Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3295 |
|---|---|
| ensemblid | ENSG00000133835.18 |
| hgncid | 5213 |
| symbol | HSD17B4 |
| name | hydroxysteroid 17-beta dehydrogenase 4 |
| refseq_nuc | NM_000414.4 |
| refseq_prot | NP_000405.1 |
| ensembl_nuc | ENST00000510025.7 |
| ensembl_prot | ENSP00000424940.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 119452497 |
| end | 119542332 |
| strand | + |
| ver | v1.2 |
| region | chr5:119452497-119542332 |
| region5000 | chr5:119447497-119547332 |
| regionname0 | HSD17B4_chr5_119452497_119542332 |
| regionname5000 | HSD17B4_chr5_119447497_119547332 |
| 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 | 736 | 169 | 36 | 30 | 80 | 6 | 16 | 62 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0002 | 0/1 | 736 | 93 | 4 | 13 | 59 | 8 | 8 | 44 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0003 | 0/0 | 736 | 42 | 11 | 9 | 19 | 0 | 3 | 18 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0004 | 0/0 | 736 | 38 | 23 | 7 | 1 | 2 | 5 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0005 | 0/0 | 736 | 10 | 0 | 0 | 10 | 0 | 0 | 6 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0006 | 0/0 | 736 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0007 | 0/0 | 736 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0008 | 0/0 | 736 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009 | 0/0 | 736 | 5 | 0 | 2 | 2 | 0 | 1 | 2 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0010 | 0/0 | 736 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0011 | 0/0 | 736 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0012 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0013 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0014 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| 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 | 2211 | 165 | 35 | 30 | 78 | 6 | 15 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0002 | 0/1 | 2211 | 93 | 4 | 13 | 59 | 8 | 8 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0003 | 0/0 | 2211 | 42 | 11 | 9 | 19 | 0 | 3 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0004 | 0/0 | 2211 | 35 | 20 | 7 | 1 | 2 | 5 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0005 | 0/0 | 2211 | 10 | 0 | 0 | 10 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0006 | 0/0 | 2211 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0007 | 0/0 | 2211 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0008 | 0/0 | 2211 | 5 | 3 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0009 | 0/0 | 2211 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0010 | 0/0 | 2211 | 3 | 0 | 1 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0011 | 0/0 | 2211 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0012 | 0/0 | 2211 | 2 | 0 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0013 | 0/0 | 2211 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0014 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0015 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0016 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0017 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0018 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| c0019 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| 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 | 418 | 168 | 28 | 27 | 90 | 6 | 16 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0002 | 0/1 | 419 | 143 | 21 | 25 | 78 | 8 | 10 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0003 | 0/0 | 419 | 44 | 36 | 5 | 1 | 0 | 2 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0004 | 0/0 | 419 | 13 | 0 | 6 | 1 | 1 | 5 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0005 | 0/0 | 419 | 3 | 0 | 1 | 0 | 1 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0006 | 0/0 | 418 | 3 | 2 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0007 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0008 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0009 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0010 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0011 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| t0012 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| 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 | 2 | 0 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| 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 | 2211 | 165 | 35 | 30 | 78 | 6 | 15 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0013 | 0/0 | 2211 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0016 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0019 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0002c0002 | 0/1 | 2211 | 93 | 4 | 13 | 59 | 8 | 8 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0003c0003 | 0/0 | 2211 | 42 | 11 | 9 | 19 | 0 | 3 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0004c0004 | 0/0 | 2211 | 35 | 20 | 7 | 1 | 2 | 5 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0004c0009 | 0/0 | 2211 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0005c0005 | 0/0 | 2211 | 10 | 0 | 0 | 10 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0006c0006 | 0/0 | 2211 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0007c0007 | 0/0 | 2211 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0008c0008 | 0/0 | 2211 | 5 | 3 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009c0010 | 0/0 | 2211 | 3 | 0 | 1 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009c0012 | 0/0 | 2211 | 2 | 0 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0010c0011 | 0/0 | 2211 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0011c0015 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0012c0018 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0013c0017 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0014c0014 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2628 | 155 | 28 | 27 | 78 | 6 | 15 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0001t0002 | 0/0 | 2629 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0001t0003 | 0/0 | 2629 | 4 | 1 | 3 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0001t0006 | 0/0 | 2628 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0001t0009 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0013t0001 | 0/0 | 2628 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0016t0001 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0001c0019t0007 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0002c0002t0002 | 0/1 | 2629 | 91 | 3 | 13 | 59 | 8 | 7 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0002c0002t0003 | 0/0 | 2629 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0002c0002t0011 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0003c0003t0002 | 0/0 | 2629 | 38 | 9 | 8 | 18 | 0 | 3 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0003c0003t0003 | 0/0 | 2629 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0003c0003t0006 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0003c0003t0010 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0004c0004t0003 | 0/0 | 2629 | 20 | 20 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0004c0004t0004 | 0/0 | 2629 | 12 | 0 | 6 | 1 | 1 | 4 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0004c0004t0005 | 0/0 | 2629 | 3 | 0 | 1 | 0 | 1 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0004c0009t0003 | 0/0 | 2629 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0005c0005t0001 | 0/0 | 2628 | 9 | 0 | 0 | 9 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0005c0005t0008 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0006c0006t0002 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0006c0006t0003 | 0/0 | 2629 | 5 | 5 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0007c0007t0002 | 0/0 | 2629 | 5 | 5 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0007c0007t0003 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0008c0008t0003 | 0/0 | 2629 | 5 | 3 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009c0010t0001 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009c0010t0002 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009c0010t0003 | 0/0 | 2629 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009c0012t0003 | 0/0 | 2629 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0009c0012t0012 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0010c0011t0002 | 0/0 | 2629 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0011c0015t0002 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0012c0018t0003 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0013c0017t0004 | 0/0 | 2629 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| a0014c0014t0002 | 0/0 | 2629 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | copy fasta | chr5 | 119447497 | 119547332 |
| 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 | 2 | 0 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0009g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0013t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0013t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0016t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0019t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0003g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0010g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0009t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0009t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0009t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0008g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0006t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0006t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0006t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0006t0003g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0006t0003g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0007t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0007t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0007t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0007t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0007t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0007t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0008t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0008t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0008t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0008t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0008t0003g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0010t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0010t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0010t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0012t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0012t0012g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0010c0011t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0010c0011t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0011c0015t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0012c0018t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0013c0017t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0014c0014t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0149 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0119 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00280 | hp1 | a0004 | c0004 | t0004 | g0346 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0158 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00323 | hp1 | a0004 | c0004 | t0005 | g0180 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0159 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0228 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00639 | hp1 | a0009 | c0010 | t0002 | g0020 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00639 | hp2 | a0003 | c0003 | t0010 | g0193 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0221 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00735 | hp1 | a0003 | c0003 | t0002 | g0208 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0137 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0145 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01081 | hp2 | a0004 | c0004 | t0005 | g0182 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0142 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01106 | hp1 | a0008 | c0008 | t0003 | g0017 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0215 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0164 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0211 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0212 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01243 | hp1 | a0008 | c0008 | t0003 | g0364 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0373 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0371 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01255 | hp2 | a0011 | c0015 | t0002 | g0207 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01256 | hp2 | a0010 | c0011 | t0002 | g0209 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01258 | hp1 | a0010 | c0011 | t0002 | g0210 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0147 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01496 | hp1 | a0009 | c0012 | t0012 | g0374 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01496 | hp2 | a0004 | c0004 | t0004 | g0348 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0192 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0003 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0003 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0366 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01884 | hp2 | a0007 | c0007 | t0002 | g0205 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01891 | hp1 | a0008 | c0008 | t0003 | g0021 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01891 | hp2 | a0001 | c0019 | t0007 | g0013 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0133 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01934 | hp2 | a0004 | c0004 | t0004 | g0359 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0237 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0206 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01993 | hp1 | a0004 | c0004 | t0004 | g0360 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02004 | hp1 | a0004 | c0004 | t0004 | g0361 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02027 | hp1 | a0005 | c0005 | t0008 | g0241 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02040 | hp2 | a0005 | c0005 | t0001 | g0268 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02055 | hp2 | a0004 | c0009 | t0003 | g0340 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02056 | hp2 | a0005 | c0005 | t0001 | g0265 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02145 | hp1 | a0003 | c0003 | t0002 | g0213 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02145 | hp2 | a0003 | c0003 | t0002 | g0183 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02148 | hp2 | a0004 | c0004 | t0004 | g0357 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02155 | hp2 | a0005 | c0005 | t0001 | g0293 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02257 | hp1 | a0002 | c0002 | t0011 | g0152 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02257 | hp2 | a0004 | c0004 | t0003 | g0342 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02258 | hp1 | a0006 | c0006 | t0003 | g0369 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0372 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02280 | hp1 | a0004 | c0004 | t0003 | g0338 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02280 | hp2 | a0004 | c0004 | t0003 | g0330 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02300 | hp2 | a0004 | c0004 | t0004 | g0358 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02451 | hp1 | a0004 | c0009 | t0003 | g0339 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02602 | hp2 | a0003 | c0003 | t0002 | g0214 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02615 | hp2 | a0004 | c0004 | t0003 | g0351 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02622 | hp1 | a0004 | c0004 | t0003 | g0362 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02622 | hp2 | a0003 | c0003 | t0002 | g0194 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02630 | hp1 | a0004 | c0004 | t0003 | g0344 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02647 | hp1 | a0004 | c0004 | t0003 | g0334 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02647 | hp2 | a0007 | c0007 | t0003 | g0199 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0095 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02886 | hp1 | a0004 | c0004 | t0003 | g0333 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0112 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02896 | hp1 | a0003 | c0003 | t0002 | g0196 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02896 | hp2 | a0006 | c0006 | t0003 | g0005 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02897 | hp2 | a0006 | c0006 | t0003 | g0005 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02922 | hp1 | a0004 | c0004 | t0003 | g0355 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02970 | hp1 | a0006 | c0006 | t0003 | g0368 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0309 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0185 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03017 | hp2 | a0003 | c0003 | t0002 | g0219 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03041 | hp2 | a0007 | c0007 | t0002 | g0204 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0197 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03130 | hp2 | a0004 | c0004 | t0003 | g0347 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03209 | hp1 | a0004 | c0009 | t0003 | g0352 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03209 | hp2 | a0006 | c0006 | t0002 | g0202 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03225 | hp1 | a0004 | c0004 | t0003 | g0341 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03239 | hp1 | a0004 | c0004 | t0004 | g0337 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03453 | hp2 | a0004 | c0004 | t0003 | g0335 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03486 | hp2 | a0004 | c0004 | t0003 | g0353 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03490 | hp2 | a0004 | c0004 | t0004 | g0004 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03492 | hp2 | a0004 | c0004 | t0004 | g0004 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03516 | hp2 | a0004 | c0004 | t0003 | g0345 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03540 | hp1 | a0008 | c0008 | t0003 | g0019 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03540 | hp2 | a0004 | c0004 | t0003 | g0350 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0093 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03654 | hp1 | a0004 | c0004 | t0005 | g0181 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03654 | hp2 | a0001 | c0016 | t0001 | g0036 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0113 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03834 | hp1 | a0013 | c0017 | t0004 | g0331 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0110 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03927 | hp2 | a0002 | c0002 | t0003 | g0329 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0223 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0120 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04115 | hp2 | a0004 | c0004 | t0004 | g0336 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04204 | hp2 | a0009 | c0012 | t0003 | g0015 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18522 | hp1 | a0004 | c0004 | t0003 | g0354 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18522 | hp2 | a0007 | c0007 | t0002 | g0203 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | CHB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | CHB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0367 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18940 | hp1 | a0005 | c0005 | t0001 | g0315 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18940 | hp2 | a0003 | c0003 | t0006 | g0151 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18947 | hp2 | a0004 | c0004 | t0004 | g0343 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18961 | hp2 | a0009 | c0010 | t0001 | g0278 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0236 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18963 | hp2 | a0003 | c0003 | t0002 | g0226 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0230 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18966 | hp2 | a0005 | c0005 | t0001 | g0246 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18972 | hp2 | a0005 | c0005 | t0001 | g0266 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0216 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18984 | hp1 | a0005 | c0005 | t0001 | g0269 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18985 | hp1 | a0003 | c0003 | t0002 | g0231 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0232 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18990 | hp2 | a0001 | c0013 | t0001 | g0282 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18993 | hp1 | a0003 | c0003 | t0002 | g0217 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18994 | hp1 | a0001 | c0013 | t0001 | g0264 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18994 | hp2 | a0003 | c0003 | t0002 | g0235 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18999 | hp1 | a0003 | c0003 | t0002 | g0222 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19001 | hp2 | a0005 | c0005 | t0001 | g0291 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0238 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0227 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0220 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19030 | hp2 | a0008 | c0008 | t0003 | g0016 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19043 | hp1 | a0004 | c0004 | t0003 | g0356 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19055 | hp2 | a0003 | c0003 | t0002 | g0198 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0234 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19060 | hp1 | a0005 | c0005 | t0001 | g0243 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19064 | hp2 | a0014 | c0014 | t0002 | g0130 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19077 | hp2 | a0009 | c0010 | t0003 | g0018 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19083 | hp2 | a0003 | c0003 | t0002 | g0233 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19086 | hp1 | a0003 | c0003 | t0002 | g0229 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19087 | hp2 | a0003 | c0003 | t0002 | g0225 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19240 | hp1 | a0006 | c0006 | t0003 | g0370 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ASW | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20129 | hp2 | a0004 | c0004 | t0003 | g0332 | AFR | ASW | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0141 | EUR | TSI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0102 | SAS | GIH | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0224 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0375 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02486 | hp1 | a0004 | c0004 | t0003 | g0349 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02486 | hp2 | a0012 | c0018 | t0003 | g0365 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0195 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02559 | hp2 | a0004 | c0004 | t0003 | g0328 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG06807 | hp2 | a0007 | c0007 | t0002 | g0200 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20300 | hp1 | a0003 | c0003 | t0002 | g0184 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20300 | hp2 | a0003 | c0003 | t0002 | g0218 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA21309 | hp2 | a0007 | c0007 | t0002 | g0201 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0092 | REF | REF | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0078 | REF | REF | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119474448
|
T | C | 1 | a0014 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.268T>C | p.Phe90Leu | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/24 | 347/2628 | 268/2211 | 90/736 | chr5 | 119474448 | ||
| chr5:119475838
|
G | A | 5 | a0002a0003a0010others(2): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
missense_variant | MODERATE | c.317G>A | p.Arg106His | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/24 | 396/2628 | 317/2211 | 106/736 | chr5 | 119475838 | ||
| chr5:119477487
|
A | T | 1 | a0007 | 6 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
missense_variant | MODERATE | c.420A>T | p.Lys140Asn | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/24 | 499/2628 | 420/2211 | 140/736 | chr5 | 119477487 | ||
| chr5:119496549
|
C | G | 2 | a0008a0012 | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
missense_variant | MODERATE | c.875C>G | p.Thr292Ser | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/24 | 954/2628 | 875/2211 | 292/736 | chr5 | 119496549 | ||
| chr5:119515014
|
G | A | 1 | a0010 | 2 | HG01256.hp2 HG01258.hp1 |
missense_variant | MODERATE | c.1471G>A | p.Ala491Thr | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/24 | 1550/2628 | 1471/2211 | 491/736 | chr5 | 119515014 | ||
| chr5:119525243
|
T | C | 4 | a0004a0006a0007others(1): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
missense_variant | MODERATE | c.1531T>C | p.Trp511Arg | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/24 | 1610/2628 | 1531/2211 | 511/736 | chr5 | 119525243 | ||
| chr5:119525968
|
G | A | 1 | a0013 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1625G>A | p.Arg542Lys | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/24 | 1704/2628 | 1625/2211 | 542/736 | chr5 | 119525968 | ||
| chr5:119525971
|
G | A | 1 | a0011 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1628G>A | p.Arg543His | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/24 | 1707/2628 | 1628/2211 | 543/736 | chr5 | 119525971 | ||
| chr5:119526018
|
A | G | 7 | a0002a0004a0006others(4): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
missense_variant | MODERATE | c.1675A>G | p.Ile559Val | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/24 | 1754/2628 | 1675/2211 | 559/736 | chr5 | 119526018 | ||
| chr5:119536489
|
C | T | 1 | a0005 | 10 | HG02027.hp1 HG02040.hp2 HG02056.hp2 others(7): Show |
missense_variant | MODERATE | c.2060C>T | p.Thr687Ile | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/24 | 2139/2628 | 2060/2211 | 687/736 | chr5 | 119536489 | ||
| chr5:119541959
|
C | G | 1 | a0012 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.2176C>G | p.Leu726Val | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 2255/2628 | 2176/2211 | 726/736 | chr5 | 119541959 | ||
| chr5:119541965
|
A | G | 2 | a0006a0007 | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
missense_variant | MODERATE | c.2182A>G | p.Met728Val | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 2261/2628 | 2182/2211 | 728/736 | chr5 | 119541965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119489235
|
C | G | 1 | a0001c0019 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.666C>G | p.Val222Val | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/24 | 745/2628 | 666/2211 | 222/736 | chr5 | 119489235 | ||
| chr5:119496622
|
A | G | 1 | a0001c0013 | 2 | NA18990.hp2 NA18994.hp1 |
synonymous_variant | LOW | c.948A>G | p.Ala316Ala | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/24 | 1027/2628 | 948/2211 | 316/736 | chr5 | 119496622 | ||
| chr5:119499403
|
G | A | 2 | a0001c0016a0004c0009 | 4 | HG02055.hp2 HG02451.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.1059G>A | p.Ala353Ala | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/24 | 1138/2628 | 1059/2211 | 353/736 | chr5 | 119499403 | ||
| chr5:119529917
|
C | T | 2 | a0008c0008a0012c0018 | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
synonymous_variant | LOW | c.1791C>T | p.Val597Val | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/24 | 1870/2628 | 1791/2211 | 597/736 | chr5 | 119529917 | ||
| chr5:119541982
|
C | T | 3 | a0006c0006a0007c0007a0009c0012 | 14 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
synonymous_variant | LOW | c.2199C>T | p.Tyr733Tyr | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 2278/2628 | 2199/2211 | 733/736 | chr5 | 119541982 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119452501
|
C | G | 14 | a0001c0001t0002a0001c0001t0006a0002c0002t0002others(11): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-75C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/24 | 75 | chr5 | 119452501 | |||||
| chr5:119452549
|
G | C | 1 | a0001c0019t0007 | 1 | HG01891.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-27G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/24 | chr5 | 119452549 | ||||||
| chr5:119542000
|
A | G | 1 | a0009c0012t0012 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 6 | chr5 | 119542000 | |||||
| chr5:119542087
|
G | A | 1 | a0005c0005t0008 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*93G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 93 | chr5 | 119542087 | |||||
| chr5:119542128
|
C | T | 1 | a0002c0002t0011 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 134 | chr5 | 119542128 | |||||
| chr5:119542238
|
T | TA | 27 | a0001c0001t0002a0001c0001t0003a0001c0019t0007others(24): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*250dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 251 | INFO_REALIGN_3_PRIME | chr5 | 119542238 | ||||
| chr5:119542245
|
T | A | 1 | a0001c0001t0009 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 251 | chr5 | 119542245 | |||||
| chr5:119542254
|
A | G | 3 | a0004c0004t0004a0004c0004t0005a0013c0017t0004 | 16 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*260A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 260 | chr5 | 119542254 | |||||
| chr5:119542272
|
T | A | 1 | a0003c0003t0010 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 24/24 | 278 | chr5 | 119542272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119452828
|
C | T | 1 | a0003c0003t0002g0375 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58+195C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119452828 | ||||||
| chr5:119452893
|
G | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.58+260G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119452893 | ||||||
| chr5:119452911
|
C | G | 11 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373others(8): Show | 12 | HG01243.hp1 HG01243.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+278C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119452911 | ||||||
| chr5:119453325
|
A | T | 177 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0239others(174): Show | 178 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.58+692A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119453325 | ||||||
| chr5:119453412
|
A | G | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.58+779A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119453412 | ||||||
| chr5:119453459
|
G | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.58+826G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119453459 | ||||||
| chr5:119453474
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58+841G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119453474 | ||||||
| chr5:119453643
|
A | G | 176 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(173): Show | 177 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.58+1010A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119453643 | ||||||
| chr5:119453718
|
G | A | 48 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(45): Show | 48 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.58+1085G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119453718 | ||||||
| chr5:119453862
|
C | T | 1 | a0004c0004t0003g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58+1229C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119453862 | ||||||
| chr5:119454015
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58+1382T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454015 | ||||||
| chr5:119454221
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58+1588A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454221 | ||||||
| chr5:119454261
|
T | C | 2 | a0002c0002t0002g0011a0002c0002t0002g0012 | 2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.58+1628T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454261 | ||||||
| chr5:119454273
|
T | C | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.58+1640T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454273 | ||||||
| chr5:119454307
|
A | AT | 173 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(170): Show | 174 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.58+1688dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119454307 | |||||
| chr5:119454393
|
A | C | 42 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(39): Show | 43 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.58+1760A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454393 | ||||||
| chr5:119454400
|
G | C | 1 | a0001c0001t0001g0327 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58+1767G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454400 | ||||||
| chr5:119454466
|
C | T | 36 | a0001c0001t0001g0327a0002c0002t0003g0329a0004c0004t0003g0328others(33): Show | 37 | HG00280.hp1 HG01496.hp2 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.58+1833C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454466 | ||||||
| chr5:119454717
|
G | T | 10 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373others(7): Show | 11 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-1598G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454717 | ||||||
| chr5:119454773
|
CA | C | 5 | a0004c0004t0004g0357a0004c0004t0004g0358a0004c0004t0004g0359others(2): Show | 5 | HG01934.hp2 HG01993.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1541delA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454773 | ||||||
| chr5:119454812
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.59-1503G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454812 | ||||||
| chr5:119454848
|
C | T | 6 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(3): Show | 6 | NA18960.hp1 NA18970.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1467C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119454848 | ||||||
| chr5:119455284
|
C | T | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.59-1031C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455284 | ||||||
| chr5:119455309
|
G | A | 48 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(45): Show | 48 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.59-1006G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455309 | ||||||
| chr5:119455327
|
G | A | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.59-988G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455327 | ||||||
| chr5:119455336
|
G | A | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-979G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455336 | ||||||
| chr5:119455366
|
A | T | 1 | a0002c0002t0002g0177 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.59-949A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455366 | ||||||
| chr5:119455378
|
G | A | 98 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0242others(95): Show | 99 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.59-937G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455378 | ||||||
| chr5:119455393
|
T | A | 1 | a0002c0002t0002g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.59-922T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455393 | ||||||
| chr5:119455409
|
C | T | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.59-906C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455409 | ||||||
| chr5:119455411
|
C | T | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-904C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455411 | ||||||
| chr5:119455473
|
T | C | 299 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 303 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.59-842T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455473 | ||||||
| chr5:119455508
|
C | G | 37 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0198others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.59-807C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455508 | ||||||
| chr5:119455516
|
C | CA | 48 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(45): Show | 48 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.59-790dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455516 | |||||
| chr5:119455542
|
T | TTCTC | 6 | a0002c0002t0002g0165a0002c0002t0002g0166a0002c0002t0002g0167others(3): Show | 6 | HG01167.hp1 HG02155.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-749_59-746dupCT others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455542 | |||||
| chr5:119455542
|
T | TTCTCTC | 7 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0002g0174others(4): Show | 7 | HG02129.hp1 HG02165.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-751_59-746dupCT others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455542 | |||||
| chr5:119455542
|
TTC | T | 81 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0242others(78): Show | 82 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.59-747_59-746delCT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455542 | |||||
| chr5:119455542
|
TTCTC | T | 3 | a0001c0001t0002g0178a0003c0003t0003g0366a0003c0003t0003g0367 | 3 | HG01884.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.59-749_59-746delCT others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455542 | |||||
| chr5:119455562
|
C | A | 1 | a0003c0003t0002g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.59-753C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455562 | ||||||
| chr5:119455564
|
C | A | 19 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0239others(16): Show | 19 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.59-751C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455564 | ||||||
| chr5:119455566
|
C | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(43): Show | 47 | HG00423.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.59-749C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455566 | ||||||
| chr5:119455566
|
C | CTA | 4 | a0001c0001t0001g0059a0001c0001t0001g0327a0001c0019t0007g0013others(1): Show | 4 | HG01192.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-748_59-747insAT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455566 | |||||
| chr5:119455566
|
C | CTATA | 23 | a0002c0002t0002g0002a0002c0002t0002g0096a0002c0002t0002g0097others(20): Show | 24 | HG00597.hp2 HG01123.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-748_59-747insAT others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455566 | |||||
| chr5:119455568
|
C | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(130): Show | 136 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.59-747C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455568 | ||||||
| chr5:119455568
|
C | CTATA | 34 | a0002c0002t0002g0003a0002c0002t0002g0011a0002c0002t0002g0092others(31): Show | 35 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.59-734_59-731dupTA others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455568 | |||||
| chr5:119455568
|
C | CTATATA | 10 | a0001c0001t0003g0010a0002c0002t0002g0143a0004c0004t0003g0332others(7): Show | 11 | HG00323.hp1 HG00741.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-736_59-731dupTA others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455568 | |||||
| chr5:119455568
|
C | CTCTA | 16 | a0002c0002t0002g0012a0002c0002t0002g0144a0002c0002t0002g0145others(13): Show | 16 | HG00099.hp2 HG01069.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-746_59-745insCT others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455568 | |||||
| chr5:119455568
|
C | CTCTATA | 24 | a0002c0002t0002g0158a0002c0002t0002g0159a0002c0002t0002g0160others(21): Show | 24 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.59-746_59-745insCT others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455568 | |||||
| chr5:119455568
|
C | CTCTCTA | 9 | a0002c0002t0002g0171a0004c0004t0003g0349a0004c0004t0003g0350others(6): Show | 9 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-746_59-745insCT others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455568 | |||||
| chr5:119455568
|
CTA | C | 14 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(11): Show | 14 | HG00558.hp1 HG01243.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-732_59-731delTA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr5 | 119455568 | |||||
| chr5:119455570
|
A | C | 12 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(9): Show | 12 | HG00609.hp2 HG00673.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-745A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455570 | ||||||
| chr5:119455572
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59-743A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455572 | ||||||
| chr5:119455601
|
A | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-714A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455601 | ||||||
| chr5:119455652
|
G | A | 1 | a0011c0015t0002g0207 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.59-663G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455652 | ||||||
| chr5:119455668
|
G | A | 295 | a0001c0001t0001g0009a0001c0001t0001g0239a0001c0001t0001g0240others(292): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.59-647G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455668 | ||||||
| chr5:119455699
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.59-616T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455699 | ||||||
| chr5:119455764
|
C | T | 296 | a0001c0001t0001g0009a0001c0001t0001g0239a0001c0001t0001g0240others(293): Show | 300 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.59-551C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455764 | ||||||
| chr5:119455915
|
G | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.59-400G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455915 | ||||||
| chr5:119455950
|
A | G | 98 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0242others(95): Show | 99 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.59-365A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455950 | ||||||
| chr5:119456100
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.59-215G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119456100 | ||||||
| chr5:119456137
|
G | A | 254 | a0001c0001t0001g0009a0001c0001t0001g0239a0001c0001t0001g0240others(251): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.59-178G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119456137 | ||||||
| chr5:119456228
|
A | G | 20 | a0001c0001t0001g0248a0001c0001t0001g0296a0001c0001t0001g0297others(17): Show | 20 | HG00544.hp1 HG00558.hp1 NA18747.hp2 others(17): Show |
intron_variant | MODIFIER | c.59-87A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119456228 | ||||||
| chr5:119456247
|
G | C | 1 | a0002c0002t0002g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.59-68G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119456247 | ||||||
| chr5:119456266
|
A | C | 1 | a0004c0004t0004g0361 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.59-49A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119456266 | ||||||
| chr5:119456282
|
C | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-33C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119456282 | ||||||
| chr5:119456570
|
G | A | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.112+202G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119456570 | ||||||
| chr5:119456599
|
G | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG01978.hp2 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.112+231G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119456599 | ||||||
| chr5:119456733
|
C | CA | 7 | a0001c0001t0001g0014a0001c0001t0001g0250a0001c0001t0001g0311others(4): Show | 7 | HG02698.hp1 NA18906.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+373dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119456733 | |||||
| chr5:119456807
|
G | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+439G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119456807 | ||||||
| chr5:119456838
|
G | A | 2 | a0002c0002t0002g0158a0002c0002t0002g0159 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.112+470G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119456838 | ||||||
| chr5:119456838
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.112+470G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119456838 | ||||||
| chr5:119457009
|
A | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA18987.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.112+641A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457009 | ||||||
| chr5:119457026
|
A | G | 88 | a0001c0001t0001g0327a0001c0001t0002g0363a0001c0001t0006g0185others(85): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.112+658A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457026 | ||||||
| chr5:119457109
|
G | T | 1 | a0007c0007t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.112+741G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457109 | ||||||
| chr5:119457187
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.112+819A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457187 | ||||||
| chr5:119457228
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.112+860C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457228 | ||||||
| chr5:119457268
|
C | G | 37 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0198others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.112+900C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457268 | ||||||
| chr5:119457300
|
A | G | 1 | a0005c0005t0001g0293 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112+932A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457300 | ||||||
| chr5:119457458
|
A | G | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.112+1090A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457458 | ||||||
| chr5:119457615
|
A | C | 1 | a0002c0002t0002g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.112+1247A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457615 | ||||||
| chr5:119457662
|
T | A | 1 | a0001c0001t0002g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112+1294T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457662 | ||||||
| chr5:119457669
|
C | CT | 255 | a0001c0001t0001g0009a0001c0001t0001g0082a0001c0001t0001g0239others(252): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.112+1301_112+1302i others(3): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457669 | ||||||
| chr5:119457713
|
G | A | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1345G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457713 | ||||||
| chr5:119457752
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.112+1384C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457752 | ||||||
| chr5:119457895
|
T | C | 3 | a0002c0002t0002g0143a0002c0002t0002g0160a0002c0002t0002g0161 | 3 | NA18951.hp2 NA18970.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.112+1527T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457895 | ||||||
| chr5:119457927
|
C | G | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1559C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119457927 | ||||||
| chr5:119458082
|
A | G | 1 | a0003c0003t0002g0234 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.112+1714A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458082 | ||||||
| chr5:119458221
|
C | T | 1 | a0004c0004t0003g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112+1853C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458221 | ||||||
| chr5:119458464
|
C | T | 94 | a0001c0001t0001g0292a0002c0002t0002g0002a0002c0002t0002g0003others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.112+2096C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458464 | ||||||
| chr5:119458508
|
A | AT | 99 | a0001c0001t0001g0009a0001c0001t0001g0292a0001c0001t0002g0178others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.112+2159dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119458508 | |||||
| chr5:119458508
|
AT | A | 40 | a0001c0001t0001g0037a0001c0001t0001g0327a0002c0002t0003g0329others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.112+2159delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119458508 | |||||
| chr5:119458537
|
T | G | 40 | a0001c0001t0001g0327a0002c0002t0003g0329a0004c0004t0003g0328others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.112+2169T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458537 | ||||||
| chr5:119458596
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.112+2228C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458596 | ||||||
| chr5:119458694
|
T | C | 14 | a0004c0004t0003g0332a0004c0004t0003g0338a0004c0004t0003g0341others(11): Show | 14 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+2326T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458694 | ||||||
| chr5:119458754
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.112+2386A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458754 | ||||||
| chr5:119458834
|
T | G | 1 | a0004c0004t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112+2466T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458834 | ||||||
| chr5:119459064
|
T | C | 5 | a0004c0004t0003g0338a0004c0004t0003g0349a0004c0004t0003g0350others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+2696T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459064 | ||||||
| chr5:119459289
|
G | A | 50 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(47): Show | 50 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.112+2921G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459289 | ||||||
| chr5:119459389
|
G | C | 2 | a0002c0002t0002g0097a0002c0002t0002g0146 | 2 | NA19058.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.112+3021G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459389 | ||||||
| chr5:119459439
|
T | A | 1 | a0004c0004t0005g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.112+3071T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459439 | ||||||
| chr5:119459582
|
T | A | 1 | a0002c0002t0002g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.112+3214T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459582 | ||||||
| chr5:119459696
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.112+3328A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459696 | ||||||
| chr5:119459719
|
C | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.112+3351C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459719 | ||||||
| chr5:119459740
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18956.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.112+3372A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459740 | ||||||
| chr5:119459846
|
C | T | 9 | a0002c0002t0002g0003a0002c0002t0002g0112a0002c0002t0002g0113others(6): Show | 10 | HG01069.hp2 HG01099.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.112+3478C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459846 | ||||||
| chr5:119459873
|
C | CT | 6 | a0001c0001t0001g0313a0002c0002t0002g0170a0004c0004t0003g0347others(3): Show | 6 | HG01891.hp1 HG03130.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+3520dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119459873 | |||||
| chr5:119459935
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.112+3567A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459935 | ||||||
| chr5:119459995
|
T | C | 54 | a0001c0001t0001g0009a0001c0001t0002g0363a0001c0001t0003g0010others(51): Show | 54 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.112+3627T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119459995 | ||||||
| chr5:119460048
|
T | C | 35 | a0003c0003t0002g0198a0003c0003t0002g0206a0003c0003t0002g0208others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.112+3680T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460048 | ||||||
| chr5:119460117
|
C | T | 37 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0198others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.112+3749C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460117 | ||||||
| chr5:119460219
|
A | G | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.112+3851A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460219 | ||||||
| chr5:119460259
|
G | C | 37 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0198others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.112+3891G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460259 | ||||||
| chr5:119460278
|
C | T | 4 | a0001c0001t0001g0247a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | HG00642.hp1 HG01074.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+3910C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460278 | ||||||
| chr5:119460285
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.112+3917C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460285 | ||||||
| chr5:119460446
|
A | G | 40 | a0001c0001t0001g0327a0002c0002t0003g0329a0004c0004t0003g0328others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.112+4078A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460446 | ||||||
| chr5:119460501
|
C | T | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+4133C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460501 | ||||||
| chr5:119460603
|
A | C | 40 | a0001c0001t0001g0327a0002c0002t0003g0329a0004c0004t0003g0328others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.112+4235A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460603 | ||||||
| chr5:119460677
|
C | T | 1 | a0002c0002t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.112+4309C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460677 | ||||||
| chr5:119460692
|
G | A | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.112+4324G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460692 | ||||||
| chr5:119460785
|
T | C | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.112+4417T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460785 | ||||||
| chr5:119460807
|
G | GA | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+4446dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119460807 | |||||
| chr5:119460837
|
C | CTGAAAGA others(5): Show |
48 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(45): Show | 48 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.112+4470_112+4471i others(14): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119460837 | |||||
| chr5:119460837
|
C | G | 3 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02630.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.112+4469C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460837 | ||||||
| chr5:119460892
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.112+4524G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460892 | ||||||
| chr5:119460894
|
G | A | 48 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(45): Show | 48 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.112+4526G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460894 | ||||||
| chr5:119460909
|
A | G | 48 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(45): Show | 48 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.112+4541A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460909 | ||||||
| chr5:119460942
|
G | T | 197 | a0001c0001t0001g0082a0001c0001t0001g0190a0001c0001t0001g0239others(194): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.112+4574G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460942 | ||||||
| chr5:119460944
|
A | T | 197 | a0001c0001t0001g0082a0001c0001t0001g0190a0001c0001t0001g0239others(194): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.112+4576A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460944 | ||||||
| chr5:119460993
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.112+4625C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460993 | ||||||
| chr5:119461124
|
A | G | 99 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(96): Show | 100 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.112+4756A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461124 | ||||||
| chr5:119461187
|
T | C | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.112+4819T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461187 | ||||||
| chr5:119461291
|
C | T | 1 | a0002c0002t0002g0111 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.112+4923C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461291 | ||||||
| chr5:119461319
|
A | C | 100 | a0001c0001t0001g0082a0001c0001t0001g0292a0001c0001t0002g0178others(97): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.112+4951A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461319 | ||||||
| chr5:119461358
|
TC | T | 8 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG00621.hp1 NA18946.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+4991delC | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461358 | ||||||
| chr5:119461359
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.112+4991C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461359 | ||||||
| chr5:119461546
|
C | G | 48 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(45): Show | 48 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.112+5178C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461546 | ||||||
| chr5:119461633
|
A | G | 44 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0198others(41): Show | 44 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.112+5265A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461633 | ||||||
| chr5:119461652
|
C | T | 40 | a0001c0001t0001g0327a0002c0002t0003g0329a0004c0004t0003g0328others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.112+5284C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461652 | ||||||
| chr5:119461672
|
A | G | 4 | a0003c0003t0002g0216a0003c0003t0002g0217a0003c0003t0002g0218others(1): Show | 4 | HG01255.hp2 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+5304A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461672 | ||||||
| chr5:119461721
|
C | CA | 55 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0251others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.112+5370dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119461721 | |||||
| chr5:119461907
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0081 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.112+5539A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461907 | ||||||
| chr5:119461994
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(5): Show | 8 | HG00642.hp1 HG01074.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+5626C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461994 | ||||||
| chr5:119462053
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.112+5685C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462053 | ||||||
| chr5:119462248
|
A | AT | 40 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0035others(37): Show | 40 | HG00323.hp1 HG00423.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+5915dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
A | ATT | 25 | a0001c0001t0002g0363a0001c0016t0001g0036a0001c0019t0007g0013others(22): Show | 26 | HG00280.hp1 HG01167.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.112+5914_112+5915d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
A | ATTT | 7 | a0001c0001t0001g0327a0004c0004t0004g0337a0004c0004t0004g0343others(4): Show | 7 | HG01934.hp2 HG01993.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+5913_112+5915d others(5): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
AT | A | 64 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0034others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+5915delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
ATT | A | 74 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0026others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.112+5914_112+5915d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
ATTT | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0002g0178others(2): Show | 6 | HG00408.hp1 HG01993.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+5913_112+5915d others(5): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0001g0083a0009c0010t0003g0018a0009c0012t0003g0015 | 3 | HG02027.hp2 HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.112+5904_112+5915d others(14): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
ATTTTTTT others(10): Show |
A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.112+5899_112+5915d others(19): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0001g0313 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.112+5897_112+5915d others(21): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
ATTTTTTT others(13): Show |
A | 98 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(95): Show | 99 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.112+5896_112+5915d others(22): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462248
|
ATTTTTTT others(14): Show |
A | 1 | a0001c0001t0001g0296 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.112+5895_112+5915d others(23): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119462248 | |||||
| chr5:119462333
|
C | T | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+5965C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462333 | ||||||
| chr5:119462462
|
C | T | 98 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(95): Show | 99 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.112+6094C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462462 | ||||||
| chr5:119462464
|
A | G | 1 | a0002c0002t0002g0153 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.112+6096A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462464 | ||||||
| chr5:119462532
|
T | C | 1 | a0003c0003t0002g0375 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+6164T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462532 | ||||||
| chr5:119462871
|
C | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.112+6503C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462871 | ||||||
| chr5:119462880
|
A | G | 1 | a0007c0007t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.112+6512A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462880 | ||||||
| chr5:119462905
|
G | C | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112+6537G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119462905 | ||||||
| chr5:119463098
|
C | A | 194 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(191): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.112+6730C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463098 | ||||||
| chr5:119463213
|
C | G | 93 | a0001c0001t0001g0292a0002c0002t0002g0002a0002c0002t0002g0003others(90): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.112+6845C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463213 | ||||||
| chr5:119463249
|
G | T | 88 | a0001c0001t0001g0327a0001c0001t0002g0363a0001c0001t0006g0185others(85): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.112+6881G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463249 | ||||||
| chr5:119463255
|
G | A | 1 | a0004c0004t0004g0343 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.112+6887G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463255 | ||||||
| chr5:119463271
|
G | A | 2 | a0004c0004t0003g0338a0004c0004t0003g0349 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.112+6903G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463271 | ||||||
| chr5:119463422
|
A | G | 88 | a0001c0001t0001g0327a0001c0001t0002g0363a0001c0001t0006g0185others(85): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.112+7054A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463422 | ||||||
| chr5:119463522
|
A | AT | 103 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(100): Show | 103 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.112+7168dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463522 | |||||
| chr5:119463522
|
A | ATT | 8 | a0001c0001t0002g0178a0001c0001t0002g0179a0003c0003t0002g0229others(5): Show | 8 | HG01975.hp2 HG03225.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+7167_112+7168d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463522 | |||||
| chr5:119463522
|
AT | A | 12 | a0001c0001t0006g0091a0002c0002t0002g0114a0002c0002t0002g0143others(9): Show | 12 | HG01243.hp1 HG02486.hp2 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.112+7168delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463522 | |||||
| chr5:119463540
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+7172T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463540 | ||||||
| chr5:119463655
|
C | CT | 8 | a0001c0001t0001g0054a0002c0002t0002g0146a0003c0003t0002g0198others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+7317dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463655
|
C | CTT | 18 | a0001c0001t0001g0053a0003c0003t0002g0211a0003c0003t0002g0213others(15): Show | 18 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.112+7316_112+7317d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463655
|
C | CTTT | 24 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(21): Show | 24 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.112+7315_112+7317d others(5): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463655
|
CT | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0014others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.112+7317delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463655
|
CTT | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0084others(95): Show | 99 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.112+7316_112+7317d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463655
|
CTTT | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0314a0001c0001t0002g0178others(12): Show | 15 | HG00741.hp1 HG01106.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.112+7315_112+7317d others(5): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463655
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0002g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.112+7306_112+7317d others(14): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463655
|
CTTTTTTT others(6): Show |
C | 25 | a0001c0001t0001g0242a0001c0001t0001g0327a0004c0004t0003g0328others(22): Show | 25 | HG00558.hp2 HG02055.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.112+7305_112+7317d others(15): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119463655 | |||||
| chr5:119463749
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.112+7381G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463749 | ||||||
| chr5:119463771
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.112+7403C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463771 | ||||||
| chr5:119463808
|
A | T | 37 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0198others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.112+7440A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463808 | ||||||
| chr5:119463825
|
C | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.112+7457C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463825 | ||||||
| chr5:119464149
|
A | G | 1 | a0001c0001t0006g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.112+7781A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464149 | ||||||
| chr5:119464255
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.112+7887C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464255 | ||||||
| chr5:119464287
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.112+7919C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464287 | ||||||
| chr5:119464306
|
G | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+7938G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464306 | ||||||
| chr5:119464379
|
G | A | 96 | a0001c0001t0001g0082a0002c0002t0002g0002a0002c0002t0002g0003others(93): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.112+8011G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464379 | ||||||
| chr5:119464411
|
T | A | 1 | a0004c0004t0004g0361 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.112+8043T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464411 | ||||||
| chr5:119464444
|
T | G | 1 | a0005c0005t0001g0243 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.112+8076T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464444 | ||||||
| chr5:119464468
|
T | C | 8 | a0001c0001t0002g0178a0001c0001t0002g0179a0008c0008t0003g0016others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+8100T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464468 | ||||||
| chr5:119464527
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.112+8159A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464527 | ||||||
| chr5:119464537
|
A | G | 1 | a0004c0004t0003g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.112+8169A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464537 | ||||||
| chr5:119464545
|
A | G | 7 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373others(4): Show | 8 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+8177A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464545 | ||||||
| chr5:119464598
|
T | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0077 | 2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.112+8230T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464598 | ||||||
| chr5:119464619
|
A | G | 88 | a0001c0001t0001g0327a0001c0001t0002g0363a0001c0001t0006g0185others(85): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.112+8251A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464619 | ||||||
| chr5:119464623
|
C | T | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.112+8255C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464623 | ||||||
| chr5:119464694
|
G | A | 7 | a0003c0003t0002g0222a0003c0003t0002g0229a0003c0003t0002g0230others(4): Show | 7 | HG01975.hp2 NA18962.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+8326G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464694 | ||||||
| chr5:119464775
|
T | A | 1 | a0001c0001t0001g0308 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.112+8407T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464775 | ||||||
| chr5:119464796
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0031 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.112+8428A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464796 | ||||||
| chr5:119464796
|
AT | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+8429delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464796 | ||||||
| chr5:119464815
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.112+8447C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464815 | ||||||
| chr5:119464883
|
C | T | 1 | a0002c0002t0002g0148 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.112+8515C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464883 | ||||||
| chr5:119464884
|
G | A | 2 | a0002c0002t0002g0096a0002c0002t0002g0122 | 2 | NA18968.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.112+8516G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464884 | ||||||
| chr5:119464889
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.112+8521C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464889 | ||||||
| chr5:119464978
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.112+8610G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119464978 | ||||||
| chr5:119465005
|
T | A | 7 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373others(4): Show | 8 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+8637T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119465005 | ||||||
| chr5:119465086
|
C | T | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+8718C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119465086 | ||||||
| chr5:119465300
|
A | T | 44 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0198others(41): Show | 44 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.113-8608A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119465300 | ||||||
| chr5:119465316
|
A | G | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113-8592A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119465316 | ||||||
| chr5:119465872
|
C | T | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.113-8036C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119465872 | ||||||
| chr5:119465891
|
T | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.113-8017T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119465891 | ||||||
| chr5:119465970
|
T | C | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-7938T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119465970 | ||||||
| chr5:119466065
|
T | C | 49 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(46): Show | 49 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.113-7843T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466065 | ||||||
| chr5:119466078
|
T | C | 1 | a0004c0004t0004g0357 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.113-7830T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466078 | ||||||
| chr5:119466103
|
G | C | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.113-7805G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466103 | ||||||
| chr5:119466165
|
G | T | 5 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(2): Show | 5 | HG01496.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-7743G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466165 | ||||||
| chr5:119466169
|
G | A | 254 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(251): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.113-7739G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466169 | ||||||
| chr5:119466211
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0083 | 2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.113-7697T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466211 | ||||||
| chr5:119466240
|
A | C | 1 | a0003c0003t0002g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.113-7668A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466240 | ||||||
| chr5:119466246
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.113-7662A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466246 | ||||||
| chr5:119466252
|
CTTCAGTT | C | 9 | a0001c0001t0002g0363a0001c0001t0006g0185a0006c0006t0002g0202others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-7652_113-7646d others(9): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119466252 | |||||
| chr5:119466386
|
G | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.113-7522G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466386 | ||||||
| chr5:119466427
|
C | T | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7481C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466427 | ||||||
| chr5:119466471
|
C | T | 14 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-7437C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466471 | ||||||
| chr5:119466526
|
T | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0039others(12): Show | 16 | HG00639.hp1 HG00735.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.113-7382T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466526 | ||||||
| chr5:119466690
|
T | G | 295 | a0001c0001t0001g0009a0001c0001t0001g0082a0001c0001t0001g0190others(292): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.113-7218T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466690 | ||||||
| chr5:119466977
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.113-6931T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119466977 | ||||||
| chr5:119467197
|
T | C | 14 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-6711T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119467197 | ||||||
| chr5:119467276
|
C | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.113-6632C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119467276 | ||||||
| chr5:119467403
|
T | A | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-6505T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119467403 | ||||||
| chr5:119467726
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.113-6182G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119467726 | ||||||
| chr5:119467745
|
G | A | 1 | a0002c0002t0002g0154 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.113-6163G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119467745 | ||||||
| chr5:119467765
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.113-6143T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119467765 | ||||||
| chr5:119468054
|
T | G | 1 | a0002c0002t0002g0134 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.113-5854T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468054 | ||||||
| chr5:119468062
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.113-5846T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468062 | ||||||
| chr5:119468079
|
G | T | 1 | a0004c0004t0004g0357 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.113-5829G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468079 | ||||||
| chr5:119468126
|
A | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.113-5782A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468126 | ||||||
| chr5:119468180
|
T | C | 94 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(91): Show | 95 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.113-5728T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468180 | ||||||
| chr5:119468368
|
A | T | 1 | a0002c0002t0002g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.113-5540A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468368 | ||||||
| chr5:119468641
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.113-5267G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468641 | ||||||
| chr5:119468739
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.113-5169A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468739 | ||||||
| chr5:119468844
|
T | A | 66 | a0001c0001t0001g0009a0001c0001t0001g0327a0001c0001t0002g0178others(63): Show | 67 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.113-5064T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468844 | ||||||
| chr5:119468888
|
C | A | 129 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(126): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.113-5020C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468888 | ||||||
| chr5:119468951
|
C | G | 3 | a0001c0001t0002g0178a0001c0001t0002g0179a0004c0004t0003g0362 | 3 | HG02622.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.113-4957C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119468951 | ||||||
| chr5:119469045
|
A | C | 5 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(2): Show | 5 | HG01496.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-4863A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119469045 | ||||||
| chr5:119469212
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.113-4696G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119469212 | ||||||
| chr5:119469285
|
C | T | 14 | a0001c0001t0002g0363a0001c0001t0006g0185a0003c0003t0002g0194others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-4623C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119469285 | ||||||
| chr5:119469301
|
C | CT | 7 | a0001c0001t0001g0089a0001c0001t0002g0363a0001c0001t0006g0185others(4): Show | 7 | HG01496.hp1 HG02015.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-4595dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119469301 | |||||
| chr5:119469547
|
G | A | 1 | a0002c0002t0002g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.113-4361G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119469547 | ||||||
| chr5:119469552
|
A | G | 53 | a0001c0001t0001g0327a0001c0001t0002g0363a0001c0001t0006g0185others(50): Show | 54 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.113-4356A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119469552 | ||||||
| chr5:119469657
|
T | C | 39 | a0001c0001t0001g0327a0002c0002t0003g0329a0004c0004t0003g0328others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.113-4251T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119469657 | ||||||
| chr5:119469920
|
C | A | 132 | a0001c0001t0002g0178a0001c0001t0002g0179a0002c0002t0002g0002others(129): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.113-3988C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119469920 | ||||||
| chr5:119470340
|
G | T | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.113-3568G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119470340 | ||||||
| chr5:119470725
|
C | T | 127 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(124): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.113-3183C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119470725 | ||||||
| chr5:119470768
|
G | C | 130 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.113-3140G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119470768 | ||||||
| chr5:119470889
|
A | G | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-3019A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119470889 | ||||||
| chr5:119470974
|
A | G | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0290others(1): Show | 4 | HG02132.hp1 NA18961.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2934A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119470974 | ||||||
| chr5:119471006
|
T | C | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.113-2902T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119471006 | ||||||
| chr5:119471075
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.113-2833T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119471075 | ||||||
| chr5:119471095
|
T | G | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.113-2813T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119471095 | ||||||
| chr5:119471348
|
A | G | 7 | a0001c0001t0001g0249a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | NA18942.hp2 NA18959.hp2 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-2560A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119471348 | ||||||
| chr5:119471350
|
C | A | 1 | a0001c0001t0001g0252 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.113-2558C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119471350 | ||||||
| chr5:119471441
|
A | G | 344 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(341): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.113-2467A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119471441 | ||||||
| chr5:119471469
|
A | G | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113-2439A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119471469 | ||||||
| chr5:119471753
|
CT | C | 4 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-2150delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119471753 | |||||
| chr5:119472268
|
G | A | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1640G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472268 | ||||||
| chr5:119472353
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.113-1555A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472353 | ||||||
| chr5:119472436
|
A | AC | 10 | a0001c0001t0002g0363a0001c0001t0006g0185a0006c0006t0002g0202others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-1472_113-1471i others(3): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472436 | ||||||
| chr5:119472436
|
A | AT | 24 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(21): Show | 25 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.113-1458dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119472436 | |||||
| chr5:119472541
|
C | T | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.113-1367C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472541 | ||||||
| chr5:119472594
|
C | G | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-1314C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472594 | ||||||
| chr5:119472611
|
T | A | 1 | a0002c0002t0002g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.113-1297T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472611 | ||||||
| chr5:119472686
|
G | A | 1 | a0004c0004t0003g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.113-1222G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472686 | ||||||
| chr5:119472705
|
A | C | 8 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-1203A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472705 | ||||||
| chr5:119472729
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.113-1179C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472729 | ||||||
| chr5:119472780
|
C | T | 1 | a0004c0004t0004g0361 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.113-1128C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472780 | ||||||
| chr5:119472856
|
A | G | 16 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.113-1052A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472856 | ||||||
| chr5:119472991
|
T | A | 10 | a0001c0001t0002g0363a0001c0001t0006g0185a0006c0006t0002g0202others(7): Show | 10 | HG01496.hp1 HG01884.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-917T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119472991 | ||||||
| chr5:119473017
|
A | T | 1 | a0002c0002t0002g0133 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.113-891A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473017 | ||||||
| chr5:119473068
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.113-840A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473068 | ||||||
| chr5:119473076
|
G | C | 2 | a0007c0007t0002g0201a0007c0007t0003g0199 | 2 | HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.113-832G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473076 | ||||||
| chr5:119473099
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.113-809A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473099 | ||||||
| chr5:119473238
|
A | AT | 5 | a0001c0001t0001g0247a0001c0001t0001g0285a0001c0001t0001g0286others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-664dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473238 | |||||
| chr5:119473273
|
C | CT | 186 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0051others(183): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.113-612dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473273 | |||||
| chr5:119473273
|
C | CTT | 94 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0244others(91): Show | 94 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.113-613_113-612dup others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473273 | |||||
| chr5:119473273
|
C | CTTT | 7 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(4): Show | 7 | HG00558.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-614_113-612dup others(3): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473273 | |||||
| chr5:119473273
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0034a0001c0001t0001g0087 | 2 | HG00609.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.113-622_113-612del others(11): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473273 | |||||
| chr5:119473273
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179 | 3 | HG03225.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.113-623_113-612del others(12): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473273 | |||||
| chr5:119473314
|
C | CT | 18 | a0001c0001t0001g0042a0001c0001t0001g0054a0001c0001t0001g0063others(15): Show | 18 | HG01243.hp2 HG01255.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.113-574dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473314 | |||||
| chr5:119473314
|
CT | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-574delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473314 | |||||
| chr5:119473473
|
A | G | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.113-435A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473473 | ||||||
| chr5:119473703
|
T | C | 129 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(126): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.113-205T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473703 | ||||||
| chr5:119473735
|
A | C | 1 | a0001c0001t0001g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.113-173A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473735 | ||||||
| chr5:119473751
|
C | G | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.113-157C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473751 | ||||||
| chr5:119473791
|
C | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.113-117C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473791 | ||||||
| chr5:119473838
|
CCA | C | 254 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(251): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.113-53_113-52delCA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr5 | 119473838 | |||||
| chr5:119473855
|
C | T | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-53C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119473855 | ||||||
| chr5:119474041
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.220+26A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 3/23 | chr5 | 119474041 | ||||||
| chr5:119474111
|
A | T | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.220+96A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 3/23 | chr5 | 119474111 | ||||||
| chr5:119474194
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.220+179C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 3/23 | chr5 | 119474194 | ||||||
| chr5:119474575
|
T | A | 1 | a0001c0001t0006g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.280+115T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119474575 | ||||||
| chr5:119474615
|
A | G | 1 | a0003c0003t0002g0222 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.280+155A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119474615 | ||||||
| chr5:119474696
|
C | T | 105 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(102): Show | 106 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.280+236C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119474696 | ||||||
| chr5:119474701
|
G | A | 1 | a0004c0004t0003g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.280+241G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119474701 | ||||||
| chr5:119474721
|
A | T | 289 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(286): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.280+261A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119474721 | ||||||
| chr5:119474798
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280+338G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119474798 | ||||||
| chr5:119474899
|
A | G | 1 | a0004c0004t0004g0357 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.280+439A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119474899 | ||||||
| chr5:119475097
|
T | A | 1 | a0003c0003t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.281-609T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475097 | ||||||
| chr5:119475124
|
T | G | 3 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373 | 3 | HG01243.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.281-582T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475124 | ||||||
| chr5:119475230
|
A | G | 1 | a0003c0003t0003g0367 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-476A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475230 | ||||||
| chr5:119475269
|
A | G | 144 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(141): Show | 146 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.281-437A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475269 | ||||||
| chr5:119475274
|
A | G | 2 | a0002c0002t0002g0011a0002c0002t0002g0012 | 2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.281-432A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475274 | ||||||
| chr5:119475308
|
C | CT | 106 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(103): Show | 107 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.281-393dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr5 | 119475308 | |||||
| chr5:119475431
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.281-275T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475431 | ||||||
| chr5:119475618
|
C | T | 138 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(135): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.281-88C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475618 | ||||||
| chr5:119475619
|
G | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0066others(9): Show | 12 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.281-87G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475619 | ||||||
| chr5:119475687
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.281-19G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 4/23 | chr5 | 119475687 | ||||||
| chr5:119475814
|
G | T | 1 | a0002c0002t0002g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.303-10G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 5/23 | chr5 | 119475814 | ||||||
| chr5:119475909
|
T | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+39T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119475909 | ||||||
| chr5:119475961
|
G | T | 3 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179 | 3 | HG03225.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.349+91G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119475961 | ||||||
| chr5:119475993
|
A | T | 5 | a0004c0004t0003g0328a0004c0004t0003g0333a0004c0004t0003g0334others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+123A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119475993 | ||||||
| chr5:119476204
|
C | A | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+334C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476204 | ||||||
| chr5:119476373
|
T | C | 4 | a0001c0001t0001g0250a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 4 | NA18957.hp2 NA18968.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+503T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476373 | ||||||
| chr5:119476391
|
C | T | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.349+521C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476391 | ||||||
| chr5:119476485
|
A | G | 257 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(254): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.349+615A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476485 | ||||||
| chr5:119476688
|
A | C | 106 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(103): Show | 107 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.350-729A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476688 | ||||||
| chr5:119476857
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0082 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.350-560C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476857 | ||||||
| chr5:119476900
|
C | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.350-517C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476900 | ||||||
| chr5:119476953
|
T | C | 141 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(138): Show | 143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.350-464T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476953 | ||||||
| chr5:119477055
|
A | G | 95 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(92): Show | 96 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.350-362A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119477055 | ||||||
| chr5:119477134
|
G | A | 295 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(292): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.350-283G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119477134 | ||||||
| chr5:119477152
|
G | A | 2 | a0002c0002t0002g0123a0002c0002t0002g0147 | 2 | HG01261.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.350-265G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119477152 | ||||||
| chr5:119477155
|
C | T | 1 | a0002c0002t0011g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-262C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119477155 | ||||||
| chr5:119477256
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.350-161C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119477256 | ||||||
| chr5:119477323
|
A | G | 3 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179 | 3 | HG03225.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.350-94A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119477323 | ||||||
| chr5:119477545
|
T | C | 135 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0292others(132): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.434+44T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477545 | ||||||
| chr5:119477581
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0087 | 2 | HG00609.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.434+80A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477581 | ||||||
| chr5:119477621
|
A | G | 257 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(254): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.434+120A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477621 | ||||||
| chr5:119477673
|
G | A | 1 | a0003c0003t0002g0237 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.434+172G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477673 | ||||||
| chr5:119477680
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.434+179A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477680 | ||||||
| chr5:119477684
|
G | T | 1 | a0002c0002t0002g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.434+183G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477684 | ||||||
| chr5:119477830
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434+329G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477830 | ||||||
| chr5:119477868
|
C | T | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.434+367C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119477868 | ||||||
| chr5:119478058
|
A | G | 2 | a0002c0002t0002g0096a0002c0002t0002g0122 | 2 | NA18968.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.434+557A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119478058 | ||||||
| chr5:119478104
|
A | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+603A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119478104 | ||||||
| chr5:119478492
|
C | A | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-342C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119478492 | ||||||
| chr5:119478526
|
G | A | 1 | a0007c0007t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.435-308G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119478526 | ||||||
| chr5:119478532
|
A | G | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.435-302A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119478532 | ||||||
| chr5:119478573
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.435-261T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119478573 | ||||||
| chr5:119478758
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.435-76T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 7/23 | chr5 | 119478758 | ||||||
| chr5:119479069
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.622+48T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479069 | ||||||
| chr5:119479132
|
A | G | 3 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179 | 3 | HG03225.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.622+111A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479132 | ||||||
| chr5:119479282
|
A | G | 93 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(90): Show | 94 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.622+261A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479282 | ||||||
| chr5:119479471
|
C | T | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.622+450C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479471 | ||||||
| chr5:119479588
|
A | T | 43 | a0001c0001t0001g0244a0001c0001t0001g0248a0001c0001t0001g0249others(40): Show | 43 | HG00544.hp1 HG00558.hp1 HG02040.hp1 others(40): Show |
intron_variant | MODIFIER | c.622+567A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479588 | ||||||
| chr5:119479695
|
T | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+674T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479695 | ||||||
| chr5:119479700
|
C | T | 1 | a0002c0002t0002g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.622+679C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479700 | ||||||
| chr5:119479804
|
A | G | 3 | a0007c0007t0002g0203a0007c0007t0002g0204a0007c0007t0002g0205 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.622+783A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479804 | ||||||
| chr5:119479868
|
G | T | 1 | a0002c0002t0002g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.622+847G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479868 | ||||||
| chr5:119479869
|
G | A | 1 | a0002c0002t0002g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.622+848G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119479869 | ||||||
| chr5:119480079
|
C | T | 1 | a0001c0013t0001g0264 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.622+1058C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480079 | ||||||
| chr5:119480086
|
C | T | 1 | a0001c0001t0001g0327 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.622+1065C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480086 | ||||||
| chr5:119480120
|
T | G | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.622+1099T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480120 | ||||||
| chr5:119480491
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.622+1470G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480491 | ||||||
| chr5:119480616
|
A | G | 8 | a0003c0003t0002g0206a0003c0003t0002g0208a0003c0003t0002g0211others(5): Show | 8 | HG00735.hp1 HG01123.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+1595A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480616 | ||||||
| chr5:119480703
|
T | C | 1 | a0004c0004t0004g0343 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.622+1682T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480703 | ||||||
| chr5:119480740
|
T | C | 1 | a0002c0002t0002g0144 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.622+1719T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480740 | ||||||
| chr5:119480793
|
C | T | 1 | a0002c0002t0002g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.622+1772C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480793 | ||||||
| chr5:119480799
|
G | A | 1 | a0002c0002t0002g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.622+1778G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480799 | ||||||
| chr5:119480801
|
G | T | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.622+1780G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480801 | ||||||
| chr5:119480859
|
T | A | 1 | a0004c0004t0003g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.622+1838T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480859 | ||||||
| chr5:119480914
|
A | G | 10 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(7): Show | 10 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.622+1893A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480914 | ||||||
| chr5:119480962
|
A | G | 1 | a0009c0010t0003g0018 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.622+1941A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119480962 | ||||||
| chr5:119481001
|
T | A | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.622+1980T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481001 | ||||||
| chr5:119481093
|
A | G | 1 | a0004c0004t0003g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.622+2072A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481093 | ||||||
| chr5:119481101
|
T | A | 1 | a0001c0001t0001g0327 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.622+2080T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481101 | ||||||
| chr5:119481304
|
T | C | 1 | a0002c0002t0002g0146 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.622+2283T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481304 | ||||||
| chr5:119481349
|
C | T | 8 | a0001c0001t0001g0327a0006c0006t0002g0202a0007c0007t0002g0200others(5): Show | 8 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+2328C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481349 | ||||||
| chr5:119481404
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.622+2383C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481404 | ||||||
| chr5:119481445
|
A | G | 1 | a0003c0003t0003g0367 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.622+2424A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481445 | ||||||
| chr5:119481453
|
A | G | 5 | a0004c0004t0004g0357a0004c0004t0004g0358a0004c0004t0004g0359others(2): Show | 5 | HG01934.hp2 HG01993.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.622+2432A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481453 | ||||||
| chr5:119481562
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.622+2541A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481562 | ||||||
| chr5:119481688
|
G | A | 8 | a0001c0001t0001g0327a0006c0006t0002g0202a0007c0007t0002g0200others(5): Show | 8 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+2667G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481688 | ||||||
| chr5:119481771
|
G | A | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+2750G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481771 | ||||||
| chr5:119481852
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.622+2831A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481852 | ||||||
| chr5:119481888
|
C | T | 1 | a0002c0002t0002g0146 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.622+2867C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481888 | ||||||
| chr5:119481910
|
A | AT | 9 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 9 | HG00621.hp1 NA18946.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.622+2897dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 119481910 | |||||
| chr5:119481936
|
C | G | 1 | a0004c0004t0003g0349 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622+2915C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481936 | ||||||
| chr5:119481973
|
C | T | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+2952C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119481973 | ||||||
| chr5:119482083
|
C | T | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.622+3062C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119482083 | ||||||
| chr5:119482252
|
T | G | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.622+3231T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119482252 | ||||||
| chr5:119482463
|
T | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+3442T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119482463 | ||||||
| chr5:119482858
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0087 | 2 | HG00609.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.622+3837C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119482858 | ||||||
| chr5:119482951
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.622+3930A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119482951 | ||||||
| chr5:119483120
|
A | G | 8 | a0004c0004t0003g0328a0004c0004t0003g0333a0004c0004t0003g0334others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.622+4099A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483120 | ||||||
| chr5:119483190
|
C | T | 1 | a0002c0002t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.622+4169C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483190 | ||||||
| chr5:119483285
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0039others(11): Show | 15 | HG00735.hp2 HG01257.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.622+4264T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483285 | ||||||
| chr5:119483353
|
T | A | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.622+4332T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483353 | ||||||
| chr5:119483600
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.622+4579G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483600 | ||||||
| chr5:119483686
|
A | G | 3 | a0004c0004t0005g0180a0004c0004t0005g0181a0004c0004t0005g0182 | 3 | HG00323.hp1 HG01081.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.622+4665A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483686 | ||||||
| chr5:119483693
|
G | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+4672G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483693 | ||||||
| chr5:119483809
|
A | G | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.622+4788A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483809 | ||||||
| chr5:119483980
|
C | G | 245 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0065others(242): Show | 248 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.622+4959C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483980 | ||||||
| chr5:119483987
|
C | T | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.622+4966C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119483987 | ||||||
| chr5:119484017
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.622+4996T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484017 | ||||||
| chr5:119484024
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.622+5003C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484024 | ||||||
| chr5:119484060
|
A | G | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.622+5039A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484060 | ||||||
| chr5:119484238
|
G | T | 1 | a0002c0002t0002g0162 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.623-4954G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484238 | ||||||
| chr5:119484244
|
A | G | 1 | a0001c0001t0001g0307 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.623-4948A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484244 | ||||||
| chr5:119484315
|
C | T | 1 | a0004c0004t0004g0336 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.623-4877C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484315 | ||||||
| chr5:119484336
|
A | G | 1 | a0003c0003t0002g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.623-4856A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484336 | ||||||
| chr5:119484351
|
G | C | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.623-4841G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484351 | ||||||
| chr5:119484490
|
C | A | 1 | a0003c0003t0002g0234 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.623-4702C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484490 | ||||||
| chr5:119484499
|
A | G | 1 | a0003c0003t0002g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.623-4693A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484499 | ||||||
| chr5:119484638
|
A | T | 3 | a0007c0007t0002g0203a0007c0007t0002g0204a0007c0007t0002g0205 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.623-4554A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484638 | ||||||
| chr5:119484693
|
A | G | 2 | a0001c0001t0002g0363a0002c0002t0002g0146 | 2 | NA19030.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.623-4499A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484693 | ||||||
| chr5:119484833
|
T | A | 89 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(86): Show | 89 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.623-4359T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484833 | ||||||
| chr5:119484834
|
T | A | 89 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(86): Show | 89 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.623-4358T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484834 | ||||||
| chr5:119484840
|
CCT | C | 7 | a0006c0006t0002g0202a0007c0007t0002g0200a0007c0007t0002g0201others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.623-4351_623-4350d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484840 | ||||||
| chr5:119484922
|
A | T | 1 | a0004c0004t0005g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.623-4270A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119484922 | ||||||
| chr5:119485144
|
C | G | 1 | a0002c0002t0002g0134 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.623-4048C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485144 | ||||||
| chr5:119485151
|
C | A | 2 | a0001c0001t0002g0363a0001c0001t0006g0185 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.623-4041C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485151 | ||||||
| chr5:119485264
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0283 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.623-3928C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485264 | ||||||
| chr5:119485269
|
G | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-3923G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485269 | ||||||
| chr5:119485300
|
G | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.623-3892G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485300 | ||||||
| chr5:119485311
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.623-3881T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485311 | ||||||
| chr5:119485400
|
G | C | 3 | a0004c0004t0005g0180a0004c0004t0005g0181a0004c0004t0005g0182 | 3 | HG00323.hp1 HG01081.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.623-3792G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485400 | ||||||
| chr5:119485582
|
T | G | 1 | a0004c0004t0003g0338 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.623-3610T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485582 | ||||||
| chr5:119485664
|
A | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.623-3528A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485664 | ||||||
| chr5:119485726
|
C | G | 1 | a0002c0002t0002g0122 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.623-3466C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485726 | ||||||
| chr5:119485888
|
C | G | 1 | a0002c0002t0002g0148 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.623-3304C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485888 | ||||||
| chr5:119485985
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.623-3207G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119485985 | ||||||
| chr5:119486070
|
C | T | 1 | a0004c0004t0004g0337 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.623-3122C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119486070 | ||||||
| chr5:119486694
|
C | T | 36 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(33): Show | 37 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.623-2498C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119486694 | ||||||
| chr5:119486735
|
G | T | 1 | a0002c0002t0002g0111 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.623-2457G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119486735 | ||||||
| chr5:119487070
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.623-2122C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487070 | ||||||
| chr5:119487104
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0048 | 2 | NA19001.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.623-2088G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487104 | ||||||
| chr5:119487148
|
C | T | 1 | a0003c0003t0002g0234 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.623-2044C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487148 | ||||||
| chr5:119487168
|
G | A | 1 | a0002c0002t0002g0124 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.623-2024G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487168 | ||||||
| chr5:119487198
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.623-1994C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487198 | ||||||
| chr5:119487240
|
A | AT | 141 | a0001c0001t0001g0026a0001c0001t0001g0062a0001c0001t0001g0085others(138): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.623-1934dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 119487240 | |||||
| chr5:119487240
|
A | ATT | 10 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0022others(7): Show | 10 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.623-1935_623-1934d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr5 | 119487240 | |||||
| chr5:119487431
|
A | C | 1 | a0004c0004t0003g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.623-1761A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487431 | ||||||
| chr5:119487526
|
C | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.623-1666C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487526 | ||||||
| chr5:119487784
|
A | G | 3 | a0001c0001t0001g0060a0002c0002t0002g0123a0002c0002t0002g0147 | 3 | HG01261.hp2 HG01943.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.623-1408A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487784 | ||||||
| chr5:119487870
|
A | G | 3 | a0003c0003t0002g0198a0003c0003t0002g0227a0003c0003t0002g0231 | 3 | NA18985.hp1 NA19011.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.623-1322A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119487870 | ||||||
| chr5:119488045
|
A | T | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.623-1147A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488045 | ||||||
| chr5:119488105
|
A | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-1087A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488105 | ||||||
| chr5:119488109
|
T | C | 2 | a0008c0008t0003g0019a0008c0008t0003g0021 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.623-1083T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488109 | ||||||
| chr5:119488110
|
T | G | 92 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(89): Show | 92 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.623-1082T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488110 | ||||||
| chr5:119488111
|
G | C | 10 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(7): Show | 11 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.623-1081G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488111 | ||||||
| chr5:119488293
|
A | T | 1 | a0003c0003t0002g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.623-899A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488293 | ||||||
| chr5:119488301
|
C | T | 2 | a0002c0002t0002g0003a0002c0002t0002g0141 | 3 | HG01516.hp2 HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.623-891C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488301 | ||||||
| chr5:119488376
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.623-816C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488376 | ||||||
| chr5:119488427
|
A | G | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.623-765A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488427 | ||||||
| chr5:119488440
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.623-752A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488440 | ||||||
| chr5:119488574
|
G | A | 1 | a0002c0002t0002g0170 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.623-618G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488574 | ||||||
| chr5:119488903
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.623-289A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119488903 | ||||||
| chr5:119489116
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.623-76T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119489116 | ||||||
| chr5:119489148
|
A | G | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.623-44A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 8/23 | chr5 | 119489148 | ||||||
| chr5:119489356
|
G | C | 131 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(128): Show | 132 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.714+73G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489356 | ||||||
| chr5:119489622
|
T | C | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.714+339T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489622 | ||||||
| chr5:119489648
|
G | A | 80 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(77): Show | 80 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.714+365G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489648 | ||||||
| chr5:119489712
|
A | G | 2 | a0003c0003t0002g0216a0003c0003t0002g0217 | 2 | NA18980.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.714+429A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489712 | ||||||
| chr5:119489713
|
A | G | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.714+430A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489713 | ||||||
| chr5:119489734
|
A | C | 374 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(371): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.714+451A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489734 | ||||||
| chr5:119489833
|
G | GT | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+558dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr5 | 119489833 | |||||
| chr5:119489875
|
A | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.714+592A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489875 | ||||||
| chr5:119490009
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.714+726A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490009 | ||||||
| chr5:119490024
|
A | AC | 113 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0066others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.714+750dupC | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr5 | 119490024 | |||||
| chr5:119490024
|
AC | A | 39 | a0001c0001t0002g0363a0002c0002t0002g0105a0002c0002t0002g0144others(36): Show | 39 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.714+750delC | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr5 | 119490024 | |||||
| chr5:119490095
|
T | C | 47 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(44): Show | 48 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.714+812T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490095 | ||||||
| chr5:119490263
|
T | G | 1 | a0001c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.714+980T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490263 | ||||||
| chr5:119490297
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.714+1014A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490297 | ||||||
| chr5:119490399
|
A | G | 103 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(100): Show | 104 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.714+1116A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490399 | ||||||
| chr5:119490425
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0076 | 2 | HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.714+1142C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490425 | ||||||
| chr5:119490618
|
G | A | 2 | a0002c0002t0002g0093a0002c0002t0002g0118 | 2 | HG02735.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.714+1335G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490618 | ||||||
| chr5:119490661
|
C | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.714+1378C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490661 | ||||||
| chr5:119490843
|
T | C | 1 | a0005c0005t0001g0266 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.715-1257T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490843 | ||||||
| chr5:119490935
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.715-1165T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119490935 | ||||||
| chr5:119491231
|
C | A | 1 | a0002c0002t0011g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.715-869C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491231 | ||||||
| chr5:119491240
|
C | T | 3 | a0007c0007t0002g0203a0007c0007t0002g0204a0007c0007t0002g0205 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.715-860C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491240 | ||||||
| chr5:119491273
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.715-827G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491273 | ||||||
| chr5:119491318
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.715-782C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491318 | ||||||
| chr5:119491461
|
CT | C | 283 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0190others(280): Show | 287 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.715-621delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr5 | 119491461 | |||||
| chr5:119491461
|
CTT | C | 9 | a0001c0001t0001g0249a0001c0001t0001g0275a0001c0001t0001g0310others(6): Show | 9 | HG00099.hp2 HG01255.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-622_715-621del others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr5 | 119491461 | |||||
| chr5:119491521
|
G | GA | 293 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(290): Show | 297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.715-575dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr5 | 119491521 | |||||
| chr5:119491685
|
A | G | 3 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373 | 3 | HG01243.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.715-415A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491685 | ||||||
| chr5:119491707
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.715-393G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491707 | ||||||
| chr5:119491887
|
A | G | 1 | a0002c0002t0002g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-213A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491887 | ||||||
| chr5:119491906
|
C | T | 191 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0327others(188): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.715-194C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491906 | ||||||
| chr5:119491916
|
C | T | 1 | a0002c0002t0002g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.715-184C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491916 | ||||||
| chr5:119491940
|
C | G | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-160C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491940 | ||||||
| chr5:119491942
|
T | A | 88 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.715-158T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119491942 | ||||||
| chr5:119492075
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.715-25A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119492075 | ||||||
| chr5:119492147
|
T | C | 92 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(89): Show | 92 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.739+23T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492147 | ||||||
| chr5:119492199
|
T | G | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.739+75T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492199 | ||||||
| chr5:119492454
|
T | C | 1 | a0002c0002t0002g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.739+330T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492454 | ||||||
| chr5:119492571
|
T | C | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.739+447T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492571 | ||||||
| chr5:119492794
|
C | A | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.739+670C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492794 | ||||||
| chr5:119492828
|
G | A | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.739+704G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492828 | ||||||
| chr5:119492852
|
C | G | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.739+728C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492852 | ||||||
| chr5:119492990
|
T | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0058 | 2 | HG00735.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.740-828T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119492990 | ||||||
| chr5:119493093
|
A | G | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.740-725A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493093 | ||||||
| chr5:119493189
|
A | G | 1 | a0002c0002t0002g0137 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.740-629A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493189 | ||||||
| chr5:119493212
|
C | T | 1 | a0002c0002t0002g0133 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.740-606C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493212 | ||||||
| chr5:119493380
|
G | A | 35 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.740-438G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493380 | ||||||
| chr5:119493527
|
T | A | 35 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.740-291T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493527 | ||||||
| chr5:119493568
|
C | T | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.740-250C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493568 | ||||||
| chr5:119493695
|
T | C | 1 | a0001c0001t0001g0327 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.740-123T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493695 | ||||||
| chr5:119493718
|
C | T | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.740-100C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493718 | ||||||
| chr5:119493802
|
T | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.740-16T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 10/23 | chr5 | 119493802 | ||||||
| chr5:119494095
|
A | G | 93 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.868+149A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494095 | ||||||
| chr5:119494149
|
T | C | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.868+203T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494149 | ||||||
| chr5:119494153
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.868+207A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494153 | ||||||
| chr5:119494174
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.868+228G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494174 | ||||||
| chr5:119494321
|
TTTCTTTT others(1): Show |
T | 3 | a0004c0004t0004g0337a0004c0004t0004g0346a0004c0004t0005g0180 | 3 | HG00280.hp1 HG00323.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.868+378_868+385del others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494321 | |||||
| chr5:119494321
|
TTTCTTTT others(13): Show |
T | 1 | a0004c0004t0004g0004 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.868+378_868+397del others(20): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494321 | |||||
| chr5:119494324
|
C | CCTTTCTT others(5): Show |
1 | a0002c0002t0002g0162 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.868+378_868+379ins others(12): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494324 | ||||||
| chr5:119494324
|
C | T | 2 | a0004c0004t0004g0348a0004c0004t0005g0181 | 2 | HG01496.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.868+378C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494324 | ||||||
| chr5:119494325
|
T | C | 3 | a0002c0002t0002g0162a0004c0004t0004g0348a0004c0004t0005g0181 | 3 | HG01496.hp2 HG03654.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.868+379T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494325 | ||||||
| chr5:119494325
|
T | TTTCTTTC others(4): Show |
1 | a0005c0005t0001g0266 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.868+381_868+382ins others(11): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
T | TTTTC | 98 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0033others(95): Show | 99 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.868+441_868+444dup others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
T | TTTTCTTT others(1): Show |
49 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0045others(46): Show | 49 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.868+437_868+444dup others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
T | TTTTCTTT others(5): Show |
11 | a0001c0001t0001g0240a0001c0001t0001g0258a0001c0001t0001g0292others(8): Show | 11 | HG00544.hp1 HG00741.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.868+433_868+444dup others(12): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
T | TTTTCTTT others(9): Show |
2 | a0001c0001t0001g0051a0001c0001t0001g0054 | 2 | HG02074.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.868+429_868+444dup others(16): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
TTTTC | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0028others(58): Show | 63 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.868+441_868+444del others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
TTTTCTTT others(1): Show |
T | 24 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0039others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.868+437_868+444del others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
TTTTCTTT others(5): Show |
T | 10 | a0001c0001t0001g0041a0001c0001t0002g0363a0002c0002t0002g0012others(7): Show | 10 | HG00639.hp1 HG01934.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.868+433_868+444del others(12): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494325
|
TTTTCTTT others(9): Show |
T | 1 | a0001c0001t0001g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.868+429_868+444del others(16): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494325 | |||||
| chr5:119494328
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.868+382T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494328 | ||||||
| chr5:119494329
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.868+383C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494329 | ||||||
| chr5:119494338
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.868+392T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494338 | ||||||
| chr5:119494376
|
T | TCTTTCTT others(17): Show |
1 | a0003c0003t0002g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.868+444_868+445ins others(24): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119494376 | |||||
| chr5:119494390
|
T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0283 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.868+444_868+445ins others(11): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494390 | ||||||
| chr5:119494679
|
C | A | 1 | a0002c0002t0002g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.868+733C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494679 | ||||||
| chr5:119494791
|
G | C | 1 | a0002c0002t0002g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.868+845G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494791 | ||||||
| chr5:119494792
|
G | C | 1 | a0002c0002t0002g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.868+846G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494792 | ||||||
| chr5:119494825
|
A | C | 39 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.868+879A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119494825 | ||||||
| chr5:119495037
|
C | T | 1 | a0002c0002t0002g0137 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.868+1091C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495037 | ||||||
| chr5:119495038
|
G | GT | 39 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.868+1092_868+1093i others(3): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495038 | ||||||
| chr5:119495039
|
G | GT | 106 | a0001c0001t0001g0052a0001c0001t0001g0190a0001c0001t0001g0239others(103): Show | 106 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.868+1103dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119495039 | |||||
| chr5:119495039
|
G | T | 40 | a0001c0001t0001g0049a0001c0001t0001g0327a0004c0004t0003g0328others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.868+1093G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495039 | ||||||
| chr5:119495039
|
GT | G | 10 | a0006c0006t0003g0005a0006c0006t0003g0368a0006c0006t0003g0369others(7): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.868+1103delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119495039 | |||||
| chr5:119495126
|
C | A | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.868+1180C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495126 | ||||||
| chr5:119495177
|
A | G | 1 | a0004c0004t0003g0351 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.868+1231A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495177 | ||||||
| chr5:119495241
|
AG | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0065 | 3 | HG01257.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.868+1297delG | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | 119495241 | |||||
| chr5:119495243
|
G | A | 1 | a0002c0002t0002g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.868+1297G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495243 | ||||||
| chr5:119495260
|
T | C | 1 | a0003c0003t0002g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.869-1283T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495260 | ||||||
| chr5:119495265
|
A | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.869-1278A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495265 | ||||||
| chr5:119495340
|
G | A | 281 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(278): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.869-1203G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495340 | ||||||
| chr5:119495394
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.869-1149G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495394 | ||||||
| chr5:119495408
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.869-1135T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495408 | ||||||
| chr5:119495500
|
A | G | 101 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(98): Show | 101 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.869-1043A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495500 | ||||||
| chr5:119495539
|
C | G | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.869-1004C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495539 | ||||||
| chr5:119495594
|
A | G | 1 | a0003c0003t0002g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.869-949A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495594 | ||||||
| chr5:119495765
|
G | A | 35 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.869-778G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495765 | ||||||
| chr5:119495774
|
G | A | 1 | a0002c0002t0002g0145 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.869-769G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495774 | ||||||
| chr5:119495827
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.869-716C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495827 | ||||||
| chr5:119495942
|
A | G | 93 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.869-601A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119495942 | ||||||
| chr5:119496168
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.869-375G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496168 | ||||||
| chr5:119496174
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.869-369A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496174 | ||||||
| chr5:119496231
|
A | C | 283 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(280): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.869-312A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496231 | ||||||
| chr5:119496272
|
C | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.869-271C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496272 | ||||||
| chr5:119496278
|
C | T | 3 | a0004c0004t0003g0344a0004c0004t0003g0347a0004c0004t0003g0355 | 3 | HG02630.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.869-265C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496278 | ||||||
| chr5:119496331
|
C | T | 3 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373 | 3 | HG01243.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.869-212C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496331 | ||||||
| chr5:119496341
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0003g0010 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.869-202G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496341 | ||||||
| chr5:119496368
|
C | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.869-175C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | 119496368 | ||||||
| chr5:119496690
|
TTTCCCTC others(5): Show |
T | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+55_972+66delTC others(10): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr5 | 119496690 | |||||
| chr5:119497112
|
G | C | 3 | a0007c0007t0002g0203a0007c0007t0002g0204a0007c0007t0002g0205 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.972+466G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497112 | ||||||
| chr5:119497128
|
G | A | 1 | a0003c0003t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.972+482G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497128 | ||||||
| chr5:119497150
|
T | C | 284 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.972+504T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497150 | ||||||
| chr5:119497209
|
T | TG | 281 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(278): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.972+569dupG | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr5 | 119497209 | |||||
| chr5:119497210
|
G | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.972+564G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497210 | ||||||
| chr5:119497270
|
C | G | 35 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.972+624C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497270 | ||||||
| chr5:119497377
|
T | C | 1 | a0005c0005t0001g0269 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.972+731T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497377 | ||||||
| chr5:119497440
|
C | T | 2 | a0002c0002t0002g0157a0002c0002t0002g0171 | 2 | NA19056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.972+794C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497440 | ||||||
| chr5:119497445
|
A | G | 1 | a0002c0002t0002g0162 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.972+799A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497445 | ||||||
| chr5:119497482
|
C | G | 136 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.972+836C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497482 | ||||||
| chr5:119497619
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.972+973C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497619 | ||||||
| chr5:119497689
|
T | C | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.972+1043T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497689 | ||||||
| chr5:119497758
|
A | C | 1 | a0002c0002t0002g0115 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.972+1112A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497758 | ||||||
| chr5:119497788
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.972+1142A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497788 | ||||||
| chr5:119497833
|
T | C | 1 | a0002c0002t0002g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.972+1187T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497833 | ||||||
| chr5:119497834
|
A | C | 1 | a0002c0002t0002g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.972+1188A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497834 | ||||||
| chr5:119497842
|
G | A | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.972+1196G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497842 | ||||||
| chr5:119497847
|
T | C | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.972+1201T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497847 | ||||||
| chr5:119497849
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.972+1203A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497849 | ||||||
| chr5:119497929
|
A | T | 1 | a0004c0004t0005g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.972+1283A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497929 | ||||||
| chr5:119497955
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.972+1309C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497955 | ||||||
| chr5:119497978
|
G | A | 1 | a0002c0002t0002g0134 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.972+1332G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497978 | ||||||
| chr5:119497983
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.973-1334T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497983 | ||||||
| chr5:119497997
|
A | C | 88 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.973-1320A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497997 | ||||||
| chr5:119498030
|
T | C | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.973-1287T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498030 | ||||||
| chr5:119498097
|
G | A | 1 | a0002c0002t0002g0115 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.973-1220G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498097 | ||||||
| chr5:119498102
|
C | A | 1 | a0004c0004t0003g0344 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.973-1215C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498102 | ||||||
| chr5:119498253
|
A | G | 101 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(98): Show | 102 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.973-1064A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498253 | ||||||
| chr5:119498348
|
G | T | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.973-969G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498348 | ||||||
| chr5:119498475
|
T | C | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.973-842T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498475 | ||||||
| chr5:119498553
|
G | C | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.973-764G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498553 | ||||||
| chr5:119498591
|
TGAGG | T | 35 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.973-723_973-720del others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr5 | 119498591 | |||||
| chr5:119498678
|
C | A | 188 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(185): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.973-639C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498678 | ||||||
| chr5:119498683
|
C | T | 45 | a0001c0001t0001g0327a0003c0003t0002g0194a0003c0003t0002g0195others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.973-634C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498683 | ||||||
| chr5:119498741
|
A | G | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.973-576A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498741 | ||||||
| chr5:119498775
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.973-542G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498775 | ||||||
| chr5:119498813
|
G | A | 1 | a0004c0004t0004g0343 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.973-504G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498813 | ||||||
| chr5:119498831
|
G | C | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.973-486G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498831 | ||||||
| chr5:119498866
|
C | T | 1 | a0002c0002t0002g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.973-451C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498866 | ||||||
| chr5:119498911
|
A | G | 188 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(185): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.973-406A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498911 | ||||||
| chr5:119498980
|
C | A | 7 | a0003c0003t0002g0206a0003c0003t0002g0208a0003c0003t0002g0211others(4): Show | 7 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-337C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498980 | ||||||
| chr5:119499076
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.973-241G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119499076 | ||||||
| chr5:119499655
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0320 | 2 | HG01106.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1209+102A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119499655 | ||||||
| chr5:119499952
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1209+399A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119499952 | ||||||
| chr5:119500070
|
A | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1209+517A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500070 | ||||||
| chr5:119500209
|
A | C | 1 | a0008c0008t0003g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1209+656A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500209 | ||||||
| chr5:119500309
|
T | G | 41 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0065others(38): Show | 41 | HG00408.hp2 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1209+756T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500309 | ||||||
| chr5:119500311
|
G | T | 139 | a0001c0001t0001g0079a0001c0001t0001g0303a0001c0001t0001g0327others(136): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1209+758G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500311 | ||||||
| chr5:119500313
|
G | T | 1 | a0007c0007t0003g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1209+760G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500313 | ||||||
| chr5:119500332
|
ATATACAT others(10): Show |
A | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1209+805_1209+821d others(19): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr5 | 119500332 | |||||
| chr5:119500339
|
T | G | 1 | a0002c0002t0002g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1209+786T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500339 | ||||||
| chr5:119500396
|
A | G | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1209+843A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500396 | ||||||
| chr5:119500515
|
G | A | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209+962G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500515 | ||||||
| chr5:119500917
|
G | T | 6 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(3): Show | 6 | NA18960.hp1 NA18970.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-1124G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500917 | ||||||
| chr5:119500926
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1210-1115G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500926 | ||||||
| chr5:119500963
|
G | A | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1210-1078G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119500963 | ||||||
| chr5:119501113
|
A | G | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1210-928A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501113 | ||||||
| chr5:119501259
|
A | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1210-782A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501259 | ||||||
| chr5:119501329
|
TA | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 8 | HG00741.hp1 HG02735.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1210-708delA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr5 | 119501329 | |||||
| chr5:119501330
|
A | T | 286 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0190others(283): Show | 290 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1210-711A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501330 | ||||||
| chr5:119501764
|
G | T | 2 | a0002c0002t0002g0098a0002c0002t0002g0100 | 2 | NA18998.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1210-277G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501764 | ||||||
| chr5:119501800
|
A | G | 3 | a0004c0009t0003g0339a0004c0009t0003g0340a0004c0009t0003g0352 | 3 | HG02055.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1210-241A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501800 | ||||||
| chr5:119501957
|
T | C | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1210-84T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501957 | ||||||
| chr5:119501963
|
T | C | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1210-78T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501963 | ||||||
| chr5:119501991
|
C | A | 1 | a0002c0002t0002g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1210-50C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 13/23 | chr5 | 119501991 | ||||||
| chr5:119502106
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0009g0309 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1261+14A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502106 | ||||||
| chr5:119502138
|
C | T | 100 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(97): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1261+46C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502138 | ||||||
| chr5:119502139
|
A | G | 151 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(148): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1261+47A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502139 | ||||||
| chr5:119502358
|
C | A | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1261+266C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502358 | ||||||
| chr5:119502373
|
G | A | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1261+281G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502373 | ||||||
| chr5:119502466
|
A | G | 1 | a0004c0004t0004g0359 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1261+374A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502466 | ||||||
| chr5:119502505
|
C | CT | 34 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(31): Show | 34 | HG00408.hp2 HG00735.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1261+422dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119502505 | |||||
| chr5:119502505
|
CT | C | 7 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261+422delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119502505 | |||||
| chr5:119502533
|
T | TCTG | 190 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(187): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1261+443_1261+444i others(5): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119502533 | |||||
| chr5:119502780
|
C | A | 44 | a0001c0001t0001g0244a0001c0001t0001g0248a0001c0001t0001g0249others(41): Show | 44 | HG00544.hp1 HG00558.hp1 HG02040.hp1 others(41): Show |
intron_variant | MODIFIER | c.1261+688C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502780 | ||||||
| chr5:119502865
|
G | T | 188 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(185): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1261+773G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502865 | ||||||
| chr5:119502900
|
C | T | 3 | a0003c0003t0002g0198a0003c0003t0002g0227a0003c0003t0002g0231 | 3 | NA18985.hp1 NA19011.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1261+808C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502900 | ||||||
| chr5:119502962
|
A | G | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1261+870A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502962 | ||||||
| chr5:119503076
|
T | TTG | 33 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0045others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1261+1022_1261+102 others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTG | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261+1020_1261+102 others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTGTG | 24 | a0001c0001t0001g0263a0001c0001t0001g0307a0003c0003t0002g0183others(21): Show | 24 | HG01496.hp2 HG02055.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1261+1018_1261+102 others(10): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTGTGT others(1): Show |
22 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0259others(19): Show | 23 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1261+1016_1261+102 others(12): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTGTGT others(3): Show |
30 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(27): Show | 30 | HG00621.hp1 HG00642.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1261+1014_1261+102 others(14): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTGTGT others(5): Show |
20 | a0001c0001t0001g0009a0001c0001t0001g0242a0001c0001t0001g0260others(17): Show | 20 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1261+1012_1261+102 others(16): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTGTGT others(7): Show |
31 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0248others(28): Show | 31 | HG00558.hp1 HG02056.hp2 HG02165.hp2 others(28): Show |
intron_variant | MODIFIER | c.1261+1010_1261+102 others(18): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0292a0005c0005t0001g0291 | 2 | HG02074.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1261+1008_1261+102 others(20): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0295a0005c0005t0001g0268 | 2 | HG02040.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1261+1006_1261+102 others(22): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
TTG | T | 9 | a0001c0001t0001g0042a0001c0001t0001g0062a0002c0002t0002g0095others(6): Show | 9 | HG00408.hp1 HG00735.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261+1022_1261+102 others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
TTGTG | T | 19 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0049others(16): Show | 19 | HG00642.hp2 HG01081.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1261+1020_1261+102 others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503076
|
TTGTGTG | T | 20 | a0001c0001t0002g0363a0003c0003t0002g0216a0003c0003t0002g0217others(17): Show | 20 | HG00408.hp2 HG01255.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.1261+1018_1261+102 others(10): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503076 | |||||
| chr5:119503180
|
A | G | 1 | a0002c0002t0002g0131 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1261+1088A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503180 | ||||||
| chr5:119503265
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1261+1173G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503265 | ||||||
| chr5:119503283
|
C | T | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261+1191C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503283 | ||||||
| chr5:119503360
|
C | T | 7 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261+1268C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503360 | ||||||
| chr5:119503368
|
T | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(7): Show | 10 | HG00738.hp2 HG00741.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1261+1276T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503368 | ||||||
| chr5:119503459
|
T | A | 1 | a0002c0002t0002g0126 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1261+1367T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503459 | ||||||
| chr5:119503603
|
A | C | 7 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261+1511A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503603 | ||||||
| chr5:119503718
|
C | T | 1 | a0002c0002t0002g0148 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1261+1626C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503718 | ||||||
| chr5:119503743
|
G | GT | 127 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(124): Show | 127 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.1261+1663dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119503743 | |||||
| chr5:119503918
|
G | A | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1261+1826G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503918 | ||||||
| chr5:119503944
|
C | CCCCATTG others(189): Show |
1 | a0001c0001t0002g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1261+1852_1261+185 others(200): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119503944 | ||||||
| chr5:119504012
|
G | A | 149 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1261+1920G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504012 | ||||||
| chr5:119504098
|
G | A | 129 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(126): Show | 129 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.1261+2006G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504098 | ||||||
| chr5:119504104
|
C | G | 1 | a0002c0002t0002g0131 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1261+2012C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504104 | ||||||
| chr5:119504130
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1261+2038C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504130 | ||||||
| chr5:119504136
|
A | G | 1 | a0003c0003t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1261+2044A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504136 | ||||||
| chr5:119504249
|
CAT | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261+2160_1261+216 others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119504249 | |||||
| chr5:119504653
|
G | A | 1 | a0005c0005t0001g0293 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1262-2165G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504653 | ||||||
| chr5:119504689
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1262-2129A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504689 | ||||||
| chr5:119504761
|
C | G | 2 | a0002c0002t0002g0003a0002c0002t0002g0141 | 3 | HG01516.hp2 HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1262-2057C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504761 | ||||||
| chr5:119504990
|
C | T | 1 | a0002c0002t0002g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1262-1828C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504990 | ||||||
| chr5:119505120
|
T | C | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1262-1698T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505120 | ||||||
| chr5:119505191
|
GT | G | 196 | a0001c0001t0001g0327a0001c0001t0002g0178a0001c0001t0002g0179others(193): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1262-1615delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr5 | 119505191 | |||||
| chr5:119505231
|
T | C | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1262-1587T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505231 | ||||||
| chr5:119505243
|
C | T | 1 | a0001c0001t0002g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1262-1575C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505243 | ||||||
| chr5:119505258
|
A | G | 3 | a0005c0005t0001g0243a0005c0005t0001g0246a0005c0005t0008g0241 | 3 | HG02027.hp1 NA18966.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1262-1560A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505258 | ||||||
| chr5:119505439
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0083 | 2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1262-1379C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505439 | ||||||
| chr5:119505488
|
T | C | 1 | a0002c0002t0002g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1262-1330T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505488 | ||||||
| chr5:119505690
|
G | A | 1 | a0009c0010t0001g0278 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1262-1128G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505690 | ||||||
| chr5:119505713
|
T | C | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1262-1105T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505713 | ||||||
| chr5:119505734
|
A | T | 1 | a0004c0004t0003g0345 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1262-1084A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119505734 | ||||||
| chr5:119506035
|
A | G | 3 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373 | 3 | HG01243.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1262-783A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506035 | ||||||
| chr5:119506064
|
T | A | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1262-754T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506064 | ||||||
| chr5:119506124
|
G | A | 1 | a0002c0002t0002g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1262-694G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506124 | ||||||
| chr5:119506133
|
A | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1262-685A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506133 | ||||||
| chr5:119506155
|
AT | A | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262-662delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506155 | ||||||
| chr5:119506190
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0049 | 3 | HG01081.hp1 HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1262-628C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506190 | ||||||
| chr5:119506207
|
C | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1262-611C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506207 | ||||||
| chr5:119506229
|
G | A | 151 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(148): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1262-589G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506229 | ||||||
| chr5:119506259
|
G | A | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262-559G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506259 | ||||||
| chr5:119506263
|
G | A | 10 | a0006c0006t0003g0005a0006c0006t0003g0368a0006c0006t0003g0369others(7): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1262-555G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506263 | ||||||
| chr5:119506405
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1262-413C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506405 | ||||||
| chr5:119506443
|
C | T | 149 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1262-375C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506443 | ||||||
| chr5:119506545
|
C | A | 1 | a0004c0004t0003g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1262-273C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506545 | ||||||
| chr5:119506548
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0001g0306others(2): Show | 5 | NA18612.hp2 NA18990.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1262-270G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506548 | ||||||
| chr5:119506646
|
G | A | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1262-172G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119506646 | ||||||
| chr5:119507028
|
A | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1333+139A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507028 | ||||||
| chr5:119507127
|
A | G | 12 | a0001c0001t0001g0248a0001c0001t0001g0261a0001c0001t0001g0296others(9): Show | 12 | HG00544.hp1 NA18747.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.1333+238A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507127 | ||||||
| chr5:119507135
|
A | G | 1 | a0004c0004t0003g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1333+246A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507135 | ||||||
| chr5:119507317
|
G | A | 149 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1333+428G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507317 | ||||||
| chr5:119507463
|
A | G | 5 | a0002c0002t0002g0104a0002c0002t0002g0110a0002c0002t0002g0123others(2): Show | 5 | HG00621.hp2 HG01261.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333+574A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507463 | ||||||
| chr5:119507502
|
C | T | 1 | a0004c0004t0003g0350 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1333+613C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507502 | ||||||
| chr5:119507527
|
T | A | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1333+638T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507527 | ||||||
| chr5:119507611
|
G | A | 50 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(47): Show | 52 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1333+722G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507611 | ||||||
| chr5:119507627
|
C | CA | 10 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0244others(7): Show | 10 | HG00639.hp2 HG01175.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333+748dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr5 | 119507627 | |||||
| chr5:119507639
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1333+750C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507639 | ||||||
| chr5:119507668
|
C | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1333+779C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507668 | ||||||
| chr5:119507701
|
G | A | 1 | a0002c0002t0002g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1333+812G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507701 | ||||||
| chr5:119507781
|
A | AT | 10 | a0001c0001t0003g0010a0003c0003t0002g0198a0003c0003t0002g0226others(7): Show | 10 | HG00408.hp2 HG00741.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333+892_1333+893i others(3): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507781 | ||||||
| chr5:119507782
|
C | T | 284 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(281): Show | 288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1333+893C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507782 | ||||||
| chr5:119507783
|
C | A | 10 | a0001c0001t0003g0010a0003c0003t0002g0198a0003c0003t0002g0226others(7): Show | 10 | HG00408.hp2 HG00741.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333+894C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507783 | ||||||
| chr5:119507783
|
CA | C | 52 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(49): Show | 54 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1333+909delA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr5 | 119507783 | |||||
| chr5:119507799
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1333+910T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507799 | ||||||
| chr5:119507866
|
A | G | 1 | a0002c0002t0002g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1333+977A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507866 | ||||||
| chr5:119507888
|
A | G | 100 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(97): Show | 100 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1333+999A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119507888 | ||||||
| chr5:119508192
|
C | G | 90 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1334-949C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508192 | ||||||
| chr5:119508230
|
C | CA | 240 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(237): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1334-900dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr5 | 119508230 | |||||
| chr5:119508249
|
C | T | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1334-892C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508249 | ||||||
| chr5:119508432
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1334-709T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508432 | ||||||
| chr5:119508434
|
A | C | 15 | a0004c0004t0004g0004a0004c0004t0004g0336a0004c0004t0004g0337others(12): Show | 16 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1334-707A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508434 | ||||||
| chr5:119508455
|
A | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334-686A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508455 | ||||||
| chr5:119508465
|
A | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1334-676A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508465 | ||||||
| chr5:119508476
|
C | G | 88 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0001g0240others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1334-665C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508476 | ||||||
| chr5:119508537
|
G | C | 1 | a0002c0002t0002g0127 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1334-604G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508537 | ||||||
| chr5:119508543
|
C | G | 36 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(33): Show | 36 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1334-598C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508543 | ||||||
| chr5:119508585
|
C | G | 41 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(38): Show | 41 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1334-556C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508585 | ||||||
| chr5:119508596
|
C | A | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1334-545C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508596 | ||||||
| chr5:119508656
|
G | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0031 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1334-485G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508656 | ||||||
| chr5:119508791
|
C | T | 149 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1334-350C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508791 | ||||||
| chr5:119508799
|
G | T | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1334-342G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508799 | ||||||
| chr5:119508912
|
A | T | 41 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(38): Show | 41 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1334-229A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508912 | ||||||
| chr5:119508924
|
T | G | 1 | a0002c0002t0002g0148 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1334-217T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508924 | ||||||
| chr5:119508936
|
T | C | 41 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(38): Show | 41 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1334-205T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508936 | ||||||
| chr5:119508976
|
T | C | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1334-165T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119508976 | ||||||
| chr5:119509010
|
C | T | 6 | a0006c0006t0003g0005a0006c0006t0003g0368a0006c0006t0003g0369others(3): Show | 7 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334-131C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119509010 | ||||||
| chr5:119509013
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01192.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1334-128G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119509013 | ||||||
| chr5:119509058
|
A | G | 1 | a0002c0002t0002g0134 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1334-83A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 15/23 | chr5 | 119509058 | ||||||
| chr5:119509269
|
A | C | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1437+25A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509269 | ||||||
| chr5:119509307
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1437+63G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509307 | ||||||
| chr5:119509394
|
G | A | 149 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1437+150G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509394 | ||||||
| chr5:119509404
|
T | TTCCTCCT others(8): Show |
1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1437+169_1437+183d others(17): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr5 | 119509404 | |||||
| chr5:119509444
|
G | A | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1437+200G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509444 | ||||||
| chr5:119509550
|
T | A | 50 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(47): Show | 52 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1437+306T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509550 | ||||||
| chr5:119509669
|
T | A | 2 | a0004c0004t0004g0004a0004c0004t0004g0337 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1437+425T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509669 | ||||||
| chr5:119509861
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1437+617A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509861 | ||||||
| chr5:119509890
|
A | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1437+646A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509890 | ||||||
| chr5:119509939
|
T | C | 50 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(47): Show | 52 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1437+695T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509939 | ||||||
| chr5:119510060
|
A | G | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1437+816A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119510060 | ||||||
| chr5:119510340
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0009g0309 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1437+1096C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119510340 | ||||||
| chr5:119510423
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1437+1179C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119510423 | ||||||
| chr5:119510482
|
T | G | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1437+1238T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119510482 | ||||||
| chr5:119510545
|
C | T | 2 | a0003c0003t0002g0229a0003c0003t0002g0230 | 2 | NA18965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1437+1301C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119510545 | ||||||
| chr5:119510671
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1437+1427T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119510671 | ||||||
| chr5:119510736
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1437+1492C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119510736 | ||||||
| chr5:119511028
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1437+1784C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511028 | ||||||
| chr5:119511044
|
C | T | 1 | a0002c0002t0002g0163 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1437+1800C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511044 | ||||||
| chr5:119511057
|
T | C | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1437+1813T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511057 | ||||||
| chr5:119511066
|
A | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1437+1822A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511066 | ||||||
| chr5:119511172
|
G | A | 1 | a0003c0003t0002g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1437+1928G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511172 | ||||||
| chr5:119511294
|
A | G | 1 | a0002c0002t0002g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1437+2050A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511294 | ||||||
| chr5:119511365
|
A | G | 50 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(47): Show | 52 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1437+2121A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511365 | ||||||
| chr5:119511403
|
C | G | 35 | a0001c0001t0002g0363a0003c0003t0002g0198a0003c0003t0002g0206others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1437+2159C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511403 | ||||||
| chr5:119511445
|
C | T | 149 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1437+2201C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511445 | ||||||
| chr5:119511576
|
G | C | 39 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1437+2332G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511576 | ||||||
| chr5:119511637
|
G | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1437+2393G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511637 | ||||||
| chr5:119511642
|
C | T | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0256 | 3 | NA18951.hp1 NA18982.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1437+2398C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511642 | ||||||
| chr5:119511746
|
C | T | 40 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(37): Show | 40 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1437+2502C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511746 | ||||||
| chr5:119511808
|
T | A | 1 | a0001c0001t0001g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1437+2564T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511808 | ||||||
| chr5:119511866
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | NA18986.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1437+2622A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511866 | ||||||
| chr5:119511867
|
CAG | C | 10 | a0006c0006t0003g0005a0006c0006t0003g0368a0006c0006t0003g0369others(7): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1437+2624_1437+262 others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511867 | ||||||
| chr5:119511869
|
G | A | 39 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1437+2625G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511869 | ||||||
| chr5:119511888
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1437+2644C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119511888 | ||||||
| chr5:119512009
|
T | C | 2 | a0002c0002t0002g0157a0002c0002t0002g0171 | 2 | NA19056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1437+2765T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512009 | ||||||
| chr5:119512067
|
A | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1437+2823A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512067 | ||||||
| chr5:119512181
|
T | C | 1 | a0001c0001t0001g0311 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1438-2800T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512181 | ||||||
| chr5:119512222
|
G | A | 10 | a0006c0006t0003g0005a0006c0006t0003g0368a0006c0006t0003g0369others(7): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1438-2759G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512222 | ||||||
| chr5:119512230
|
C | T | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1438-2751C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512230 | ||||||
| chr5:119512455
|
C | T | 2 | a0002c0002t0002g0191a0002c0002t0002g0192 | 2 | HG01515.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1438-2526C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512455 | ||||||
| chr5:119512533
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1438-2448A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512533 | ||||||
| chr5:119512833
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1438-2148A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512833 | ||||||
| chr5:119512999
|
T | C | 33 | a0001c0001t0001g0244a0001c0001t0001g0248a0001c0001t0001g0249others(30): Show | 33 | HG00544.hp1 HG00558.hp1 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.1438-1982T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119512999 | ||||||
| chr5:119513078
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1438-1903T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513078 | ||||||
| chr5:119513109
|
G | A | 12 | a0001c0001t0001g0250a0001c0001t0001g0262a0001c0001t0001g0281others(9): Show | 12 | HG02027.hp1 HG02040.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1438-1872G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513109 | ||||||
| chr5:119513130
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1438-1851C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513130 | ||||||
| chr5:119513131
|
G | A | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1438-1850G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513131 | ||||||
| chr5:119513137
|
T | C | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1438-1844T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513137 | ||||||
| chr5:119513243
|
G | C | 3 | a0004c0009t0003g0339a0004c0009t0003g0340a0004c0009t0003g0352 | 3 | HG02055.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1438-1738G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513243 | ||||||
| chr5:119513452
|
C | T | 3 | a0004c0009t0003g0339a0004c0009t0003g0340a0004c0009t0003g0352 | 3 | HG02055.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1438-1529C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513452 | ||||||
| chr5:119513479
|
A | G | 242 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(239): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1438-1502A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513479 | ||||||
| chr5:119513547
|
C | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1438-1434C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513547 | ||||||
| chr5:119513565
|
G | A | 7 | a0001c0001t0001g0292a0001c0001t0001g0321a0001c0001t0001g0322others(4): Show | 7 | HG02074.hp1 NA18960.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1438-1416G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513565 | ||||||
| chr5:119513572
|
C | T | 1 | a0003c0003t0002g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1438-1409C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513572 | ||||||
| chr5:119513682
|
G | A | 8 | a0003c0003t0002g0206a0003c0003t0002g0208a0003c0003t0002g0211others(5): Show | 8 | HG00735.hp1 HG01123.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.1438-1299G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513682 | ||||||
| chr5:119513722
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1438-1259G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513722 | ||||||
| chr5:119513799
|
A | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1438-1182A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119513799 | ||||||
| chr5:119514048
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0039others(11): Show | 15 | HG00735.hp2 HG01257.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1438-933A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514048 | ||||||
| chr5:119514116
|
A | T | 1 | a0002c0002t0002g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1438-865A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514116 | ||||||
| chr5:119514130
|
A | G | 80 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(77): Show | 80 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1438-851A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514130 | ||||||
| chr5:119514205
|
CT | C | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1438-769delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr5 | 119514205 | |||||
| chr5:119514228
|
C | T | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1438-753C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514228 | ||||||
| chr5:119514270
|
C | T | 100 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(97): Show | 100 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1438-711C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514270 | ||||||
| chr5:119514349
|
A | C | 90 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1438-632A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514349 | ||||||
| chr5:119514439
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1438-542A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514439 | ||||||
| chr5:119514558
|
A | C | 2 | a0007c0007t0002g0201a0007c0007t0003g0199 | 2 | HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1438-423A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514558 | ||||||
| chr5:119514673
|
T | C | 3 | a0004c0004t0003g0344a0004c0004t0003g0347a0004c0004t0003g0355 | 3 | HG02630.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1438-308T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514673 | ||||||
| chr5:119514870
|
A | T | 2 | a0004c0004t0004g0358a0004c0004t0004g0359 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1438-111A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119514870 | ||||||
| chr5:119515058
|
T | G | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1503+12T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515058 | ||||||
| chr5:119515188
|
G | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1503+142G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515188 | ||||||
| chr5:119515282
|
C | A | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1503+236C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515282 | ||||||
| chr5:119515300
|
A | G | 8 | a0004c0004t0003g0328a0004c0004t0003g0333a0004c0004t0003g0334others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1503+254A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515300 | ||||||
| chr5:119515717
|
A | C | 17 | a0001c0001t0001g0327a0004c0004t0003g0330a0004c0004t0004g0004others(14): Show | 18 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1503+671A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515717 | ||||||
| chr5:119515815
|
A | T | 1 | a0001c0001t0001g0250 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1503+769A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515815 | ||||||
| chr5:119515822
|
G | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02040.hp1 NA18943.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1503+776G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515822 | ||||||
| chr5:119515964
|
C | T | 1 | a0009c0010t0002g0020 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1503+918C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119515964 | ||||||
| chr5:119516039
|
T | C | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1503+993T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516039 | ||||||
| chr5:119516144
|
A | G | 8 | a0003c0003t0002g0206a0003c0003t0002g0208a0003c0003t0002g0211others(5): Show | 8 | HG00735.hp1 HG01123.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.1503+1098A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516144 | ||||||
| chr5:119516164
|
G | A | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1503+1118G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516164 | ||||||
| chr5:119516241
|
A | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+1195A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516241 | ||||||
| chr5:119516258
|
A | T | 1 | a0002c0002t0002g0192 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1503+1212A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516258 | ||||||
| chr5:119516427
|
A | G | 1 | a0003c0003t0002g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1503+1381A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516427 | ||||||
| chr5:119516451
|
G | T | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1503+1405G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516451 | ||||||
| chr5:119516462
|
A | G | 1 | a0007c0007t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1503+1416A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516462 | ||||||
| chr5:119516486
|
T | C | 1 | a0003c0003t0002g0198 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1503+1440T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516486 | ||||||
| chr5:119516735
|
C | G | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1503+1689C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516735 | ||||||
| chr5:119516818
|
C | T | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1503+1772C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516818 | ||||||
| chr5:119516892
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1503+1846G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516892 | ||||||
| chr5:119516909
|
A | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1503+1863A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516909 | ||||||
| chr5:119516936
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1503+1890C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516936 | ||||||
| chr5:119516937
|
G | A | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1503+1891G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119516937 | ||||||
| chr5:119517002
|
C | T | 94 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1503+1956C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517002 | ||||||
| chr5:119517016
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1503+1970C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517016 | ||||||
| chr5:119517024
|
C | T | 1 | a0002c0002t0002g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1503+1978C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517024 | ||||||
| chr5:119517077
|
C | G | 1 | a0001c0001t0001g0263 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1503+2031C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517077 | ||||||
| chr5:119517162
|
C | T | 1 | a0003c0003t0002g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1503+2116C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517162 | ||||||
| chr5:119517188
|
C | G | 50 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(47): Show | 52 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1503+2142C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517188 | ||||||
| chr5:119517211
|
C | T | 143 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(140): Show | 145 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1503+2165C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517211 | ||||||
| chr5:119517261
|
G | A | 90 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1503+2215G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517261 | ||||||
| chr5:119517310
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1503+2264C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517310 | ||||||
| chr5:119517318
|
C | T | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1503+2272C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517318 | ||||||
| chr5:119517319
|
G | A | 2 | a0002c0002t0002g0003a0002c0002t0002g0141 | 3 | HG01516.hp2 HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1503+2273G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517319 | ||||||
| chr5:119517384
|
C | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1503+2338C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517384 | ||||||
| chr5:119517414
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1503+2368C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517414 | ||||||
| chr5:119517433
|
C | G | 23 | a0001c0001t0003g0010a0004c0004t0003g0328a0004c0004t0003g0332others(20): Show | 23 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1503+2387C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517433 | ||||||
| chr5:119517438
|
C | A | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1503+2392C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517438 | ||||||
| chr5:119517448
|
C | T | 97 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(94): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1503+2402C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517448 | ||||||
| chr5:119517475
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1503+2429G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517475 | ||||||
| chr5:119517501
|
C | T | 94 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1503+2455C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517501 | ||||||
| chr5:119517622
|
A | G | 1 | a0002c0002t0002g0155 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1503+2576A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517622 | ||||||
| chr5:119517665
|
C | G | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1503+2619C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517665 | ||||||
| chr5:119517711
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1503+2665C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517711 | ||||||
| chr5:119517738
|
C | A | 1 | a0005c0005t0001g0293 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1503+2692C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517738 | ||||||
| chr5:119517759
|
G | T | 1 | a0001c0001t0001g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1503+2713G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517759 | ||||||
| chr5:119517770
|
G | C | 39 | a0001c0001t0001g0327a0004c0004t0003g0328a0004c0004t0003g0330others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1503+2724G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517770 | ||||||
| chr5:119517962
|
A | C | 1 | a0004c0009t0003g0352 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1503+2916A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119517962 | ||||||
| chr5:119518147
|
C | G | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1503+3101C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518147 | ||||||
| chr5:119518167
|
C | G | 2 | a0002c0002t0002g0095a0002c0002t0002g0120 | 2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1503+3121C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518167 | ||||||
| chr5:119518240
|
C | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1503+3194C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518240 | ||||||
| chr5:119518278
|
C | T | 14 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(11): Show | 15 | HG01192.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1503+3232C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518278 | ||||||
| chr5:119518308
|
C | T | 2 | a0003c0003t0002g0211a0003c0003t0002g0215 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1503+3262C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518308 | ||||||
| chr5:119518342
|
A | G | 106 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(103): Show | 107 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1503+3296A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518342 | ||||||
| chr5:119518397
|
T | C | 145 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(142): Show | 147 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1503+3351T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518397 | ||||||
| chr5:119518454
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0088 | 2 | NA18959.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1503+3408G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518454 | ||||||
| chr5:119518973
|
T | G | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1503+3927T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518973 | ||||||
| chr5:119518983
|
A | T | 7 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503+3937A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119518983 | ||||||
| chr5:119519131
|
C | G | 3 | a0002c0002t0002g0102a0002c0002t0002g0140a0002c0002t0003g0329 | 3 | HG02602.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1503+4085C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519131 | ||||||
| chr5:119519226
|
G | A | 7 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1503+4180G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519226 | ||||||
| chr5:119519297
|
C | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1503+4251C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519297 | ||||||
| chr5:119519313
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1503+4267C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519313 | ||||||
| chr5:119519335
|
A | G | 15 | a0004c0004t0004g0004a0004c0004t0004g0336a0004c0004t0004g0337others(12): Show | 16 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1503+4289A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519335 | ||||||
| chr5:119519580
|
A | C | 38 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(35): Show | 38 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1503+4534A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519580 | ||||||
| chr5:119519587
|
G | A | 4 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(1): Show | 4 | HG01106.hp1 HG01891.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+4541G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519587 | ||||||
| chr5:119519744
|
C | T | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1503+4698C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119519744 | ||||||
| chr5:119520153
|
GT | G | 131 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0190others(128): Show | 132 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1504-5050delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr5 | 119520153 | |||||
| chr5:119520194
|
T | A | 94 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1504-5022T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119520194 | ||||||
| chr5:119520334
|
A | C | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1504-4882A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119520334 | ||||||
| chr5:119520576
|
A | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0046others(5): Show | 9 | HG00735.hp2 HG01257.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1504-4640A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119520576 | ||||||
| chr5:119520863
|
C | T | 1 | a0002c0002t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1504-4353C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119520863 | ||||||
| chr5:119520889
|
G | C | 13 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(10): Show | 14 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1504-4327G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119520889 | ||||||
| chr5:119521012
|
G | A | 13 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(10): Show | 14 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1504-4204G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521012 | ||||||
| chr5:119521368
|
G | A | 1 | a0003c0003t0002g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1504-3848G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521368 | ||||||
| chr5:119521394
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1504-3822G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521394 | ||||||
| chr5:119521398
|
G | A | 3 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373 | 3 | HG01243.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1504-3818G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521398 | ||||||
| chr5:119521426
|
T | C | 3 | a0003c0003t0002g0198a0003c0003t0002g0227a0003c0003t0002g0231 | 3 | NA18985.hp1 NA19011.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1504-3790T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521426 | ||||||
| chr5:119521443
|
A | G | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1504-3773A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521443 | ||||||
| chr5:119521454
|
ATTAG | A | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1504-3759_1504-375 others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr5 | 119521454 | |||||
| chr5:119521782
|
T | C | 1 | a0001c0001t0001g0310 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1504-3434T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521782 | ||||||
| chr5:119521802
|
T | C | 109 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(106): Show | 110 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1504-3414T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521802 | ||||||
| chr5:119521868
|
G | C | 100 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(97): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1504-3348G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521868 | ||||||
| chr5:119521919
|
G | T | 4 | a0001c0001t0003g0010a0004c0004t0003g0332a0004c0004t0003g0351others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1504-3297G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521919 | ||||||
| chr5:119521954
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1504-3262T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521954 | ||||||
| chr5:119521978
|
G | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1504-3238G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119521978 | ||||||
| chr5:119522061
|
T | C | 1 | a0001c0013t0001g0282 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1504-3155T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522061 | ||||||
| chr5:119522163
|
C | T | 34 | a0003c0003t0002g0198a0003c0003t0002g0206a0003c0003t0002g0208others(31): Show | 34 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1504-3053C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522163 | ||||||
| chr5:119522251
|
C | T | 1 | a0002c0002t0002g0110 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1504-2965C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522251 | ||||||
| chr5:119522367
|
G | C | 1 | a0002c0002t0011g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1504-2849G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522367 | ||||||
| chr5:119522480
|
G | T | 93 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(90): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1504-2736G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522480 | ||||||
| chr5:119522630
|
A | C | 1 | a0004c0004t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1504-2586A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522630 | ||||||
| chr5:119522784
|
G | C | 203 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(200): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1504-2432G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522784 | ||||||
| chr5:119522852
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1504-2364T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522852 | ||||||
| chr5:119522943
|
C | A | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1504-2273C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119522943 | ||||||
| chr5:119523006
|
A | G | 81 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(78): Show | 81 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1504-2210A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523006 | ||||||
| chr5:119523027
|
GTGGTGTT others(20): Show |
G | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 100 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1504-2187_1504-216 others(31): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr5 | 119523027 | |||||
| chr5:119523092
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1504-2124T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523092 | ||||||
| chr5:119523148
|
C | T | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1504-2068C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523148 | ||||||
| chr5:119523212
|
T | C | 13 | a0002c0002t0002g0098a0002c0002t0002g0100a0002c0002t0002g0103others(10): Show | 13 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1504-2004T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523212 | ||||||
| chr5:119523259
|
A | G | 96 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(93): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1504-1957A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523259 | ||||||
| chr5:119523271
|
C | T | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1504-1945C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523271 | ||||||
| chr5:119523281
|
C | T | 3 | a0004c0009t0003g0339a0004c0009t0003g0340a0009c0010t0003g0018 | 3 | HG02055.hp2 HG02451.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1504-1935C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523281 | ||||||
| chr5:119523459
|
A | G | 1 | a0002c0002t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1504-1757A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523459 | ||||||
| chr5:119523474
|
C | T | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1504-1742C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523474 | ||||||
| chr5:119523573
|
T | C | 144 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(141): Show | 146 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1504-1643T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523573 | ||||||
| chr5:119523574
|
A | G | 1 | a0001c0001t0006g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1504-1642A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523574 | ||||||
| chr5:119523680
|
A | G | 3 | a0007c0007t0002g0203a0007c0007t0002g0204a0007c0007t0002g0205 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1504-1536A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523680 | ||||||
| chr5:119523795
|
A | T | 1 | a0001c0013t0001g0282 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1504-1421A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523795 | ||||||
| chr5:119523851
|
A | G | 144 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(141): Show | 146 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1504-1365A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523851 | ||||||
| chr5:119523871
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1504-1345A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523871 | ||||||
| chr5:119523963
|
T | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0039others(11): Show | 15 | HG00735.hp2 HG01257.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1504-1253T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119523963 | ||||||
| chr5:119524137
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1504-1079A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524137 | ||||||
| chr5:119524142
|
A | G | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1504-1074A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524142 | ||||||
| chr5:119524182
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1504-1034A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524182 | ||||||
| chr5:119524263
|
A | G | 94 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1504-953A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524263 | ||||||
| chr5:119524443
|
G | A | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1504-773G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524443 | ||||||
| chr5:119524474
|
C | A | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1504-742C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524474 | ||||||
| chr5:119524521
|
A | G | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1504-695A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524521 | ||||||
| chr5:119524628
|
C | T | 1 | a0002c0002t0002g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1504-588C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524628 | ||||||
| chr5:119524865
|
T | C | 1 | a0009c0010t0003g0018 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1504-351T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119524865 | ||||||
| chr5:119525089
|
TA | T | 3 | a0007c0007t0002g0203a0007c0007t0002g0204a0007c0007t0002g0205 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1504-123delA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr5 | 119525089 | |||||
| chr5:119525380
|
G | C | 1 | a0002c0002t0002g0137 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1573+95G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | chr5 | 119525380 | ||||||
| chr5:119525390
|
TA | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1573+112delA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 119525390 | |||||
| chr5:119525415
|
C | T | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1573+130C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | chr5 | 119525415 | ||||||
| chr5:119525450
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1573+165G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | chr5 | 119525450 | ||||||
| chr5:119525525
|
C | A | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1573+240C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | chr5 | 119525525 | ||||||
| chr5:119525532
|
G | A | 94 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1573+247G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | chr5 | 119525532 | ||||||
| chr5:119525713
|
G | GTT | 48 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(45): Show | 50 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1574-193_1574-192d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr5 | 119525713 | |||||
| chr5:119525732
|
T | G | 8 | a0003c0003t0002g0183a0003c0003t0002g0184a0008c0008t0003g0016others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1574-185T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | chr5 | 119525732 | ||||||
| chr5:119526105
|
T | C | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1680+82T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526105 | ||||||
| chr5:119526110
|
A | G | 1 | a0009c0010t0003g0018 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1680+87A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526110 | ||||||
| chr5:119526118
|
T | A | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1680+95T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526118 | ||||||
| chr5:119526195
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1680+172C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526195 | ||||||
| chr5:119526209
|
C | T | 38 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.1680+186C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526209 | ||||||
| chr5:119526282
|
T | TTATATAT others(7): Show |
1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1680+272_1680+273i others(16): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr5 | 119526282 | |||||
| chr5:119526282
|
T | TTTTATAT others(7): Show |
1 | a0003c0003t0002g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1680+260_1680+261i others(16): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr5 | 119526282 | |||||
| chr5:119526284
|
A | ATATATAT others(5): Show |
292 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(289): Show | 296 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1680+272_1680+273i others(14): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr5 | 119526284 | |||||
| chr5:119526284
|
A | G | 1 | a0003c0003t0002g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1680+261A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526284 | ||||||
| chr5:119526448
|
T | G | 4 | a0001c0001t0003g0010a0001c0019t0007g0013a0003c0003t0002g0183others(1): Show | 4 | HG00741.hp1 HG01891.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1680+425T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526448 | ||||||
| chr5:119526545
|
C | G | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1680+522C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526545 | ||||||
| chr5:119526594
|
A | G | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1681-539A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526594 | ||||||
| chr5:119526643
|
A | T | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1681-490A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526643 | ||||||
| chr5:119526696
|
A | G | 2 | a0010c0011t0002g0209a0010c0011t0002g0210 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1681-437A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119526696 | ||||||
| chr5:119527040
|
T | C | 37 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1681-93T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 19/23 | chr5 | 119527040 | ||||||
| chr5:119527227
|
T | C | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
splice_region_variant&intron_variant | LOW | c.1767+8T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527227 | ||||||
| chr5:119527276
|
C | T | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1767+57C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527276 | ||||||
| chr5:119527280
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1767+61T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527280 | ||||||
| chr5:119527435
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1767+216C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527435 | ||||||
| chr5:119527502
|
C | T | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1767+283C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527502 | ||||||
| chr5:119527586
|
G | T | 1 | a0006c0006t0002g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1767+367G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527586 | ||||||
| chr5:119527607
|
A | G | 3 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373 | 3 | HG01243.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1767+388A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527607 | ||||||
| chr5:119527643
|
A | G | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1767+424A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527643 | ||||||
| chr5:119527698
|
G | A | 1 | a0001c0001t0006g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1767+479G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527698 | ||||||
| chr5:119527717
|
A | G | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1767+498A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527717 | ||||||
| chr5:119527755
|
T | C | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1767+536T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527755 | ||||||
| chr5:119527846
|
A | C | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1767+627A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527846 | ||||||
| chr5:119527936
|
T | G | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1767+717T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119527936 | ||||||
| chr5:119528064
|
G | T | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1767+845G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528064 | ||||||
| chr5:119528133
|
G | A | 1 | a0002c0002t0002g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1767+914G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528133 | ||||||
| chr5:119528253
|
C | G | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1767+1034C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528253 | ||||||
| chr5:119528351
|
T | C | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1767+1132T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528351 | ||||||
| chr5:119528356
|
C | A | 1 | a0001c0001t0001g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1767+1137C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528356 | ||||||
| chr5:119528373
|
A | T | 10 | a0006c0006t0003g0005a0006c0006t0003g0368a0006c0006t0003g0369others(7): Show | 11 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1767+1154A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528373 | ||||||
| chr5:119528590
|
T | G | 1 | a0002c0002t0002g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1768-1304T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528590 | ||||||
| chr5:119528625
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1768-1269A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528625 | ||||||
| chr5:119528895
|
C | T | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1768-999C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528895 | ||||||
| chr5:119528897
|
T | C | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1768-997T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119528897 | ||||||
| chr5:119529041
|
C | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1768-853C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529041 | ||||||
| chr5:119529061
|
A | G | 1 | a0003c0003t0002g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1768-833A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529061 | ||||||
| chr5:119529136
|
A | G | 2 | a0004c0004t0004g0004a0004c0004t0004g0337 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1768-758A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529136 | ||||||
| chr5:119529183
|
T | C | 14 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(11): Show | 15 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1768-711T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529183 | ||||||
| chr5:119529199
|
C | T | 101 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(98): Show | 101 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1768-695C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529199 | ||||||
| chr5:119529204
|
C | G | 3 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373 | 3 | HG01243.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1768-690C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529204 | ||||||
| chr5:119529225
|
C | A | 2 | a0002c0002t0002g0011a0002c0002t0002g0012 | 2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1768-669C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529225 | ||||||
| chr5:119529269
|
G | T | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1768-625G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529269 | ||||||
| chr5:119529391
|
C | T | 16 | a0004c0004t0003g0330a0004c0004t0004g0004a0004c0004t0004g0336others(13): Show | 17 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1768-503C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529391 | ||||||
| chr5:119529567
|
TGCCCAAA others(8): Show |
T | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1768-321_1768-307d others(17): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr5 | 119529567 | |||||
| chr5:119529630
|
C | T | 34 | a0003c0003t0002g0198a0003c0003t0002g0206a0003c0003t0002g0208others(31): Show | 34 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1768-264C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529630 | ||||||
| chr5:119529640
|
T | C | 1 | a0002c0002t0002g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1768-254T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529640 | ||||||
| chr5:119529718
|
C | T | 80 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(77): Show | 80 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1768-176C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 20/23 | chr5 | 119529718 | ||||||
| chr5:119530062
|
G | A | 1 | a0001c0001t0001g0327 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1854+82G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530062 | ||||||
| chr5:119530153
|
A | G | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1854+173A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530153 | ||||||
| chr5:119530353
|
A | G | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1854+373A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530353 | ||||||
| chr5:119530399
|
A | C | 295 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(292): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1854+419A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530399 | ||||||
| chr5:119530407
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1854+427G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530407 | ||||||
| chr5:119530463
|
G | C | 101 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(98): Show | 101 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1854+483G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530463 | ||||||
| chr5:119530555
|
G | GA | 94 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1854+586dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr5 | 119530555 | |||||
| chr5:119530563
|
A | G | 11 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(8): Show | 12 | HG01884.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1854+583A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530563 | ||||||
| chr5:119530574
|
C | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1854+594C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530574 | ||||||
| chr5:119530580
|
C | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1854+600C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530580 | ||||||
| chr5:119530845
|
C | CA | 86 | a0001c0001t0001g0045a0001c0001t0001g0065a0001c0001t0001g0066others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.1855-403dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr5 | 119530845 | |||||
| chr5:119530845
|
C | CAA | 23 | a0001c0001t0001g0274a0001c0001t0001g0283a0002c0002t0002g0002others(20): Show | 24 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1855-404_1855-403d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr5 | 119530845 | |||||
| chr5:119530845
|
C | CAAAAAAA others(15): Show |
1 | a0009c0010t0003g0018 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1855-403_1855-402i others(24): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr5 | 119530845 | |||||
| chr5:119530854
|
AAAAAAAA others(10): Show |
A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1855-403_1855-387d others(19): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr5 | 119530854 | |||||
| chr5:119530857
|
A | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1855-409A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530857 | ||||||
| chr5:119530860
|
AAAAC | A | 6 | a0006c0006t0002g0202a0007c0007t0002g0201a0007c0007t0002g0203others(3): Show | 6 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1855-402_1855-399d others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr5 | 119530860 | |||||
| chr5:119530860
|
AAAACAAA others(4): Show |
A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | NA18943.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1855-402_1855-392d others(13): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr5 | 119530860 | |||||
| chr5:119530861
|
A | C | 37 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1855-405A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530861 | ||||||
| chr5:119530862
|
A | C | 2 | a0003c0003t0002g0212a0003c0003t0002g0226 | 2 | HG01175.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1855-404A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530862 | ||||||
| chr5:119530863
|
AC | A | 112 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1855-402delC | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530863 | ||||||
| chr5:119530864
|
C | A | 166 | a0001c0001t0001g0045a0001c0001t0001g0240a0001c0001t0001g0244others(163): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1855-402C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530864 | ||||||
| chr5:119530865
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1855-401A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530865 | ||||||
| chr5:119530866
|
A | C | 11 | a0001c0001t0001g0242a0001c0001t0001g0245a0001c0001t0001g0251others(8): Show | 11 | HG00558.hp2 HG00621.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.1855-400A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530866 | ||||||
| chr5:119530871
|
C | A | 93 | a0001c0001t0001g0058a0001c0001t0001g0242a0001c0001t0001g0244others(90): Show | 94 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1855-395C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530871 | ||||||
| chr5:119530929
|
T | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0299 | 2 | NA18747.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1855-337T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530929 | ||||||
| chr5:119531184
|
T | A | 95 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(92): Show | 95 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1855-82T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119531184 | ||||||
| chr5:119531216
|
A | T | 1 | a0002c0002t0002g0163 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1855-50A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119531216 | ||||||
| chr5:119531237
|
T | C | 1 | a0003c0003t0002g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1855-29T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119531237 | ||||||
| chr5:119531478
|
G | C | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1993+74G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531478 | ||||||
| chr5:119531563
|
AGG | A | 93 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(90): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1993+164_1993+165d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119531563 | |||||
| chr5:119531566
|
G | GGT | 42 | a0001c0001t0003g0010a0003c0003t0002g0183a0003c0003t0002g0184others(39): Show | 43 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1993+163_1993+164i others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119531566 | |||||
| chr5:119531566
|
G | GGTGT | 55 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(52): Show | 55 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1993+163_1993+164i others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119531566 | |||||
| chr5:119531566
|
G | GGTGTGT | 77 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(74): Show | 77 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1993+163_1993+164i others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119531566 | |||||
| chr5:119531566
|
GGGGT | G | 12 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(9): Show | 13 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1993+164_1993+167d others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119531566 | |||||
| chr5:119531568
|
G | GGT | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(10): Show | 13 | HG00738.hp2 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1993+191_1993+192d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119531568 | |||||
| chr5:119531568
|
G | T | 188 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0190others(185): Show | 189 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1993+164G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531568 | ||||||
| chr5:119531597
|
T | G | 2 | a0002c0002t0002g0157a0002c0002t0002g0171 | 2 | NA19056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1993+193T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531597 | ||||||
| chr5:119531607
|
G | A | 1 | a0002c0002t0002g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1993+203G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531607 | ||||||
| chr5:119531693
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1993+289T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531693 | ||||||
| chr5:119531758
|
A | G | 1 | a0001c0001t0006g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1993+354A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531758 | ||||||
| chr5:119531789
|
C | G | 30 | a0004c0004t0003g0330a0004c0004t0004g0004a0004c0004t0004g0336others(27): Show | 32 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1993+385C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531789 | ||||||
| chr5:119531903
|
T | C | 15 | a0004c0004t0004g0004a0004c0004t0004g0336a0004c0004t0004g0337others(12): Show | 16 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1993+499T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531903 | ||||||
| chr5:119532243
|
G | A | 295 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(292): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1993+839G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532243 | ||||||
| chr5:119532252
|
G | T | 1 | a0001c0001t0001g0327 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1993+848G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532252 | ||||||
| chr5:119532331
|
C | T | 1 | a0001c0001t0002g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1993+927C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532331 | ||||||
| chr5:119532401
|
T | C | 30 | a0004c0004t0003g0330a0004c0004t0004g0004a0004c0004t0004g0336others(27): Show | 32 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1993+997T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532401 | ||||||
| chr5:119532559
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1993+1155T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532559 | ||||||
| chr5:119532566
|
G | GAAATATG others(1): Show |
89 | a0001c0001t0001g0047a0001c0001t0001g0190a0001c0001t0001g0239others(86): Show | 89 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1993+1165_1993+117 others(12): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119532566 | |||||
| chr5:119532637
|
A | G | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1993+1233A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532637 | ||||||
| chr5:119532707
|
C | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1993+1303C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532707 | ||||||
| chr5:119532898
|
G | C | 344 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(341): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1993+1494G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119532898 | ||||||
| chr5:119533049
|
T | A | 1 | a0014c0014t0002g0130 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1993+1645T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533049 | ||||||
| chr5:119533158
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1993+1754A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533158 | ||||||
| chr5:119533289
|
C | CCT | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1993+1885_1993+188 others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533289 | ||||||
| chr5:119533289
|
C | CT | 246 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0024others(243): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1993+1898dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119533289 | |||||
| chr5:119533289
|
C | CTT | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 17 | HG01069.hp1 HG01071.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1993+1897_1993+189 others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119533289 | |||||
| chr5:119533289
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0023others(8): Show | 11 | HG00738.hp2 HG00741.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1993+1885C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533289 | ||||||
| chr5:119533336
|
G | A | 2 | a0002c0002t0002g0011a0002c0002t0002g0012 | 2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1993+1932G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533336 | ||||||
| chr5:119533354
|
C | T | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1993+1950C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533354 | ||||||
| chr5:119533745
|
A | G | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1993+2341A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533745 | ||||||
| chr5:119533827
|
T | C | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1993+2423T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533827 | ||||||
| chr5:119533835
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1993+2431C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533835 | ||||||
| chr5:119533942
|
G | A | 344 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(341): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1994-2481G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533942 | ||||||
| chr5:119533960
|
G | A | 2 | a0009c0012t0003g0015a0009c0012t0012g0374 | 2 | HG01496.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1994-2463G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119533960 | ||||||
| chr5:119533984
|
AATAT | A | 37 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1994-2436_1994-243 others(8): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119533984 | |||||
| chr5:119534069
|
A | G | 37 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1994-2354A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534069 | ||||||
| chr5:119534311
|
G | A | 3 | a0002c0002t0002g0173a0009c0010t0003g0018a0009c0012t0003g0015 | 3 | HG02129.hp1 HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1994-2112G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534311 | ||||||
| chr5:119534338
|
G | C | 97 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(94): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1994-2085G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534338 | ||||||
| chr5:119534376
|
AC | A | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1994-2046delC | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534376 | ||||||
| chr5:119534440
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1994-1983T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534440 | ||||||
| chr5:119534757
|
G | A | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1994-1666G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534757 | ||||||
| chr5:119534854
|
G | A | 8 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG00621.hp1 NA18946.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.1994-1569G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534854 | ||||||
| chr5:119534886
|
A | G | 97 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(94): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1994-1537A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534886 | ||||||
| chr5:119534966
|
CT | C | 203 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(200): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1994-1449delT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119534966 | |||||
| chr5:119535246
|
T | C | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1994-1177T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535246 | ||||||
| chr5:119535260
|
TA | T | 37 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(34): Show | 37 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1994-1162delA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535260 | ||||||
| chr5:119535328
|
A | T | 1 | a0001c0019t0007g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1994-1095A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535328 | ||||||
| chr5:119535328
|
AATT | A | 81 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(78): Show | 81 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1994-1088_1994-108 others(7): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119535328 | |||||
| chr5:119535492
|
A | G | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1994-931A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535492 | ||||||
| chr5:119535533
|
C | G | 10 | a0001c0001t0003g0371a0001c0001t0003g0372a0001c0001t0003g0373others(7): Show | 10 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1994-890C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535533 | ||||||
| chr5:119535628
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1994-795C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535628 | ||||||
| chr5:119535670
|
T | TTA | 99 | a0001c0001t0003g0010a0001c0001t0003g0371a0001c0001t0003g0372others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1994-737_1994-736d others(4): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119535670 | |||||
| chr5:119535670
|
T | TTATA | 21 | a0004c0004t0003g0328a0004c0004t0003g0332a0004c0004t0003g0333others(18): Show | 21 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.1994-739_1994-736d others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr5 | 119535670 | |||||
| chr5:119535672
|
A | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0084a0003c0003t0003g0366others(1): Show | 4 | HG01516.hp1 HG01884.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1994-751A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535672 | ||||||
| chr5:119535921
|
T | C | 1 | a0003c0003t0002g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1994-502T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535921 | ||||||
| chr5:119535953
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1994-470C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119535953 | ||||||
| chr5:119536058
|
G | A | 30 | a0004c0004t0003g0330a0004c0004t0004g0004a0004c0004t0004g0336others(27): Show | 32 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1994-365G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119536058 | ||||||
| chr5:119536133
|
T | C | 1 | a0004c0004t0003g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1994-290T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119536133 | ||||||
| chr5:119536208
|
C | T | 2 | a0002c0002t0002g0104a0002c0002t0002g0110 | 2 | HG03834.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1994-215C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119536208 | ||||||
| chr5:119536330
|
A | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1994-93A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119536330 | ||||||
| chr5:119536397
|
C | T | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1994-26C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119536397 | ||||||
| chr5:119536606
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2121+56T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119536606 | ||||||
| chr5:119536640
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2121+90T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119536640 | ||||||
| chr5:119536816
|
T | A | 8 | a0004c0004t0003g0328a0004c0004t0003g0333a0004c0004t0003g0334others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2121+266T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119536816 | ||||||
| chr5:119536999
|
T | A | 2 | a0003c0003t0002g0183a0003c0003t0002g0184 | 2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2121+449T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119536999 | ||||||
| chr5:119537070
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2121+520A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537070 | ||||||
| chr5:119537231
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01069.hp1 HG01071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2121+681A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537231 | ||||||
| chr5:119537470
|
A | T | 1 | a0002c0002t0002g0129 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2121+920A>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537470 | ||||||
| chr5:119537563
|
T | G | 2 | a0009c0010t0003g0018a0009c0012t0003g0015 | 2 | HG04204.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2121+1013T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537563 | ||||||
| chr5:119537618
|
C | T | 2 | a0002c0002t0002g0092a0003c0003t0002g0224 | 2 | HG01123.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2121+1068C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537618 | ||||||
| chr5:119537626
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2121+1076A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537626 | ||||||
| chr5:119537668
|
A | G | 1 | a0001c0001t0002g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2121+1118A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537668 | ||||||
| chr5:119537731
|
A | G | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2121+1181A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537731 | ||||||
| chr5:119537802
|
T | G | 2 | a0003c0003t0003g0366a0003c0003t0003g0367 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2121+1252T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537802 | ||||||
| chr5:119537819
|
C | T | 1 | a0002c0002t0002g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2121+1269C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537819 | ||||||
| chr5:119537834
|
T | C | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2121+1284T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537834 | ||||||
| chr5:119537972
|
T | C | 4 | a0002c0002t0002g0114a0002c0002t0002g0143a0002c0002t0002g0160others(1): Show | 4 | NA18612.hp1 NA18951.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2121+1422T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119537972 | ||||||
| chr5:119538031
|
C | A | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2121+1481C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538031 | ||||||
| chr5:119538065
|
A | G | 103 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0190others(100): Show | 103 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.2121+1515A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538065 | ||||||
| chr5:119538156
|
C | T | 1 | a0004c0004t0003g0344 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2121+1606C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538156 | ||||||
| chr5:119538255
|
G | C | 1 | a0002c0002t0002g0175 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2121+1705G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538255 | ||||||
| chr5:119538264
|
C | T | 13 | a0006c0006t0002g0202a0006c0006t0003g0005a0006c0006t0003g0368others(10): Show | 14 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.2121+1714C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538264 | ||||||
| chr5:119538326
|
C | T | 3 | a0007c0007t0002g0203a0007c0007t0002g0204a0007c0007t0002g0205 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2121+1776C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538326 | ||||||
| chr5:119538592
|
C | T | 95 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.2121+2042C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538592 | ||||||
| chr5:119538618
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2121+2068C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538618 | ||||||
| chr5:119538635
|
C | T | 1 | a0005c0005t0001g0293 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2121+2085C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538635 | ||||||
| chr5:119538786
|
GC | G | 2 | a0004c0004t0004g0004a0004c0004t0004g0337 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2121+2237delC | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538786 | ||||||
| chr5:119538802
|
C | A | 1 | a0003c0003t0010g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2121+2252C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538802 | ||||||
| chr5:119538802
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2121+2252C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119538802 | ||||||
| chr5:119539096
|
C | T | 2 | a0002c0002t0002g0125a0002c0002t0002g0177 | 2 | NA18946.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2121+2546C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119539096 | ||||||
| chr5:119539323
|
A | G | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2122-2582A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119539323 | ||||||
| chr5:119539353
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2122-2552G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119539353 | ||||||
| chr5:119539444
|
AG | A | 107 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(104): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2122-2454delG | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119539444 | |||||
| chr5:119539546
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2122-2359C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119539546 | ||||||
| chr5:119539708
|
G | A | 2 | a0001c0001t0003g0010a0001c0019t0007g0013 | 2 | HG00741.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.2122-2197G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119539708 | ||||||
| chr5:119539717
|
G | A | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2122-2188G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119539717 | ||||||
| chr5:119539922
|
C | CA | 132 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 133 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.2122-1962dupA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119539922 | |||||
| chr5:119539922
|
C | CAA | 76 | a0001c0001t0001g0043a0001c0001t0001g0058a0001c0001t0001g0066others(73): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2122-1963_2122-196 others(6): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119539922 | |||||
| chr5:119539922
|
C | CAAA | 90 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(87): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2122-1964_2122-196 others(7): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119539922 | |||||
| chr5:119539922
|
CAAAAAAA others(1): Show |
C | 36 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0363others(33): Show | 36 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.2122-1969_2122-196 others(12): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119539922 | |||||
| chr5:119540072
|
G | A | 1 | a0001c0001t0003g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2122-1833G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540072 | ||||||
| chr5:119540182
|
G | T | 2 | a0002c0002t0002g0095a0002c0002t0002g0120 | 2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2122-1723G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540182 | ||||||
| chr5:119540193
|
C | T | 1 | a0002c0002t0002g0096 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2122-1712C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540193 | ||||||
| chr5:119540277
|
C | T | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2122-1628C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540277 | ||||||
| chr5:119540278
|
T | A | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2122-1627T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540278 | ||||||
| chr5:119540279
|
C | T | 50 | a0001c0001t0009g0309a0004c0004t0003g0328a0004c0004t0003g0330others(47): Show | 52 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2122-1626C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540279 | ||||||
| chr5:119540280
|
C | T | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2122-1625C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540280 | ||||||
| chr5:119540281
|
C | A | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2122-1624C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540281 | ||||||
| chr5:119540282
|
A | C | 1 | a0001c0001t0009g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2122-1623A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540282 | ||||||
| chr5:119540331
|
C | T | 1 | a0004c0004t0005g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2122-1574C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540331 | ||||||
| chr5:119540346
|
C | CAGA | 49 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(46): Show | 51 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.2122-1558_2122-155 others(7): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119540346 | |||||
| chr5:119540473
|
C | A | 1 | a0002c0002t0002g0192 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2122-1432C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540473 | ||||||
| chr5:119540509
|
T | C | 97 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0011others(94): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.2122-1396T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540509 | ||||||
| chr5:119540515
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2122-1390A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540515 | ||||||
| chr5:119540518
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2122-1387G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540518 | ||||||
| chr5:119540769
|
G | T | 1 | a0004c0004t0003g0353 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2122-1136G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540769 | ||||||
| chr5:119540900
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0084 | 2 | HG01516.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2122-1005G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540900 | ||||||
| chr5:119540940
|
G | A | 294 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.2122-965G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540940 | ||||||
| chr5:119540982
|
T | A | 3 | a0004c0009t0003g0339a0004c0009t0003g0340a0004c0009t0003g0352 | 3 | HG02055.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2122-923T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119540982 | ||||||
| chr5:119541067
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2122-838A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541067 | ||||||
| chr5:119541311
|
G | C | 1 | a0004c0004t0003g0330 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2122-594G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541311 | ||||||
| chr5:119541325
|
G | A | 15 | a0004c0004t0004g0004a0004c0004t0004g0336a0004c0004t0004g0337others(12): Show | 16 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2122-580G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541325 | ||||||
| chr5:119541338
|
G | A | 4 | a0003c0003t0002g0194a0003c0003t0002g0195a0003c0003t0002g0196others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2122-567G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541338 | ||||||
| chr5:119541386
|
C | T | 11 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0066others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2122-519C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541386 | ||||||
| chr5:119541411
|
C | T | 2 | a0002c0002t0002g0106a0002c0002t0002g0108 | 2 | NA18989.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2122-494C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541411 | ||||||
| chr5:119541715
|
C | CT | 38 | a0004c0004t0003g0328a0004c0004t0003g0330a0004c0004t0003g0332others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2122-182dupT | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119541715 | |||||
| chr5:119541821
|
G | A | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2122-84G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541821 | ||||||
| chr5:119541834
|
TA | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0253a0001c0001t0001g0290others(16): Show | 19 | HG01934.hp2 HG01993.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.2122-57delA | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119541834 | |||||
| chr5:119541834
|
TAA | T | 6 | a0008c0008t0003g0016a0008c0008t0003g0017a0008c0008t0003g0019others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.2122-58_2122-57del others(2): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr5 | 119541834 | |||||
| chr5:119541853
|
T | G | 101 | a0001c0001t0001g0009a0001c0001t0001g0190a0001c0001t0001g0239others(98): Show | 101 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.2122-52T>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541853 | ||||||
| chr5:119541863
|
C | T | 1 | a0009c0012t0012g0374 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2122-42C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541863 | ||||||
| chr5:119541871
|
C | T | 34 | a0003c0003t0002g0198a0003c0003t0002g0206a0003c0003t0002g0208others(31): Show | 34 | HG00408.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2122-34C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541871 | ||||||
| chr5:119541896
|
T | C | 1 | a0009c0012t0003g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2122-9T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541896 |