Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3294 |
| ensemblid | ENSG00000086696.11 |
| hgncid | 5211 |
| symbol | HSD17B2 |
| name | hydroxysteroid 17-beta dehydrogenase 2 |
| refseq_nuc | NM_002153.3 |
| refseq_prot | NP_002144.1 |
| ensembl_nuc | ENST00000199936.9 |
| ensembl_prot | ENSP00000199936.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 82035253 |
| end | 82098534 |
| strand | + |
| ver | v1.2 |
| region | chr16:82035253-82098534 |
| region5000 | chr16:82030253-82103534 |
| regionname0 | HSD17B2_chr16_82035253_82098534 |
| regionname5000 | HSD17B2_chr16_82030253_82103534 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 387 | 356 | 86 | 49 | 169 | 12 | 38 | 131 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | MSTFF others(382): Show |
chr16 | 82030253 | 82103534 |
| a0002 | 0/0 | 387 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | MSTFF others(382): Show |
chr16 | 82030253 | 82103534 |
| a0003 | 0/0 | 387 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | MSTFF others(382): Show |
chr16 | 82030253 | 82103534 |
| a0004 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | MSTFF others(382): Show |
chr16 | 82030253 | 82103534 |
| a0005 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | MSTFF others(382): Show |
chr16 | 82030253 | 82103534 |
| a0006 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | MSTFF others(382): Show |
chr16 | 82030253 | 82103534 |
| a0007 | 0/0 | 387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | MSTFF others(382): Show |
chr16 | 82030253 | 82103534 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1161 | 334 | 82 | 48 | 152 | 12 | 38 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0001c0002 | 0/0 | 1161 | 11 | 2 | 1 | 8 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0001c0003 | 0/0 | 1161 | 9 | 0 | 0 | 9 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0001c0008 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0001c0011 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0002c0004 | 0/0 | 1161 | 4 | 4 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0003c0005 | 0/0 | 1161 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0004c0009 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0005c0010 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0006c0006 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 | ||
| a0007c0007 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ATGAG others(1156): Show |
chr16 | 82030253 | 82103534 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1434 | 187 | 50 | 30 | 78 | 8 | 20 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0001t0002 | 1/0 | 1434 | 134 | 25 | 17 | 69 | 4 | 18 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0001t0003 | 0/0 | 1434 | 6 | 5 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0001t0004 | 0/0 | 1434 | 7 | 2 | 0 | 5 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0002t0001 | 0/0 | 1434 | 4 | 2 | 1 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0002t0003 | 0/0 | 1434 | 7 | 0 | 0 | 7 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0003t0002 | 0/0 | 1434 | 9 | 0 | 0 | 9 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0008t0001 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0001c0011t0001 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0002c0004t0001 | 0/0 | 1434 | 4 | 4 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0003c0005t0001 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0004c0009t0001 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0005c0010t0002 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0006c0006t0001 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| a0007c0007t0002 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | ACCCA others(1429): Show |
chr16 | 82030253 | 82103534 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0001c0011t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0002c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0002c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0002c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0002c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0003c0005t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0003c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0004c0009t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0005c0010t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0006c0006t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| a0007c0007t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | FIN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0296 | EUR | FIN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0017 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0017 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01175 | hp2 | a0004 | c0009 | t0001 | g0225 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01192 | hp2 | a0005 | c0010 | t0002 | g0098 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01346 | hp1 | a0006 | c0006 | t0001 | g0280 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | IBS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02055 | hp1 | a0002 | c0004 | t0001 | g0311 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | CDX | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0303 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02630 | hp1 | a0001 | c0011 | t0001 | g0323 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02818 | hp1 | a0002 | c0004 | t0001 | g0316 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02970 | hp1 | a0002 | c0004 | t0001 | g0304 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03041 | hp1 | a0003 | c0005 | t0001 | g0324 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03130 | hp2 | a0003 | c0005 | t0001 | g0325 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03209 | hp1 | a0002 | c0004 | t0001 | g0027 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03579 | hp2 | a0001 | c0008 | t0001 | g0161 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0123 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18972 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18978 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0133 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0135 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18995 | hp1 | a0007 | c0007 | t0002 | g0181 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19000 | hp1 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ASW | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ASW | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | GIH | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0199 | REF | REF | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0147 | REF | REF | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:82068265 | G | A | 1 | a0003 | 2 | HG03041.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.361G>A | p.Ala121Thr | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/5 | 533/1434 | 361/1164 | 121/387 | chr16 | 82068265 | |||
| chr16:82068331 | G | A | 1 | a0006 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.427G>A | p.Val143Met | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/5 | 599/1434 | 427/1164 | 143/387 | chr16 | 82068331 | |||
| chr16:82071127 | G | A | 1 | a0007 | 1 | NA18995.hp1 | missense_variant&splice_region_variant | MODERATE | c.664G>A | p.Gly222Arg | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/5 | 836/1434 | 664/1164 | 222/387 | chr16 | 82071127 | |||
| chr16:82090913 | A | G | 1 | a0005 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.676A>G | p.Met226Val | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/5 | 848/1434 | 676/1164 | 226/387 | chr16 | 82090913 | |||
| chr16:82090956 | C | G | 1 | a0002 | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.719C>G | p.Thr240Ser | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/5 | 891/1434 | 719/1164 | 240/387 | chr16 | 82090956 | |||
| chr16:82098083 | G | T | 1 | a0004 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.811G>T | p.Gly271Cys | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 5/5 | 983/1434 | 811/1164 | 271/387 | chr16 | 82098083 | |||
| chr16:82098435 | A | G | 1 | a0001 | 20 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(17): Show |
stop_lost | HIGH | c.1163A>G | p.Ter388Trpext*? | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 5/5 | 1335/1434 | 1163/1164 | 388/387 | chr16 | 82098435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:82035679 | C | G | 1 | a0001c0011 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.255C>G | p.Val85Val | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/5 | 427/1434 | 255/1164 | 85/387 | chr16 | 82035679 | |||
| chr16:82068222 | C | T | 1 | a0001c0002 | 11 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(8): Show |
synonymous_variant | LOW | c.318C>T | p.Gly106Gly | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/5 | 490/1434 | 318/1164 | 106/387 | chr16 | 82068222 | |||
| chr16:82098197 | T | C | 1 | a0001c0003 | 9 | NA18943.hp1 NA18951.hp1 NA18966.hp1 others(6): Show |
synonymous_variant | LOW | c.925T>C | p.Leu309Leu | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 5/5 | 1097/1434 | 925/1164 | 309/387 | chr16 | 82098197 | |||
| chr16:82098265 | G | A | 1 | a0001c0008 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.993G>A | p.Ala331Ala | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 5/5 | 1165/1434 | 993/1164 | 331/387 | chr16 | 82098265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:82035292 | T | C | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(7): Show |
213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
5_prime_UTR_variant | MODIFIER | c.-133T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/5 | 133 | chr16 | 82035292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:82035756 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.265+67T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82035756 | |||||||
| chr16:82035846 | G | GT | 35 | a0001c0001t0001g0027 a0001c0001t0001g0302 a0001c0001t0001g0307 others(32): Show |
35 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.265+163dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82035846 | ||||||
| chr16:82035983 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0301 |
3 | HG00140.hp2 HG01099.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.265+294A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82035983 | |||||||
| chr16:82036060 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+371T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036060 | |||||||
| chr16:82036104 | C | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.265+415C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036104 | |||||||
| chr16:82036118 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.265+429C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036118 | |||||||
| chr16:82036298 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.265+609G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036298 | |||||||
| chr16:82036320 | T | TTG | 24 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0068 others(21): Show |
26 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.265+673_265+674dup others(2): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | T | TTGTG | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0002g0038 others(7): Show |
10 | HG00609.hp1 HG02015.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.265+671_265+674dup others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | T | TTGTGTG | 7 | a0001c0001t0001g0037 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG02523.hp2 HG02738.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+669_265+674dup others(6): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | TTG | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0029 others(22): Show |
28 | HG00639.hp1 HG01081.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.265+673_265+674del others(2): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | TTGTG | T | 29 | a0001c0001t0001g0027 a0001c0001t0001g0182 a0001c0001t0001g0308 others(26): Show |
30 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.265+671_265+674del others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | TTGTGTG | T | 23 | a0001c0001t0001g0016 a0001c0001t0001g0183 a0001c0001t0001g0185 others(20): Show |
25 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.265+669_265+674del others(6): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | TTGTGTGT others(1): Show |
T | 13 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(10): Show |
13 | HG00735.hp1 HG00738.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+667_265+674del others(8): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | TTGTGTGT others(3): Show |
T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
117 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.265+665_265+674del others(10): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0001g0294 a0001c0001t0001g0334 a0001c0001t0003g0295 |
3 | HG02922.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.265+663_265+674del others(12): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036320 | TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0001g0296 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.265+659_265+674del others(16): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036320 | ||||||
| chr16:82036354 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0030 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.265+667_265+676del others(10): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82036354 | ||||||
| chr16:82036356 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.265+667G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036356 | |||||||
| chr16:82036383 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.265+694G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036383 | |||||||
| chr16:82036523 | C | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(15): Show |
19 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+834C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036523 | |||||||
| chr16:82036585 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.265+896G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036585 | |||||||
| chr16:82036678 | T | C | 35 | a0001c0001t0001g0027 a0001c0001t0001g0307 a0001c0001t0001g0308 others(32): Show |
35 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.265+989T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036678 | |||||||
| chr16:82036745 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.265+1056A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036745 | |||||||
| chr16:82036873 | C | A | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG01891.hp2 HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.265+1184C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036873 | |||||||
| chr16:82036886 | A | G | 1 | a0001c0001t0003g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.265+1197A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036886 | |||||||
| chr16:82036909 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+1220C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036909 | |||||||
| chr16:82036925 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.265+1236T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036925 | |||||||
| chr16:82036950 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.265+1261C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82036950 | |||||||
| chr16:82037131 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0046 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.265+1442T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037131 | |||||||
| chr16:82037141 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
6 | NA18960.hp1 NA18966.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1452T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037141 | |||||||
| chr16:82037302 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0002g0069 |
2 | HG01255.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.265+1613T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037302 | |||||||
| chr16:82037332 | C | G | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.265+1643C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037332 | |||||||
| chr16:82037414 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.265+1725C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037414 | |||||||
| chr16:82037489 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.265+1800C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037489 | |||||||
| chr16:82037600 | G | T | 1 | a0001c0001t0001g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.265+1911G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037600 | |||||||
| chr16:82037685 | G | T | 9 | a0001c0001t0002g0044 a0001c0001t0002g0066 a0001c0001t0002g0153 others(6): Show |
9 | HG01069.hp2 HG02148.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+1996G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037685 | |||||||
| chr16:82037719 | A | C | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.265+2030A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037719 | |||||||
| chr16:82037926 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.265+2237T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037926 | |||||||
| chr16:82037942 | G | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(2): Show |
6 | HG00639.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+2253G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037942 | |||||||
| chr16:82037980 | C | G | 50 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(47): Show |
52 | HG00639.hp1 HG01081.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.265+2291C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037980 | |||||||
| chr16:82037986 | A | G | 50 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(47): Show |
52 | HG00639.hp1 HG01081.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.265+2297A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82037986 | |||||||
| chr16:82038119 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+2430G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038119 | |||||||
| chr16:82038173 | C | T | 50 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(47): Show |
52 | HG00639.hp1 HG01081.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.265+2484C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038173 | |||||||
| chr16:82038301 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.265+2612A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038301 | |||||||
| chr16:82038323 | G | T | 1 | a0001c0001t0001g0292 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.265+2634G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038323 | |||||||
| chr16:82038325 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+2636A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038325 | |||||||
| chr16:82038326 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.265+2637T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038326 | |||||||
| chr16:82038341 | A | G | 7 | a0001c0001t0001g0183 a0001c0002t0001g0065 a0001c0002t0003g0017 others(4): Show |
8 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+2652A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038341 | |||||||
| chr16:82038355 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+2666C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038355 | |||||||
| chr16:82038407 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+2718T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038407 | |||||||
| chr16:82038477 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.265+2788G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038477 | |||||||
| chr16:82038492 | G | C | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+2803G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038492 | |||||||
| chr16:82038494 | C | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+2805C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038494 | |||||||
| chr16:82038599 | G | A | 1 | a0002c0004t0001g0311 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.265+2910G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038599 | |||||||
| chr16:82038607 | T | A | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+2918T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038607 | |||||||
| chr16:82038643 | G | C | 26 | a0001c0001t0001g0027 a0001c0001t0001g0294 a0001c0001t0001g0308 others(23): Show |
26 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.265+2954G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038643 | |||||||
| chr16:82038665 | G | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0038 |
2 | NA18945.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.265+2976G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038665 | |||||||
| chr16:82038724 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+3035T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038724 | |||||||
| chr16:82038785 | C | A | 2 | a0001c0001t0001g0327 a0001c0001t0001g0333 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.265+3096C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038785 | |||||||
| chr16:82039081 | G | C | 2 | a0001c0001t0004g0048 a0001c0001t0004g0049 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.265+3392G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039081 | |||||||
| chr16:82039139 | C | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.265+3450C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039139 | |||||||
| chr16:82039154 | A | G | 2 | a0001c0001t0001g0334 a0001c0002t0003g0197 |
2 | HG02071.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.265+3465A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039154 | |||||||
| chr16:82039160 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.265+3471A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039160 | |||||||
| chr16:82039198 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.265+3509T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039198 | |||||||
| chr16:82039214 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.265+3525G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039214 | |||||||
| chr16:82039248 | T | TAC | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.265+3582_265+3583d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82039248 | ||||||
| chr16:82039248 | T | TACAC | 10 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(7): Show |
11 | HG00408.hp1 HG00544.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.265+3580_265+3583d others(6): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82039248 | ||||||
| chr16:82039248 | T | TACACAC | 4 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0001g0198 others(1): Show |
5 | HG00438.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+3578_265+3583d others(8): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82039248 | ||||||
| chr16:82039330 | T | TGA | 6 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0067 others(3): Show |
7 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+3661_265+3662d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82039330 | ||||||
| chr16:82039330 | TGAGA | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.265+3659_265+3662d others(6): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82039330 | ||||||
| chr16:82039354 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.265+3665A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039354 | |||||||
| chr16:82039581 | C | G | 1 | a0001c0001t0002g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.265+3892C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039581 | |||||||
| chr16:82039589 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+3900T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039589 | |||||||
| chr16:82039616 | G | T | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.265+3927G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039616 | |||||||
| chr16:82039634 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+3945G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039634 | |||||||
| chr16:82039671 | C | T | 17 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(14): Show |
17 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.265+3982C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039671 | |||||||
| chr16:82039783 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+4094C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039783 | |||||||
| chr16:82039839 | C | A | 1 | a0001c0001t0001g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.265+4150C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039839 | |||||||
| chr16:82039839 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.265+4150C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039839 | |||||||
| chr16:82039903 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.265+4214C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039903 | |||||||
| chr16:82039977 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+4288A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82039977 | |||||||
| chr16:82040026 | A | C | 1 | a0001c0001t0002g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.265+4337A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040026 | |||||||
| chr16:82040068 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.265+4379G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040068 | |||||||
| chr16:82040081 | A | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(15): Show |
19 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+4392A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040081 | |||||||
| chr16:82040144 | T | G | 1 | a0002c0004t0001g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.265+4455T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040144 | |||||||
| chr16:82040195 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+4506G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040195 | |||||||
| chr16:82040218 | ATTACTGA others(4): Show |
A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0004c0009t0001g0225 |
3 | HG00639.hp2 HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.265+4531_265+4541d others(13): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82040218 | ||||||
| chr16:82040260 | G | C | 1 | a0001c0001t0002g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.265+4571G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040260 | |||||||
| chr16:82040355 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.265+4666C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040355 | |||||||
| chr16:82040622 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+4933A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040622 | |||||||
| chr16:82040853 | G | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(15): Show |
19 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+5164G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040853 | |||||||
| chr16:82040959 | T | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(15): Show |
19 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+5270T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040959 | |||||||
| chr16:82040986 | C | T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02622.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+5297C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82040986 | |||||||
| chr16:82041042 | T | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(16): Show |
20 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.265+5353T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041042 | |||||||
| chr16:82041079 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.265+5390T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041079 | |||||||
| chr16:82041114 | C | A | 30 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(27): Show |
31 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.265+5425C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041114 | |||||||
| chr16:82041165 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.265+5476G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041165 | |||||||
| chr16:82041175 | A | T | 1 | a0007c0007t0002g0181 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.265+5486A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041175 | |||||||
| chr16:82041267 | G | C | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.265+5578G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041267 | |||||||
| chr16:82041279 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.265+5590T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041279 | |||||||
| chr16:82041306 | T | C | 6 | a0001c0002t0003g0017 a0001c0002t0003g0152 a0001c0002t0003g0194 others(3): Show |
7 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+5617T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041306 | |||||||
| chr16:82041316 | T | C | 1 | a0001c0001t0003g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.265+5627T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041316 | |||||||
| chr16:82041320 | A | G | 1 | a0001c0001t0002g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.265+5631A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041320 | |||||||
| chr16:82041419 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+5730C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041419 | |||||||
| chr16:82041446 | G | A | 1 | a0001c0002t0003g0195 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.265+5757G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041446 | |||||||
| chr16:82041525 | T | A | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02622.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+5836T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041525 | |||||||
| chr16:82041558 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0046 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.265+5869C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041558 | |||||||
| chr16:82041664 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+5975C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041664 | |||||||
| chr16:82041665 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.265+5976G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041665 | |||||||
| chr16:82041712 | C | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.265+6023C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041712 | |||||||
| chr16:82041750 | T | G | 30 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(27): Show |
31 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.265+6061T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041750 | |||||||
| chr16:82041848 | G | C | 8 | a0001c0001t0001g0183 a0001c0001t0001g0326 a0001c0002t0001g0065 others(5): Show |
9 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(6): Show |
intron_variant | MODIFIER | c.265+6159G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041848 | |||||||
| chr16:82041886 | C | A | 48 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(45): Show |
50 | HG00639.hp1 HG01081.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.265+6197C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041886 | |||||||
| chr16:82041954 | T | A | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02622.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+6265T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041954 | |||||||
| chr16:82041975 | C | T | 8 | a0001c0001t0001g0183 a0001c0001t0001g0326 a0001c0002t0001g0065 others(5): Show |
9 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(6): Show |
intron_variant | MODIFIER | c.265+6286C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041975 | |||||||
| chr16:82041997 | C | CT | 8 | a0001c0001t0001g0287 a0001c0001t0001g0299 a0001c0001t0001g0334 others(5): Show |
9 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(6): Show |
intron_variant | MODIFIER | c.265+6322dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82041997 | ||||||
| chr16:82042002 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+6313T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042002 | |||||||
| chr16:82042129 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.265+6440G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042129 | |||||||
| chr16:82042220 | G | GGCTTGAA others(24): Show |
4 | a0001c0002t0003g0017 a0001c0002t0003g0195 a0001c0002t0003g0196 others(1): Show |
5 | HG00408.hp1 HG00544.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+6534_265+6564d others(33): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82042220 | ||||||
| chr16:82042229 | C | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.265+6540C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042229 | |||||||
| chr16:82042279 | A | G | 2 | a0003c0005t0001g0324 a0003c0005t0001g0325 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.265+6590A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042279 | |||||||
| chr16:82042280 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265+6591C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042280 | |||||||
| chr16:82042306 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.265+6617C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042306 | |||||||
| chr16:82042329 | G | A | 29 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(26): Show |
30 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.265+6640G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042329 | |||||||
| chr16:82042426 | G | T | 1 | a0001c0001t0002g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.265+6737G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042426 | |||||||
| chr16:82042608 | A | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(15): Show |
19 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+6919A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042608 | |||||||
| chr16:82042716 | G | C | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.265+7027G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042716 | |||||||
| chr16:82042782 | CAGCTAA | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(2): Show |
6 | HG00639.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+7094_265+7099d others(8): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042782 | |||||||
| chr16:82042831 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.265+7142G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042831 | |||||||
| chr16:82042913 | A | T | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265+7224A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042913 | |||||||
| chr16:82042955 | A | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(15): Show |
19 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+7266A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82042955 | |||||||
| chr16:82043008 | T | C | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+7319T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043008 | |||||||
| chr16:82043104 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.265+7415T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043104 | |||||||
| chr16:82043132 | C | A | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.265+7443C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043132 | |||||||
| chr16:82043171 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | NA19007.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.265+7482G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043171 | |||||||
| chr16:82043251 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.265+7562T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043251 | |||||||
| chr16:82043387 | TAAAAATC others(315): Show |
T | 46 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(43): Show |
48 | HG00639.hp1 HG01081.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.265+7714_265+8035d others(2): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82043387 | ||||||
| chr16:82043400 | G | A | 3 | a0001c0001t0002g0059 a0001c0001t0002g0093 a0001c0001t0002g0119 |
3 | HG00741.hp2 HG01496.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.265+7711G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043400 | |||||||
| chr16:82043601 | G | T | 1 | a0001c0002t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.265+7912G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043601 | |||||||
| chr16:82043684 | C | CA | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
103 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.265+8025dupA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82043684 | ||||||
| chr16:82043684 | C | CAA | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(53): Show |
62 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.265+8024_265+8025d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82043684 | ||||||
| chr16:82043684 | C | CAAA | 17 | a0001c0001t0001g0186 a0001c0001t0001g0269 a0001c0001t0002g0039 others(14): Show |
17 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.265+8023_265+8025d others(5): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82043684 | ||||||
| chr16:82043684 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.265+8009_265+8025d others(19): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82043684 | ||||||
| chr16:82043684 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265+8000_265+8025d others(28): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82043684 | ||||||
| chr16:82043684 | CA | C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0165 a0001c0001t0001g0235 others(10): Show |
13 | HG00741.hp1 HG02486.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+8025delA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82043684 | ||||||
| chr16:82043731 | T | C | 30 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(27): Show |
31 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.265+8042T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043731 | |||||||
| chr16:82043773 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+8084C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043773 | |||||||
| chr16:82043950 | C | G | 1 | a0001c0002t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.265+8261C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82043950 | |||||||
| chr16:82044083 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.265+8394A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044083 | |||||||
| chr16:82044187 | C | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(13): Show |
17 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.265+8498C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044187 | |||||||
| chr16:82044255 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265+8566C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044255 | |||||||
| chr16:82044308 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.265+8619G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044308 | |||||||
| chr16:82044529 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.265+8840G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044529 | |||||||
| chr16:82044574 | G | T | 1 | a0001c0001t0002g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.265+8885G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044574 | |||||||
| chr16:82044648 | A | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0067 others(3): Show |
7 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+8959A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044648 | |||||||
| chr16:82044677 | A | G | 1 | a0001c0002t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.265+8988A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044677 | |||||||
| chr16:82044817 | C | T | 42 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(39): Show |
43 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+9128C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044817 | |||||||
| chr16:82044840 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.265+9151G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82044840 | |||||||
| chr16:82045076 | T | C | 1 | a0002c0004t0001g0311 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.265+9387T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045076 | |||||||
| chr16:82045085 | C | T | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.265+9396C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045085 | |||||||
| chr16:82045094 | G | T | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.265+9405G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045094 | |||||||
| chr16:82045121 | C | CA | 13 | a0001c0001t0001g0151 a0001c0001t0001g0213 a0001c0001t0002g0062 others(10): Show |
13 | HG04204.hp2 NA18940.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.265+9454dupA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82045121 | ||||||
| chr16:82045121 | CA | C | 46 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(43): Show |
48 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.265+9454delA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82045121 | ||||||
| chr16:82045121 | CAAA | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(14): Show |
18 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+9452_265+9454d others(5): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82045121 | ||||||
| chr16:82045296 | C | A | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265+9607C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045296 | |||||||
| chr16:82045353 | C | T | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.265+9664C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045353 | |||||||
| chr16:82045368 | CAT | C | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+9680_265+9681d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045368 | |||||||
| chr16:82045465 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.265+9776A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045465 | |||||||
| chr16:82045486 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
191 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.265+9797G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045486 | |||||||
| chr16:82045779 | G | A | 40 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(37): Show |
41 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.265+10090G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045779 | |||||||
| chr16:82045886 | A | C | 22 | a0001c0001t0001g0027 a0001c0001t0001g0308 a0001c0001t0001g0309 others(19): Show |
22 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.265+10197A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82045886 | |||||||
| chr16:82046055 | C | T | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.265+10366C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046055 | |||||||
| chr16:82046165 | G | A | 24 | a0001c0001t0001g0027 a0001c0001t0001g0308 a0001c0001t0001g0309 others(21): Show |
24 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.265+10476G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046165 | |||||||
| chr16:82046176 | A | C | 10 | a0001c0001t0002g0060 a0001c0001t0002g0080 a0001c0001t0002g0081 others(7): Show |
10 | HG00621.hp2 NA18940.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.265+10487A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046176 | |||||||
| chr16:82046272 | C | G | 40 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(37): Show |
41 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.265+10583C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046272 | |||||||
| chr16:82046323 | G | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.265+10634G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046323 | |||||||
| chr16:82046393 | A | C | 39 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(36): Show |
40 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.265+10704A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046393 | |||||||
| chr16:82046410 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.265+10721G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046410 | |||||||
| chr16:82046486 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.265+10797G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046486 | |||||||
| chr16:82046531 | T | C | 2 | a0001c0001t0001g0328 a0001c0001t0002g0164 |
2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.265+10842T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046531 | |||||||
| chr16:82046535 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.265+10846G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046535 | |||||||
| chr16:82046641 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.265+10952T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046641 | |||||||
| chr16:82046654 | T | C | 24 | a0001c0001t0001g0027 a0001c0001t0001g0308 a0001c0001t0001g0309 others(21): Show |
24 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.265+10965T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046654 | |||||||
| chr16:82046680 | GA | G | 44 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(41): Show |
46 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.265+11002delA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82046680 | ||||||
| chr16:82046725 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.265+11036C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046725 | |||||||
| chr16:82046814 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.265+11125C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046814 | |||||||
| chr16:82046958 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265+11269C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82046958 | |||||||
| chr16:82047027 | C | T | 1 | a0006c0006t0001g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.265+11338C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047027 | |||||||
| chr16:82047045 | C | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0312 a0001c0001t0001g0313 others(1): Show |
4 | HG01255.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+11356C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047045 | |||||||
| chr16:82047046 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0067 others(3): Show |
7 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+11357T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047046 | |||||||
| chr16:82047078 | G | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(13): Show |
17 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.265+11389G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047078 | |||||||
| chr16:82047085 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0046 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.265+11396C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047085 | |||||||
| chr16:82047096 | A | G | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.265+11407A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047096 | |||||||
| chr16:82047110 | C | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.265+11421C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047110 | |||||||
| chr16:82047289 | T | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.265+11600T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047289 | |||||||
| chr16:82047370 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0327 a0001c0001t0001g0333 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+11681G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047370 | |||||||
| chr16:82047379 | T | C | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+11690T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047379 | |||||||
| chr16:82047406 | T | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+11717T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047406 | |||||||
| chr16:82047432 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.265+11743G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047432 | |||||||
| chr16:82047476 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+11787C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047476 | |||||||
| chr16:82047591 | G | A | 1 | a0002c0004t0001g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.265+11902G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047591 | |||||||
| chr16:82047598 | G | C | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(60): Show |
66 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.265+11909G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047598 | |||||||
| chr16:82047635 | G | A | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(60): Show |
66 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.265+11946G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047635 | |||||||
| chr16:82047826 | G | A | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.265+12137G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047826 | |||||||
| chr16:82047830 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.265+12141G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047830 | |||||||
| chr16:82047859 | G | A | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.265+12170G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047859 | |||||||
| chr16:82047892 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.265+12203C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047892 | |||||||
| chr16:82047900 | T | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.265+12211T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047900 | |||||||
| chr16:82047963 | C | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.265+12274C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82047963 | |||||||
| chr16:82048002 | A | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+12313A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048002 | |||||||
| chr16:82048094 | A | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(38): Show |
42 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.265+12405A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048094 | |||||||
| chr16:82048110 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.265+12421G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048110 | |||||||
| chr16:82048223 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
122 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.265+12534C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048223 | |||||||
| chr16:82048241 | C | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+12552C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048241 | |||||||
| chr16:82048256 | G | T | 23 | a0001c0001t0001g0027 a0001c0001t0001g0308 a0001c0001t0001g0309 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.265+12567G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048256 | |||||||
| chr16:82048405 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
190 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.265+12716C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048405 | |||||||
| chr16:82048447 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+12758T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048447 | |||||||
| chr16:82048524 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.265+12835T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048524 | |||||||
| chr16:82048667 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.265+12978A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048667 | |||||||
| chr16:82048875 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.265+13186A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048875 | |||||||
| chr16:82048879 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.265+13190T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048879 | |||||||
| chr16:82048921 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.265+13232C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048921 | |||||||
| chr16:82048982 | A | C | 1 | a0001c0001t0001g0193 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.265+13293A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82048982 | |||||||
| chr16:82049022 | C | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+13333C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049022 | |||||||
| chr16:82049024 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.265+13335G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049024 | |||||||
| chr16:82049024 | G | C | 6 | a0001c0001t0001g0307 a0001c0001t0001g0329 a0001c0001t0003g0303 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+13335G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049024 | |||||||
| chr16:82049104 | T | G | 4 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0125 others(1): Show |
4 | NA18940.hp1 NA19009.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+13415T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049104 | |||||||
| chr16:82049132 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.265+13443C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049132 | |||||||
| chr16:82049235 | C | G | 55 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(52): Show |
57 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.265+13546C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049235 | |||||||
| chr16:82049270 | G | T | 1 | a0004c0009t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.265+13581G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049270 | |||||||
| chr16:82049328 | T | A | 40 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(37): Show |
41 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.265+13639T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049328 | |||||||
| chr16:82049373 | C | G | 31 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(28): Show |
32 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.265+13684C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049373 | |||||||
| chr16:82049382 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.265+13693G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049382 | |||||||
| chr16:82049456 | C | T | 2 | a0001c0003t0002g0010 a0001c0003t0002g0123 |
3 | NA18951.hp1 NA18966.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.265+13767C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049456 | |||||||
| chr16:82049507 | G | A | 23 | a0001c0001t0001g0027 a0001c0001t0001g0308 a0001c0001t0001g0309 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.265+13818G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049507 | |||||||
| chr16:82049549 | A | T | 1 | a0001c0001t0002g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.265+13860A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049549 | |||||||
| chr16:82049582 | G | A | 40 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0037 others(37): Show |
41 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.265+13893G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049582 | |||||||
| chr16:82049624 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.265+13935G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049624 | |||||||
| chr16:82049652 | C | T | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG01891.hp2 HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.265+13963C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049652 | |||||||
| chr16:82049732 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.265+14043C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049732 | |||||||
| chr16:82049926 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+14237C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82049926 | |||||||
| chr16:82050049 | C | A | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265+14360C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050049 | |||||||
| chr16:82050049 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.265+14360C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050049 | |||||||
| chr16:82050239 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.265+14550G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050239 | |||||||
| chr16:82050341 | G | A | 1 | a0001c0003t0002g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.265+14652G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050341 | |||||||
| chr16:82050397 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.265+14708T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050397 | |||||||
| chr16:82050621 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.265+14932C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050621 | |||||||
| chr16:82050708 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.265+15019C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050708 | |||||||
| chr16:82050741 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265+15052G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050741 | |||||||
| chr16:82050876 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.265+15187T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050876 | |||||||
| chr16:82050934 | A | G | 7 | a0001c0003t0002g0010 a0001c0003t0002g0123 a0001c0003t0002g0131 others(4): Show |
8 | NA18951.hp1 NA18966.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+15245A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050934 | |||||||
| chr16:82050947 | T | G | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+15258T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050947 | |||||||
| chr16:82050991 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.265+15302G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82050991 | |||||||
| chr16:82051014 | A | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.265+15325A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051014 | |||||||
| chr16:82051101 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265+15412T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051101 | |||||||
| chr16:82051208 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0183 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.265+15519A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051208 | |||||||
| chr16:82051385 | A | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+15696A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051385 | |||||||
| chr16:82051522 | C | A | 1 | a0001c0001t0001g0326 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.265+15833C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051522 | |||||||
| chr16:82051613 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+15924A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051613 | |||||||
| chr16:82051643 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265+15954G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051643 | |||||||
| chr16:82051801 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+16112T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051801 | |||||||
| chr16:82051825 | T | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
121 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.265+16136T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051825 | |||||||
| chr16:82051851 | A | G | 1 | a0001c0003t0002g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.265+16162A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051851 | |||||||
| chr16:82051993 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.266-16177A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82051993 | |||||||
| chr16:82052004 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.266-16166T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052004 | |||||||
| chr16:82052052 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.266-16118T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052052 | |||||||
| chr16:82052055 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.266-16115G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052055 | |||||||
| chr16:82052078 | C | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0183 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.266-16092C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052078 | |||||||
| chr16:82052217 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.266-15953G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052217 | |||||||
| chr16:82052220 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-15950G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052220 | |||||||
| chr16:82052326 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-15844T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052326 | |||||||
| chr16:82052388 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-15782A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052388 | |||||||
| chr16:82052428 | C | T | 6 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-15742C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052428 | |||||||
| chr16:82052494 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.266-15676C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052494 | |||||||
| chr16:82052716 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.266-15454T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052716 | |||||||
| chr16:82052945 | G | C | 1 | a0001c0001t0002g0034 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.266-15225G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052945 | |||||||
| chr16:82052973 | C | G | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.266-15197C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82052973 | |||||||
| chr16:82053015 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.266-15155C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053015 | |||||||
| chr16:82053193 | C | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-14977C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053193 | |||||||
| chr16:82053195 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.266-14975G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053195 | |||||||
| chr16:82053230 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.266-14940C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053230 | |||||||
| chr16:82053232 | T | G | 1 | a0001c0001t0002g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.266-14938T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053232 | |||||||
| chr16:82053323 | A | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(14): Show |
18 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.266-14847A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053323 | |||||||
| chr16:82053458 | A | T | 23 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0037 others(20): Show |
25 | HG00639.hp1 HG01081.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.266-14712A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053458 | |||||||
| chr16:82053575 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.266-14595C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053575 | |||||||
| chr16:82053635 | T | C | 30 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0037 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.266-14535T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053635 | |||||||
| chr16:82053985 | A | C | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG03491.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.266-14185A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82053985 | |||||||
| chr16:82054058 | C | T | 30 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0037 others(27): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.266-14112C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054058 | |||||||
| chr16:82054076 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-14094G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054076 | |||||||
| chr16:82054139 | T | G | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-14031T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054139 | |||||||
| chr16:82054208 | G | GA | 7 | a0001c0001t0001g0029 a0001c0001t0001g0302 a0001c0001t0001g0312 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-13947dupA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82054208 | ||||||
| chr16:82054208 | GA | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(18): Show |
22 | HG01081.hp2 HG01109.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.266-13947delA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82054208 | ||||||
| chr16:82054212 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-13958A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054212 | |||||||
| chr16:82054327 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.266-13843C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054327 | |||||||
| chr16:82054369 | G | C | 7 | a0001c0001t0001g0307 a0001c0001t0001g0329 a0001c0001t0002g0120 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-13801G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054369 | |||||||
| chr16:82054376 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-13794G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054376 | |||||||
| chr16:82054421 | T | G | 1 | a0001c0001t0004g0126 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.266-13749T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054421 | |||||||
| chr16:82054440 | G | A | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.266-13730G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054440 | |||||||
| chr16:82054529 | G | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.266-13641G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054529 | |||||||
| chr16:82054560 | G | C | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.266-13610G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054560 | |||||||
| chr16:82054575 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-13595C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054575 | |||||||
| chr16:82054679 | C | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-13491C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054679 | |||||||
| chr16:82054705 | A | C | 1 | a0001c0001t0001g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.266-13465A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054705 | |||||||
| chr16:82054739 | T | C | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG01891.hp2 HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.266-13431T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054739 | |||||||
| chr16:82054807 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(18): Show |
22 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.266-13363G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054807 | |||||||
| chr16:82054858 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.266-13312T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054858 | |||||||
| chr16:82054949 | G | A | 1 | a0001c0003t0002g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.266-13221G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054949 | |||||||
| chr16:82054985 | G | C | 7 | a0001c0001t0001g0307 a0001c0001t0001g0329 a0001c0001t0002g0120 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-13185G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82054985 | |||||||
| chr16:82055112 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.266-13058A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055112 | |||||||
| chr16:82055204 | G | C | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.266-12966G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055204 | |||||||
| chr16:82055406 | G | C | 1 | a0002c0004t0001g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.266-12764G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055406 | |||||||
| chr16:82055409 | T | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(64): Show |
70 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.266-12761T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055409 | |||||||
| chr16:82055415 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-12755G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055415 | |||||||
| chr16:82055445 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.266-12725C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055445 | |||||||
| chr16:82055487 | A | G | 2 | a0003c0005t0001g0324 a0003c0005t0001g0325 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.266-12683A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055487 | |||||||
| chr16:82055593 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-12577G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055593 | |||||||
| chr16:82055654 | T | C | 2 | a0001c0001t0004g0048 a0001c0001t0004g0049 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.266-12516T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055654 | |||||||
| chr16:82055682 | C | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(18): Show |
22 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.266-12488C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055682 | |||||||
| chr16:82055849 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-12321T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055849 | |||||||
| chr16:82055921 | G | C | 9 | a0001c0001t0001g0183 a0001c0002t0001g0065 a0001c0002t0001g0283 others(6): Show |
10 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(7): Show |
intron_variant | MODIFIER | c.266-12249G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055921 | |||||||
| chr16:82055965 | G | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 others(1): Show |
4 | HG02622.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-12205G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82055965 | |||||||
| chr16:82056119 | T | C | 1 | a0001c0001t0003g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.266-12051T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82056119 | |||||||
| chr16:82056456 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.266-11714A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82056456 | |||||||
| chr16:82056457 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-11713G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82056457 | |||||||
| chr16:82056533 | T | C | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 others(2): Show |
5 | HG02622.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-11637T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82056533 | |||||||
| chr16:82056582 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(7): Show |
11 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-11588G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82056582 | |||||||
| chr16:82056904 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.266-11266C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82056904 | |||||||
| chr16:82056978 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-11192T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82056978 | |||||||
| chr16:82057028 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.266-11142A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057028 | |||||||
| chr16:82057088 | C | G | 28 | a0001c0001t0001g0027 a0001c0001t0001g0174 a0001c0001t0001g0175 others(25): Show |
28 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.266-11082C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057088 | |||||||
| chr16:82057143 | G | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(21): Show |
25 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.266-11027G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057143 | |||||||
| chr16:82057204 | C | CT | 12 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 others(9): Show |
12 | HG02257.hp2 HG02451.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-10953dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82057204 | ||||||
| chr16:82057204 | C | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.266-10966C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057204 | |||||||
| chr16:82057216 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.266-10954T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057216 | |||||||
| chr16:82057217 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.266-10953T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057217 | |||||||
| chr16:82057228 | C | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0300 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.266-10942C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057228 | |||||||
| chr16:82057302 | G | A | 7 | a0001c0001t0001g0307 a0001c0001t0001g0329 a0001c0001t0002g0120 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-10868G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057302 | |||||||
| chr16:82057339 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.266-10831C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057339 | |||||||
| chr16:82057346 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(7): Show |
11 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-10824G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057346 | |||||||
| chr16:82057419 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.266-10751G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057419 | |||||||
| chr16:82057422 | T | C | 69 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(66): Show |
72 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.266-10748T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057422 | |||||||
| chr16:82057451 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.266-10719C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057451 | |||||||
| chr16:82057455 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.266-10715C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057455 | |||||||
| chr16:82057483 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-10687C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057483 | |||||||
| chr16:82057703 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.266-10467C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057703 | |||||||
| chr16:82057740 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-10430A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057740 | |||||||
| chr16:82057792 | T | C | 14 | a0001c0001t0001g0183 a0001c0001t0001g0298 a0001c0001t0001g0299 others(11): Show |
15 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.266-10378T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057792 | |||||||
| chr16:82057831 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.266-10339T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057831 | |||||||
| chr16:82057855 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.266-10315G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057855 | |||||||
| chr16:82057909 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.266-10261A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82057909 | |||||||
| chr16:82058040 | T | A | 1 | a0001c0001t0001g0237 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.266-10130T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058040 | |||||||
| chr16:82058059 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-10111T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058059 | |||||||
| chr16:82058071 | A | AT | 12 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0001t0001g0272 others(9): Show |
12 | HG00438.hp1 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-10081dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82058071 | ||||||
| chr16:82058071 | AT | A | 34 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(31): Show |
35 | HG01070.hp2 HG01081.hp2 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.266-10081delT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82058071 | ||||||
| chr16:82058092 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-10078G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058092 | |||||||
| chr16:82058219 | T | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-9951T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058219 | |||||||
| chr16:82058477 | G | A | 9 | a0001c0001t0001g0307 a0001c0001t0001g0312 a0001c0001t0001g0313 others(6): Show |
9 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.266-9693G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058477 | |||||||
| chr16:82058508 | G | C | 3 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01433.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.266-9662G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058508 | |||||||
| chr16:82058604 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-9566C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058604 | |||||||
| chr16:82058714 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-9456G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058714 | |||||||
| chr16:82058720 | T | A | 3 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01433.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.266-9450T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058720 | |||||||
| chr16:82058745 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-9425T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058745 | |||||||
| chr16:82058849 | G | A | 4 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | NA18970.hp2 NA18989.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-9321G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058849 | |||||||
| chr16:82058853 | A | T | 1 | a0001c0001t0003g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.266-9317A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058853 | |||||||
| chr16:82058895 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.266-9275C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058895 | |||||||
| chr16:82058986 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.266-9184C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82058986 | |||||||
| chr16:82059094 | A | G | 9 | a0001c0001t0001g0307 a0001c0001t0001g0312 a0001c0001t0001g0313 others(6): Show |
9 | HG02257.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.266-9076A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059094 | |||||||
| chr16:82059295 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.266-8875C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059295 | |||||||
| chr16:82059339 | C | T | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.266-8831C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059339 | |||||||
| chr16:82059392 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.266-8778G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059392 | |||||||
| chr16:82059403 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.266-8767T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059403 | |||||||
| chr16:82059482 | T | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(7): Show |
11 | HG00639.hp1 HG02486.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-8688T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059482 | |||||||
| chr16:82059578 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-8592T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059578 | |||||||
| chr16:82059583 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-8587G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059583 | |||||||
| chr16:82059610 | C | T | 30 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0037 others(27): Show |
32 | HG00639.hp1 HG01081.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.266-8560C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059610 | |||||||
| chr16:82059620 | G | T | 1 | a0001c0001t0002g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.266-8550G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059620 | |||||||
| chr16:82059678 | G | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.266-8492G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059678 | |||||||
| chr16:82059721 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-8449C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059721 | |||||||
| chr16:82059755 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.266-8415A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059755 | |||||||
| chr16:82059789 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.266-8381C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059789 | |||||||
| chr16:82059802 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-8368T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059802 | |||||||
| chr16:82059969 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-8201C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82059969 | |||||||
| chr16:82060196 | C | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-7974C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060196 | |||||||
| chr16:82060250 | C | A | 1 | a0001c0001t0002g0180 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.266-7920C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060250 | |||||||
| chr16:82060381 | T | A | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-7789T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060381 | |||||||
| chr16:82060466 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.266-7704T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060466 | |||||||
| chr16:82060515 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.266-7655C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060515 | |||||||
| chr16:82060638 | C | T | 69 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(66): Show |
72 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.266-7532C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060638 | |||||||
| chr16:82060672 | A | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(11): Show |
15 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.266-7498A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060672 | |||||||
| chr16:82060737 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.266-7433C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060737 | |||||||
| chr16:82060991 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(7): Show |
11 | HG00639.hp1 HG02486.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-7179C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82060991 | |||||||
| chr16:82061104 | C | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(7): Show |
11 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-7066C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061104 | |||||||
| chr16:82061147 | T | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0307 a0001c0001t0003g0303 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-7023T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061147 | |||||||
| chr16:82061168 | G | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-7002G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061168 | |||||||
| chr16:82061255 | C | CA | 10 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0244 others(7): Show |
10 | NA18945.hp2 NA18946.hp1 NA18977.hp1 others(7): Show |
intron_variant | MODIFIER | c.266-6900dupA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82061255 | ||||||
| chr16:82061255 | CA | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0019 others(28): Show |
34 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.266-6900delA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82061255 | ||||||
| chr16:82061362 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-6808C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061362 | |||||||
| chr16:82061456 | G | A | 1 | a0001c0001t0002g0013 | 2 | NA18991.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.266-6714G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061456 | |||||||
| chr16:82061515 | A | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-6655A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061515 | |||||||
| chr16:82061519 | T | A | 1 | a0001c0001t0002g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.266-6651T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061519 | |||||||
| chr16:82061618 | A | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-6552A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061618 | |||||||
| chr16:82061650 | G | T | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-6520G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061650 | |||||||
| chr16:82061748 | T | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0307 a0001c0001t0003g0303 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-6422T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061748 | |||||||
| chr16:82061914 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0002g0184 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.266-6256A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061914 | |||||||
| chr16:82061919 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.266-6251T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061919 | |||||||
| chr16:82061972 | T | G | 10 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 others(7): Show |
11 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.266-6198T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82061972 | |||||||
| chr16:82062049 | T | G | 1 | a0003c0005t0001g0324 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.266-6121T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062049 | |||||||
| chr16:82062090 | C | A | 1 | a0001c0001t0002g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.266-6080C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062090 | |||||||
| chr16:82062265 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.266-5905C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062265 | |||||||
| chr16:82062405 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(10): Show |
14 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.266-5765C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062405 | |||||||
| chr16:82062406 | T | G | 6 | a0001c0001t0002g0070 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG02040.hp1 NA18942.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-5764T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062406 | |||||||
| chr16:82062434 | G | C | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.266-5736G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062434 | |||||||
| chr16:82062489 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.266-5681T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062489 | |||||||
| chr16:82062607 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.266-5563C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062607 | |||||||
| chr16:82062665 | G | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.266-5505G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062665 | |||||||
| chr16:82062674 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.266-5496A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062674 | |||||||
| chr16:82062675 | G | A | 10 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 others(7): Show |
11 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.266-5495G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062675 | |||||||
| chr16:82062695 | T | C | 1 | a0001c0001t0002g0035 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.266-5475T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062695 | |||||||
| chr16:82062797 | C | G | 1 | a0001c0001t0002g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.266-5373C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062797 | |||||||
| chr16:82062798 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.266-5372G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062798 | |||||||
| chr16:82062814 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.266-5356T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062814 | |||||||
| chr16:82062833 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG02040.hp1 HG02647.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.266-5337T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062833 | |||||||
| chr16:82062861 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-5309G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062861 | |||||||
| chr16:82062935 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.266-5235C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062935 | |||||||
| chr16:82062940 | A | C | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-5230A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062940 | |||||||
| chr16:82062947 | G | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(10): Show |
14 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.266-5223G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062947 | |||||||
| chr16:82062975 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.266-5195C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062975 | |||||||
| chr16:82062976 | G | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0314 a0001c0001t0001g0315 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.266-5194G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82062976 | |||||||
| chr16:82063019 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.266-5151C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063019 | |||||||
| chr16:82063078 | T | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0307 a0001c0001t0003g0303 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-5092T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063078 | |||||||
| chr16:82063195 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.266-4975T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063195 | |||||||
| chr16:82063210 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(10): Show |
14 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.266-4960G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063210 | |||||||
| chr16:82063252 | A | G | 6 | a0001c0001t0001g0302 a0001c0001t0001g0307 a0001c0001t0003g0303 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-4918A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063252 | |||||||
| chr16:82063381 | C | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0213 others(30): Show |
35 | HG00621.hp2 HG00741.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.266-4789C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063381 | |||||||
| chr16:82063403 | G | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0307 a0001c0001t0003g0303 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-4767G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063403 | |||||||
| chr16:82063434 | A | G | 1 | a0001c0001t0002g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.266-4736A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063434 | |||||||
| chr16:82063450 | G | A | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-4720G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063450 | |||||||
| chr16:82063458 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(7): Show |
11 | HG00639.hp1 HG02486.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-4712C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063458 | |||||||
| chr16:82063468 | C | T | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.266-4702C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063468 | |||||||
| chr16:82063506 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(7): Show |
11 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-4664A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063506 | |||||||
| chr16:82063516 | G | A | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG01891.hp2 HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.266-4654G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063516 | |||||||
| chr16:82063557 | A | C | 1 | a0001c0001t0002g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.266-4613A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063557 | |||||||
| chr16:82063560 | T | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-4610T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063560 | |||||||
| chr16:82063857 | G | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(8): Show |
12 | HG00639.hp1 HG02486.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-4313G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063857 | |||||||
| chr16:82063862 | CTT | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-4306_266-4305d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82063862 | ||||||
| chr16:82063880 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-4290G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063880 | |||||||
| chr16:82063961 | C | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(8): Show |
12 | HG00639.hp1 HG02486.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-4209C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82063961 | |||||||
| chr16:82064009 | T | A | 1 | a0001c0001t0002g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.266-4161T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064009 | |||||||
| chr16:82064145 | A | C | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.266-4025A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064145 | |||||||
| chr16:82064154 | G | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-4016G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064154 | |||||||
| chr16:82064162 | G | A | 10 | a0001c0001t0002g0011 a0001c0001t0002g0044 a0001c0001t0002g0066 others(7): Show |
11 | HG01069.hp2 HG02148.hp1 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-4008G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064162 | |||||||
| chr16:82064351 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0003g0297 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.266-3819C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064351 | |||||||
| chr16:82064544 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-3626G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064544 | |||||||
| chr16:82064629 | A | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.266-3541A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064629 | |||||||
| chr16:82064703 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.266-3467A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064703 | |||||||
| chr16:82064777 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.266-3393T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064777 | |||||||
| chr16:82064830 | C | T | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-3340C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064830 | |||||||
| chr16:82064909 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-3261T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064909 | |||||||
| chr16:82064930 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-3240G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82064930 | |||||||
| chr16:82065059 | T | G | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-3111T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065059 | |||||||
| chr16:82065101 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.266-3069C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065101 | |||||||
| chr16:82065174 | A | G | 2 | a0001c0001t0004g0114 a0001c0001t0004g0168 |
2 | NA18944.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.266-2996A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065174 | |||||||
| chr16:82065209 | G | A | 7 | a0001c0002t0001g0283 a0001c0002t0003g0017 a0001c0002t0003g0152 others(4): Show |
8 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-2961G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065209 | |||||||
| chr16:82065222 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-2948G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065222 | |||||||
| chr16:82065328 | G | C | 1 | a0001c0001t0004g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.266-2842G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065328 | |||||||
| chr16:82065338 | T | C | 4 | a0001c0001t0001g0294 a0001c0001t0001g0298 a0001c0001t0001g0299 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-2832T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065338 | |||||||
| chr16:82065364 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.266-2806C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065364 | |||||||
| chr16:82065431 | G | T | 1 | a0001c0001t0001g0332 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.266-2739G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065431 | |||||||
| chr16:82065442 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.266-2728T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065442 | |||||||
| chr16:82065448 | A | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-2722A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065448 | |||||||
| chr16:82065455 | TA | T | 7 | a0001c0002t0001g0283 a0001c0002t0003g0017 a0001c0002t0003g0152 others(4): Show |
8 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-2714delA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065455 | |||||||
| chr16:82065469 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.266-2701G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065469 | |||||||
| chr16:82065557 | CT | C | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0334 |
3 | HG02717.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.266-2612delT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065557 | |||||||
| chr16:82065678 | C | G | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-2492C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065678 | |||||||
| chr16:82065755 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.266-2415G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065755 | |||||||
| chr16:82065790 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.266-2380G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065790 | |||||||
| chr16:82065845 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.266-2325G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065845 | |||||||
| chr16:82065914 | T | G | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-2256T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065914 | |||||||
| chr16:82065923 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.266-2247C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82065923 | |||||||
| chr16:82066139 | T | G | 1 | a0001c0001t0001g0227 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.266-2031T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066139 | |||||||
| chr16:82066304 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.266-1866C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066304 | |||||||
| chr16:82066434 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.266-1736T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066434 | |||||||
| chr16:82066510 | T | G | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-1660T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066510 | |||||||
| chr16:82066519 | G | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(11): Show |
15 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.266-1651G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066519 | |||||||
| chr16:82066528 | G | T | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.266-1642G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066528 | |||||||
| chr16:82066703 | CCTT | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(8): Show |
12 | HG00639.hp1 HG01109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.266-1463_266-1461d others(5): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82066703 | ||||||
| chr16:82066735 | AATT | A | 7 | a0001c0002t0001g0283 a0001c0002t0003g0017 a0001c0002t0003g0152 others(4): Show |
8 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-1426_266-1424d others(5): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 82066735 | ||||||
| chr16:82066751 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.266-1419C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066751 | |||||||
| chr16:82066833 | G | T | 1 | a0001c0001t0002g0128 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.266-1337G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066833 | |||||||
| chr16:82066884 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-1286T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82066884 | |||||||
| chr16:82067249 | G | T | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-921G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067249 | |||||||
| chr16:82067260 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-910T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067260 | |||||||
| chr16:82067355 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.266-815A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067355 | |||||||
| chr16:82067512 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.266-658A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067512 | |||||||
| chr16:82067601 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.266-569T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067601 | |||||||
| chr16:82067711 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.266-459T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067711 | |||||||
| chr16:82067713 | A | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-457A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067713 | |||||||
| chr16:82067734 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.266-436G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82067734 | |||||||
| chr16:82068002 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.266-168T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82068002 | |||||||
| chr16:82068123 | T | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(11): Show |
15 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.266-47T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82068123 | |||||||
| chr16:82068390 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19068.hp1 | splice_region_variant&intron_variant | LOW | c.478+8C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068390 | |||||||
| chr16:82068442 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.478+60C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068442 | |||||||
| chr16:82068492 | T | G | 1 | a0001c0001t0001g0247 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.478+110T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068492 | |||||||
| chr16:82068554 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.478+172G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068554 | |||||||
| chr16:82068583 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+201C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068583 | |||||||
| chr16:82068684 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.478+302G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068684 | |||||||
| chr16:82068836 | G | A | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.478+454G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068836 | |||||||
| chr16:82068902 | G | T | 50 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(47): Show |
52 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.478+520G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82068902 | |||||||
| chr16:82069026 | T | G | 2 | a0001c0001t0002g0011 a0007c0007t0002g0181 |
3 | NA18995.hp1 NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.478+644T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069026 | |||||||
| chr16:82069069 | C | T | 1 | a0001c0011t0001g0323 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.478+687C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069069 | |||||||
| chr16:82069113 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478+731G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069113 | |||||||
| chr16:82069120 | T | A | 36 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(33): Show |
37 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.478+738T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069120 | |||||||
| chr16:82069156 | C | T | 29 | a0001c0001t0001g0027 a0001c0001t0001g0174 a0001c0001t0001g0175 others(26): Show |
29 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.478+774C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069156 | |||||||
| chr16:82069187 | A | G | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+805A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069187 | |||||||
| chr16:82069198 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
118 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.478+816G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069198 | |||||||
| chr16:82069225 | C | A | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.478+843C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069225 | |||||||
| chr16:82069354 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.478+972G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069354 | |||||||
| chr16:82069368 | C | T | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.478+986C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069368 | |||||||
| chr16:82069426 | A | T | 1 | a0004c0009t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.478+1044A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069426 | |||||||
| chr16:82069431 | G | C | 2 | a0001c0001t0002g0129 a0001c0001t0003g0295 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.478+1049G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069431 | |||||||
| chr16:82069467 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.478+1085C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069467 | |||||||
| chr16:82069471 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.478+1089C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069471 | |||||||
| chr16:82069476 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.478+1094T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069476 | |||||||
| chr16:82069493 | T | C | 5 | a0001c0001t0001g0307 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.478+1111T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069493 | |||||||
| chr16:82069503 | C | T | 7 | a0001c0002t0001g0283 a0001c0002t0003g0017 a0001c0002t0003g0152 others(4): Show |
8 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+1121C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069503 | |||||||
| chr16:82069541 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+1159C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069541 | |||||||
| chr16:82069721 | C | G | 1 | a0001c0011t0001g0323 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.479-1221C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069721 | |||||||
| chr16:82069723 | T | C | 58 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(55): Show |
60 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.479-1219T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069723 | |||||||
| chr16:82069806 | G | A | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0003g0305 |
3 | HG02717.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.479-1136G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069806 | |||||||
| chr16:82069811 | A | G | 10 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 others(7): Show |
11 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.479-1131A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069811 | |||||||
| chr16:82069880 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.479-1062C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069880 | |||||||
| chr16:82069924 | T | C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(67): Show |
73 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.479-1018T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069924 | |||||||
| chr16:82069990 | G | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0189 |
3 | HG00735.hp2 HG01070.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.479-952G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82069990 | |||||||
| chr16:82070041 | G | A | 31 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0037 others(28): Show |
33 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.479-901G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070041 | |||||||
| chr16:82070052 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.479-890C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070052 | |||||||
| chr16:82070056 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.479-886C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070056 | |||||||
| chr16:82070168 | G | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.479-774G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070168 | |||||||
| chr16:82070392 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(9): Show |
13 | HG00639.hp1 HG01109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.479-550G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070392 | |||||||
| chr16:82070474 | A | G | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.479-468A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070474 | |||||||
| chr16:82070481 | C | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.479-461C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070481 | |||||||
| chr16:82070509 | A | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(36): Show |
40 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.479-433A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070509 | |||||||
| chr16:82070534 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.479-408G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070534 | |||||||
| chr16:82070577 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-365T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070577 | |||||||
| chr16:82070850 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.479-92G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 2/4 | chr16 | 82070850 | |||||||
| chr16:82071166 | T | A | 1 | a0001c0001t0003g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.664+39T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071166 | |||||||
| chr16:82071367 | T | A | 1 | a0001c0001t0002g0061 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.664+240T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071367 | |||||||
| chr16:82071501 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.664+374A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071501 | |||||||
| chr16:82071532 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0002g0120 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.664+405C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071532 | |||||||
| chr16:82071537 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+410T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071537 | |||||||
| chr16:82071593 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.664+466G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071593 | |||||||
| chr16:82071668 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.664+541C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071668 | |||||||
| chr16:82071692 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.664+565G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071692 | |||||||
| chr16:82071709 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.664+582C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071709 | |||||||
| chr16:82071802 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.664+675T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071802 | |||||||
| chr16:82071824 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+697C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071824 | |||||||
| chr16:82071851 | G | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0093 |
2 | HG00140.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.664+724G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071851 | |||||||
| chr16:82071884 | C | T | 47 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(44): Show |
48 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.664+757C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071884 | |||||||
| chr16:82071966 | G | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
118 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.664+839G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82071966 | |||||||
| chr16:82072018 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.664+891T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072018 | |||||||
| chr16:82072069 | T | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+942T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072069 | |||||||
| chr16:82072077 | A | G | 2 | a0001c0001t0001g0298 a0001c0001t0001g0300 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.664+950A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072077 | |||||||
| chr16:82072102 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.664+975A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072102 | |||||||
| chr16:82072211 | G | GGA | 9 | a0001c0001t0001g0027 a0001c0001t0001g0314 a0001c0001t0001g0315 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.664+1101_664+1102d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82072211 | ||||||
| chr16:82072295 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.664+1168T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072295 | |||||||
| chr16:82072346 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0272 |
2 | HG00438.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.664+1219G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072346 | |||||||
| chr16:82072474 | C | T | 4 | a0001c0001t0003g0303 a0001c0001t0003g0305 a0001c0001t0003g0306 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1347C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072474 | |||||||
| chr16:82072484 | C | G | 3 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01433.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.664+1357C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072484 | |||||||
| chr16:82072694 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
193 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.664+1567G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072694 | |||||||
| chr16:82072718 | G | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1591G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072718 | |||||||
| chr16:82072927 | T | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+1800T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072927 | |||||||
| chr16:82072990 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+1863G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82072990 | |||||||
| chr16:82073093 | C | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+1966C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073093 | |||||||
| chr16:82073142 | T | C | 3 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01433.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.664+2015T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073142 | |||||||
| chr16:82073274 | G | C | 2 | a0001c0001t0001g0328 a0001c0011t0001g0323 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.664+2147G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073274 | |||||||
| chr16:82073286 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.664+2159G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073286 | |||||||
| chr16:82073306 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+2179G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073306 | |||||||
| chr16:82073310 | C | T | 40 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(37): Show |
41 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.664+2183C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073310 | |||||||
| chr16:82073433 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.664+2306C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073433 | |||||||
| chr16:82073466 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.664+2339T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073466 | |||||||
| chr16:82073482 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+2355C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073482 | |||||||
| chr16:82073549 | A | G | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664+2422A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073549 | |||||||
| chr16:82073796 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.664+2669G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073796 | |||||||
| chr16:82073881 | C | A | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664+2754C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073881 | |||||||
| chr16:82073923 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.664+2796G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82073923 | |||||||
| chr16:82073990 | GTACAAAA others(5): Show |
G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+2870_664+2881d others(14): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82073990 | ||||||
| chr16:82074095 | T | C | 41 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(38): Show |
42 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.664+2968T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074095 | |||||||
| chr16:82074150 | G | C | 11 | a0001c0001t0002g0078 a0001c0002t0001g0065 a0001c0002t0001g0087 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.664+3023G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074150 | |||||||
| chr16:82074255 | TC | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+3129delC | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074255 | |||||||
| chr16:82074258 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+3131C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074258 | |||||||
| chr16:82074262 | C | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+3135C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074262 | |||||||
| chr16:82074266 | C | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+3139C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074266 | |||||||
| chr16:82074344 | T | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+3217T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074344 | |||||||
| chr16:82074461 | G | T | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0329 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+3334G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074461 | |||||||
| chr16:82074500 | G | A | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664+3373G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074500 | |||||||
| chr16:82074568 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.664+3441T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074568 | |||||||
| chr16:82074588 | G | A | 1 | a0001c0002t0003g0195 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.664+3461G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074588 | |||||||
| chr16:82074665 | A | G | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.664+3538A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074665 | |||||||
| chr16:82074734 | C | A | 6 | a0001c0002t0001g0283 a0001c0002t0003g0017 a0001c0002t0003g0152 others(3): Show |
7 | HG00408.hp1 HG00544.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.664+3607C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074734 | |||||||
| chr16:82074789 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0252 a0001c0001t0001g0272 |
3 | HG00438.hp1 NA18974.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.664+3662T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074789 | |||||||
| chr16:82074819 | T | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+3692T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074819 | |||||||
| chr16:82074826 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.664+3699T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074826 | |||||||
| chr16:82074921 | T | C | 1 | a0001c0001t0002g0011 | 2 | NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.664+3794T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82074921 | |||||||
| chr16:82075062 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(56): Show |
61 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664+3935T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075062 | |||||||
| chr16:82075183 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+4056G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075183 | |||||||
| chr16:82075221 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0046 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.664+4094C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075221 | |||||||
| chr16:82075222 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.664+4095G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075222 | |||||||
| chr16:82075347 | A | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+4220A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075347 | |||||||
| chr16:82075395 | A | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0038 |
2 | NA18945.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.664+4268A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075395 | |||||||
| chr16:82075401 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(56): Show |
61 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664+4274G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075401 | |||||||
| chr16:82075442 | G | T | 1 | a0001c0001t0001g0331 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.664+4315G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075442 | |||||||
| chr16:82075456 | GAGACTAA others(5): Show |
G | 3 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01433.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.664+4357_664+4368d others(14): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82075456 | ||||||
| chr16:82075498 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+4371G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075498 | |||||||
| chr16:82075504 | C | A | 1 | a0001c0001t0002g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.664+4377C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075504 | |||||||
| chr16:82075556 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0183 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.664+4429C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075556 | |||||||
| chr16:82075600 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.664+4473C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075600 | |||||||
| chr16:82075626 | T | C | 1 | a0001c0001t0002g0011 | 2 | NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.664+4499T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075626 | |||||||
| chr16:82075631 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+4504A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075631 | |||||||
| chr16:82075666 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.664+4539G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075666 | |||||||
| chr16:82075686 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(56): Show |
61 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664+4559T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075686 | |||||||
| chr16:82075869 | C | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
199 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.664+4742C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075869 | |||||||
| chr16:82075908 | T | TA | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.664+4797dupA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82075908 | ||||||
| chr16:82075908 | T | TAA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0160 others(10): Show |
17 | HG00639.hp1 HG01891.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.664+4796_664+4797d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82075908 | ||||||
| chr16:82075966 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+4839G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075966 | |||||||
| chr16:82076030 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0234 a0001c0001t0001g0265 |
3 | HG01175.hp1 HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.664+4903A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076030 | |||||||
| chr16:82076180 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.664+5053T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076180 | |||||||
| chr16:82076182 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.664+5055C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076182 | |||||||
| chr16:82076373 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.664+5246G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076373 | |||||||
| chr16:82076441 | T | C | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664+5314T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076441 | |||||||
| chr16:82076443 | G | C | 1 | a0001c0001t0002g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.664+5316G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076443 | |||||||
| chr16:82076454 | G | C | 1 | a0001c0001t0002g0050 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.664+5327G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076454 | |||||||
| chr16:82076481 | A | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(56): Show |
61 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664+5354A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076481 | |||||||
| chr16:82076635 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.664+5508C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076635 | |||||||
| chr16:82076673 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(56): Show |
61 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664+5546T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076673 | |||||||
| chr16:82076675 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.664+5548G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076675 | |||||||
| chr16:82076724 | G | A | 5 | a0001c0001t0001g0246 a0001c0001t0003g0303 a0001c0001t0003g0305 others(2): Show |
5 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+5597G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076724 | |||||||
| chr16:82076785 | G | T | 1 | a0001c0001t0002g0032 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.664+5658G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076785 | |||||||
| chr16:82076791 | G | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(7): Show |
11 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.664+5664G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076791 | |||||||
| chr16:82076819 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(56): Show |
61 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664+5692T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076819 | |||||||
| chr16:82076989 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.664+5862T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82076989 | |||||||
| chr16:82077078 | A | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+5951A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077078 | |||||||
| chr16:82077139 | C | T | 1 | a0006c0006t0001g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.664+6012C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077139 | |||||||
| chr16:82077149 | A | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.664+6022A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077149 | |||||||
| chr16:82077152 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(3): Show |
7 | HG00639.hp1 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.664+6025A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077152 | |||||||
| chr16:82077339 | A | G | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG00544.hp2 HG00597.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+6212A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077339 | |||||||
| chr16:82077350 | A | G | 54 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0027 others(51): Show |
56 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.664+6223A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077350 | |||||||
| chr16:82077600 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+6473T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077600 | |||||||
| chr16:82077605 | C | A | 1 | a0001c0001t0003g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.664+6478C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077605 | |||||||
| chr16:82077674 | C | A | 89 | a0001c0001t0001g0018 a0001c0001t0001g0072 a0001c0001t0001g0082 others(86): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.664+6547C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077674 | |||||||
| chr16:82077722 | C | A | 38 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0160 others(35): Show |
39 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.664+6595C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077722 | |||||||
| chr16:82077735 | G | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+6608G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077735 | |||||||
| chr16:82077747 | GAAGAAAG others(6): Show |
G | 1 | a0001c0001t0002g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.664+6635_664+6647d others(15): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82077747 | ||||||
| chr16:82077791 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.664+6664G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077791 | |||||||
| chr16:82077805 | G | C | 4 | a0001c0001t0003g0303 a0001c0001t0003g0305 a0001c0001t0003g0306 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+6678G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82077805 | |||||||
| chr16:82078021 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.664+6894C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078021 | |||||||
| chr16:82078196 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+7069T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078196 | |||||||
| chr16:82078204 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(8): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+7077T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078204 | |||||||
| chr16:82078227 | A | G | 3 | a0001c0002t0001g0065 a0001c0002t0001g0087 a0001c0002t0001g0088 |
3 | HG01433.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.664+7100A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078227 | |||||||
| chr16:82078369 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.664+7242C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078369 | |||||||
| chr16:82078394 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.664+7267G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078394 | |||||||
| chr16:82078440 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.664+7313T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078440 | |||||||
| chr16:82078469 | A | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
8 | HG00639.hp1 HG01109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+7342A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078469 | |||||||
| chr16:82078511 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.664+7384G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078511 | |||||||
| chr16:82078559 | C | A | 1 | a0001c0001t0001g0307 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.664+7432C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078559 | |||||||
| chr16:82078637 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(8): Show |
12 | HG00639.hp1 HG01109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.664+7510G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078637 | |||||||
| chr16:82078644 | A | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(8): Show |
12 | HG00639.hp1 HG01109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.664+7517A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078644 | |||||||
| chr16:82078725 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+7598G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078725 | |||||||
| chr16:82078761 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+7634C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82078761 | |||||||
| chr16:82079103 | G | T | 1 | a0001c0001t0003g0297 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664+7976G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079103 | |||||||
| chr16:82079241 | G | T | 1 | a0001c0001t0002g0107 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.664+8114G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079241 | |||||||
| chr16:82079314 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0314 a0001c0001t0001g0315 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.664+8187C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079314 | |||||||
| chr16:82079322 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(2): Show |
6 | HG00639.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+8195C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079322 | |||||||
| chr16:82079335 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.664+8208G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079335 | |||||||
| chr16:82079389 | C | T | 2 | a0001c0001t0001g0331 a0001c0001t0002g0150 |
2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.664+8262C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079389 | |||||||
| chr16:82079551 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.664+8424C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079551 | |||||||
| chr16:82079568 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.664+8441G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079568 | |||||||
| chr16:82079584 | T | A | 16 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0037 others(13): Show |
18 | HG00639.hp1 HG01081.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.664+8457T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079584 | |||||||
| chr16:82079585 | A | G | 4 | a0001c0001t0003g0303 a0001c0001t0003g0305 a0001c0001t0003g0306 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+8458A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079585 | |||||||
| chr16:82079586 | C | T | 41 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
44 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.664+8459C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079586 | |||||||
| chr16:82079619 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0198 |
3 | HG02622.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.664+8492G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079619 | |||||||
| chr16:82079731 | G | A | 2 | a0001c0001t0001g0309 a0001c0001t0002g0069 |
2 | HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.664+8604G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079731 | |||||||
| chr16:82079756 | A | G | 1 | a0001c0001t0003g0303 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+8629A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079756 | |||||||
| chr16:82079866 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
190 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.664+8739C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079866 | |||||||
| chr16:82079882 | T | A | 1 | a0001c0001t0001g0189 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.664+8755T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079882 | |||||||
| chr16:82079983 | G | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0102 others(2): Show |
7 | HG01943.hp2 HG02132.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.664+8856G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82079983 | |||||||
| chr16:82080007 | C | G | 1 | a0001c0001t0002g0033 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.664+8880C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080007 | |||||||
| chr16:82080417 | G | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(9): Show |
13 | HG01081.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.664+9290G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080417 | |||||||
| chr16:82080629 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.664+9502G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080629 | |||||||
| chr16:82080757 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.664+9630T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080757 | |||||||
| chr16:82080837 | T | C | 6 | a0001c0002t0003g0017 a0001c0002t0003g0152 a0001c0002t0003g0194 others(3): Show |
7 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.664+9710T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080837 | |||||||
| chr16:82080841 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.664+9714A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080841 | |||||||
| chr16:82080847 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.664+9720C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080847 | |||||||
| chr16:82080852 | T | C | 65 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0029 others(62): Show |
67 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.664+9725T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080852 | |||||||
| chr16:82080878 | T | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0314 a0001c0001t0001g0315 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.664+9751T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82080878 | |||||||
| chr16:82081136 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
79 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.665-9766G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081136 | |||||||
| chr16:82081174 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0236 a0001c0001t0001g0238 others(4): Show |
9 | NA18939.hp1 NA18942.hp2 NA18989.hp1 others(6): Show |
intron_variant | MODIFIER | c.665-9728G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081174 | |||||||
| chr16:82081227 | C | T | 3 | a0001c0001t0003g0297 a0001c0001t0004g0048 a0001c0001t0004g0049 |
3 | HG01109.hp2 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.665-9675C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081227 | |||||||
| chr16:82081245 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.665-9657C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081245 | |||||||
| chr16:82081275 | GT | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
72 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.665-9625delT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82081275 | ||||||
| chr16:82081338 | A | T | 9 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.665-9564A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081338 | |||||||
| chr16:82081543 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
76 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.665-9359C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081543 | |||||||
| chr16:82081638 | T | G | 2 | a0001c0001t0002g0045 a0001c0001t0002g0176 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.665-9264T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081638 | |||||||
| chr16:82081670 | T | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
76 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.665-9232T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081670 | |||||||
| chr16:82081704 | G | C | 1 | a0001c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.665-9198G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081704 | |||||||
| chr16:82081739 | G | A | 2 | a0001c0001t0001g0183 a0001c0011t0001g0323 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.665-9163G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081739 | |||||||
| chr16:82081823 | T | G | 2 | a0001c0001t0001g0330 a0001c0001t0002g0062 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-9079T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081823 | |||||||
| chr16:82081937 | C | T | 106 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(103): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.665-8965C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081937 | |||||||
| chr16:82081956 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0001g0173 others(2): Show |
6 | HG01081.hp2 HG01255.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-8946G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081956 | |||||||
| chr16:82081959 | G | C | 1 | a0001c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.665-8943G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081959 | |||||||
| chr16:82081985 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.665-8917T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081985 | |||||||
| chr16:82081989 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.665-8913G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82081989 | |||||||
| chr16:82082054 | C | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
75 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.665-8848C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082054 | |||||||
| chr16:82082128 | C | T | 59 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(56): Show |
61 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.665-8774C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082128 | |||||||
| chr16:82082223 | C | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.665-8679C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082223 | |||||||
| chr16:82082317 | T | A | 1 | a0001c0001t0002g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.665-8585T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082317 | |||||||
| chr16:82082466 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.665-8436G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082466 | |||||||
| chr16:82082500 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.665-8402C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082500 | |||||||
| chr16:82082538 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.665-8364A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082538 | |||||||
| chr16:82082666 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.665-8236A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082666 | |||||||
| chr16:82082772 | T | C | 9 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.665-8130T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082772 | |||||||
| chr16:82082781 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.665-8121G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082781 | |||||||
| chr16:82082799 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665-8103G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082799 | |||||||
| chr16:82082900 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0198 |
2 | HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.665-8002C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082900 | |||||||
| chr16:82082954 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665-7948C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82082954 | |||||||
| chr16:82083000 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
77 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.665-7902C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083000 | |||||||
| chr16:82083024 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0046 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.665-7878G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083024 | |||||||
| chr16:82083166 | T | C | 62 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(59): Show |
64 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.665-7736T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083166 | |||||||
| chr16:82083396 | C | G | 1 | a0001c0001t0002g0009 | 2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.665-7506C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083396 | |||||||
| chr16:82083409 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.665-7493G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083409 | |||||||
| chr16:82083430 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.665-7472C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083430 | |||||||
| chr16:82083520 | G | C | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0002g0050 |
3 | HG02717.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.665-7382G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083520 | |||||||
| chr16:82083651 | T | G | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0002g0050 |
3 | HG02717.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.665-7251T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083651 | |||||||
| chr16:82083731 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0332 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.665-7171C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083731 | |||||||
| chr16:82083773 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.665-7129T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82083773 | |||||||
| chr16:82084009 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0302 others(3): Show |
6 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-6893G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084009 | |||||||
| chr16:82084033 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.665-6869A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084033 | |||||||
| chr16:82084057 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0089 a0001c0001t0002g0105 |
4 | NA18955.hp2 NA18977.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-6845G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084057 | |||||||
| chr16:82084159 | G | A | 47 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(44): Show |
49 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.665-6743G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084159 | |||||||
| chr16:82084280 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.665-6622C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084280 | |||||||
| chr16:82084371 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0206 a0001c0001t0001g0254 |
5 | HG01099.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-6531T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084371 | |||||||
| chr16:82084457 | C | A | 147 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(144): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.665-6445C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084457 | |||||||
| chr16:82084459 | G | C | 1 | a0001c0001t0002g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.665-6443G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084459 | |||||||
| chr16:82084461 | T | C | 1 | a0001c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.665-6441T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084461 | |||||||
| chr16:82084503 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0162 others(1): Show |
5 | HG00639.hp1 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-6399C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084503 | |||||||
| chr16:82084557 | A | AT | 49 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(46): Show |
51 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.665-6337dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82084557 | ||||||
| chr16:82084557 | A | T | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.665-6345A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084557 | |||||||
| chr16:82084560 | T | A | 1 | a0001c0002t0003g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.665-6342T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084560 | |||||||
| chr16:82084566 | A | AT | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-6329dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82084566 | ||||||
| chr16:82084629 | A | T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0213 a0001c0001t0001g0219 others(21): Show |
25 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.665-6273A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084629 | |||||||
| chr16:82084645 | G | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0176 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.665-6257G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084645 | |||||||
| chr16:82084746 | C | G | 147 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(144): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.665-6156C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084746 | |||||||
| chr16:82084752 | A | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-6150A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084752 | |||||||
| chr16:82084753 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0276 |
3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.665-6149A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084753 | |||||||
| chr16:82084770 | G | T | 77 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(74): Show |
80 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.665-6132G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084770 | |||||||
| chr16:82084836 | G | C | 66 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(63): Show |
68 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.665-6066G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084836 | |||||||
| chr16:82084846 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.665-6056C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084846 | |||||||
| chr16:82084926 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.665-5976G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084926 | |||||||
| chr16:82084926 | G | C | 156 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(153): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.665-5976G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084926 | |||||||
| chr16:82085005 | T | G | 1 | a0001c0001t0001g0242 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.665-5897T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085005 | |||||||
| chr16:82085105 | A | T | 1 | a0001c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.665-5797A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085105 | |||||||
| chr16:82085167 | C | T | 42 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(39): Show |
44 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.665-5735C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085167 | |||||||
| chr16:82085495 | G | A | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(43): Show |
48 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.665-5407G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085495 | |||||||
| chr16:82085568 | G | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-5334G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085568 | |||||||
| chr16:82085599 | T | G | 70 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(67): Show |
73 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.665-5303T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085599 | |||||||
| chr16:82085630 | C | A | 1 | a0001c0002t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.665-5272C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085630 | |||||||
| chr16:82085637 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.665-5265G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085637 | |||||||
| chr16:82085677 | G | T | 1 | a0001c0001t0002g0167 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.665-5225G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085677 | |||||||
| chr16:82085749 | G | T | 52 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(49): Show |
54 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.665-5153G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085749 | |||||||
| chr16:82085782 | C | T | 3 | a0001c0001t0001g0302 a0001c0001t0001g0332 a0001c0002t0001g0088 |
3 | HG02280.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.665-5120C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085782 | |||||||
| chr16:82085788 | T | G | 51 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(48): Show |
53 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.665-5114T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085788 | |||||||
| chr16:82085791 | T | C | 55 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(52): Show |
57 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.665-5111T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085791 | |||||||
| chr16:82085795 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.665-5107C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085795 | |||||||
| chr16:82085952 | TA | T | 56 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(53): Show |
58 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.665-4940delA | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82085952 | ||||||
| chr16:82086023 | G | C | 1 | a0001c0001t0002g0050 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.665-4879G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82086023 | |||||||
| chr16:82086065 | G | A | 155 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(152): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.665-4837G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82086065 | |||||||
| chr16:82086218 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.665-4684A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82086218 | |||||||
| chr16:82086587 | G | A | 159 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(156): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.665-4315G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82086587 | |||||||
| chr16:82086609 | G | C | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0002g0050 |
3 | HG02717.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.665-4293G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82086609 | |||||||
| chr16:82086707 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-4195A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82086707 | |||||||
| chr16:82086753 | T | C | 13 | a0001c0001t0001g0329 a0001c0001t0002g0120 a0001c0001t0004g0114 others(10): Show |
14 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.665-4149T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82086753 | |||||||
| chr16:82087030 | T | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.665-3872T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82087030 | |||||||
| chr16:82087438 | C | G | 1 | a0001c0002t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.665-3464C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82087438 | |||||||
| chr16:82087438 | C | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-3464C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82087438 | |||||||
| chr16:82087439 | G | A | 3 | a0001c0001t0001g0294 a0001c0001t0001g0327 a0001c0001t0001g0333 |
3 | HG01884.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.665-3463G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82087439 | |||||||
| chr16:82087798 | C | T | 283 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.665-3104C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82087798 | |||||||
| chr16:82087973 | T | G | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.665-2929T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82087973 | |||||||
| chr16:82088161 | C | G | 1 | a0001c0001t0002g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.665-2741C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088161 | |||||||
| chr16:82088311 | G | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-2591G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088311 | |||||||
| chr16:82088376 | G | A | 161 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(158): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.665-2526G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088376 | |||||||
| chr16:82088380 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.665-2522C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088380 | |||||||
| chr16:82088394 | A | G | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-2508A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088394 | |||||||
| chr16:82088479 | C | A | 1 | a0001c0001t0002g0042 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.665-2423C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088479 | |||||||
| chr16:82088479 | C | T | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.665-2423C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088479 | |||||||
| chr16:82088603 | T | A | 1 | a0001c0001t0001g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.665-2299T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088603 | |||||||
| chr16:82088753 | T | C | 332 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.665-2149T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088753 | |||||||
| chr16:82088914 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665-1988C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82088914 | |||||||
| chr16:82089097 | A | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
73 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.665-1805A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089097 | |||||||
| chr16:82089297 | G | C | 1 | a0001c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.665-1605G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089297 | |||||||
| chr16:82089332 | A | G | 8 | a0001c0003t0002g0010 a0001c0003t0002g0057 a0001c0003t0002g0123 others(5): Show |
9 | NA18943.hp1 NA18951.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.665-1570A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089332 | |||||||
| chr16:82089385 | C | G | 162 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.665-1517C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089385 | |||||||
| chr16:82089420 | G | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-1482G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089420 | |||||||
| chr16:82089444 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.665-1458G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089444 | |||||||
| chr16:82089447 | T | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0097 |
3 | HG02027.hp1 NA18948.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.665-1455T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089447 | |||||||
| chr16:82089597 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.665-1305T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089597 | |||||||
| chr16:82089605 | G | A | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-1297G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089605 | |||||||
| chr16:82089621 | G | A | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0002g0050 |
3 | HG02717.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.665-1281G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089621 | |||||||
| chr16:82089660 | C | T | 8 | a0001c0001t0001g0279 a0001c0001t0002g0054 a0001c0001t0002g0101 others(5): Show |
8 | HG02738.hp1 HG03239.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-1242C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089660 | |||||||
| chr16:82089661 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.665-1241G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089661 | |||||||
| chr16:82089690 | C | T | 288 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.665-1212C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089690 | |||||||
| chr16:82090035 | A | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.665-867A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090035 | |||||||
| chr16:82090071 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0243 |
2 | NA18989.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.665-831T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090071 | |||||||
| chr16:82090121 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.665-781T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090121 | |||||||
| chr16:82090192 | C | T | 277 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.665-710C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090192 | |||||||
| chr16:82090302 | G | GT | 51 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0037 others(48): Show |
55 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.665-566dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTT | 27 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0001g0172 others(24): Show |
30 | HG00140.hp2 HG00621.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.665-567_665-566dup others(2): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTTT | 19 | a0001c0001t0001g0022 a0001c0001t0001g0160 a0001c0001t0001g0163 others(16): Show |
20 | HG01175.hp2 HG01884.hp1 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.665-568_665-566dup others(3): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTTTT | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0183 others(5): Show |
8 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-569_665-566dup others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTTTTT | 5 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0239 others(2): Show |
6 | HG02486.hp2 HG02630.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-570_665-566dup others(5): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTTTTTTT | 7 | a0001c0001t0001g0248 a0001c0001t0001g0302 a0001c0001t0001g0310 others(4): Show |
7 | HG01255.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.665-572_665-566dup others(7): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.665-577_665-566dup others(12): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.665-579_665-566dup others(14): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.665-582_665-566dup others(17): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GT | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0203 a0001c0001t0001g0208 others(22): Show |
28 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.665-566delT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTT | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0186 others(28): Show |
35 | HG00408.hp2 HG00621.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.665-567_665-566del others(2): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTT | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0185 others(19): Show |
23 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.665-568_665-566del others(3): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTT | G | 8 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(5): Show |
9 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(6): Show |
intron_variant | MODIFIER | c.665-570_665-566del others(5): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTTTT others(1): Show |
G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
47 | HG00280.hp1 HG00741.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.665-573_665-566del others(8): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTTTT others(2): Show |
G | 7 | a0001c0001t0001g0238 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01167.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.665-574_665-566del others(9): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0002g0039 a0002c0004t0001g0316 |
2 | HG00609.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.665-575_665-566del others(10): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0001g0329 a0001c0001t0002g0120 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.665-577_665-566del others(12): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0002g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.665-578_665-566del others(13): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0002g0015 a0001c0001t0002g0071 a0001c0001t0002g0177 |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-579_665-566del others(14): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090302 | GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0055 |
2 | HG00099.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.665-580_665-566del others(15): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 82090302 | ||||||
| chr16:82090459 | C | T | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(262): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.665-443C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090459 | |||||||
| chr16:82090465 | T | C | 1 | a0001c0003t0002g0133 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.665-437T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090465 | |||||||
| chr16:82090592 | T | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0332 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.665-310T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090592 | |||||||
| chr16:82090670 | T | C | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-232T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090670 | |||||||
| chr16:82090772 | C | A | 2 | a0001c0001t0001g0329 a0001c0001t0002g0120 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.665-130C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090772 | |||||||
| chr16:82090789 | T | C | 8 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0303 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.665-113T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090789 | |||||||
| chr16:82090873 | T | G | 17 | a0001c0001t0001g0027 a0001c0001t0001g0172 a0001c0001t0001g0174 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.665-29T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090873 | |||||||
| chr16:82091100 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.802+61T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091100 | |||||||
| chr16:82091125 | C | A | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.802+86C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091125 | |||||||
| chr16:82091242 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.802+203G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091242 | |||||||
| chr16:82091302 | G | C | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.802+263G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091302 | |||||||
| chr16:82091379 | A | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0214 a0001c0001t0001g0215 |
4 | NA18946.hp2 NA18947.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+340A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091379 | |||||||
| chr16:82091394 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0296 |
2 | HG00280.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.802+355T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091394 | |||||||
| chr16:82091397 | C | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG00597.hp2 HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.802+358C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091397 | |||||||
| chr16:82091421 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+382A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091421 | |||||||
| chr16:82091446 | C | G | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+407C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091446 | |||||||
| chr16:82091676 | C | A | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.802+637C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091676 | |||||||
| chr16:82091745 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.802+706A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091745 | |||||||
| chr16:82091749 | C | T | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.802+710C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091749 | |||||||
| chr16:82091791 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.802+752T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091791 | |||||||
| chr16:82091858 | G | C | 5 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(2): Show |
5 | HG02056.hp2 NA18990.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+819G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091858 | |||||||
| chr16:82091945 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
126 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.802+906G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091945 | |||||||
| chr16:82091957 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.802+918C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091957 | |||||||
| chr16:82092035 | T | C | 7 | a0001c0001t0001g0063 a0001c0001t0002g0080 a0001c0001t0002g0109 others(4): Show |
7 | HG02056.hp2 NA18940.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+996T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092035 | |||||||
| chr16:82092152 | G | C | 297 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.802+1113G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092152 | |||||||
| chr16:82092179 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
127 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.802+1140C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092179 | |||||||
| chr16:82092280 | C | G | 2 | a0001c0001t0001g0302 a0001c0001t0001g0332 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.802+1241C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092280 | |||||||
| chr16:82092296 | C | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
126 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.802+1257C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092296 | |||||||
| chr16:82092314 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.802+1275C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092314 | |||||||
| chr16:82092359 | A | C | 1 | a0001c0001t0002g0050 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.802+1320A>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092359 | |||||||
| chr16:82092361 | T | C | 17 | a0001c0001t0001g0027 a0001c0001t0001g0172 a0001c0001t0001g0174 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+1322T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092361 | |||||||
| chr16:82092390 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
127 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.802+1351C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092390 | |||||||
| chr16:82092432 | G | C | 6 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(3): Show |
6 | HG02056.hp2 HG04199.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+1393G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092432 | |||||||
| chr16:82092463 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.802+1424C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092463 | |||||||
| chr16:82092561 | G | C | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.802+1522G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092561 | |||||||
| chr16:82092791 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.802+1752T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092791 | |||||||
| chr16:82093059 | T | A | 1 | a0005c0010t0002g0098 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.802+2020T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093059 | |||||||
| chr16:82093060 | GT | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(47): Show |
59 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.802+2023delT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82093060 | ||||||
| chr16:82093119 | G | T | 177 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(174): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.802+2080G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093119 | |||||||
| chr16:82093225 | C | G | 158 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(155): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.802+2186C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093225 | |||||||
| chr16:82093311 | C | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.802+2272C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093311 | |||||||
| chr16:82093351 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0276 |
3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.802+2312G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093351 | |||||||
| chr16:82093403 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+2364T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093403 | |||||||
| chr16:82093548 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.802+2509A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093548 | |||||||
| chr16:82093608 | C | T | 158 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(155): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.802+2569C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093608 | |||||||
| chr16:82093610 | G | A | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.802+2571G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093610 | |||||||
| chr16:82093676 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.802+2637T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093676 | |||||||
| chr16:82093685 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0259 |
3 | HG01069.hp1 HG01071.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.802+2646G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093685 | |||||||
| chr16:82093884 | A | G | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+2845A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093884 | |||||||
| chr16:82093901 | C | T | 159 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(156): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.802+2862C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093901 | |||||||
| chr16:82093946 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+2907A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093946 | |||||||
| chr16:82093992 | C | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+2953C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82093992 | |||||||
| chr16:82094022 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.802+2983G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094022 | |||||||
| chr16:82094086 | C | G | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.802+3047C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094086 | |||||||
| chr16:82094089 | C | A | 1 | a0001c0001t0002g0180 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.802+3050C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094089 | |||||||
| chr16:82094222 | C | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+3183C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094222 | |||||||
| chr16:82094256 | A | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0219 a0001c0001t0001g0249 others(10): Show |
14 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.802+3217A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094256 | |||||||
| chr16:82094259 | G | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.802+3220G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094259 | |||||||
| chr16:82094270 | A | G | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+3231A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094270 | |||||||
| chr16:82094319 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.802+3280C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094319 | |||||||
| chr16:82094466 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.802+3427G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094466 | |||||||
| chr16:82094489 | C | T | 157 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(154): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.802+3450C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094489 | |||||||
| chr16:82094490 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0001g0298 others(3): Show |
7 | HG01081.hp2 HG01255.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+3451G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094490 | |||||||
| chr16:82094494 | T | A | 1 | a0001c0001t0002g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.802+3455T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094494 | |||||||
| chr16:82094494 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0002g0069 |
4 | HG01081.hp2 HG01255.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3455T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094494 | |||||||
| chr16:82094495 | G | C | 17 | a0001c0001t0001g0027 a0001c0001t0001g0172 a0001c0001t0001g0174 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+3456G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094495 | |||||||
| chr16:82094496 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802+3457G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094496 | |||||||
| chr16:82094538 | T | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | NA18988.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.802+3499T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094538 | |||||||
| chr16:82094563 | C | A | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.803-3512C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094563 | |||||||
| chr16:82094592 | C | G | 221 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(218): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.803-3483C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094592 | |||||||
| chr16:82094636 | G | C | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.803-3439G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094636 | |||||||
| chr16:82094732 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.803-3343G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094732 | |||||||
| chr16:82094738 | C | G | 173 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(170): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.803-3337C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094738 | |||||||
| chr16:82094817 | T | C | 157 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(154): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.803-3258T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094817 | |||||||
| chr16:82094906 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.803-3169G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82094906 | |||||||
| chr16:82095048 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.803-3027G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095048 | |||||||
| chr16:82095172 | C | T | 61 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0037 others(58): Show |
63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.803-2903C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095172 | |||||||
| chr16:82095212 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.803-2863T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095212 | |||||||
| chr16:82095259 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.803-2816T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095259 | |||||||
| chr16:82095270 | A | G | 1 | a0001c0003t0002g0123 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.803-2805A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095270 | |||||||
| chr16:82095271 | T | C | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-2804T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095271 | |||||||
| chr16:82095327 | C | T | 1 | a0001c0002t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.803-2748C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095327 | |||||||
| chr16:82095352 | G | T | 1 | a0001c0001t0002g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.803-2723G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095352 | |||||||
| chr16:82095422 | G | C | 226 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.803-2653G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095422 | |||||||
| chr16:82095591 | T | G | 14 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(11): Show |
14 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-2484T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095591 | |||||||
| chr16:82095683 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.803-2392T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095683 | |||||||
| chr16:82095699 | T | C | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-2376T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095699 | |||||||
| chr16:82095747 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
71 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.803-2328A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095747 | |||||||
| chr16:82095876 | C | T | 14 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(11): Show |
14 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-2199C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095876 | |||||||
| chr16:82095880 | T | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(160): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.803-2195T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82095880 | |||||||
| chr16:82096020 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0002t0001g0088 |
3 | HG02818.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803-2055A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096020 | |||||||
| chr16:82096070 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.803-2005T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096070 | |||||||
| chr16:82096125 | TTA | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0222 a0001c0001t0001g0232 others(1): Show |
5 | NA18956.hp1 NA18963.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1948_803-1947d others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82096125 | ||||||
| chr16:82096131 | G | C | 1 | a0001c0001t0002g0066 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.803-1944G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096131 | |||||||
| chr16:82096199 | G | C | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.803-1876G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096199 | |||||||
| chr16:82096275 | G | A | 10 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(7): Show |
11 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-1800G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096275 | |||||||
| chr16:82096385 | G | A | 1 | a0001c0002t0003g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.803-1690G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096385 | |||||||
| chr16:82096425 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0332 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.803-1650T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096425 | |||||||
| chr16:82096455 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.803-1620C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096455 | |||||||
| chr16:82096464 | T | C | 25 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0063 others(22): Show |
27 | HG00621.hp2 HG02015.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.803-1611T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096464 | |||||||
| chr16:82096728 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0214 a0001c0001t0001g0215 |
4 | NA18946.hp2 NA18947.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1347G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096728 | |||||||
| chr16:82096766 | G | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02615.hp2 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.803-1309G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096766 | |||||||
| chr16:82096780 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0002t0001g0088 |
3 | HG02818.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803-1295C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096780 | |||||||
| chr16:82096872 | A | G | 27 | a0001c0001t0001g0022 a0001c0001t0001g0220 a0001c0001t0001g0222 others(24): Show |
31 | HG00099.hp2 HG00609.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.803-1203A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096872 | |||||||
| chr16:82096895 | T | C | 3 | a0001c0001t0001g0302 a0001c0001t0001g0332 a0001c0001t0002g0129 |
3 | HG02109.hp2 HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.803-1180T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096895 | |||||||
| chr16:82096962 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.803-1113T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82096962 | |||||||
| chr16:82097005 | G | GT | 6 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0302 others(3): Show |
6 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-1059dupT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097005 | ||||||
| chr16:82097005 | G | T | 1 | a0001c0001t0002g0013 | 2 | NA18991.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.803-1070G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097005 | |||||||
| chr16:82097005 | GT | G | 12 | a0001c0001t0002g0032 a0001c0001t0004g0114 a0001c0001t0004g0126 others(9): Show |
13 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.803-1059delT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097005 | ||||||
| chr16:82097016 | T | C | 1 | a0004c0009t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.803-1059T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097016 | |||||||
| chr16:82097038 | C | G | 1 | a0004c0009t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.803-1037C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097038 | |||||||
| chr16:82097160 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.803-915C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097160 | |||||||
| chr16:82097206 | ATATGTC | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0171 others(18): Show |
25 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-809_803-804del others(6): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097206 | ||||||
| chr16:82097206 | ATATGTCT others(5): Show |
A | 156 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.803-815_803-804del others(12): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097206 | ||||||
| chr16:82097206 | ATATGTCT others(11): Show |
A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
72 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.803-821_803-804del others(18): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097206 | ||||||
| chr16:82097206 | ATATGTCT others(17): Show |
A | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-827_803-804del others(24): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097206 | ||||||
| chr16:82097254 | C | G | 10 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-821C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097254 | |||||||
| chr16:82097256 | A | G | 10 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-819A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097256 | |||||||
| chr16:82097260 | C | A | 10 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-815C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097260 | |||||||
| chr16:82097260 | C | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0267 others(2): Show |
5 | HG02083.hp2 HG02280.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-815C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097260 | |||||||
| chr16:82097262 | A | G | 15 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0267 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-813A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097262 | |||||||
| chr16:82097266 | C | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0267 others(2): Show |
5 | HG02083.hp2 HG02280.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-809C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097266 | |||||||
| chr16:82097266 | C | G | 31 | a0001c0001t0001g0023 a0001c0001t0001g0189 a0001c0001t0001g0200 others(28): Show |
32 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.803-809C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097266 | |||||||
| chr16:82097268 | A | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0189 others(34): Show |
38 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.803-807A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097268 | |||||||
| chr16:82097270 | G | C | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-805G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097270 | |||||||
| chr16:82097272 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0189 a0001c0001t0001g0200 others(18): Show |
22 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.803-803G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097272 | |||||||
| chr16:82097274 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.803-801G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097274 | |||||||
| chr16:82097276 | G | A | 10 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-799G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097276 | |||||||
| chr16:82097277 | T | TATATATA others(5): Show |
10 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-796_803-795ins others(12): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097277 | ||||||
| chr16:82097277 | T | TGTGTATA others(11): Show |
5 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0267 others(2): Show |
5 | HG02083.hp2 HG02280.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-798_803-797ins others(18): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097277 | |||||||
| chr16:82097278 | A | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0189 a0001c0001t0001g0200 others(19): Show |
23 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.803-797A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097278 | |||||||
| chr16:82097280 | G | A | 15 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0267 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-795G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097280 | |||||||
| chr16:82097282 | G | A | 15 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0267 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-793G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097282 | |||||||
| chr16:82097284 | G | A | 15 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0267 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-791G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097284 | |||||||
| chr16:82097284 | G | GTGTATAT others(17): Show |
21 | a0001c0001t0001g0023 a0001c0001t0001g0189 a0001c0001t0001g0200 others(18): Show |
22 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.803-788_803-787ins others(24): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097284 | ||||||
| chr16:82097284 | G | GTGTGTGT others(23): Show |
7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0250 others(4): Show |
7 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-765_803-736dup others(30): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097284 | ||||||
| chr16:82097292 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.803-783G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097292 | |||||||
| chr16:82097350 | T | TAC | 38 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0025 others(35): Show |
41 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.803-699_803-698dup others(2): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | T | TACAC | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
55 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.803-701_803-698dup others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | T | TACACAC | 19 | a0001c0001t0001g0029 a0001c0001t0001g0232 a0001c0001t0002g0045 others(16): Show |
20 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.803-703_803-698dup others(6): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | T | TACACACA others(1): Show |
103 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0020 others(100): Show |
111 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.803-705_803-698dup others(8): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | T | TACACACA others(3): Show |
12 | a0001c0001t0001g0183 a0001c0001t0001g0213 a0001c0001t0001g0314 others(9): Show |
12 | HG01884.hp1 HG01928.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.803-707_803-698dup others(10): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | T | TACACACA others(5): Show |
4 | a0001c0001t0001g0296 a0001c0001t0002g0103 a0001c0001t0002g0111 others(1): Show |
4 | HG00280.hp2 HG01192.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-709_803-698dup others(12): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | TAC | T | 13 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0163 others(10): Show |
13 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.803-699_803-698del others(2): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | TACAC | T | 5 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0001t0002g0034 others(2): Show |
5 | HG02818.hp2 HG02895.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-701_803-698del others(4): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(2): Show |
5 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-707_803-698del others(10): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097350 | TACACACA others(5): Show |
T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0185 others(33): Show |
37 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.803-709_803-698del others(12): Show |
HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 82097350 | ||||||
| chr16:82097376 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0171 a0001c0001t0002g0069 |
4 | HG01081.hp2 HG01255.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-699C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097376 | |||||||
| chr16:82097454 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.803-621C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097454 | |||||||
| chr16:82097570 | T | C | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-505T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097570 | |||||||
| chr16:82097578 | C | T | 11 | a0001c0001t0004g0114 a0001c0001t0004g0126 a0001c0001t0004g0166 others(8): Show |
12 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-497C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097578 | |||||||
| chr16:82097664 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.803-411C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097664 | |||||||
| chr16:82097720 | A | G | 2 | a0001c0001t0001g0302 a0001c0001t0001g0332 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.803-355A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097720 | |||||||
| chr16:82097742 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-333C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097742 | |||||||
| chr16:82097753 | A | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0301 |
3 | HG00140.hp2 HG01099.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.803-322A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097753 | |||||||
| chr16:82097764 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.803-311C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097764 | |||||||
| chr16:82097795 | C | A | 8 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0303 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-280C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097795 | |||||||
| chr16:82097795 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.803-280C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097795 | |||||||
| chr16:82097949 | A | T | 1 | a0001c0001t0001g0330 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.803-126A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097949 | |||||||
| chr16:82097951 | A | T | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-124A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097951 | |||||||
| chr16:82097952 | AT | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0117 a0001c0001t0002g0177 |
3 | HG01243.hp2 HG02258.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.803-122delT | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097952 | |||||||
| chr16:82097953 | T | A | 155 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(152): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.803-122T>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097953 | |||||||
| chr16:82097957 | A | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
8 | HG01515.hp2 HG02723.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-118A>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097957 | |||||||
| chr16:82097973 | C | G | 212 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(209): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.803-102C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097973 | |||||||
| chr16:82098012 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.803-63C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82098012 | |||||||
| chr16:82098018 | C | G | 36 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0185 others(33): Show |
37 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.803-57C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82098018 |