | C | 5 | a0001c0001t0004g0008a0001c0001t0004g0359a0001c0001t0004g0360others(2): Show | 6 | HG00099.hp2 HG03239.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+3402A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378853 | ||||||
| chr4:87378853
|
TATAAATA others(100): Show |
T | 1 | a0001c0002t0004g0345 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.318+3295_318+3401d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378853 | ||||||
| chr4:87378854
|
ATAAATAT others(100): Show |
A | 5 | a0001c0001t0016g0149a0001c0002t0001g0187a0001c0002t0002g0077others(2): Show | 5 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+3294_318+3400d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378854 | ||||||
| chr4:87378854
|
ATAAATAT others(103): Show |
A | 1 | a0001c0003t0013g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.318+3291_318+3400d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378854 | ||||||
| chr4:87378855
|
T | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(119): Show | 127 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.318+3400A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378855 | ||||||
| chr4:87378855
|
TAAATATA others(94): Show |
T | 1 | a0001c0002t0004g0376 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.318+3299_318+3399d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378855 | ||||||
| chr4:87378855
|
TAAATATA others(96): Show |
T | 2 | a0001c0002t0001g0258a0001c0002t0004g0378 | 2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.318+3297_318+3399d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378855 | ||||||
| chr4:87378855
|
TAAATATA others(98): Show |
T | 7 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(4): Show | 9 | HG00099.hp1 HG01261.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+3295_318+3399d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378855 | ||||||
| chr4:87378856
|
AAATATAT others(98): Show |
A | 10 | a0001c0002t0001g0184a0001c0002t0002g0017a0001c0002t0002g0024others(7): Show | 10 | HG00323.hp1 HG00741.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+3294_318+3398d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378856 | ||||||
| chr4:87378856
|
AAATATAT others(100): Show |
A | 1 | a0001c0002t0004g0367 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.318+3292_318+3398d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378856 | ||||||
| chr4:87378856
|
AAATATAT others(103): Show |
A | 3 | a0001c0003t0003g0131a0001c0003t0003g0132a0001c0003t0003g0133 | 3 | HG02572.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.318+3289_318+3398d others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378856 | ||||||
| chr4:87378857
|
A | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(129): Show | 138 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.318+3398T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378857 | ||||||
| chr4:87378857
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0001g0226a0001c0001t0004g0372 | 2 | HG02273.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.318+3386_318+3397d others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378857 | ||||||
| chr4:87378867
|
A | C | 1 | a0001c0001t0002g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318+3388T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378867 | ||||||
| chr4:87378867
|
A | T | 17 | a0001c0001t0001g0315a0001c0001t0002g0048a0001c0001t0002g0049others(14): Show | 19 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.318+3388T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378867 | ||||||
| chr4:87378869
|
T | A | 8 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0073others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3386A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378869 | ||||||
| chr4:87378869
|
TATATATA others(19): Show |
T | 4 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0001g0244others(1): Show | 4 | HG00423.hp1 NA18939.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3360_318+3385d others(28): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378869 | ||||||
| chr4:87378869
|
TATATATA others(29): Show |
T | 4 | a0001c0001t0002g0014a0001c0001t0003g0086a0001c0001t0003g0122others(1): Show | 4 | HG00408.hp1 NA18954.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3350_318+3385d others(38): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378869 | ||||||
| chr4:87378871
|
T | A | 6 | a0001c0001t0001g0315a0001c0001t0004g0008a0001c0001t0004g0359others(3): Show | 7 | HG00099.hp2 HG00621.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+3384A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378871 | ||||||
| chr4:87378871
|
TATATATA others(17): Show |
T | 37 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0188others(34): Show | 37 | HG00544.hp1 HG00621.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.318+3360_318+3383d others(26): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378871 | ||||||
| chr4:87378873
|
T | TATATTA | 8 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0158others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3381_318+3382i others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378873 | ||||||
| chr4:87378873
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0001g0223 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.318+3360_318+3381d others(24): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378873 | ||||||
| chr4:87378877
|
T | A | 8 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0277others(5): Show | 8 | HG00280.hp2 HG01074.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3378A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378877 | ||||||
| chr4:87378877
|
TATAAATA others(72): Show |
T | 2 | a0001c0002t0003g0146a0001c0002t0003g0147 | 2 | HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.318+3299_318+3377d others(81): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378877 | ||||||
| chr4:87378877
|
TATAAATA others(76): Show |
T | 1 | a0001c0002t0001g0006 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.318+3295_318+3377d others(85): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378877 | ||||||
| chr4:87378879
|
TAAATATA others(43): Show |
T | 1 | a0001c0002t0001g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.318+3326_318+3375d others(52): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378879 | ||||||
| chr4:87378880
|
A | G | 2 | a0001c0001t0001g0325a0001c0001t0001g0335 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.318+3375T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378880 | ||||||
| chr4:87378880
|
A | T | 9 | a0001c0001t0002g0029a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG00639.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+3375T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378880 | ||||||
| chr4:87378881
|
A | T | 18 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0158others(15): Show | 18 | HG00280.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.318+3374T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378881 | ||||||
| chr4:87378881
|
AAT | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0189a0001c0001t0001g0194others(58): Show | 64 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.318+3372_318+3373d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378881 | ||||||
| chr4:87378881
|
AATATATA others(19): Show |
A | 5 | a0001c0001t0001g0205a0001c0001t0003g0089a0001c0001t0003g0090others(2): Show | 5 | HG02738.hp2 HG03491.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3348_318+3373d others(28): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378881 | ||||||
| chr4:87378883
|
T | A | 9 | a0001c0001t0001g0204a0001c0001t0005g0156a0001c0001t0005g0157others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+3372A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378883 | ||||||
| chr4:87378883
|
T | TATATATA others(1): Show |
3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | NA18971.hp2 NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.318+3371_318+3372i others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378883 | ||||||
| chr4:87378883
|
TATATATA others(39): Show |
T | 1 | a0001c0001t0003g0142 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.318+3326_318+3371d others(48): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378883 | ||||||
| chr4:87378885
|
T | TATATAAA others(103): Show |
3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0053 | 3 | HG01168.hp1 HG01346.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.318+3369_318+3370i others(112): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(115): Show |
1 | a0001c0001t0002g0003 | 2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.318+3369_318+3370i others(124): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(103): Show |
1 | a0001c0001t0002g0038 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.318+3369_318+3370i others(112): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(93): Show |
8 | a0001c0001t0002g0015a0001c0001t0002g0040a0001c0001t0002g0052others(5): Show | 8 | HG01167.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3369_318+3370i others(102): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(105): Show |
33 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0241others(30): Show | 34 | HG00280.hp1 HG00673.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.318+3369_318+3370i others(114): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(117): Show |
1 | a0001c0001t0002g0067 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.318+3369_318+3370i others(126): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(117): Show |
1 | a0001c0001t0002g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318+3369_318+3370i others(126): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(111): Show |
1 | a0001c0001t0001g0276 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+3369_318+3370i others(120): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(117): Show |
1 | a0001c0001t0002g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.318+3369_318+3370i others(126): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATAAA others(133): Show |
3 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137 | 3 | HG02976.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318+3369_318+3370i others(142): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
T | TATATATA others(1): Show |
3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0073 | 3 | HG01070.hp1 HG01071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.318+3369_318+3370i others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378885
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0004g0372 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.318+3360_318+3369d others(12): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378885 | ||||||
| chr4:87378889
|
T | A | 1 | a0001c0003t0004g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.318+3366A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378889 | ||||||
| chr4:87378891
|
T | A | 11 | a0001c0001t0001g0193a0001c0001t0001g0226a0001c0001t0002g0033others(8): Show | 11 | HG00639.hp2 HG01069.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.318+3364A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378891 | ||||||
| chr4:87378893
|
T | A | 5 | a0001c0001t0001g0249a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG00597.hp2 HG02083.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+3362A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378893 | ||||||
| chr4:87378893
|
TAA | T | 4 | a0001c0001t0005g0155a0001c0001t0005g0162a0001c0001t0005g0163others(1): Show | 4 | HG00639.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3360_318+3361d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378893 | ||||||
| chr4:87378893
|
TAAATATA others(19): Show |
T | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.318+3336_318+3361d others(28): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378893 | ||||||
| chr4:87378895
|
A | T | 18 | a0001c0001t0001g0193a0001c0001t0001g0226a0001c0001t0001g0249others(15): Show | 18 | HG00597.hp2 HG01069.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.318+3360T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378895 | ||||||
| chr4:87378895
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0001g0180a0001c0001t0001g0334 | 2 | HG00609.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.318+3348_318+3359d others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378895 | ||||||
| chr4:87378895
|
AATATATA others(7): Show |
A | 1 | a0001c0001t0006g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.318+3346_318+3359d others(16): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378895 | ||||||
| chr4:87378897
|
T | A | 1 | a0001c0002t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.318+3358A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378897 | ||||||
| chr4:87378901
|
T | A | 3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | NA18971.hp2 NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.318+3354A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378901 | ||||||
| chr4:87378903
|
T | A | 1 | a0001c0001t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.318+3352A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378903 | ||||||
| chr4:87378903
|
TAA | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0190others(50): Show | 54 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.318+3350_318+3351d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378903 | ||||||
| chr4:87378903
|
TAAATATA others(50): Show |
T | 1 | a0001c0002t0001g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.318+3295_318+3351d others(59): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378903 | ||||||
| chr4:87378904
|
A | T | 1 | a0001c0001t0004g0372 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.318+3351T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378904 | ||||||
| chr4:87378904
|
AAATATAT others(50): Show |
A | 1 | a0001c0002t0002g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.318+3294_318+3350d others(59): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378904 | ||||||
| chr4:87378905
|
A | T | 29 | a0001c0001t0001g0337a0001c0001t0003g0108a0001c0001t0003g0127others(26): Show | 30 | HG00099.hp2 HG01074.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.318+3350T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378905 | ||||||
| chr4:87378905
|
AATATATA others(19): Show |
A | 1 | a0001c0001t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.318+3324_318+3349d others(28): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378905 | ||||||
| chr4:87378907
|
T | A | 6 | a0001c0001t0003g0108a0001c0001t0003g0127a0001c0001t0003g0128others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+3348A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378907 | ||||||
| chr4:87378907
|
T | TAA | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3347_318+3348i others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378907 | ||||||
| chr4:87378907
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0323 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.318+3347_318+3348i others(24): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378907 | ||||||
| chr4:87378907
|
TATATATA others(15): Show |
T | 42 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(39): Show | 42 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.318+3326_318+3347d others(24): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378907 | ||||||
| chr4:87378909
|
T | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0190others(55): Show | 59 | HG00673.hp2 HG00738.hp2 HG01168.hp2 others(56): Show |
intron_variant | MODIFIER | c.318+3346A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378909 | ||||||
| chr4:87378909
|
TATATATA others(13): Show |
T | 15 | a0001c0001t0001g0001a0001c0001t0001g0189a0001c0001t0001g0245others(12): Show | 18 | HG00597.hp1 HG00738.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.318+3326_318+3345d others(22): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378909 | ||||||
| chr4:87378911
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0003g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.318+3326_318+3343d others(20): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378911 | ||||||
| chr4:87378913
|
T | A | 1 | a0001c0001t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.318+3342A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378913 | ||||||
| chr4:87378915
|
T | A | 7 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(4): Show | 7 | HG00597.hp2 HG01496.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+3340A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378915 | ||||||
| chr4:87378915
|
TATAAATA others(7): Show |
T | 1 | a0001c0001t0004g0373 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.318+3326_318+3339d others(16): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378915 | ||||||
| chr4:87378917
|
T | A | 3 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137 | 3 | HG02976.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318+3338A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378917 | ||||||
| chr4:87378917
|
TAAATATA others(5): Show |
T | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | HG00597.hp2 HG01496.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3326_318+3337d others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378917 | ||||||
| chr4:87378919
|
A | AAT | 3 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0009g0346 | 3 | HG02717.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.318+3334_318+3335d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378919 | ||||||
| chr4:87378919
|
A | T | 18 | a0001c0001t0001g0208a0001c0001t0002g0029a0001c0001t0003g0092others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG02976.hp2 others(15): Show |
intron_variant | MODIFIER | c.318+3336T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378919 | ||||||
| chr4:87378921
|
TATATATA others(1): Show |
T | 44 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0190others(41): Show | 45 | HG00738.hp2 HG01168.hp2 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.318+3326_318+3333d others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378921 | ||||||
| chr4:87378923
|
TATATAA | T | 4 | a0001c0001t0001g0299a0001c0001t0001g0309a0001c0001t0003g0094others(1): Show | 4 | NA18747.hp2 NA18949.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+3326_318+3331d others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378923 | ||||||
| chr4:87378925
|
T | A | 3 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286 | 3 | HG03486.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.318+3330A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378925 | ||||||
| chr4:87378926
|
A | T | 2 | a0001c0001t0001g0208a0001c0001t0006g0171 | 2 | NA19006.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.318+3329T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378926 | ||||||
| chr4:87378927
|
T | A | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.318+3328A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378927 | ||||||
| chr4:87378928
|
A | T | 7 | a0001c0001t0003g0092a0001c0001t0003g0111a0001c0001t0003g0112others(4): Show | 7 | NA18977.hp2 NA18990.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+3327T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378928 | ||||||
| chr4:87378929
|
A | AAT | 12 | a0001c0001t0001g0323a0001c0001t0002g0043a0001c0001t0002g0054others(9): Show | 13 | HG00099.hp2 HG01123.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.318+3324_318+3325d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378929 | ||||||
| chr4:87378929
|
A | AATAT | 3 | a0001c0001t0001g0241a0001c0001t0001g0283a0001c0001t0002g0004 | 4 | HG01256.hp1 HG01258.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3322_318+3325d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378929 | ||||||
| chr4:87378929
|
A | AATATATA others(45): Show |
1 | a0001c0001t0001g0315 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.318+3325_318+3326i others(54): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378929 | ||||||
| chr4:87378929
|
A | T | 43 | a0001c0001t0001g0177a0001c0001t0001g0208a0001c0001t0001g0324others(40): Show | 43 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.318+3326T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378929 | ||||||
| chr4:87378929
|
AAT | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0232a0001c0001t0003g0084 | 3 | HG00423.hp1 NA18939.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.318+3324_318+3325d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378929 | ||||||
| chr4:87378931
|
T | A | 3 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137 | 3 | HG02976.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318+3324A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378931 | ||||||
| chr4:87378935
|
T | A | 10 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0290others(7): Show | 10 | HG00323.hp2 HG00741.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.318+3320A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378935 | ||||||
| chr4:87378935
|
T | TATATAAA others(91): Show |
3 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | NA18971.hp2 NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.318+3319_318+3320i others(100): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378935 | ||||||
| chr4:87378936
|
A | T | 1 | a0001c0001t0003g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.318+3319T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378936 | ||||||
| chr4:87378937
|
T | TATAAATA others(109): Show |
1 | a0001c0001t0007g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.318+3317_318+3318i others(118): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378937 | ||||||
| chr4:87378938
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.318+3317T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378938 | ||||||
| chr4:87378939
|
T | A | 3 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0010g0013 | 3 | HG00642.hp1 HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.318+3316A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378939 | ||||||
| chr4:87378940
|
A | T | 1 | a0001c0001t0001g0324 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.318+3315T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378940 | ||||||
| chr4:87378941
|
T | A | 3 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137 | 3 | HG02976.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318+3314A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378941 | ||||||
| chr4:87378942
|
A | T | 1 | a0001c0001t0003g0096 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.318+3313T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378942 | ||||||
| chr4:87378942
|
ATATATTT others(16): Show |
A | 2 | a0001c0001t0001g0208a0001c0001t0006g0171 | 2 | NA19006.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.318+3290_318+3312d others(25): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378942 | ||||||
| chr4:87378943
|
T | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+3312A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378943 | ||||||
| chr4:87378944
|
ATATT | A | 5 | a0001c0001t0001g0238a0001c0001t0002g0041a0001c0001t0002g0053others(2): Show | 5 | HG00673.hp1 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3307_318+3310d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378944 | ||||||
| chr4:87378944
|
ATATTTAT others(14): Show |
A | 7 | a0001c0001t0003g0092a0001c0001t0003g0111a0001c0001t0003g0112others(4): Show | 7 | NA18977.hp2 NA18990.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+3290_318+3310d others(23): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378944 | ||||||
| chr4:87378946
|
A | T | 3 | a0001c0001t0001g0309a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG06807.hp2 NA18949.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.318+3309T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378946 | ||||||
| chr4:87378946
|
ATT | A | 29 | a0001c0001t0001g0236a0001c0001t0001g0276a0001c0001t0001g0297others(26): Show | 30 | HG00280.hp1 HG00544.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.318+3307_318+3308d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378946 | ||||||
| chr4:87378947
|
T | A | 2 | a0001c0002t0005g0153a0001c0002t0011g0152 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.318+3308A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378947 | ||||||
| chr4:87378948
|
T | A | 96 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(93): Show | 97 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.318+3307A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378948 | ||||||
| chr4:87378949
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0004g0373 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.318+3295_318+3305d others(13): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378949 | ||||||
| chr4:87378955
|
TATATA | T | 13 | a0001c0001t0002g0042a0001c0001t0002g0066a0001c0002t0001g0255others(10): Show | 13 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.318+3295_318+3299d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378955 | ||||||
| chr4:87378956
|
A | T | 2 | a0001c0001t0005g0155a0001c0002t0009g0356 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.318+3299T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378956 | ||||||
| chr4:87378957
|
TATA | T | 3 | a0001c0001t0002g0068a0001c0002t0001g0259a0001c0002t0001g0278 | 3 | HG01516.hp1 HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.318+3295_318+3297d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378957 | ||||||
| chr4:87378958
|
A | T | 7 | a0001c0001t0001g0222a0001c0001t0002g0038a0001c0001t0005g0155others(4): Show | 7 | HG00544.hp2 HG01256.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+3297T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378958 | ||||||
| chr4:87378959
|
TA | T | 10 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0265others(7): Show | 10 | HG00323.hp2 HG00741.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.318+3295delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378959 | ||||||
| chr4:87378960
|
A | T | 27 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0242others(24): Show | 27 | HG00544.hp2 HG00673.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.318+3295T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378960 | ||||||
| chr4:87378960
|
AT | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(58): Show | 64 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.318+3294delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378960 | ||||||
| chr4:87378961
|
T | TA | 4 | a0001c0001t0001g0221a0001c0001t0002g0037a0001c0001t0002g0081others(1): Show | 4 | HG01175.hp1 HG01255.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+3293_318+3294i others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378961 | ||||||
| chr4:87378962
|
T | A | 106 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(103): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.318+3293A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378962 | ||||||
| chr4:87378963
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0197a0001c0001t0001g0198others(47): Show | 53 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.318+3292A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378963 | ||||||
| chr4:87378964
|
T | A | 14 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(11): Show | 14 | HG00609.hp2 HG02055.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+3291A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378964 | ||||||
| chr4:87378965
|
T | A | 2 | a0001c0001t0001g0249a0001c0001t0007g0119 | 2 | HG02965.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.318+3290A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378965 | ||||||
| chr4:87378966
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.318+3289A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87378966 | ||||||
| chr4:87379131
|
C | T | 20 | a0001c0002t0001g0296a0001c0002t0005g0153a0001c0002t0011g0150others(17): Show | 20 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.318+3124G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379131 | ||||||
| chr4:87379251
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.318+3004C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379251 | ||||||
| chr4:87379263
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+2992A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379263 | ||||||
| chr4:87379288
|
G | A | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+2967C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379288 | ||||||
| chr4:87379376
|
C | T | 23 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(20): Show | 25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.318+2879G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379376 | ||||||
| chr4:87379384
|
T | C | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2871A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379384 | ||||||
| chr4:87379388
|
T | G | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.318+2867A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379388 | ||||||
| chr4:87379393
|
C | T | 4 | a0001c0001t0001g0211a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | HG00423.hp1 HG02273.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+2862G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379393 | ||||||
| chr4:87379410
|
T | G | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2845A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379410 | ||||||
| chr4:87379449
|
G | A | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+2806C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379449 | ||||||
| chr4:87379449
|
G | GAT | 8 | a0001c0001t0001g0007a0001c0001t0001g0319a0001c0001t0001g0320others(5): Show | 9 | HG02040.hp2 NA18939.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+2804_318+2805d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379449 | ||||||
| chr4:87379451
|
T | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0228 | 3 | HG01978.hp2 HG01993.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.318+2804A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379451 | ||||||
| chr4:87379472
|
G | A | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2783C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379472 | ||||||
| chr4:87379564
|
T | C | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.318+2691A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379564 | ||||||
| chr4:87379583
|
C | T | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2672G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379583 | ||||||
| chr4:87379664
|
ATAT | A | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+2588_318+2590d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379664 | ||||||
| chr4:87379674
|
T | C | 60 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(57): Show | 62 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.318+2581A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379674 | ||||||
| chr4:87379689
|
G | GTAT | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2563_318+2565d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379689 | ||||||
| chr4:87379702
|
T | C | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+2553A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379702 | ||||||
| chr4:87379772
|
ATATAGTA others(9): Show |
A | 27 | a0001c0002t0001g0006a0001c0002t0001g0255a0001c0002t0001g0256others(24): Show | 28 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.318+2467_318+2482d others(18): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379772 | ||||||
| chr4:87379783
|
GTATAT | G | 80 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(77): Show | 82 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.318+2467_318+2471d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379783 | ||||||
| chr4:87379784
|
T | TATA | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2468_318+2470d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379784 | ||||||
| chr4:87379788
|
T | A | 55 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0181others(52): Show | 57 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.318+2467A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379788 | ||||||
| chr4:87379797
|
AAT | A | 3 | a0001c0003t0002g0028a0001c0003t0004g0364a0001c0003t0004g0365 | 3 | HG01192.hp2 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.318+2456_318+2457d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379797 | ||||||
| chr4:87379799
|
T | TATA | 11 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.318+2453_318+2455d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379799 | ||||||
| chr4:87379833
|
ATTATAC | A | 96 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(93): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.318+2416_318+2421d others(8): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379833 | ||||||
| chr4:87379842
|
TTA | T | 96 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(93): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.318+2411_318+2412d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379842 | ||||||
| chr4:87379853
|
TATG | T | 92 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(89): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.318+2399_318+2401d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379853 | ||||||
| chr4:87379853
|
TATGTA | T | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+2397_318+2401d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379853 | ||||||
| chr4:87379866
|
T | A | 96 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(93): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.318+2389A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379866 | ||||||
| chr4:87379869
|
ACTATTAA others(7): Show |
A | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2372_318+2385d others(16): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379869 | ||||||
| chr4:87379870
|
CTATTAAT others(7): Show |
C | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.318+2371_318+2384d others(16): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379870 | ||||||
| chr4:87379906
|
CATATT | C | 19 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.318+2344_318+2348d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379906 | ||||||
| chr4:87379936
|
A | G | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2319T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87379936 | ||||||
| chr4:87380037
|
GGAGGCGG others(10): Show |
G | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2201_318+2217d others(19): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380037 | ||||||
| chr4:87380059
|
C | G | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+2196G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380059 | ||||||
| chr4:87380089
|
T | A | 60 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(57): Show | 62 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.318+2166A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380089 | ||||||
| chr4:87380110
|
C | CA | 88 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(85): Show | 91 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.318+2144dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380110 | ||||||
| chr4:87380110
|
C | CAA | 9 | a0001c0001t0001g0202a0001c0001t0001g0310a0001c0001t0002g0083others(6): Show | 9 | HG00642.hp2 HG02055.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+2143_318+2144d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380110 | ||||||
| chr4:87380209
|
G | T | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2046C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380209 | ||||||
| chr4:87380235
|
G | A | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+2020C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380235 | ||||||
| chr4:87380246
|
A | G | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+2009T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380246 | ||||||
| chr4:87380254
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0197others(65): Show | 71 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.318+2001G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380254 | ||||||
| chr4:87380396
|
C | T | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+1859G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380396 | ||||||
| chr4:87380437
|
C | T | 5 | a0001c0001t0016g0149a0001c0002t0002g0077a0001c0002t0004g0345others(2): Show | 5 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+1818G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380437 | ||||||
| chr4:87380470
|
C | CA | 66 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0180others(63): Show | 69 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.318+1784dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380470 | ||||||
| chr4:87380478
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318+1777T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380478 | ||||||
| chr4:87380478
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0004g0377 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.318+1766_318+1776d others(13): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380478 | ||||||
| chr4:87380484
|
A | AAAAAG | 9 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(6): Show | 9 | HG01361.hp1 HG01952.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+1766_318+1770d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380484 | ||||||
| chr4:87380484
|
A | AAAAG | 45 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(42): Show | 47 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.318+1770_318+1771i others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380484 | ||||||
| chr4:87380484
|
A | AAG | 7 | a0001c0001t0002g0029a0001c0001t0007g0135a0001c0001t0007g0136others(4): Show | 7 | HG02258.hp1 HG02602.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1770_318+1771i others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380484 | ||||||
| chr4:87380484
|
A | AG | 75 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(72): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.318+1770_318+1771i others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380484 | ||||||
| chr4:87380484
|
A | G | 4 | a0001c0002t0002g0020a0001c0002t0012g0257a0001c0002t0017g0185others(1): Show | 4 | HG01069.hp1 HG01081.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1771T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380484 | ||||||
| chr4:87380485
|
A | G | 9 | a0001c0003t0003g0131a0001c0003t0003g0132a0001c0003t0003g0133others(6): Show | 9 | HG02486.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+1770T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380485 | ||||||
| chr4:87380654
|
C | G | 96 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(93): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.318+1601G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380654 | ||||||
| chr4:87380715
|
A | G | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+1540T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380715 | ||||||
| chr4:87380738
|
A | G | 14 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(11): Show | 14 | HG01192.hp2 HG02055.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+1517T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380738 | ||||||
| chr4:87380863
|
C | CA | 23 | a0001c0001t0001g0179a0001c0001t0001g0193a0001c0001t0001g0203others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.318+1391dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0194 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.318+1381_318+1391d others(13): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0195a0001c0001t0002g0078a0001c0006t0004g0368 | 3 | HG02896.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.318+1380_318+1391d others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.318+1379_318+1391d others(15): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0196a0001c0001t0015g0080 | 2 | HG00609.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.318+1377_318+1391d others(17): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0189 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.318+1376_318+1391d others(18): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.318+1375_318+1391d others(19): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CA | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(53): Show | 58 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.318+1391delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CAAA | C | 7 | a0001c0002t0001g0286a0001c0002t0008g0288a0001c0003t0008g0291others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1389_318+1391d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CAAAA | C | 31 | a0001c0002t0001g0006a0001c0002t0001g0255a0001c0002t0001g0256others(28): Show | 32 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.318+1388_318+1391d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CAAAAA | C | 37 | a0001c0002t0001g0002a0001c0002t0001g0181a0001c0002t0001g0182others(34): Show | 39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.318+1387_318+1391d others(7): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CAAAAAAA others(1): Show |
C | 17 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0005g0154others(14): Show | 17 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.318+1384_318+1391d others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0197a0001c0001t0002g0029 | 2 | HG00735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.318+1381_318+1391d others(13): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0001g0242a0001c0001t0007g0135a0001c0001t0007g0136others(3): Show | 6 | HG01192.hp2 HG02129.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+1380_318+1391d others(14): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380863
|
CAAAAAAA others(6): Show |
C | 67 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(64): Show | 69 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.318+1379_318+1391d others(15): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380863 | ||||||
| chr4:87380920
|
C | A | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.318+1335G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380920 | ||||||
| chr4:87380920
|
C | T | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | NA18952.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.318+1335G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380920 | ||||||
| chr4:87380935
|
C | CT | 3 | a0001c0003t0003g0131a0001c0003t0003g0132a0001c0003t0003g0133 | 3 | HG02572.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.318+1319dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87380935 | ||||||
| chr4:87381149
|
T | A | 72 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(69): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.318+1106A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381149 | ||||||
| chr4:87381165
|
C | T | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1090G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381165 | ||||||
| chr4:87381186
|
C | CA | 30 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(27): Show | 30 | HG00639.hp2 HG01884.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.318+1068dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381186 | ||||||
| chr4:87381186
|
C | CCA | 52 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(49): Show | 54 | HG00544.hp2 HG00673.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.318+1068_318+1069i others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381186 | ||||||
| chr4:87381186
|
C | CCAA | 7 | a0001c0001t0001g0283a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG00280.hp1 HG01167.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1068_318+1069i others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381186 | ||||||
| chr4:87381186
|
CA | C | 7 | a0001c0001t0002g0019a0001c0001t0004g0357a0001c0003t0003g0131others(4): Show | 7 | HG01257.hp2 HG01496.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1068delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381186 | ||||||
| chr4:87381186
|
CAAAAAAA others(1): Show |
C | 66 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(63): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.318+1061_318+1068d others(10): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381186 | ||||||
| chr4:87381219
|
A | T | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+1036T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381219 | ||||||
| chr4:87381387
|
G | A | 4 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+868C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381387 | ||||||
| chr4:87381389
|
G | A | 4 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+866C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381389 | ||||||
| chr4:87381397
|
G | A | 1 | a0001c0001t0003g0120 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.318+858C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381397 | ||||||
| chr4:87381475
|
TCTG | T | 9 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00609.hp2 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+777_318+779del others(3): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381475 | ||||||
| chr4:87381495
|
T | C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+760A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381495 | ||||||
| chr4:87381556
|
G | A | 1 | a0001c0001t0006g0170 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.318+699C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381556 | ||||||
| chr4:87381633
|
C | T | 14 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0266others(11): Show | 14 | HG00280.hp2 HG01192.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.318+622G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381633 | ||||||
| chr4:87381705
|
A | G | 5 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(2): Show | 5 | HG00621.hp1 NA18963.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+550T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381705 | ||||||
| chr4:87381708
|
G | A | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+547C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381708 | ||||||
| chr4:87381752
|
C | T | 3 | a0001c0003t0002g0028a0001c0003t0004g0364a0001c0003t0004g0365 | 3 | HG01192.hp2 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.318+503G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381752 | ||||||
| chr4:87381760
|
CA | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(168): Show | 176 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.318+494delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381760 | ||||||
| chr4:87381760
|
CAA | C | 146 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(143): Show | 151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.318+493_318+494del others(2): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381760 | ||||||
| chr4:87381931
|
T | G | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+324A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381931 | ||||||
| chr4:87381940
|
T | C | 2 | a0001c0002t0001g0266a0001c0002t0001g0267 | 2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.318+315A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381940 | ||||||
| chr4:87381955
|
G | C | 1 | a0001c0001t0001g0339 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.318+300C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381955 | ||||||
| chr4:87381968
|
T | C | 176 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(173): Show | 181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.318+287A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87381968 | ||||||
| chr4:87382013
|
G | C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+242C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87382013 | ||||||
| chr4:87382066
|
G | C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+189C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 2/6 | chr4 | 87382066 | ||||||
| chr4:87382416
|
C | T | 23 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0004g0372others(20): Show | 23 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.211-54G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87382416 | ||||||
| chr4:87382460
|
A | T | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-98T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87382460 | ||||||
| chr4:87382543
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211-181G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87382543 | ||||||
| chr4:87382751
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.211-389T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87382751 | ||||||
| chr4:87382772
|
A | G | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.211-410T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87382772 | ||||||
| chr4:87382831
|
C | T | 1 | a0001c0002t0004g0349 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.211-469G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87382831 | ||||||
| chr4:87382963
|
A | G | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-601T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87382963 | ||||||
| chr4:87383015
|
G | A | 1 | a0001c0008t0009g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.211-653C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383015 | ||||||
| chr4:87383206
|
G | T | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-844C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383206 | ||||||
| chr4:87383260
|
C | CA | 4 | a0001c0001t0007g0135a0001c0001t0007g0136a0001c0001t0007g0137others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-899dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383260 | ||||||
| chr4:87383261
|
A | G | 4 | a0001c0002t0005g0153a0001c0002t0011g0150a0001c0002t0011g0151others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-899T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383261 | ||||||
| chr4:87383313
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0244 | 2 | HG03710.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.211-951C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383313 | ||||||
| chr4:87383356
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246 | 5 | NA18941.hp1 NA18959.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-994C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383356 | ||||||
| chr4:87383366
|
G | A | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-1004C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383366 | ||||||
| chr4:87383478
|
A | G | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-1116T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383478 | ||||||
| chr4:87383510
|
G | A | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-1148C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383510 | ||||||
| chr4:87383527
|
T | C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1165A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383527 | ||||||
| chr4:87383561
|
A | G | 1 | a0001c0002t0004g0348 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.211-1199T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383561 | ||||||
| chr4:87383594
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.211-1232A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383594 | ||||||
| chr4:87383650
|
G | A | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1288C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383650 | ||||||
| chr4:87383651
|
C | T | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-1289G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383651 | ||||||
| chr4:87383746
|
C | CT | 52 | a0001c0001t0001g0189a0001c0001t0001g0194a0001c0001t0001g0195others(49): Show | 52 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.211-1385dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383746 | ||||||
| chr4:87383746
|
C | CTT | 11 | a0001c0001t0004g0372a0001c0001t0004g0373a0001c0002t0002g0074others(8): Show | 11 | HG01167.hp1 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-1386_211-1385d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383746 | ||||||
| chr4:87383839
|
T | A | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-1477A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383839 | ||||||
| chr4:87383898
|
G | C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1536C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383898 | ||||||
| chr4:87383971
|
G | A | 2 | a0001c0001t0004g0372a0001c0001t0004g0373 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.211-1609C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87383971 | ||||||
| chr4:87384028
|
A | G | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-1666T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384028 | ||||||
| chr4:87384055
|
A | G | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1693T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384055 | ||||||
| chr4:87384088
|
G | T | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-1726C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384088 | ||||||
| chr4:87384141
|
C | T | 4 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG02738.hp2 HG03704.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-1779G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384141 | ||||||
| chr4:87384263
|
C | G | 1 | a0001c0002t0001g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.211-1901G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384263 | ||||||
| chr4:87384280
|
C | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG00597.hp2 NA18968.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-1918G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384280 | ||||||
| chr4:87384400
|
G | A | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-2038C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384400 | ||||||
| chr4:87384451
|
A | G | 1 | a0001c0002t0009g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.211-2089T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384451 | ||||||
| chr4:87384528
|
C | T | 4 | a0001c0002t0002g0077a0001c0002t0004g0345a0001c0002t0004g0379others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2166G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384528 | ||||||
| chr4:87384546
|
C | T | 2 | a0001c0003t0004g0364a0001c0003t0004g0365 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.211-2184G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384546 | ||||||
| chr4:87384594
|
T | C | 88 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(85): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.211-2232A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384594 | ||||||
| chr4:87384613
|
C | T | 7 | a0001c0001t0004g0008a0001c0001t0004g0357a0001c0001t0004g0358others(4): Show | 8 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-2251G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384613 | ||||||
| chr4:87384622
|
T | C | 88 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(85): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.211-2260A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384622 | ||||||
| chr4:87384715
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.211-2353A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384715 | ||||||
| chr4:87384735
|
C | T | 5 | a0001c0001t0002g0029a0001c0001t0007g0135a0001c0001t0007g0136others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-2373G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384735 | ||||||
| chr4:87384736
|
G | A | 1 | a0001c0002t0005g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211-2374C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384736 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2680): Show |
1 | a0001c0003t0004g0365 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2689): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2677): Show |
1 | a0001c0003t0004g0364 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2686): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2682): Show |
1 | a0001c0003t0002g0028 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2691): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2675): Show |
1 | a0001c0005t0004g0369 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2684): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2676): Show |
2 | a0001c0005t0004g0370a0001c0005t0004g0374 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.211-2395_211-2394i others(2685): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2674): Show |
1 | a0001c0003t0003g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2683): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2674): Show |
1 | a0001c0003t0003g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2683): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2675): Show |
1 | a0001c0003t0003g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2684): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384756
|
T | TAAGATGT others(2675): Show |
1 | a0001c0003t0013g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.211-2395_211-2394i others(2684): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384756 | ||||||
| chr4:87384848
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.211-2486G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384848 | ||||||
| chr4:87384932
|
C | T | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-2570G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384932 | ||||||
| chr4:87384957
|
T | C | 19 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0005g0156others(16): Show | 19 | HG00639.hp2 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.211-2595A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384957 | ||||||
| chr4:87384999
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.211-2637G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87384999 | ||||||
| chr4:87385074
|
A | T | 3 | a0001c0002t0001g0284a0001c0002t0001g0285a0001c0002t0001g0286 | 3 | HG03486.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.211-2712T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385074 | ||||||
| chr4:87385281
|
T | C | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-2919A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385281 | ||||||
| chr4:87385413
|
A | C | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-3051T>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385413 | ||||||
| chr4:87385419
|
G | A | 10 | a0001c0003t0002g0028a0001c0003t0003g0131a0001c0003t0003g0132others(7): Show | 10 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-3057C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385419 | ||||||
| chr4:87385559
|
A | G | 1 | a0001c0001t0006g0168 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.211-3197T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385559 | ||||||
| chr4:87385563
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.211-3201T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385563 | ||||||
| chr4:87385576
|
T | G | 1 | a0001c0001t0003g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.211-3214A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385576 | ||||||
| chr4:87385679
|
G | A | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-3317C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385679 | ||||||
| chr4:87385887
|
T | C | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-3525A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385887 | ||||||
| chr4:87385890
|
G | A | 5 | a0001c0002t0001g0290a0001c0002t0004g0376a0001c0002t0004g0377others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-3528C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385890 | ||||||
| chr4:87385902
|
G | A | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-3540C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385902 | ||||||
| chr4:87385902
|
G | T | 1 | a0001c0002t0003g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.211-3540C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385902 | ||||||
| chr4:87385914
|
C | CA | 20 | a0001c0001t0001g0248a0001c0001t0002g0069a0001c0001t0003g0125others(17): Show | 22 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.211-3553dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385914 | ||||||
| chr4:87385914
|
C | CAA | 11 | a0001c0001t0001g0341a0001c0003t0002g0028a0001c0003t0003g0131others(8): Show | 11 | HG01192.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-3554_211-3553d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385914 | ||||||
| chr4:87385914
|
CA | C | 34 | a0001c0001t0001g0193a0001c0001t0004g0008a0001c0001t0004g0357others(31): Show | 35 | HG00099.hp2 HG00639.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.211-3553delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87385914 | ||||||
| chr4:87386100
|
T | G | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-3738A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386100 | ||||||
| chr4:87386125
|
C | T | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-3763G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386125 | ||||||
| chr4:87386204
|
C | CT | 83 | a0001c0001t0001g0341a0001c0001t0016g0149a0001c0002t0001g0002others(80): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.211-3843dupA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386204 | ||||||
| chr4:87386233
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.211-3871G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386233 | ||||||
| chr4:87386234
|
G | A | 1 | a0001c0001t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.211-3872C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386234 | ||||||
| chr4:87386391
|
C | T | 4 | a0001c0002t0004g0345a0001c0005t0004g0369a0001c0005t0004g0370others(1): Show | 4 | HG02717.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-4029G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386391 | ||||||
| chr4:87386485
|
G | A | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-4123C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386485 | ||||||
| chr4:87386535
|
G | C | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-4173C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386535 | ||||||
| chr4:87386561
|
G | T | 60 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(57): Show | 61 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.211-4199C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386561 | ||||||
| chr4:87386596
|
CA | C | 84 | a0001c0001t0001g0188a0001c0001t0001g0298a0001c0001t0016g0149others(81): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.211-4235delT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386596 | ||||||
| chr4:87386617
|
C | T | 82 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(79): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.210+4244G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386617 | ||||||
| chr4:87386626
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.210+4235C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386626 | ||||||
| chr4:87386767
|
T | C | 83 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(80): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.210+4094A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386767 | ||||||
| chr4:87386800
|
GT | G | 5 | a0001c0002t0004g0379a0001c0002t0005g0153a0001c0002t0011g0150others(2): Show | 5 | HG02055.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+4060delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386800 | ||||||
| chr4:87386834
|
T | C | 83 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(80): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.210+4027A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386834 | ||||||
| chr4:87386899
|
C | T | 5 | a0001c0002t0004g0379a0001c0002t0005g0153a0001c0002t0011g0150others(2): Show | 5 | HG02055.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+3962G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386899 | ||||||
| chr4:87386905
|
C | T | 79 | a0001c0001t0016g0149a0001c0002t0001g0002a0001c0002t0001g0006others(76): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.210+3956G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386905 | ||||||
| chr4:87386977
|
C | T | 2 | a0001c0001t0001g0297a0001c0002t0001g0289 | 2 | HG02451.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.210+3884G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386977 | ||||||
| chr4:87386979
|
T | C | 5 | a0001c0002t0004g0379a0001c0002t0005g0153a0001c0002t0011g0150others(2): Show | 5 | HG02055.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+3882A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87386979 | ||||||
| chr4:87387082
|
C | T | 5 | a0001c0003t0008g0291a0001c0003t0008g0292a0001c0003t0008g0293others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3779G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387082 | ||||||
| chr4:87387083
|
G | A | 44 | a0001c0001t0001g0007a0001c0001t0001g0176a0001c0001t0001g0180others(41): Show | 45 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.210+3778C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387083 | ||||||
| chr4:87387090
|
A | G | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+3771T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387090 | ||||||
| chr4:87387156
|
G | A | 6 | a0001c0002t0001g0277a0001c0002t0001g0278a0001c0002t0001g0279others(3): Show | 6 | HG01074.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+3705C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387156 | ||||||
| chr4:87387263
|
G | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0176others(300): Show | 310 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.210+3598C>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387263 | ||||||
| chr4:87387367
|
T | C | 4 | a0001c0001t0003g0127a0001c0001t0003g0128a0001c0001t0003g0129others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+3494A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387367 | ||||||
| chr4:87387633
|
G | A | 8 | a0001c0002t0001g0289a0001c0002t0001g0290a0001c0002t0004g0354others(5): Show | 8 | HG02451.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+3228C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387633 | ||||||
| chr4:87387983
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.210+2878A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87387983 | ||||||
| chr4:87388013
|
C | A | 6 | a0001c0002t0001g0296a0001c0003t0008g0291a0001c0003t0008g0292others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+2848G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388013 | ||||||
| chr4:87388166
|
C | CA | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0014others(73): Show | 78 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.210+2694dupT | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388166 | ||||||
| chr4:87388166
|
C | CAA | 103 | a0001c0001t0001g0287a0001c0001t0002g0015a0001c0001t0002g0073others(100): Show | 104 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.210+2693_210+2694d others(4): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388166 | ||||||
| chr4:87388166
|
C | CAAA | 75 | a0001c0001t0001g0007a0001c0001t0001g0180a0001c0001t0001g0297others(72): Show | 77 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.210+2692_210+2694d others(5): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388166 | ||||||
| chr4:87388166
|
C | CAAAA | 7 | a0001c0001t0001g0176a0001c0001t0001g0341a0001c0001t0001g0342others(4): Show | 7 | HG02109.hp2 HG03486.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+2691_210+2694d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388166 | ||||||
| chr4:87388181
|
C | A | 12 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0007g0134others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+2680G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388181 | ||||||
| chr4:87388228
|
C | A | 10 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0007g0134others(7): Show | 10 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+2633G>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388228 | ||||||
| chr4:87388310
|
A | G | 12 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0007g0134others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+2551T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388310 | ||||||
| chr4:87388610
|
G | C | 12 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0007g0134others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+2251C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388610 | ||||||
| chr4:87388829
|
A | G | 5 | a0001c0001t0006g0167a0001c0002t0001g0181a0001c0002t0001g0182others(2): Show | 5 | HG00099.hp1 HG01081.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+2032T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388829 | ||||||
| chr4:87388983
|
A | G | 65 | a0001c0001t0002g0015a0001c0001t0002g0078a0001c0001t0002g0079others(62): Show | 66 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.210+1878T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87388983 | ||||||
| chr4:87389023
|
G | A | 9 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0081others(6): Show | 9 | HG01167.hp1 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+1838C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389023 | ||||||
| chr4:87389099
|
C | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.210+1762G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389099 | ||||||
| chr4:87389102
|
A | G | 10 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0007g0134others(7): Show | 10 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+1759T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389102 | ||||||
| chr4:87389225
|
AATTT | A | 8 | a0001c0001t0004g0372a0001c0001t0004g0373a0001c0002t0004g0371others(5): Show | 8 | HG02258.hp2 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+1632_210+1635d others(6): Show |
HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389225 | ||||||
| chr4:87389229
|
T | A | 63 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0014others(60): Show | 65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.210+1632A>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389229 | ||||||
| chr4:87389334
|
T | C | 3 | a0001c0002t0004g0376a0001c0002t0004g0377a0001c0002t0004g0378 | 3 | HG02630.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.210+1527A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389334 | ||||||
| chr4:87389346
|
A | T | 2 | a0001c0001t0001g0180a0001c0001t0006g0166 | 2 | HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.210+1515T>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389346 | ||||||
| chr4:87389371
|
C | G | 56 | a0001c0001t0002g0015a0001c0001t0002g0083a0001c0001t0003g0005others(53): Show | 57 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.210+1490G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389371 | ||||||
| chr4:87389375
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.210+1486T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389375 | ||||||
| chr4:87389379
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.210+1482G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389379 | ||||||
| chr4:87389425
|
T | G | 1 | a0001c0001t0006g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.210+1436A>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389425 | ||||||
| chr4:87389468
|
C | T | 1 | a0001c0001t0006g0165 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.210+1393G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389468 | ||||||
| chr4:87389475
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.210+1386G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389475 | ||||||
| chr4:87389558
|
C | T | 1 | a0001c0003t0003g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.210+1303G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389558 | ||||||
| chr4:87389671
|
A | G | 3 | a0001c0002t0004g0379a0001c0002t0004g0380a0001c0003t0013g0009 | 3 | HG02486.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.210+1190T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389671 | ||||||
| chr4:87389686
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.210+1175G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389686 | ||||||
| chr4:87389919
|
C | T | 1 | a0001c0003t0004g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.210+942G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87389919 | ||||||
| chr4:87390224
|
T | C | 1 | a0001c0002t0010g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.210+637A>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390224 | ||||||
| chr4:87390246
|
C | G | 9 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0081others(6): Show | 9 | HG01167.hp1 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+615G>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390246 | ||||||
| chr4:87390284
|
A | G | 12 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0007g0134others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+577T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390284 | ||||||
| chr4:87390375
|
C | T | 1 | a0001c0001t0009g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.210+486G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390375 | ||||||
| chr4:87390399
|
G | A | 3 | a0001c0002t0004g0379a0001c0002t0004g0380a0001c0003t0013g0009 | 3 | HG02486.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.210+462C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390399 | ||||||
| chr4:87390510
|
A | G | 4 | a0001c0002t0002g0074a0001c0002t0002g0075a0001c0002t0002g0076others(1): Show | 4 | HG01167.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+351T>C | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390510 | ||||||
| chr4:87390544
|
C | T | 1 | a0001c0002t0003g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.210+317G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390544 | ||||||
| chr4:87390583
|
G | A | 12 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0007g0134others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+278C>T | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390583 | ||||||
| chr4:87390648
|
G | C | 64 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0081others(61): Show | 65 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.210+213C>G | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390648 | ||||||
| chr4:87390715
|
C | T | 1 | a0001c0001t0016g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+146G>A | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390715 | ||||||
| chr4:87390747
|
AT | A | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.210+113delA | HSD17B11 | ENSG00000198189.11 | transcript | ENST00000358290.9 | protein_coding | 1/6 | chr4 | 87390747 |