Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0002 | 0/1 | 736 | 93 | 4 | 13 | 59 | 8 | 8 | 44 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0003 | 0/0 | 736 | 42 | 11 | 9 | 19 | 0 | 3 | 18 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0004 | 0/0 | 736 | 38 | 23 | 7 | 1 | 2 | 5 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0005 | 0/0 | 736 | 10 | 0 | 0 | 10 | 0 | 0 | 6 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0006 | 0/0 | 736 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0007 | 0/0 | 736 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0008 | 0/0 | 736 | 5 | 0 | 2 | 2 | 0 | 1 | 2 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0009 | 0/0 | 736 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0010 | 0/0 | 736 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0011 | 0/0 | 736 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0012 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0013 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| a0014 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | MGSPL others(731): Show |
chr5 | 119447497 | 119547332 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2208 | 165 | 35 | 30 | 78 | 6 | 15 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0001c0013 | 0/0 | 2208 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0001c0016 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0001c0019 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0002c0002 | 0/1 | 2208 | 93 | 4 | 13 | 59 | 8 | 8 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0003c0003 | 0/0 | 2208 | 42 | 11 | 9 | 19 | 0 | 3 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0004c0004 | 0/0 | 2208 | 35 | 20 | 7 | 1 | 2 | 5 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0004c0009 | 0/0 | 2208 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0005c0005 | 0/0 | 2208 | 10 | 0 | 0 | 10 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0006c0007 | 0/0 | 2208 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0007c0006 | 0/0 | 2208 | 6 | 6 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0008c0010 | 0/0 | 2208 | 3 | 0 | 1 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0008c0012 | 0/0 | 2208 | 2 | 0 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0009c0008 | 0/0 | 2208 | 5 | 3 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0010c0011 | 0/0 | 2208 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0011c0015 | 0/0 | 2208 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0012c0018 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0013c0017 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
chr5 | 119447497 | 119547332 | ||
| a0014c0014 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATGGG others(2203): Show |
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 | ATTCC others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0001c0001t0002 | 0/0 | 2629 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0001c0001t0003 | 0/0 | 2629 | 4 | 1 | 3 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0001c0001t0006 | 0/0 | 2628 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0001c0001t0009 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0001c0013t0001 | 0/0 | 2628 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0001c0016t0001 | 0/0 | 2628 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0001c0019t0007 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0002c0002t0002 | 0/1 | 2629 | 91 | 3 | 13 | 59 | 8 | 7 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0002c0002t0003 | 0/0 | 2629 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0002c0002t0011 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0003c0003t0002 | 0/0 | 2629 | 38 | 9 | 8 | 18 | 0 | 3 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0003c0003t0003 | 0/0 | 2629 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0003c0003t0006 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0003c0003t0010 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0004c0004t0003 | 0/0 | 2629 | 20 | 20 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0004c0004t0004 | 0/0 | 2629 | 12 | 0 | 6 | 1 | 1 | 4 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0004c0004t0005 | 0/0 | 2629 | 3 | 0 | 1 | 0 | 1 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0004c0009t0003 | 0/0 | 2629 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0005c0005t0001 | 0/0 | 2628 | 9 | 0 | 0 | 9 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0005c0005t0008 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0006c0007t0002 | 0/0 | 2629 | 5 | 5 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0006c0007t0003 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0007c0006t0002 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0007c0006t0003 | 0/0 | 2629 | 5 | 5 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0008c0010t0001 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2623): Show |
chr5 | 119447497 | 119547332 |
| a0008c0010t0002 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0008c0010t0003 | 0/0 | 2629 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0008c0012t0003 | 0/0 | 2629 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0008c0012t0012 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0009c0008t0003 | 0/0 | 2629 | 5 | 3 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0010c0011t0002 | 0/0 | 2629 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0011c0015t0002 | 0/0 | 2629 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0012c0018t0003 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0013c0017t0004 | 0/0 | 2629 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCC others(2624): Show |
chr5 | 119447497 | 119547332 |
| a0014c0014t0002 | 0/0 | 2629 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | ATTCG others(2624): Show |
chr5 | 119447497 | 119547332 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0243 | 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 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0261 | 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 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0269 | 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 |
| 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 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0291 | 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 |
| a0001c0001t0001g0293 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0315 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0001t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0013t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0013t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0016t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0001c0019t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0002c0002t0002g0130 | 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 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| 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 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0002c0002t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0187 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0210 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0003c0003t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0003c0003t0010g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0329 | 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 |
| a0004c0004t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0003g0336 | 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 |
| a0004c0004t0003g0340 | 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 |
| a0004c0004t0003g0346 | 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 |
| a0004c0004t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0004c0004t0004g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0004t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0009t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0009t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0004c0009t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0005c0005t0008g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0007t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0007t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0007t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0007t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0006c0007t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0006t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0006t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0006t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0007c0006t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0010t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0010t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0010t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0012t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0008c0012t0012g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0008t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0008t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0008t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0008t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0009c0008t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0010c0011t0002g0208 | 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 |
| a0011c0015t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0012c0018t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0013c0017t0004g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| a0014c0014t0002g0136 | 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 | g0076 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0152 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0124 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00280 | hp1 | a0004 | c0004 | t0004 | g0337 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0161 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00323 | hp1 | a0004 | c0004 | t0005 | g0183 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0162 | EUR | FIN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0227 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00639 | hp1 | a0008 | c0010 | t0002 | g0030 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00639 | hp2 | a0003 | c0003 | t0010 | g0196 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0220 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | CHS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00735 | hp1 | a0003 | c0003 | t0002 | g0207 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01081 | hp2 | a0004 | c0004 | t0005 | g0185 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0145 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01106 | hp1 | a0009 | c0008 | t0003 | g0027 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0169 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0214 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0210 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0211 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01243 | hp1 | a0009 | c0008 | t0003 | g0355 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0362 | AMR | PUR | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0360 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01255 | hp2 | a0011 | c0015 | t0002 | g0206 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01256 | hp2 | a0010 | c0011 | t0002 | g0208 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01258 | hp1 | a0010 | c0011 | t0002 | g0209 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01496 | hp1 | a0008 | c0012 | t0012 | g0363 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01496 | hp2 | a0004 | c0004 | t0004 | g0339 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0195 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | IBS | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0357 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01884 | hp2 | a0006 | c0007 | t0002 | g0204 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01891 | hp1 | a0009 | c0008 | t0003 | g0031 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01891 | hp2 | a0001 | c0019 | t0007 | g0023 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01934 | hp2 | a0004 | c0004 | t0004 | g0351 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0128 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0234 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0205 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01993 | hp1 | a0004 | c0004 | t0004 | g0349 | 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 | g0352 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02027 | hp1 | a0005 | c0005 | t0008 | g0236 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02040 | hp2 | a0005 | c0005 | t0001 | g0262 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02055 | hp2 | a0004 | c0009 | t0003 | g0331 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02056 | hp2 | a0005 | c0005 | t0001 | g0258 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | KHV | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02145 | hp1 | a0003 | c0003 | t0002 | g0212 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02145 | hp2 | a0003 | c0003 | t0002 | g0186 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02148 | hp2 | a0004 | c0004 | t0004 | g0348 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02155 | hp2 | a0005 | c0005 | t0001 | g0284 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02257 | hp1 | a0002 | c0002 | t0011 | g0155 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02257 | hp2 | a0004 | c0004 | t0003 | g0333 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02258 | hp1 | a0007 | c0006 | t0003 | g0015 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0361 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02280 | hp1 | a0004 | c0004 | t0003 | g0329 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02280 | hp2 | a0004 | c0004 | t0003 | g0321 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02300 | hp2 | a0004 | c0004 | t0004 | g0350 | AMR | PEL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02451 | hp1 | a0004 | c0009 | t0003 | g0330 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0143 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02602 | hp2 | a0003 | c0003 | t0002 | g0213 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02615 | hp2 | a0004 | c0004 | t0003 | g0344 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02622 | hp1 | a0004 | c0004 | t0003 | g0353 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02622 | hp2 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02630 | hp1 | a0004 | c0004 | t0003 | g0335 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02647 | hp1 | a0004 | c0004 | t0003 | g0325 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02647 | hp2 | a0006 | c0007 | t0003 | g0200 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0100 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02886 | hp1 | a0004 | c0004 | t0003 | g0324 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0117 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02896 | hp1 | a0003 | c0003 | t0002 | g0197 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02896 | hp2 | a0007 | c0006 | t0003 | g0014 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02897 | hp2 | a0007 | c0006 | t0003 | g0014 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02922 | hp1 | a0004 | c0004 | t0003 | g0346 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02970 | hp1 | a0007 | c0006 | t0003 | g0359 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0300 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03017 | hp2 | a0003 | c0003 | t0002 | g0218 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03041 | hp2 | a0006 | c0007 | t0002 | g0008 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0198 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03130 | hp2 | a0004 | c0004 | t0003 | g0338 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03209 | hp1 | a0004 | c0009 | t0003 | g0343 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03209 | hp2 | a0007 | c0006 | t0002 | g0203 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03225 | hp1 | a0004 | c0004 | t0003 | g0332 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03239 | hp1 | a0004 | c0004 | t0004 | g0328 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03453 | hp2 | a0004 | c0004 | t0003 | g0326 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03486 | hp2 | a0004 | c0004 | t0003 | g0342 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03490 | hp2 | a0004 | c0004 | t0004 | g0013 | 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 | g0013 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03516 | hp2 | a0004 | c0004 | t0003 | g0336 | AFR | ESN | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03540 | hp1 | a0009 | c0008 | t0003 | g0029 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03540 | hp2 | a0004 | c0004 | t0003 | g0341 | AFR | GWD | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0096 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0098 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03654 | hp1 | a0004 | c0004 | t0005 | g0184 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03654 | hp2 | a0001 | c0016 | t0001 | g0043 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03834 | hp1 | a0013 | c0017 | t0004 | g0322 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03927 | hp2 | a0002 | c0002 | t0003 | g0320 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0222 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04115 | hp2 | a0004 | c0004 | t0004 | g0327 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG04204 | hp2 | a0008 | c0012 | t0003 | g0025 | SAS | STU | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18522 | hp1 | a0004 | c0004 | t0003 | g0345 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18522 | hp2 | a0006 | c0007 | t0002 | g0008 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | CHB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0256 | 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 | g0288 | EAS | CHB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0358 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18940 | hp1 | a0005 | c0005 | t0001 | g0307 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18940 | hp2 | a0003 | c0003 | t0006 | g0153 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18947 | hp2 | a0004 | c0004 | t0004 | g0334 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18961 | hp2 | a0008 | c0010 | t0001 | g0271 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18963 | hp2 | a0003 | c0003 | t0002 | g0225 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0228 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18966 | hp2 | a0005 | c0005 | t0001 | g0241 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18972 | hp2 | a0005 | c0005 | t0001 | g0259 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0215 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18984 | hp1 | a0005 | c0005 | t0001 | g0260 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18985 | hp1 | a0003 | c0003 | t0002 | g0230 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0231 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18990 | hp2 | a0001 | c0013 | t0001 | g0275 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18993 | hp1 | a0003 | c0003 | t0002 | g0216 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18994 | hp1 | a0001 | c0013 | t0001 | g0257 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18994 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18999 | hp1 | a0003 | c0003 | t0002 | g0221 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19001 | hp2 | a0005 | c0005 | t0001 | g0282 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0235 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0226 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0219 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19030 | hp2 | a0009 | c0008 | t0003 | g0026 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19043 | hp1 | a0004 | c0004 | t0003 | g0347 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19055 | hp2 | a0003 | c0003 | t0002 | g0199 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0233 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19060 | hp1 | a0005 | c0005 | t0001 | g0238 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19064 | hp2 | a0014 | c0014 | t0002 | g0136 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19077 | hp2 | a0008 | c0010 | t0003 | g0028 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19083 | hp2 | a0003 | c0003 | t0002 | g0232 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0085 | 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 | g0315 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19087 | hp2 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19240 | hp1 | a0007 | c0006 | t0003 | g0015 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | YRI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20129 | hp2 | a0004 | c0004 | t0003 | g0323 | AFR | ASW | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0144 | EUR | TSI | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | GIH | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0106 | SAS | GIH | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0223 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | CLM | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0364 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02486 | hp1 | a0004 | c0004 | t0003 | g0340 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02486 | hp2 | a0012 | c0018 | t0003 | g0356 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG02559 | hp2 | a0004 | c0004 | t0003 | g0319 | AFR | ACB | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| HG06807 | hp2 | a0006 | c0007 | t0002 | g0201 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20300 | hp1 | a0003 | c0003 | t0002 | g0187 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA20300 | hp2 | a0003 | c0003 | t0002 | g0217 | AFR | USA | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| NA21309 | hp2 | a0006 | c0007 | t0002 | g0202 | AFR | LWK | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0097 | REF | REF | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0083 | REF | REF | HSD17B4_chr5_119447497_119547332 | HSD17B4 | chr5 | 119447497 | 119547332 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002 a0003 a0010 others(2): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): 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 | a0006 | 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 | a0009 a0012 |
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 | a0004 a0006 a0007 others(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 | a0002 a0004 a0006 others(4): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): 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 | a0006 a0007 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0016 a0004c0009 |
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 | a0009c0008 a0012c0018 |
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 | a0006c0007 a0007c0006 a0008c0012 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119452501 | C | G | 14 | a0001c0001t0002 a0001c0001t0006 a0002c0002t0002 others(11): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): 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 | a0008c0012t0012 | 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 | a0001c0001t0002 a0001c0001t0003 a0001c0019t0007 others(24): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): 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 | a0004c0004t0004 a0004c0004t0005 a0013c0017t0004 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:119452828 | C | T | 1 | a0003c0003t0002g0364 | 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 | a0008c0012t0012g0363 | 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 | 10 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(7): 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 | 171 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(168): 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 | a0001c0001t0002g0354 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | 170 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(167): 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 | 45 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(42): 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 | a0004c0004t0003g0353 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0002c0002t0002g0021 a0002c0002t0002g0022 |
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 | a0001c0019t0007g0023 | 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 | 168 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(165): 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 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0318 a0002c0002t0003g0320 a0004c0004t0003g0319 others(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 | 9 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(6): 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 | a0004c0004t0004g0348 a0004c0004t0004g0349 a0004c0004t0004g0350 others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.59-1031C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455284 | |||||||
| chr5:119455309 | G | A | 45 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(42): 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 | a0008c0012t0003g0025 | 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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | a0002c0002t0002g0180 | 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 | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): 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 | |||||||
| chr5:119455409 | C | T | 1 | a0001c0001t0006g0096 | 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 | a0001c0019t0007g0023 | 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 | 290 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(287): Show |
302 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.59-842T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 1/23 | chr5 | 119455473 | |||||||
| chr5:119455508 | C | G | 36 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0009 others(33): 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 | 45 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(42): 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 | a0002c0002t0002g0168 a0002c0002t0002g0169 a0002c0002t0002g0170 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0176 a0002c0002t0002g0177 others(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 | 77 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(74): 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 | a0001c0001t0002g0181 a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0003c0003t0002g0205 | 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 | 18 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0033 others(15): 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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(40): 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 | a0001c0001t0001g0064 a0001c0001t0001g0318 a0001c0019t0007g0023 others(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 | a0002c0002t0002g0004 a0002c0002t0002g0101 a0002c0002t0002g0102 others(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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): 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 | 32 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0021 others(29): Show |
34 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(31): 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 | a0001c0001t0003g0020 a0002c0002t0002g0146 a0004c0004t0003g0323 others(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 | a0002c0002t0002g0022 a0002c0002t0002g0147 a0002c0002t0002g0148 others(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 | a0002c0002t0002g0161 a0002c0002t0002g0162 a0002c0002t0002g0163 others(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 | a0002c0002t0002g0174 a0004c0004t0003g0340 a0004c0004t0003g0341 others(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 | a0001c0001t0001g0299 a0001c0001t0001g0301 a0001c0001t0001g0302 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0095 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0011c0015t0002g0206 | 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 | 286 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(283): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): 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 | a0001c0001t0001g0065 | 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 | 287 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(284): Show |
299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): 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 | a0008c0012t0012g0363 | 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 | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): 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 | a0001c0001t0001g0244 | 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 | 245 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(242): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(253): 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 | a0001c0001t0001g0243 a0001c0001t0001g0287 a0001c0001t0001g0288 others(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 | a0002c0002t0002g0168 | 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 | a0004c0004t0004g0352 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0245 a0001c0001t0001g0302 others(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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0002c0002t0002g0161 a0002c0002t0002g0162 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
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 | 85 | a0001c0001t0001g0318 a0001c0001t0002g0354 a0001c0001t0006g0188 others(82): 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 | a0006c0007t0002g0201 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0001c0001t0001g0062 | 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 | 36 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0009 others(33): 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 | a0005c0005t0001g0284 | 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 | a0008c0012t0012g0363 | 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 | a0002c0002t0002g0118 | 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 | a0001c0001t0002g0182 | 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 | 246 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(243): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(254): 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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0002c0002t0002g0146 a0002c0002t0002g0163 a0002c0002t0002g0164 |
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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0003c0003t0002g0233 | 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 | a0004c0004t0003g0353 | 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 | 92 | a0001c0001t0001g0283 a0002c0002t0002g0004 a0002c0002t0002g0005 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.112+2096C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119458464 | |||||||
| chr5:119458508 | A | AT | 97 | a0001c0001t0001g0019 a0001c0001t0001g0283 a0001c0001t0002g0181 others(94): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): 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 | a0001c0001t0001g0044 a0001c0001t0001g0318 a0002c0002t0003g0320 others(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 | a0001c0001t0001g0318 a0002c0002t0003g0320 a0004c0004t0003g0319 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0004c0004t0003g0323 a0004c0004t0003g0329 a0004c0004t0003g0332 others(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 | a0001c0001t0001g0281 | 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 | a0004c0004t0003g0324 | 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 | a0004c0004t0003g0329 a0004c0004t0003g0340 a0004c0004t0003g0341 others(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 | 47 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(44): 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 | a0002c0002t0002g0102 a0002c0002t0002g0149 |
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 | a0004c0004t0005g0185 | 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 | a0002c0002t0002g0124 | 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
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 | a0002c0002t0002g0006 a0002c0002t0002g0117 a0002c0002t0002g0118 others(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 | a0001c0001t0001g0304 a0002c0002t0002g0173 a0004c0004t0003g0338 others(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 | a0001c0001t0001g0280 | 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 | 52 | a0001c0001t0001g0019 a0001c0001t0002g0354 a0001c0001t0003g0020 others(49): 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 | 34 | a0003c0003t0002g0009 a0003c0003t0002g0199 a0003c0003t0002g0205 others(31): 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 | 36 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0009 others(33): 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 | a0001c0019t0007g0023 | 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 | 36 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0009 others(33): 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 | 3 | a0001c0001t0001g0012 a0001c0001t0001g0242 a0001c0001t0001g0279 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0001c0001t0001g0318 a0002c0002t0003g0320 a0004c0004t0003g0319 others(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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | a0001c0001t0001g0318 a0002c0002t0003g0320 a0004c0004t0003g0319 others(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 | a0002c0002t0002g0123 | 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 | a0007c0006t0002g0203 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 |
45 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(42): 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 | 2 | a0001c0001t0001g0010 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0045 | 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 | 45 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(42): 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 | 45 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(42): 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 | 191 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(188): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.112+4574G>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119460942 | |||||||
| chr5:119460944 | A | T | 191 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(188): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): 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 | a0001c0001t0001g0065 | 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 | 95 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0002c0002t0002g0116 | 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 | 98 | a0001c0001t0001g0087 a0001c0001t0001g0283 a0001c0001t0002g0181 others(95): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.112+4951A>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119461319 | |||||||
| chr5:119461358 | TC | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0246 a0001c0001t0001g0247 others(4): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 45 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(42): 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 | 42 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0009 others(39): 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 | a0001c0001t0001g0318 a0002c0002t0003g0320 a0004c0004t0003g0319 others(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 | a0003c0003t0002g0215 a0003c0003t0002g0216 a0003c0003t0002g0217 others(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 | 53 | a0001c0001t0001g0034 a0001c0001t0001g0066 a0001c0001t0001g0246 others(50): 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 | a0001c0001t0001g0059 a0001c0001t0001g0086 |
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 | 6 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0193 others(3): 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 | a0001c0001t0001g0094 | 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 | 39 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0042 others(36): 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 | a0001c0001t0002g0354 a0001c0016t0001g0043 a0001c0019t0007g0023 others(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 | a0001c0001t0001g0318 a0004c0004t0004g0328 a0004c0004t0004g0334 others(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 | 62 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0041 others(59): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): 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 | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(69): 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 | 4 | a0001c0001t0001g0001 a0001c0001t0002g0181 a0002c0002t0002g0125 others(1): 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 | a0001c0001t0001g0088 a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0304 | 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 | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): 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 | a0001c0001t0001g0287 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): 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 | a0002c0002t0002g0156 | 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 | a0003c0003t0002g0364 | 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 | a0008c0012t0012g0363 | 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 | a0006c0007t0002g0201 | 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 | a0001c0001t0002g0354 | 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 | 188 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(185): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.112+6730C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463098 | |||||||
| chr5:119463213 | C | G | 91 | a0001c0001t0001g0283 a0002c0002t0002g0004 a0002c0002t0002g0005 others(88): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.112+6845C>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119463213 | |||||||
| chr5:119463249 | G | T | 85 | a0001c0001t0001g0318 a0001c0001t0002g0354 a0001c0001t0006g0188 others(82): 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 | a0004c0004t0004g0334 | 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 | a0004c0004t0003g0329 a0004c0004t0003g0340 |
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 | 85 | a0001c0001t0001g0318 a0001c0001t0002g0354 a0001c0001t0006g0188 others(82): 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 | 100 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): 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 | 7 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0003c0003t0002g0009 others(4): 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 | 11 | a0001c0001t0006g0096 a0002c0002t0002g0119 a0002c0002t0002g0146 others(8): 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 | a0001c0001t0002g0181 | 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 | a0001c0001t0001g0059 a0002c0002t0002g0149 a0003c0003t0002g0199 others(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 | a0001c0001t0001g0058 a0003c0003t0002g0210 a0003c0003t0002g0212 others(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 | 21 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(18): 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 | 115 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0018 others(112): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): 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 | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): 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 | 14 | a0001c0001t0001g0019 a0001c0001t0001g0305 a0001c0001t0002g0181 others(11): 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 | a0002c0002t0002g0150 | 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 | a0001c0001t0001g0237 a0001c0001t0001g0318 a0004c0004t0003g0319 others(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 | a0001c0001t0001g0058 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 36 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0009 others(33): 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0006g0188 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0077 |
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 | 94 | a0001c0001t0001g0087 a0002c0002t0002g0004 a0002c0002t0002g0005 others(91): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): 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 | a0004c0004t0004g0352 | 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 | a0005c0005t0001g0238 | 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0009c0008t0003g0026 others(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 | a0001c0001t0001g0094 | 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 | a0004c0004t0003g0347 | 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 | 6 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(3): 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 | a0001c0001t0001g0071 a0001c0001t0001g0082 |
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 | 85 | a0001c0001t0001g0318 a0001c0001t0002g0354 a0001c0001t0006g0188 others(82): 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 | a0007c0006t0002g0203 | 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 | 6 | a0003c0003t0002g0009 a0003c0003t0002g0221 a0003c0003t0002g0228 others(3): 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0040 |
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 | 3 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0077 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0002c0002t0002g0151 | 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 | a0002c0002t0002g0101 a0002c0002t0002g0127 |
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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | 6 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(3): 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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | 42 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0009 others(39): 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 | a0007c0006t0002g0203 | 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | 46 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(43): 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 | a0004c0004t0004g0348 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | 4 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 others(1): 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 | 245 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(242): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(253): 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 | a0001c0001t0001g0078 a0001c0001t0001g0088 |
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 | a0003c0003t0002g0226 | 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 | a0001c0001t0001g0076 | 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 | 8 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0006c0007t0002g0008 others(5): 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 | a0008c0012t0012g0363 | 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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | 12 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(9): 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 | 13 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0046 others(10): 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 | 286 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(283): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): 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 | a0001c0001t0001g0253 | 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 | 12 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(9): 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 | a0008c0012t0012g0363 | 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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0002c0002t0002g0157 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0002c0002t0002g0139 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0004c0004t0004g0348 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0002c0002t0002g0098 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | 64 | a0001c0001t0001g0019 a0001c0001t0001g0318 a0001c0001t0002g0181 others(61): 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 | 126 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(123): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0004c0004t0003g0353 |
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 | 4 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 others(1): 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 | a0001c0001t0001g0033 | 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 | 12 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0003c0003t0002g0007 others(9): 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 | a0001c0001t0001g0094 a0001c0001t0002g0354 a0001c0001t0006g0188 others(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 | a0002c0002t0002g0110 | 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 | 51 | a0001c0001t0001g0318 a0001c0001t0002g0354 a0001c0001t0006g0188 others(48): 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 | a0001c0001t0001g0318 a0002c0002t0003g0320 a0004c0004t0003g0319 others(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 | 129 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0002c0002t0002g0004 others(126): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(130): 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 | a0001c0001t0001g0019 | 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 | 124 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(121): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.113-3183C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119470725 | |||||||
| chr5:119470768 | G | C | 127 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(124): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.113-3140G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 2/23 | chr5 | 119470768 | |||||||
| chr5:119470889 | A | G | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0281 others(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 | a0003c0003t0010g0196 | 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 | a0001c0001t0001g0311 | 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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0268 a0001c0001t0001g0269 others(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 | a0001c0001t0001g0247 | 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 | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(329): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): 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 | a0001c0001t0009g0300 | 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 | 3 | a0001c0001t0001g0010 a0001c0001t0001g0193 a0001c0001t0001g0278 |
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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | 9 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0006c0007t0002g0008 others(6): 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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(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 | a0001c0001t0006g0096 | 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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | a0002c0002t0002g0175 | 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 | a0004c0004t0003g0321 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 a0009c0008t0003g0026 others(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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0004c0004t0004g0352 | 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 | 15 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0048 others(12): 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 | 9 | a0001c0001t0002g0354 a0001c0001t0006g0188 a0006c0007t0002g0008 others(6): 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 | a0002c0002t0002g0138 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0006c0007t0002g0202 a0006c0007t0003g0200 |
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 | a0001c0001t0001g0189 | 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 | 4 | a0001c0001t0001g0012 a0001c0001t0001g0242 a0001c0001t0001g0278 others(1): 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 | 180 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0056 others(177): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): 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 | 92 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0065 others(89): 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 | 6 | a0001c0001t0001g0010 a0001c0001t0001g0193 a0001c0001t0001g0237 others(3): 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 | a0001c0001t0001g0041 a0001c0001t0001g0092 |
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 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0006g0096 | 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 | 126 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(123): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0006g0096 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 245 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(242): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(253): 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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0001c0001t0001g0055 | 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 | a0001c0001t0006g0188 | 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 | a0003c0003t0002g0221 | 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 | 100 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): 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 | a0004c0004t0003g0347 | 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 | 280 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(277): Show |
292 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(289): 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 | a0001c0001t0001g0019 | 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 | a0004c0004t0004g0348 | 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 | a0003c0003t0002g0212 | 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 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
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 | a0003c0003t0003g0358 | 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 | 139 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(136): 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 | a0002c0002t0002g0021 a0002c0002t0002g0022 |
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 | 101 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): 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 | a0001c0001t0001g0051 | 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 | 134 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(131): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): 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 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0041 | 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 | a0002c0002t0002g0110 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0004c0004t0003g0319 a0004c0004t0003g0324 a0004c0004t0003g0325 others(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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | a0001c0001t0001g0245 a0001c0001t0001g0254 a0001c0001t0001g0255 others(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 | a0001c0019t0007g0023 | 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 | 248 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(245): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.349+615A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 6/23 | chr5 | 119476485 | |||||||
| chr5:119476688 | A | C | 101 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): 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 | a0001c0001t0001g0077 a0001c0001t0001g0087 |
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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | 136 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(133): 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 | 91 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): 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 | 286 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(283): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): 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 | a0002c0002t0002g0128 a0002c0002t0002g0150 |
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 | a0002c0002t0011g0155 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | 132 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0283 others(129): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): 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 | a0001c0001t0001g0041 a0001c0001t0001g0092 |
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 | 248 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(245): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(256): 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 | a0003c0003t0002g0234 | 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 | a0001c0001t0001g0240 | 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 | a0002c0002t0002g0143 | 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0001c0001t0002g0354 | 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 | a0002c0002t0002g0101 a0002c0002t0002g0127 |
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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | a0006c0007t0002g0201 | 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0237 others(87): 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 | a0001c0001t0009g0300 | 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 | a0001c0001t0001g0239 a0001c0001t0001g0243 a0001c0001t0001g0244 others(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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0002c0002t0002g0141 | 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 | 2 | a0006c0007t0002g0008 a0006c0007t0002g0204 |
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 | a0002c0002t0002g0114 | 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 | a0002c0002t0002g0114 | 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 | a0001c0013t0001g0257 | 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0065 | 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 | a0003c0003t0002g0205 a0003c0003t0002g0207 a0003c0003t0002g0210 others(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 | a0004c0004t0004g0334 | 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 | a0002c0002t0002g0147 | 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 | a0002c0002t0002g0141 | 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 | a0002c0002t0002g0124 | 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 | a0001c0019t0007g0023 | 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 | a0004c0004t0003g0321 | 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 | 9 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(6): 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 | a0008c0010t0003g0028 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0004c0004t0003g0338 | 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 | a0001c0001t0001g0318 | 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 | a0002c0002t0002g0149 | 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 | 7 | a0001c0001t0001g0318 a0006c0007t0002g0008 a0006c0007t0002g0201 others(4): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0003c0003t0003g0358 | 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 | a0004c0004t0004g0348 a0004c0004t0004g0349 a0004c0004t0004g0350 others(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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | 7 | a0001c0001t0001g0318 a0006c0007t0002g0008 a0006c0007t0002g0201 others(4): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0001c0001t0001g0033 | 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 | a0002c0002t0002g0149 | 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 | 8 | a0001c0001t0001g0011 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): 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 | a0004c0004t0003g0340 | 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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0001c0001t0003g0020 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0092 |
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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0004c0004t0003g0319 a0004c0004t0003g0324 a0004c0004t0003g0325 others(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 | a0002c0002t0002g0170 | 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 | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0046 others(9): 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 | a0001c0001t0001g0276 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0004c0004t0005g0183 a0004c0004t0005g0184 a0004c0004t0005g0185 |
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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | 237 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(234): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(244): 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0050 | 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 | a0008c0012t0012g0363 | 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 | a0002c0002t0002g0165 | 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 | a0001c0001t0001g0298 | 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 | a0004c0004t0004g0327 | 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 | a0003c0003t0002g0219 | 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 | a0003c0003t0010g0196 | 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 | a0003c0003t0002g0233 | 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 | a0003c0003t0002g0226 | 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 | 2 | a0006c0007t0002g0008 a0006c0007t0002g0204 |
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 | a0001c0001t0002g0354 a0002c0002t0002g0149 |
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 | 86 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): 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 | 86 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): 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 | 6 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(3): 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 | a0004c0004t0005g0183 | 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 | a0002c0002t0002g0139 | 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 | a0001c0001t0002g0354 a0001c0001t0006g0188 |
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 | a0001c0001t0001g0267 a0001c0001t0001g0276 |
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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0064 | 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 | a0004c0004t0005g0183 a0004c0004t0005g0184 a0004c0004t0005g0185 |
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 | a0004c0004t0003g0329 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0002c0002t0002g0127 | 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 | a0002c0002t0002g0151 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0004c0004t0004g0328 | 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 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(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 | a0002c0002t0002g0116 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0053 |
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 | a0003c0003t0002g0233 | 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 | a0002c0002t0002g0129 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 138 | a0001c0001t0001g0035 a0001c0001t0001g0067 a0001c0001t0001g0090 others(135): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): 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 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0032 others(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 | a0004c0004t0003g0347 | 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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0001c0001t0001g0065 a0002c0002t0002g0128 a0002c0002t0002g0150 |
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 | a0003c0003t0002g0199 a0003c0003t0002g0226 a0003c0003t0002g0230 |
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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0009c0008t0003g0029 a0009c0008t0003g0031 |
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 | 89 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): 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 | 9 | a0006c0007t0002g0201 a0006c0007t0002g0202 a0006c0007t0003g0200 others(6): 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 | a0003c0003t0002g0230 | 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 | a0002c0002t0002g0006 a0002c0002t0002g0144 |
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 | a0001c0001t0001g0050 | 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 | a0003c0003t0010g0196 | 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 | a0001c0001t0001g0046 | 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 | a0002c0002t0002g0173 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0059 | 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 | a0007c0006t0002g0203 | 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 | 127 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(124): 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 | a0008c0012t0012g0363 | 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 | 79 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0239 others(76): 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 | a0003c0003t0002g0215 a0003c0003t0002g0216 |
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 | a0008c0012t0012g0363 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.714+430A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 9/23 | chr5 | 119489713 | |||||||
| chr5:119489833 | G | GT | 6 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0001c0001t0001g0310 | 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 | 108 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(105): 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 | 38 | a0001c0001t0002g0354 a0002c0002t0002g0110 a0002c0002t0002g0147 others(35): 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 | 46 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(43): 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0281 | 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 | 98 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(95): 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 | a0001c0001t0001g0075 a0001c0001t0001g0081 |
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 | a0002c0002t0002g0098 a0002c0002t0002g0123 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0005c0005t0001g0259 | 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0002c0002t0011g0155 | 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 | 2 | a0006c0007t0002g0008 a0006c0007t0002g0204 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0001c0001t0001g0042 | 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 | 274 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(271): Show |
286 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(283): 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 | a0001c0001t0001g0244 a0001c0001t0001g0268 a0001c0001t0001g0301 others(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 | 284 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(281): Show |
296 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(293): 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 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0002c0002t0002g0170 | 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 | 187 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0001g0318 others(184): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): 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 | a0002c0002t0002g0117 | 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 | a0007c0006t0002g0203 | 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 | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): 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 | a0001c0001t0001g0280 | 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 | 89 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): 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 | a0001c0001t0001g0019 | 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 | a0002c0002t0002g0145 | 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 | a0001c0019t0007g0023 | 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0063 |
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 | a0001c0019t0007g0023 | 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 | a0002c0002t0002g0140 | 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 | a0002c0002t0002g0138 | 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 | 34 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(31): 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 | 34 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(31): 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0318 | 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 | a0007c0006t0002g0203 | 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0001c0019t0007g0023 | 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0001c0001t0001g0289 | 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 | a0004c0004t0004g0328 a0004c0004t0004g0337 a0004c0004t0005g0183 |
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 | a0004c0004t0004g0013 | 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 | a0002c0002t0002g0165 | 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 | a0004c0004t0004g0339 a0004c0004t0005g0184 |
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 | a0002c0002t0002g0165 a0004c0004t0004g0339 a0004c0004t0005g0184 |
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 | a0005c0005t0001g0259 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(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 |
48 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0038 others(45): Show |
48 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(45): 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0283 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0042 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0003 a0001c0001t0002g0354 a0002c0002t0002g0022 others(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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0076 | 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 | a0003c0003t0002g0186 | 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 | a0001c0001t0001g0276 | 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 | a0002c0002t0002g0141 | 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 | a0002c0002t0002g0099 | 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 | a0002c0002t0002g0099 | 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 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(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 | a0002c0002t0002g0140 | 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 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(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 | 102 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): 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 | a0001c0001t0001g0054 a0001c0001t0001g0318 a0004c0004t0003g0319 others(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 | 8 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(5): 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 | a0003c0003t0010g0196 | 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 | a0004c0004t0003g0344 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0070 |
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 | a0002c0002t0002g0118 | 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 | a0003c0003t0002g0186 | 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 | 1 | a0001c0001t0001g0012 | 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 | 274 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(271): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | 97 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): 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 | a0001c0019t0007g0023 | 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 | a0003c0003t0002g0224 | 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 | 34 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(31): 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 | a0002c0002t0002g0148 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0089 | 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 | 276 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(273): Show |
285 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(282): 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 | a0008c0012t0012g0363 | 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 | a0004c0004t0003g0335 a0004c0004t0003g0338 a0004c0004t0003g0346 |
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 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
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 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | 2 | a0006c0007t0002g0008 a0006c0007t0002g0204 |
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 | a0003c0003t0002g0212 | 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 | 277 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(274): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.972+504T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119497150 | |||||||
| chr5:119497209 | T | TG | 274 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(271): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 34 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(31): 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 | a0005c0005t0001g0260 | 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 | a0002c0002t0002g0160 a0002c0002t0002g0174 |
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 | a0002c0002t0002g0165 | 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 | 133 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(130): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0003g0020 | 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 | a0002c0002t0002g0120 | 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 | a0001c0001t0001g0056 | 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 | a0002c0002t0002g0175 | 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 | a0002c0002t0002g0175 | 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 | a0001c0019t0007g0023 | 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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0001c0001t0001g0255 | 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 | a0004c0004t0005g0185 | 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 | a0001c0001t0001g0042 | 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 | a0002c0002t0002g0139 | 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 | a0001c0001t0001g0045 | 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 | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): 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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | a0002c0002t0002g0120 | 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 | a0004c0004t0003g0335 | 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 | 96 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): 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 | a0007c0006t0002g0203 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0001c0001t0003g0020 | 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 | 34 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(31): 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 | 184 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.973-639C>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 12/23 | chr5 | 119498678 | |||||||
| chr5:119498683 | C | T | 44 | a0001c0001t0001g0318 a0003c0003t0002g0007 a0003c0003t0002g0197 others(41): 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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): 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 | a0001c0001t0001g0095 | 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 | a0004c0004t0004g0334 | 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 | a0007c0006t0002g0203 | 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 | a0002c0002t0002g0108 | 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 | 184 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): 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 | a0003c0003t0002g0205 a0003c0003t0002g0207 a0003c0003t0002g0210 others(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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0299 a0001c0001t0001g0311 |
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 | a0001c0001t0001g0317 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0009c0008t0003g0027 | 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 | 40 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0070 others(37): 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 | 135 | a0001c0001t0001g0084 a0001c0001t0001g0294 a0001c0001t0001g0318 others(132): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): 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 | a0006c0007t0003g0200 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0002c0002t0002g0121 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0003c0003t0010g0196 | 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 | a0008c0012t0012g0363 | 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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0001c0001t0001g0248 a0001c0001t0001g0265 a0001c0001t0001g0266 others(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 | 278 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(275): Show |
289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): 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 | a0002c0002t0002g0103 a0002c0002t0002g0107 |
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 | a0004c0009t0003g0330 a0004c0009t0003g0331 a0004c0009t0003g0343 |
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 | a0008c0012t0012g0363 | 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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): 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 | a0002c0002t0002g0146 | 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 | a0001c0001t0001g0019 a0001c0001t0009g0300 |
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 | 98 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(95): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1261+46C>T | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119502138 | |||||||
| chr5:119502139 | A | G | 147 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(144): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): 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 | a0001c0001t0009g0300 | 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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): 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 | a0004c0004t0004g0351 | 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 | 33 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(30): 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 | 6 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 others(3): 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 | 186 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(183): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): 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 | a0001c0001t0001g0239 a0001c0001t0001g0243 a0001c0001t0001g0244 others(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 | 184 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): 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 | a0003c0003t0002g0199 a0003c0003t0002g0226 a0003c0003t0002g0230 |
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 | a0007c0006t0002g0203 | 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 | 31 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0050 others(28): 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0298 a0003c0003t0002g0186 others(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 | a0001c0001t0001g0245 a0001c0001t0001g0249 a0001c0001t0001g0252 others(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 |
27 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(24): 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 | a0001c0001t0001g0019 a0001c0001t0001g0237 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0283 a0005c0005t0001g0282 |
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 | a0001c0001t0001g0286 a0005c0005t0001g0262 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0002c0002t0002g0100 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0054 others(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 | 19 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0215 others(16): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | 6 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 others(3): 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 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(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 | a0002c0002t0002g0132 | 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 | 6 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 others(3): 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 | a0002c0002t0002g0151 | 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 | 123 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(120): 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 | a0001c0001t0002g0354 | 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 | a0001c0001t0002g0181 | 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 | 145 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1261+1920G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 14/23 | chr5 | 119504012 | |||||||
| chr5:119504098 | G | A | 125 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(122): 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0003c0003t0002g0212 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0005c0005t0001g0284 | 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 | a0001c0001t0001g0242 | 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 | a0002c0002t0002g0006 a0002c0002t0002g0144 |
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 | a0002c0002t0002g0141 | 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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | 191 | a0001c0001t0001g0318 a0001c0001t0002g0181 a0001c0001t0002g0182 others(188): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0001c0001t0002g0182 | 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 | a0005c0005t0001g0238 a0005c0005t0001g0241 a0005c0005t0008g0236 |
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 | a0001c0001t0001g0078 a0001c0001t0001g0088 |
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 | a0002c0002t0002g0098 | 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 | a0008c0010t0001g0271 | 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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): 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 | a0004c0004t0003g0336 | 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 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0002c0002t0002g0154 | 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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0054 |
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 | a0008c0012t0012g0363 | 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 | 147 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(144): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | 8 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(5): 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 | a0001c0001t0001g0042 | 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 | 145 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): 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 | a0004c0004t0003g0353 | 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 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0297 others(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 | a0003c0003t0010g0196 | 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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0001c0001t0001g0243 a0001c0001t0001g0254 a0001c0001t0001g0287 others(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 | a0004c0004t0003g0321 | 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 | 145 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): 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 | a0002c0002t0002g0109 a0002c0002t0002g0115 a0002c0002t0002g0128 others(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 | a0004c0004t0003g0341 | 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 | a0008c0012t0003g0025 | 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 | 48 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(45): 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 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0283 | 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 | a0008c0012t0012g0363 | 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 | a0002c0002t0002g0164 | 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 | a0001c0001t0003g0020 a0003c0003t0002g0199 a0003c0003t0002g0225 others(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 | 275 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(272): Show |
287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): 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 | a0001c0001t0003g0020 a0003c0003t0002g0199 a0003c0003t0002g0225 others(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 | 49 | a0001c0001t0001g0011 a0001c0001t0001g0246 a0001c0001t0001g0248 others(46): 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 | a0001c0001t0001g0189 | 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 | a0002c0002t0002g0099 | 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 | 96 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): 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 | 87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): 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 | 233 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(230): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(238): 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0001c0001t0001g0261 | 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 | a0004c0004t0004g0013 a0004c0004t0004g0327 a0004c0004t0004g0328 others(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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): 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 | a0002c0002t0002g0133 | 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 | 35 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(32): 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 | 40 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(37): 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 | a0001c0001t0006g0096 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0040 |
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 | 145 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 40 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(37): 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 | a0002c0002t0002g0151 | 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 | 40 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(37): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 5 | a0006c0007t0002g0202 a0006c0007t0003g0200 a0007c0006t0003g0014 others(2): 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 |
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 | a0002c0002t0002g0139 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0001c0001t0001g0073 | 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 | 145 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): 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 | a0007c0006t0002g0203 | 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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1437+200G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 16/23 | chr5 | 119509444 | |||||||
| chr5:119509550 | T | A | 48 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(45): 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 | a0004c0004t0004g0013 a0004c0004t0004g0328 |
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 | 4 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0077 others(1): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 48 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(45): 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0019 a0001c0001t0009g0300 |
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 | a0001c0001t0003g0020 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0003c0003t0002g0228 a0003c0003t0002g0229 |
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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0316 | 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 | a0002c0002t0002g0166 | 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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0003c0003t0002g0224 | 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 | a0002c0002t0002g0099 | 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 | 48 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(45): 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 | 34 | a0001c0001t0002g0354 a0003c0003t0002g0009 a0003c0003t0002g0199 others(31): 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 | 145 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): 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 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0251 |
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 | 39 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(36): 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
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 | 8 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(5): 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 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(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 | a0001c0001t0003g0020 | 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 | a0002c0002t0002g0160 a0002c0002t0002g0174 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0001c0001t0001g0302 | 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 | 8 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(5): 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 | a0001c0001t0006g0096 | 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 | a0002c0002t0002g0194 a0002c0002t0002g0195 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0239 a0001c0001t0001g0243 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0255 a0001c0001t0001g0274 others(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 | a0001c0001t0001g0049 | 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 | a0008c0012t0003g0025 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0004c0009t0003g0330 a0004c0009t0003g0331 a0004c0009t0003g0343 |
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 | a0004c0009t0003g0330 a0004c0009t0003g0331 a0004c0009t0003g0343 |
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 | 235 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(232): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(240): 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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0283 a0001c0001t0001g0312 a0001c0001t0001g0313 others(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 | a0003c0003t0002g0220 | 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 | a0003c0003t0002g0205 a0003c0003t0002g0207 a0003c0003t0002g0210 others(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 | a0001c0001t0001g0040 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0046 others(9): 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 | a0002c0002t0002g0102 | 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 | 79 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0239 others(76): 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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | a0001c0019t0007g0023 | 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 | 96 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): 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 | 87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): 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 | a0001c0001t0001g0095 | 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 | a0006c0007t0002g0202 a0006c0007t0003g0200 |
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 | a0004c0004t0003g0335 a0004c0004t0003g0338 a0004c0004t0003g0346 |
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 | a0004c0004t0004g0350 a0004c0004t0004g0351 |
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 | a0007c0006t0002g0203 | 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 | a0008c0012t0012g0363 | 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 | a0001c0019t0007g0023 | 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 | a0004c0004t0003g0319 a0004c0004t0003g0324 a0004c0004t0003g0325 others(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 | a0001c0001t0001g0318 a0004c0004t0003g0321 a0004c0004t0004g0013 others(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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0253 a0001c0001t0001g0265 a0001c0001t0001g0266 |
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 | a0008c0010t0002g0030 | 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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): 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 | a0003c0003t0002g0205 a0003c0003t0002g0207 a0003c0003t0002g0210 others(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 | a0001c0019t0007g0023 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0002c0002t0002g0195 | 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 | a0003c0003t0002g0224 | 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 | a0003c0003t0010g0196 | 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 | a0006c0007t0002g0201 | 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 | a0003c0003t0002g0199 | 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 | a0001c0001t0003g0020 | 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0001c0001t0001g0296 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 92 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): 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 | a0001c0001t0003g0020 | 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 | a0002c0002t0002g0099 | 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 | a0001c0001t0001g0256 | 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 | a0003c0003t0002g0186 | 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 | 48 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(45): 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 | 138 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(135): 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 | 87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): 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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | a0001c0001t0006g0096 | 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 | a0002c0002t0002g0006 a0002c0002t0002g0144 |
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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0003g0020 a0004c0004t0003g0319 a0004c0004t0003g0323 others(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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | 95 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(92): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): 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 | a0001c0001t0001g0062 | 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 | 92 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): 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 | a0002c0002t0002g0159 | 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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): 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 | a0001c0001t0001g0192 | 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 | a0005c0005t0001g0284 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0318 a0004c0004t0003g0319 a0004c0004t0003g0321 others(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 | a0004c0009t0003g0343 | 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 | a0001c0001t0003g0020 | 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 | a0002c0002t0002g0100 a0002c0002t0002g0125 |
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 | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | 12 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(9): 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 | a0003c0003t0002g0210 a0003c0003t0002g0214 |
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 | 101 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): 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 | 140 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(137): 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 | a0001c0001t0001g0085 a0001c0001t0001g0093 |
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 | a0007c0006t0002g0203 | 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 | 6 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 others(3): 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 | a0002c0002t0002g0106 a0002c0002t0002g0143 a0002c0002t0003g0320 |
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 | 6 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 others(3): 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 | a0008c0012t0012g0363 | 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 | a0001c0001t0003g0020 | 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 | a0004c0004t0004g0013 a0004c0004t0004g0327 a0004c0004t0004g0328 others(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 | 37 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(34): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0007c0006t0002g0203 | 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 | 128 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(125): 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 | 92 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1504-5022T>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 17/23 | chr5 | 119520194 | |||||||
| chr5:119520334 | A | C | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | 7 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0063 others(4): 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 | a0002c0002t0002g0123 | 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 | 11 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(8): 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 | 11 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(8): 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 | a0003c0003t0002g0219 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
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 | a0003c0003t0002g0199 a0003c0003t0002g0226 a0003c0003t0002g0230 |
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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0001c0001t0001g0301 | 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 | 104 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(101): 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 | 98 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(95): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): 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 | a0001c0001t0003g0020 a0004c0004t0003g0323 a0004c0004t0003g0344 others(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 | a0001c0001t0001g0305 | 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 | a0008c0012t0012g0363 | 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 | a0001c0013t0001g0275 | 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 | 33 | a0003c0003t0002g0009 a0003c0003t0002g0199 a0003c0003t0002g0205 others(30): 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 | a0002c0002t0002g0115 | 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 | a0002c0002t0011g0155 | 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 | 91 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(88): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): 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 | a0004c0004t0003g0324 | 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 | 196 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(193): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(202): 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 | a0001c0001t0001g0066 | 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 | a0007c0006t0002g0203 | 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 | 80 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0239 others(77): 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 | 97 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): 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 | a0001c0001t0001g0024 | 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0002c0002t0002g0103 a0002c0002t0002g0107 a0002c0002t0002g0108 others(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 | 94 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(91): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): 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 | a0001c0001t0002g0354 | 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 | a0004c0009t0003g0330 a0004c0009t0003g0331 a0008c0010t0003g0028 |
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 | a0002c0002t0002g0123 | 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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | 139 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(136): 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 | a0001c0001t0006g0188 | 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 | 2 | a0006c0007t0002g0008 a0006c0007t0002g0204 |
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 | a0001c0013t0001g0275 | 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 | 139 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(136): 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 | a0001c0001t0001g0311 | 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 | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0046 others(9): 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 | a0001c0001t0001g0024 | 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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0270 | 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 | 92 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): 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 | a0001c0001t0006g0096 | 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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | |||||||
| chr5:119524865 | T | C | 1 | a0008c0010t0003g0028 | 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 | 2 | a0006c0007t0002g0008 a0006c0007t0002g0204 |
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 | a0002c0002t0002g0140 | 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 | 15 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0048 others(12): 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 | a0007c0006t0002g0203 | 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 | a0001c0001t0001g0296 | 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | 92 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1573+247G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 18/23 | chr5 | 119525532 | |||||||
| chr5:119525713 | G | GTT | 46 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(43): 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 a0009c0008t0003g0026 others(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 | a0003c0003t0010g0196 | 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 | a0008c0010t0003g0028 | 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0076 | 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 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(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 | a0003c0003t0010g0196 | 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 | a0003c0003t0002g0224 | 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 |
283 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(280): Show |
295 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(292): 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 | a0003c0003t0002g0224 | 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 | a0001c0001t0003g0020 a0001c0019t0007g0023 a0003c0003t0002g0186 others(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 | a0007c0006t0002g0203 | 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 | a0001c0001t0003g0020 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0010c0011t0002g0208 a0010c0011t0002g0209 |
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 | 36 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(33): 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0054 | 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 | a0007c0006t0002g0203 | 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 | a0007c0006t0002g0203 | 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 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
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 | a0001c0001t0006g0096 | 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 | a0001c0001t0006g0188 | 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 | a0008c0012t0003g0025 | 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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | a0001c0001t0002g0354 | 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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): 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 | a0002c0002t0002g0154 | 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 | a0001c0001t0002g0354 | 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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0041 | 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 | 8 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(5): 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 | a0002c0002t0002g0141 | 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 | a0001c0001t0001g0313 | 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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0003c0003t0002g0219 | 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 | a0004c0004t0004g0013 a0004c0004t0004g0328 |
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 | 12 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(9): 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 | 97 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): 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 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
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 | a0002c0002t0002g0021 a0002c0002t0002g0022 |
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 | a0001c0001t0001g0276 | 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 | a0004c0004t0003g0321 a0004c0004t0004g0013 a0004c0004t0004g0327 others(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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): 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 | 33 | a0003c0003t0002g0009 a0003c0003t0002g0199 a0003c0003t0002g0205 others(30): 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 | a0002c0002t0002g0169 | 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 | 79 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0239 others(76): 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0002g0354 | 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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1854+373A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 21/23 | chr5 | 119530353 | |||||||
| chr5:119530399 | A | C | 286 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(283): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): 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 | a0001c0001t0001g0264 | 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 | 97 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): 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 | 92 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(89): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): 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 | 9 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(6): 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 | a0008c0012t0012g0363 | 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 | 26 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0032 others(23): 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 | 83 | a0001c0001t0001g0050 a0001c0001t0001g0070 a0001c0001t0001g0071 others(80): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): 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 | a0001c0001t0001g0267 a0001c0001t0001g0276 a0002c0002t0002g0004 others(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 | a0008c0010t0003g0028 | 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 | a0008c0012t0012g0363 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | 5 | a0006c0007t0002g0008 a0006c0007t0002g0202 a0006c0007t0002g0204 others(2): 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 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
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 | 36 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(33): 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 | a0003c0003t0002g0211 a0003c0003t0002g0225 |
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 | 109 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(106): 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 | 163 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0239 others(160): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0001g0263 | 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 | 10 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0240 others(7): 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 | 90 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0237 others(87): 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 | a0001c0001t0001g0288 a0001c0001t0001g0290 |
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 | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(89): 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 | a0002c0002t0002g0166 | 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 | a0003c0003t0002g0219 | 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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1993+74G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119531478 | |||||||
| chr5:119531563 | AGG | A | 91 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(88): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): 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 | a0001c0001t0003g0020 a0003c0003t0002g0186 a0003c0003t0002g0187 others(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 | 51 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0019 others(48): 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 | 76 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0239 others(73): 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 | 10 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(7): 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 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(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 | 183 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(180): 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 | a0002c0002t0002g0160 a0002c0002t0002g0174 |
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 | a0002c0002t0002g0119 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0006g0188 | 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 | 28 | a0004c0004t0003g0321 a0004c0004t0004g0013 a0004c0004t0004g0327 others(25): 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 | a0004c0004t0004g0013 a0004c0004t0004g0327 a0004c0004t0004g0328 others(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 | 286 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(283): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0002g0182 | 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 | 28 | a0004c0004t0003g0321 a0004c0004t0004g0013 a0004c0004t0004g0327 others(25): 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 | a0001c0001t0001g0055 | 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 |
86 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | a0008c0012t0012g0363 | 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 | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(329): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): 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 | a0014c0014t0002g0136 | 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 | a0001c0001t0001g0036 | 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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): 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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): 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 | 14 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(11): 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 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(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 | a0002c0002t0002g0021 a0002c0002t0002g0022 |
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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | a0001c0001t0001g0095 | 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 | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(329): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): 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 | a0008c0012t0003g0025 a0008c0012t0012g0363 |
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 | 36 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(33): 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 | 36 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(33): 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 | a0002c0002t0002g0176 a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 95 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(92): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1994-2085G>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534338 | |||||||
| chr5:119534376 | AC | A | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | a0001c0001t0001g0310 | 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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1994-1666G>A | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534757 | |||||||
| chr5:119534854 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0246 a0001c0001t0001g0247 others(4): 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 | 95 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(92): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1994-1537A>G | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 22/23 | chr5 | 119534886 | |||||||
| chr5:119534966 | CT | C | 197 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(194): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): 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 | a0008c0012t0012g0363 | 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 | 36 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(33): 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 | a0001c0019t0007g0023 | 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 | 80 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0239 others(77): 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 | a0008c0012t0012g0363 | 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 | 9 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(6): 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 | a0001c0001t0001g0246 | 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 | 97 | a0001c0001t0003g0020 a0001c0001t0003g0360 a0001c0001t0003g0361 others(94): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): 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 | a0004c0004t0003g0319 a0004c0004t0003g0323 a0004c0004t0003g0324 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0003c0003t0003g0357 others(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 | a0003c0003t0002g0219 | 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 | a0001c0001t0001g0273 | 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 | 28 | a0004c0004t0003g0321 a0004c0004t0004g0013 a0004c0004t0004g0327 others(25): 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 | a0004c0004t0003g0321 | 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 | a0002c0002t0002g0109 a0002c0002t0002g0115 |
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 | 1 | a0001c0001t0001g0012 | 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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0045 | 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 | a0004c0004t0003g0319 a0004c0004t0003g0324 a0004c0004t0003g0325 others(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 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | a0002c0002t0002g0134 | 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 | a0008c0010t0003g0028 a0008c0012t0003g0025 |
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 | 1 | a0003c0003t0002g0223 | 1 | HG01123.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 | a0001c0001t0001g0092 | 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 | a0001c0001t0002g0354 | 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 | a0008c0012t0003g0025 | 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 | a0003c0003t0003g0357 a0003c0003t0003g0358 |
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 | a0002c0002t0002g0099 | 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 | a0008c0012t0003g0025 | 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 | a0002c0002t0002g0119 a0002c0002t0002g0146 a0002c0002t0002g0163 others(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 | a0008c0012t0003g0025 | 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 | 99 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): 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 | a0004c0004t0003g0335 | 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 | a0002c0002t0002g0178 | 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 | 11 | a0006c0007t0002g0008 a0006c0007t0002g0201 a0006c0007t0002g0202 others(8): 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 | 2 | a0006c0007t0002g0008 a0006c0007t0002g0204 |
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 | 93 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): 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 | a0001c0001t0001g0064 | 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 | a0005c0005t0001g0284 | 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 | a0004c0004t0004g0013 a0004c0004t0004g0328 |
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 | a0003c0003t0010g0196 | 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 | a0001c0001t0001g0095 | 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 | a0002c0002t0002g0130 a0002c0002t0002g0180 |
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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | a0001c0001t0001g0303 | 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 | 103 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0003g0020 a0001c0019t0007g0023 |
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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): 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 | 73 | a0001c0001t0001g0048 a0001c0001t0001g0063 a0001c0001t0001g0071 others(70): 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 | 88 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(85): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): 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 | 35 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0354 others(32): 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 | a0001c0001t0003g0020 | 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 | a0002c0002t0002g0100 a0002c0002t0002g0125 |
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 | a0002c0002t0002g0101 | 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 | a0001c0001t0009g0300 | 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 | a0001c0001t0009g0300 | 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 | 48 | a0001c0001t0009g0300 a0004c0004t0003g0319 a0004c0004t0003g0321 others(45): 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 | a0001c0001t0009g0300 | 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 | a0001c0001t0009g0300 | 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 | a0001c0001t0009g0300 | 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 | a0004c0004t0005g0185 | 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 | 47 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(44): 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 | a0002c0002t0002g0195 | 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 | 95 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0006 others(92): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): 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 | a0001c0001t0002g0181 | 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 | a0001c0001t0001g0303 | 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 | a0004c0004t0003g0342 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0089 |
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 | 285 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): 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 | a0004c0009t0003g0330 a0004c0009t0003g0331 a0004c0009t0003g0343 |
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 | a0001c0001t0001g0080 | 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 | a0004c0004t0003g0321 | 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 | a0004c0004t0004g0013 a0004c0004t0004g0327 a0004c0004t0004g0328 others(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 | 3 | a0003c0003t0002g0007 a0003c0003t0002g0197 a0003c0003t0002g0198 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0071 others(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 | a0002c0002t0002g0111 a0002c0002t0002g0113 |
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 | a0004c0004t0003g0319 a0004c0004t0003g0321 a0004c0004t0003g0323 others(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 | a0008c0012t0012g0363 | 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 | 18 | a0001c0001t0001g0040 a0001c0001t0001g0248 a0001c0001t0001g0281 others(15): 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 | a0009c0008t0003g0026 a0009c0008t0003g0027 a0009c0008t0003g0029 others(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 | 97 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): 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 | a0008c0012t0012g0363 | 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 | 33 | a0003c0003t0002g0009 a0003c0003t0002g0199 a0003c0003t0002g0205 others(30): 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 | a0008c0012t0003g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2122-9T>C | HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 23/23 | chr5 | 119541896 |